Rehabilitation of in-centre haemodialysis patients

ABSTRACT

Hong Kong Med J 1995;1:97-102 | Number 2, June 1995
ORIGINAL ARTICLE
Rehabilitation of in-centre haemodialysis patients
MC Law, YH Hui, ALC Cheung, ALK Chan, PKT Li
Renal Unit, Department of Medicine, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
A study was undertaken to investigate the rehabilitation status of in-center haemodialysis patients at the Prince of Wales Hospital. Thirty-four patients (23 males and 11 females) were recruited and interviewed using a set of questionnaires. Seventy-seven per cent of patients were able to conduct normal physical activities at least part of the time. General well-being and treatment-related stress and distress were found to be important factors affecting patients' functional capacity. No significant relationship between the Karnofsky activity index and the haemoglobin, serum albumin, or pre-dialysis plasma creatinine levels was found. Fifty-two per cent of patients were employed, 27% unemployed, and 21% listed their occupation as housewives. Fifty-six per cent of unemployed patients were young (under 36 years of age). Fifty-three per cent of patients said their employment status had decreased since their illness began. Eighty-two per cent of patients and 91% advised that interests/hobbies and holidays were affected, respectively. Sixty-two per cent of patients admitted having to play a reduced role in the family.
 
Key words: Rehabilitation; Haemodialysis units, hospital; Disability evaluation
 
View this abstract indexed in MEDLINE:
 

The efficacy of gonadotropin-releasing hormone agonist administration for in vitro fertilisation

ABSTRACT

Hong Kong Med J 1995;1:93-5 | Number 2, June 1995
ORIGINAL ARTICLE
The efficacy of gonadotropin-releasing hormone agonist administration for in vitro fertilisation
CJ Haines, EPL Loong
Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
Gonadotropin-releasing hormone agonists are commonly used to achieve pituitary and ovarian downregulation in preparation for in vitro fertilisation. The purpose of this study was to examine the efficacy of gonadotropin-releasing hormone agonists in achieving downregulation prior to the commencement of ovarian stimulation. After a three week pretreatment with the gonadotropin-releasing hormone agonists, a satisfactory response as determined by ultrasound, was achieved in 164/200 cycles (82.0%). Treatment was continued for up to five additional weeks in 35 of the remaining 36 cases. Ovarian suppression was achieved in nine of 11 cases after an additional week of treatment, in nine of 14 cases after two weeks and in two of 10 in the remainder. The results of this study suggest that downregulation will be achieved in over 80% of cases after a three week pretreatment with a gonadotropin-releasing hormone agonist, and a short prolongation of treatment may be worthwhile in those cases where downregulation is not achieved in the first instance.
 
Key words: Fertilisation in vitro; GnRH agonists; Downregulation
 
View this abstract indexed in MEDLINE:
 

Type and screen of blood units at a teaching hospital

ABSTRACT

Hong Kong Med J 1995;1:27-30 | Number 1,March 1995
ORIGINAL ARTICLE
Type and screen of blood units at a teaching hospital
L Wong, G Cheng
Department of Pathology (Haematology), The University of Hong Kong, Pokfulam, Hong Kong
 
 
The Type, Screen and Save Policy and the abbreviated crossmatch procedure for blood issue were instituted in May 1993 at the Queen Mary Hospital. These crossmatch policies were found to be safe, with only one haemolytic transfusion reaction occurring out of 21 524 units transfused (0.005%). Thesepolicies also significantly reduced blood wastage by more than 50 units monthly and improved the crossmatch/transfusion ratio from 2.42 to 1.67. They allowed for efficient utilisation of blood stocks and reallocation of manpower for the investigation of complex serological problems.
 
Key words: Type, Screen and Save Policy; Abbreviated crossmatching; Crossmatch/transfusion ratio
 
View this abstract indexed in MEDLINE:
 

A survey of pregnancies that ended in haemoglobin Bart's hydrops foetalis and Cooley's anaemia

ABSTRACT

Hong Kong Med J 1995;1:22-6 | Number 1,March 1995
ORIGINAL ARTICLE
A survey of pregnancies that ended in haemoglobin Bart's hydrops foetalis and Cooley's anaemia
CS Feng, WC Tsoi
Haematology Laboratory, Prince of Wales Hospital, Shatin, Hong Kong
 
 
Recent advances now allow detection of the homozygous states of alpha- and beta-thalassemia in early pregnancy, thus giving couples at risk the option of early abortion. However, at the Prince of Wales Hospital, no reduction has occurred in the number of births of infants with haemoglobin Bart's hydrops foetalis. A survey by us has revealed a total of 33 cases during the 7-year period from 1987 to 1993. Antenatal records were available for 20 of the 33 and none of these showed that a thalassemia risk had been recognized prior to the development of hydrops. In some cases mothers had failed to attend antenatal clinics early in pregnancy. However, in others, there was apparent failure of vigilance on the part of the doctors concerned, because the thalassemia risk was not identified and appropriate referral for prenatal diagnosis was not made. During the same period, only five new cases of Cooley's anaemia were diagnosed, mostly after the first year of life. Antenatal records were unavailable for review.
 
Key words: Haemoglobin Bart's hydrops foetalis; Cooley's anaemia; Antenatal care; Prenatal diagnosis
 
View this abstract indexed in MEDLINE:
 

Towards full paramedic training in Hong Kong: defibrillation capability is just one step forward

ABSTRACT

Hong Kong Med J 1995;1:16-21 | Number 1,March 1995
ORIGINAL ARTICLE
Towards full paramedic training in Hong Kong: defibrillation capability is just one step forward
AYS Lo, A Chen, WK Hui, S Yeung, HLA Yeung
Hong Kong Adventist Hospital and Heart Centre, Stubbs Road, Hong Kong
 
 
Defibrillation training within the Hong Kong Ambulance Service commenced in January 1991. Training supervision was provided by the Ambulance Service and the Hong Kong Medical Association. Practical examinations were given in which candidates had to perform the protocol satisfactorily. Defibrillator-equipped ambulances/motorcycles were despatched when a patient was found to be unconscious or thought to be suffering from myocardial infarction. Defibrillation success was defined as pulse resumption after ambulance treatment. Comparison of the success rates of two groups of patients were made. In group 1, patients were treated by ambulance equipped with a defibrillator, while in group 2, patients were treated by ambulance not equipped with a defibrillator. There were 772 patients in group 1 and 471 in group 2; 358 group 1 patients received defibrillation treatment. Thirty two of the group 1 patients regained pulse compared with 17 of the group 2 patients (8.94% versus 3.61%, p< 0.01). However, only 15 of the 32 group 1 patients were admitted to hospital, compared with 15 of 17 Group 2 patients (47% versus 88%, p<0.01). The fact that no increase in the number of patients admitted to hospital occurred, suggests that defibrillation therapy alone is insufficient to increase the salvage rate. Future paramedic training in Hong Kong should include endotracheal intubation, intravenous access and the administration of drugs.
 
Key words: Defibrillation; Cardiopulmonary resuscitation; Cardiac arrest
 
View this abstract indexed in MEDLINE:
 

A year's experience of giardiasis on Hong Kong Island

ABSTRACT

Hong Kong Med J 1995;1:10-5 | Number 1,March 1995
ORIGINAL ARTICLE
A year's experience of giardiasis on Hong Kong Island
N Lewindon, PJ Lewindon, E Arevalo
Drs Anderson and Partners, Repulse Bay, Hong Kong
 
 
Cases of giardiasis diagnosed by stool microscopy performed in a single laboratory serving two general practices on Hong Kong Island were reviewed by retrospective analysis of case notes. From 1 September 1992 to 31 August 1993, 95 stool samples from 88 patients were found positive for Giardia lamblia. Case notes were available for analysis of 77 subjects. There were 50 children (mean age 39 months) and 27 adults (mean age 36 years) in a predominantly Caucasian population. Infection was most common in the spring months of February and March and widespread over Hong Kong island. Diarrhoea (47%) and abdominal pain (27%) were the commonest symptoms. Twenty (23%) of the stool samples positive for G. lamblia were obtained from asymptomatic members of 12 families with a symptomatic case. Treating all family members on the basis of a positive stool result for G. lamblia from one member would seem justified in view of frequent person-to-person transmission and the poor diagnostic sensitivity of stool microscopy.
 
Key words: Giardia lamblia; Hong Kong
 
View this abstract indexed in MEDLINE:
 

Current practices, attitudes, and perceived barriers for treating smokers by Hong Kong dentists

Hong Kong Med J 2014;20:94–101 | Number 2, April 2014 | Epub 14 Mar 2014
DOI: 10.12809/hkmj134027
© Hong Kong Academy of Medicine. CC BY-NC-ND 4.0
 
ORIGINAL ARTICLE
Current practices, attitudes, and perceived barriers for treating smokers by Hong Kong dentists
Kenneth WK Li, BDS1; David VK Chao, FRCGP, FHKAM (Family Medicine)2
1 Tai Po Wong Siu Ching Government Dental Clinic, 1 Po Wu Lane, Tai Po, Hong Kong
2 Department of Family Medicine and Primary Health Care, United Christian Hospital, Kwun Tong, Hong Kong
 
Corresponding author: Dr KWK Li (wkk_li@yahoo.com.hk)
 Full paper in PDF
Abstract
Objectives: To assess the attitudes of dentists towards smoking cessation advice, as well as to investigate their current practice and perceived barriers to giving such advice and the relationships among their peers regarding such activity.
 
Design: Cross-sectional survey.
 
Setting: Hong Kong.
 
Participants: Self-reporting questionnaires were mailed to 330 dentists in Hong Kong by systematic sampling. Information on their attitudes, practices, and perceived barriers towards smoking cessation advice and relevant background information was collected.
 
Results: A total of 218 questionnaires were returned (response rate, 66%). The majority (97%) reported that they would enquire into every patient’s smoking status, yet only around half of them did so routinely. Most (95%) of the dentists who always enquired about smoking status would actually offer smoking cessation advice to their patients. Multiple logistic regression of the results revealed that government dentists (odds ratio=2.7; 95% confidence interval, 1.4-5.1), those who received training in smoking cessation advice (2.5; 1.2-5.1), and those aged over 40 years (1.9; 1.0-3.4) were significantly more likely to enquire about smoking status. In most practices (93%), smoking cessation advice was offered by the dentists themselves rather than by other team members. “Lack of training”, “unlikely to be successful”, and “possibility of losing patients” were the three barriers regarded as “very important” by dentists.
 
Conclusions: Dentists in Hong Kong generally had positive attitudes towards smoking cessation advice. The dental team is in a very good position to help smokers quit. However, training and guidelines designed specifically for dental teams are paramount to overcome barriers in delivering smoking cessation advice by dental professionals.
 
 
New knowledge added by this study
  • The information gathered generally revealed a positive attitude towards delivering smoking cessation advice to smokers. However, lack of training and guidelines prevented dentists from implementing such advice in practice.
Implications for clinical practice or policy
  • This study raises the awareness of dentists about delivering smoking cessation advice to patients in their daily practice.
  • There is a need of specific guidelines for dentists to achieve this goal.
  • Practical training on such activity should be encouraged and included in both the undergraduate and postgraduate training of dentists.
 
Introduction
Tobacco smoking is one of the most significant public health problems worldwide. The adverse effects of smoking on health are well known.1 According to the World Health Organization (WHO), the annual death toll could rise to more than eight million by 2030, unless urgent action is taken against smoking.2
 
In Hong Kong, 11.1% of the population aged 15 years or above are daily smokers. Men are the high-risk group and have a 22% prevalence of being smokers, which is much higher than in women (4%).3 The situation is particularly alarming, as the smoking population is becoming younger.3 Smoking contributes a large public health and medical burden to society.
 
The Hong Kong SAR Government has implemented numerous policies and enacted legislation on many occasions to combat tobacco smoking. Such action has entailed raising tobacco tax, making amendments to the existing Smoking (Public Health) Ordinance to prohibit smoking in public places, restricting the sale of tobacco products and tobacco advertising. While strategies such as taxation and prohibition of advertising are proven to be effective, one effective strategy that should not be ignored is “smoking cessation advice” (SCA) delivered by health care professionals.
 
Smoking tobacco has been identified as an important cause of various oral diseases and pathologies. It is one of the most important factors predisposing to pre-cancerous lesions and cancer of the oral cavity, the reported pooled cancer risk being 3.4-fold higher than in non-smokers.4 It also increases the risk of periodontal diseases,5 complications after extractions,6 and increased rates of implant failures.7 Cross-sectional studies show that smokers have more tooth loss.8 Other easily recognised effects include staining of teeth,9 dental restorations, and prosthesis10 as well as alteration of taste perception11 and halitosis.12 All these have detrimental effects on the quality of life of smokers because of reduced chewing efficiency, poor aesthetics, and poor self-esteem.13
 
The benefits of smoking cessation are substantial. Evidence shows that smoking counselling given by dental professions can be effective and comparable to that offered by other primary care professionals.14 15 16 Around a quarter of the population have regular dental checkups and 53% have their teeth checked every 1 or 2 years.17 In their daily practice, dental professionals have access to a large patient population, including smokers. Besides, the detrimental effects of smoking on the oral cavity can be readily demonstrated directly and thus easily appreciated by patients; this acts as a strong motivator to quit smoking.16 Moreover, dental treatments entailing multiple visits provide good opportunities to motivate, reinforce, and support smoking cessation. Thus, dental professionals are in an excellent position for delivering advice and counselling to smokers. Notably, counselling by dentists has been reported to achieve an 8.6% cessation rate after 1 year, and over 16% when also coupled with nicotine replacement therapies.18 Despite these observations, delivery of SCA by dentists remains less than satisfactory.19 20 21 22 According to the literature, the reported barriers to such activity include lack of time, resources, remuneration, training, and fear of damaging dentist-patient rapport.23
 
In Hong Kong, a study conducted in 2006 showed that more than half of all medical doctors did not have adequate knowledge (53%) or favourable attitudes (55%) towards smoking cessation.24 Slightly over 40% lacked confidence in delivery of SCA. Although 77% of them obtained information on the smoking status of their patients, only 29% advised them to quit smoking, reflecting a low involvement of medical doctors in the promotion of smoking cessation.24
 
Local published data on the dentists’ attitudes, practices, and barriers to delivering SCA to patients are limited, except for one study by Lu et al.25 The rationale of the present study was to collect data from local dentists, and compare local results with those gleaned from international studies.
 
The objectives of the present study were: (1) to assess the attitudes of dentists towards SCA; (2) to investigate the current practice of dentists in respect of SCA; (3) to examine the perceived barriers to offering SCA; and (4) to seek possible relationships between the characteristics of dentists and their SCA activity.
 
Methods
A 17-item structured, self-administered and validated questionnaire developed by Stacey et al26 in 2006 in the UK was adopted as the survey instrument. The questionnaire consisted of three main parts: (1) smoking cessation views and activities of the dental team; (2) perceived barriers to giving SCA; and (3) perception of the importance of the smoking cessation role of the dental team and general medical practitioners. It was pilot-tested with a small convenience sample (n=20) of dentists.
 
The target population consisted of 2026 general dentists registered with the Hong Kong Dental Council, whose correspondence addresses are available on a website27 that is open to the general public. The inclusion criterion was any dentist who was currently having a dental practice in Hong Kong with a valid address at the time of this survey. A systematic sample (every 6th dentists on the list) was drawn from the 2026 registered general dentists in Hong Kong, so as to yield the desired sample size. A sample size of 324 subjects was calculated as needed based on a 5% margin of error (type I error), and 95% confidence level, assuming 50% response after distribution. Thus, 330 questionnaires were mailed in January 2012 with stamped self-addressed reply envelopes. Other means of reply allowed were by fax or by online completion of the questionnaires via a designated website. Another follow-up round of 330 questionnaires was sent to these dentists again 3 weeks after the first mailing.
 
Data analysis
A pilot study was carried out with a convenience sample (n=20) to ensure the face validity of the questionnaire. Test-retest reliability test was also performed using these 20 subjects who were asked to complete the questionnaire a second time (2 weeks later). The questionnaire was viewed by three experts in dental public health to ensure its suitability for the present study.
 
All data were analysed with the Statistical Package for the Social Sciences (Windows version 19.0; SPSS Inc, Chicago [IL], US). Frequency distributions were generated to illustrate the demographic data, their attitudes, practices, and perceived barriers in SCA. To examine any relationships between demographic variables and outcomes, unconditional logistic regression analysis was performed with each demographic variable and the outcome variables (attitudes, practices, perceived barriers). Multiple logistic regression was then performed for variables that yielded a P value of <0.25 in the individual analysis. The final model contained those statistically significant variables, using a stepwise-forward Wald logistic regression. The significance level was set at 0.05.
 
Results
Response rate and demographic backgrounds
From the 330 selected dentists, 223 questionnaires were returned (163 by mail, 39 by fax, 21 online), of which five were incomplete. Thus, 218 questionnaires were valid for analysis, yielding a response rate of 66%. Alarmingly, less than one fourth of the dentists had received training in SCA. Only 16% of them had received such training during their undergraduate training and only 12% during postgraduate training. Moreover, only approximately 60% of the dentists claimed that they knew the contact of relevant supporting agencies for SCA. Table 1 shows the background of these dentists.
 

Table 1. Demographic background of the dentists (n=218)
 
Current practices on smoking cessation
Nearly 97% of the dentists claimed that they would enquire about their patients’ smoking status, yet only around half of them would always do so as a routine (Fig 1). About 97% would enquire about smoking status whenever a patient presented with oral diseases related to smoking (eg periodontal disease and leukoplakia). The percentage of routine enquiries about smoking status when patients presented with oral white lesion (a symptom of oral pre-cancer) was slightly higher (73%) than those presented with periodontal disease (66%).
 

Figure 1. Proportion of dentists who enquired about patient’s smoking status
 
For dentists who would not routinely enquire about the smoking status, around half (53%) would always do so when patients presented with an oral white lesion, and around 40% would do so when the latter presented with periodontal disease.
 
For dentists who would always enquire about smoking status, 95% claimed they actually offered SCA. The majority of the dental practices (93%) entailed SCA offered by the dentists themselves, only 16% had dental nurses/hygienists who offered such advice and only 3% had practice managers/receptionists who did so.
 
After adjustments and exclusion of non-significant variables in the unconditional logistic regressions, only three variables were retained in the final model and were found to be statistically significant. These were the type of practice, receipt of training in SCA, and age. Government dentists, those who had received training in SCA, and those aged over 40 years were more likely to always enquire about their patients’ smoking status (outcome variable of the model, P<0.05; Table 2).
 

Table 2. Relationships between dentists who always enquire about patient’s smoking status and their demographic backgrounds (univariate and multiple logistic regression)
 
Trained dentists were more likely to always enquire about smoking when patients presented with periodontal disease than non-trained dentists, the respective odds ratio (OR) and 95% confidence interval (CI) being 3.3 and 1.5-7.2. Government dentists were also more likely to enquire about smoking when patients presented with a white oral lesion (OR=2.9; 95% CI, 1.4-6.1).
 
Similar results prevailed with respect to actually offering SCA to patients. Government dentists offered such advice more often than non-government dentists according to the logistic regression analysis (OR=8.3; 95% CI, 1.1-64.4).
 
Moreover, government dentists were more likely to know how to contact supporting agencies (OR=2.3; 95% CI, 1.1-4.6) than non-government counterparts, and trained dentists were more likely to know how to contact supporting agencies (OR=14.3; 95% CI, 4.2-48.5) than those non-trained.
 
Attitudes and perceptions of dentists on the role of delivering smoking cessation advice
A high proportion (89%) of dentists agreed or strongly agreed that the dental team has an important role in delivering SCA to patients; the percentage who agreed or strongly agreed that medical doctors had an important role was slightly higher (93%).
 
Trained dentists were 8.5 times more likely to think that it was imperative for dental teams to offer SCA (P<0.05). Almost all (98%) of those who received training thought that dentists should offer SCA, which was more than that for those who did not have such training (86%; P=0.014).
 
When dentists were asked who should offer SCA in the team, most (approximately 90%) claimed that they should be responsible, whilst 41% thought that nurses should also be involved, and 47% felt that hygienists too should be involved. However, only 16% of such personnel were actively involved in offering SCA; the percentages were even lower for receptionists (3%) and practice managers (1%).
 
Perceived barriers to delivering smoking cessation advice by dentists
Among the potential barriers listed in the questionnaire, the most important one identified by the dentists was the “possibility of losing patients” (31%), followed by the “lack of training” (25%) and the “unlikely to be successful” (14%). On the other hand, the “lack of time”, the “lack of fee”, and the “not perceived as my role” were not regarded as important (Fig 2).
 

Figure 2. Proportion of each barrier being regarded as “very important” by the dentists (n=218)
 
Discussion
This study gathered information on the current attitudes, practices, and perceived barriers among dentists in delivering SCA to Hong Kong patients, which could have implications for the development of training programmes and provide directions for future research.
 
Knowledge and attitudes towards smoking cessation advice
The present study showed that Hong Kong dentists generally had positive attitudes and knowledge about SCA, and recognised the adverse effects of smoking on oral health, as reflected by the high percentages for enquiry about a patient’s smoking status. Moreover, nearly 90% expressed positive attitudes towards SCA, in that they agreed it had an important role to play.
 
Training and guidelines are important but inadequate
Government dentists and dentists who received training were significantly more likely (approximately 3 times) to routinely enquire about a patient’s smoking status than other dentists. Trained dentists were also approximately 14 times more likely to know how to contact local supporting agencies, and more than 8 times as likely to offer SCA to the patients. They also perceived their role in offering SCA as very important and were more actively involved than other team members in its delivery. These results were similar to those for Hong Kong medical doctors,24 as well as findings of other international and local studies.20 21 22 25
 
This study reflects the importance of training and guidelines, although these were not widely available. Only a small proportion (16%) of dentists received training in SCA during their undergraduate studies. Notably, for local students the limited practical training in essential techniques for delivering SCA to patients was similar to the situation in the United States and Europe.28 29 Research has shown that to increase the effectiveness of SCA, education is needed to expand both didactic knowledge and clinical competencies to help patients quit smoking.30 Evidence also suggests that training should be provided early and continued throughout subsequent courses.31 Inclusion of both theoretical and practical training (counselling skills, problem-solving strategies) should be considered in future undergraduate curricula. Moreover, continuing professional education programmes focusing on hands-on SCA techniques could help dentists acquire better knowledge and more up-to-date techniques. According to the results, the continuing education programmes should be directed towards younger and non-government dentists.
 
The Department of Health has guidelines on SCA for the government dental officers, which includes annual updating of the patient’s smoking status, provision of SCA, and obtaining patient consent for referral to Tobacco Control Office when needed. This may be one reason government dentists were more likely to enquire about a patient’s smoking status, offer SCA, and confirm the importance of relevant guidelines. As in other countries, many dentists are not familiar with guidelines like the “5A approach”.32 Evidence suggests that dentists familiar with guidelines are more likely to engage in SCA.33 Local information and guidelines on SCA are mostly unclear, as they were not being designed specifically for dentists and may not be readily accessible to them.34 Not surprisingly, only approximately 60% of the dentists knew how to contact supporting agencies. Thus, clear, evidence-based, and easily accessible guidelines designed for the dental profession should be developed to facilitate the effective delivery of SCA by dental professionals.
 
Recently, a WHO Collaborating Centre for Smoking Cessation and Treatment of Tobacco Dependence was set up by Department of Health. It aims to provide evidence-based smoking cessation training for health care personnel. It also aims to develop, test, and evaluate models of smoking cessation to support WHO’s initiatives on assistance in the dissemination of relevant information on smoking cessation. Hopefully therefore, the dental profession will have more opportunities to receive training in SCA in the near future.35
 
Barriers
Despite their apparently positive attitudes to SCA, only around half of the dentists always enquired about each patient’s smoking status and, if indicated, offered SCA. These findings are consistent with those from Australia36 and for Hong Kong medical doctors.24 The difference in the beliefs and the actual practice of dentists suggest barriers to implementation. In the present study, “lack of training”, “possibility of losing patients”, and “unlikely to be successful” were regarded as important barriers by the dentists, and were similar to those reported in the UK26 and Malaysia.20 They suggest that dentists lack confidence in delivering SCA and reinforce the importance of adequate training. Dentists worry that by offering SCA, they might damage relationships with their patients. However, in reality, research indicates that over half of the patients expect their dentists to discuss issues related to smoking.37 Also, such discussion could cultivate rapport between the dentists and the patients. Thus, actually delivering SCA could be very cost-effective in terms of gaining patient trust. To encourage involvement of dentists in delivering SCA, efforts should be directed at reducing the above-mentioned barriers (provision of adequate training, informing the dentists about current evidence, reducing their worries about damaging relationships with patients).
 
Team approach
In this study, over 40% of the dentists expressed that other personnel in their teams (nurses, hygienists) should be involved in delivering SCA, though the percentages were lower than those in the UK.26 Thus, dentists generally recognised the importance of the team approach to delivering SCA, and the literature indicates that such team members (including administrative staff) are in a good position to do so.18 38 This is especially true for the hygienists, who are responsible for managing periodontal diseases that are smoking-related and require multiple visits, and therefore offer excellent opportunities to deliver SCA.39 40
 
The team approach should be encouraged, and as team leader, the dentist has overall responsibility and should actively involve other staff.41 In order to increase the effectiveness, training of the entire dental office team could be considered.42 The proportion of local dentists who thought practice managers and receptionists should be involved was low compared to that reported from the UK.26 Variations in dental clinic organisation in different countries may be part of the reason; for example, locally it is not common to involve dental practice managers in patient care.
 
Comparison with other studies
As mentioned previously, various aspects of our results were generally comparable to those of other studies. The response rate in the present study was just under 70%, which was higher than 60% reported from the UK,26 and 55% reported from Malaysia,20 as well as 19% reported for Hong Kong medical doctors24 and 50% in another study on Hong Kong dentists.25 Our higher questionnaire response rate could be because the questions were simple, straightforward, and not time-consuming. Notably, the locally developed questionnaire used by Lu et al25 (on Hong Kong dentists) gathered more detailed information than we did.
 
Limitations
The relatively low response rate in our study may limit the generalisability of the results, and our sample size was less than ideal. A full population survey should be conducted if resources and time permit. The tendency of respondents to provide positive, favourable responses may be a source of bias, resulting in an over-optimistic estimate of SCA implementation. The characteristics of the non-respondents were not known due to the anonymous nature of the questionnaire. The questionnaire was comparatively simple, and did not address specific aspects of knowledge on SCA, nor any specific aspects of advice offered to patients. This limited the scope of information being collected. Due to time and resource limitations, other important personnel, such as nurses and hygienists, were not surveyed.
 
Recommendations for future researches
A qualitative design could be considered to gain a deeper understanding on the beliefs and barriers to SCA with respect to the dental professions. Thereafter an updated questionnaire could be designed and validated, specifically for the local setting. This could entail specific questions on the knowledge of dentists regarding SCA and the specific activities they and their teams undertake. Further research could also focus on evaluating the effectiveness of different smoking cessation training programmes and practical approaches to SCA.
 
Conclusions
The present research showed that dentists in Hong Kong generally have positive attitudes towards their role in delivering SCA to patients. However, barriers like the relative lack of training and guidelines, the lack of confidence, and fear of damaging relationships with patients may prevent them from delivering the relevant advice. Local guidelines specifically designed for the dental profession should be developed and relevant resources made readily accessible. More importantly, adequate practical training programmes should be included in both the undergraduate curriculum and continuing education activities, especially for the private and younger dentists.
 
References
1. World Health Organization. WHO report on the global tobacco epidemic, 2011: Warning about the dangers of tobacco. Geneva: WHO; 2011.
2. WHO key facts about tobacco. Available from: http://www.who.int/mediacentre/factsheets/fs339/en. Accessed 29 Apr 2012.
3. Census and Statistics Department, Hong Kong. General household survey and thematic household survey, 2011. Available from: http://www.census2011.gov.hk/en/index.html. Accessed Feb 2014.
4. Gandini S, Botteri E, Iodice S, et al. Tobacco smoking and cancer: a meta-analysis. Int J Cancer 2008;122:155-64. CrossRef
5. Bergstrom J. Periodontitis and smoking: an evidence-based appraisal. J Evid Based Dent Pract 2006;6:33-41. CrossRef
6. Johnson NW, Bain CA. Tobacco and oral disease. EU-Working Group on Tobacco and Oral Health. Br Dent J 2000;189:200-6.
7. Reibel J. Tobacco and oral diseases. Update on the evidence, with recommendations. Med Princ Pract 2003;12 Suppl 1:22-32. CrossRef
8. Ylöstalo P, Sakki T, Laitinen J, Järvelin MR, Knuuttila M. The relation of tobacco smoking to tooth loss among young adults. Eur J Oral Sci 2004;112:121-6. CrossRef
9. Eriksen HM, Nordbo H. Extrinsic discoloration of teeth. J Clin Periodontol 1978;5:229-36. CrossRef
10. Asmuseen E, Hansen EK. Surface discoloration of restorative resins in relation to surface softening and oral hygiene. Scan J Dent Res 1986;94:174-7.
11. Pasquali B. Menstrual phase, history of smoking and taste discrimination in young women. Percept Mot Skills 1997;84:1243-6. CrossRef
12. Rosenberg M. Clinical assessment of bad breath: current concepts. J Am Dent Assoc 1996;127:475-82. CrossRef
13. Gerritsen AE, Allen PF, Witter DJ, Bronkhorst EM, Creugers NH. Tooth loss and oral health–related quality of life: a systematic review and meta-analysis. Health Qual Life Outcomes 2010;8:126. CrossRef
14. Needleman IG, Binnie VI, Ainamo A, et al. Improving the effectiveness of tobacco use cessation (TUC). Int Dent J 2010;60:50-9.
15. John J. Tobacco smoking cessation counselling interventions delivered by dental professionals may be effective in helping tobacco users to quit. Evid Based Dent 2006;7:40-1. CrossRef
16. Warnakulasuriya S. Effectiveness of tobacco counseling in the dental office. J Dent Educ 2002;66:1079-87.
17. Census and Statistics Department, Hong Kong. General household survey and thematic household survey, report no. 45. Available from: http://smokefree.hk/UserFiles/resources/smoking_risk_cessation/thematic_household_surveys/THS_45Report.pdf. Accessed Feb 2014.
18. Cohen SJ, Stookey GK, Katz BP, Drook CA, Christen AG. Helping smokers quit: a randomized controlled trial with private practice dentists. J Am Dent Assoc 1989;118:41-5.
19. Allard RH. Tobacco and oral health: attitudes and opinions of European dentists; a report of the EU working group on tobacco and oral health. Int Dent J 2000;50:99-102. CrossRef
20. Ibrahim H, Norkhafizah S. Attitudes and practices in smoking cessation counselling among dentists in Kelantan. Archives of Orofacial Sciences 2008;3:11-6.
21. Uti OG, Sofola OO. Smoking cessation counseling in dentistry: attitudes of Nigerian dentists and dental students. J Dent Educ 2010;75:406-12.
22. Victoroff KZ, Dankulich-Huryn T, Haque S. Attitudes of incoming dental students toward tobacco cessation promotion in the dental setting. J Dent Educ 2004;5:563-8.
23. Watt RG, McGlone P, Dykes J, Smith M. Barriers limiting dentists' active involvement in smoking cessation. Oral Health Prev Dent 2004;2:95-102.
24. Abdullah AS, Rahman AS, Suen CW, et al. Investigation of Hong Kong doctors' current knowledge, beliefs, attitudes, confidence and practices: implications for the treatment of tobacco dependency. J Chin Med Assoc 2006;69:461-71. CrossRef
25. Lu HX, Wong MC, Chan KF, et al. Perspectives of the dentists on smoking cessation in Hong Kong. Hong Kong Dent J 2011;8:79-86.
26. Stacey F, Heasman PA, Heasman L, Hepburn S, McCracken GI, Preshaw PM. Smoking cessation as a dental intervention—views of the profession. Br Dent J 2006;201:109-13. CrossRef
27. The Hong Kong Dental Council. Lists of Registered Dentists in Hong Kong, September 2011. DCHK website: http://www.dchk.org.hk/docs/List_of_Registered_Dentists_Local.pdf. Accessed 2 Jan 2012.
28. Geller AC, Powers CA. Teaching smoking cessation in U.S. medical schools: a long way to go. Virtual Mentor 2007;9:21-5. CrossRef
29. Raupach T, Shahab L, Baetzing S, et al. Medical students lack basic knowledge about smoking: findings from two European medical schools. Nicotine Tob Res 2009;11:92-8. CrossRef
30. Ramseier CA, Christen A, McGowan J, et al. Tobacco use prevention and cessation in dental and dental hygiene undergraduate education. Oral Health Prev Dent 2006;4:49-60.
31. Brown RL, Pfeifer JM, Gjerde CL, Seibert CS, Haq CL. Teaching patient-centered tobacco intervention to first-year medical students. J Gen Intern Med 2004;19:534-9. CrossRef
32. Succar CT, Hardigan PC, Fleisher JM, Godel JH. Survey of tobacco control among Florida dentists. J Community Health 2011;36:211-8. CrossRef
33. Hu S, Pallonen U, McAlister AL, et al. Knowing how to help tobacco users. Dentists' familiarity and compliance with the clinical practice guideline. J Am Dent Assoc 2006;137:170-9. CrossRef
34. Tobacco Control Office, Department of Health, Hong Kong. Health promotion-tobacco control resources centre. Available from: http//www.tco.gov.hk/English/health/health_tcrc.html. Accessed 1 May 2012.
35. Hong Kong Council on Smoking and Health. News update—First WHO collaborating centre for smoking cessation officially launched in Hong Kong. COSH Website: http://smokefree.hk/en/content/web.do?page=news20120410. Accessed 4 May 2012.
36. Trotter L, Worcester P. Training for dentists in smoking cessation intervention. Aust Dent J 2003;48:183-9. CrossRef
37. Rikard-Bell G, Donnelly N, Ward J. Preventive dentistry: what do Australian patients endorse and recall of smoking cessation advice by their dentists? Br Dent J 2003;94:159-64. CrossRef
38. Pizzo G, Piscopo MR, Pizzo I, Giuliana G. Smoking cessation counselling and dental team [in Italian]. Ann Ig 2006;18:155-70.
39. Severson HH, Andres JA, Lichtenstein E, Gordon JS, Barckley MF. Using the hygiene visit to deliver a tobacco cessation program: results of a randomized clinical trial. J Am Dent Assoc 1998;129:993-9. CrossRef
40. Stevens VJ, Severson H, Lichtenstein E, Little SJ, Leben J. Making the most of a teachable moment: a smokeless-tobacco cessation intervention in the dental office. Am J Public Health 1995;85:231-5. CrossRef
41. Campbell HS, Sletten M, Petty T. Patient perceptions of tobacco cessation advice in dental offices. J Am Dent Assoc 1999;130:219-26. CrossRef
42. Wood GJ, Cecchini JJ, Nathason N, Hiroshige K. Office based training in tobacco cessation for dental professionals. J Am Dent Assoc 1997;128:216-24. CrossRef

Live birth rate, multiple pregnancy rate, and obstetric outcomes of elective single and double embryo transfers: Hong Kong experience

Hong Kong Med J 2014;20:102–6 | Number 2, April 2014
DOI: 10.12809/hkmj134065
© Hong Kong Academy of Medicine. CC BY-NC-ND 4.0
 
ORIGINAL ARTICLE
Live birth rate, multiple pregnancy rate, and obstetric outcomes of elective single and double embryo transfers: Hong Kong experience
Joyce Chai, FHKAM (Obstetrics and Gynaecology); Tracy WY Yeung, FHKAM (Obstetrics and Gynaecology); Vivian CY Lee, FHKAM (Obstetrics and Gynaecology); Raymond HW Li, FHKAM (Obstetrics and Gynaecology); Estella YL Lau, PhD; William SB Yeung, PhD; PC Ho, MD, FHKAM (Obstetrics and Gynaecology); Ernest HY Ng, MD, FHKAM (Obstetrics and Gynaecology)
Department of Obstetrics and Gynaecology, Queen Mary Hospital, The University of Hong Kong, Pokfulam, Hong Kong
 
Corresponding author: Dr J Chai (jchai@hkucc.hku.hk)
Abstract
Objective: To compare the live birth rate, multiple pregnancy rate, and obstetric outcomes of elective single and double embryo transfers.
 
Design: Case series with internal comparisons.
 
Setting: University affiliated hospital, Hong Kong.
 
Participants: Between October 2009 and December 2011, 206 women underwent their first in-vitro fertilisation cycle. Elective single embryo transfer was offered to women who were aged 35 years or below, and had endometrial thickness of 8 mm or more and at least two embryos of good quality.
 
Main outcome measures: Live birth rate, multiple birth rate, and obstetric outcomes.
 
Results: Among the 206 eligible women, 74 underwent an elective single embryo transfer and 132 a double embryo transfer. The live birth rate was comparable in the two groups, being 39.2% in the elective single embryo transfer group and 43.2% in the double embryo transfer group, while the multiple pregnancy rate was significantly lower in the elective single embryo transfer group than the double embryo transfer group (6.9% vs 40.4%; P<0.001). Gestational ages and birth weights were comparable in the two groups. There was no significant difference between the two groups with respect to the rate of preterm delivery and antenatal complications (27.6% vs 43.9%, respectively; P>0.05).
 
Conclusion: In this selected population, an elective single embryo transfer policy decreases the multiple pregnancy rate without compromising the live birth rate. The non-significant difference in antenatal complications may be related to the small sample size.
 
 
New knowledge added by this study
  • Elective single embryo transfer decreased the multiple pregnancy rate without compromising the live birth rate in women with a good prognosis undergoing in-vitro fertilisation.
Implications for clinical practice or policy
  • Elective single embryo transfer should be offered to women with a good prognosis and the care provider should promote this policy through education.
 
Introduction
In-vitro fertilisation (IVF) treatment is an effective treatment for various causes of infertility and involves development of multiple follicles after ovarian stimulation, oocyte retrieval, and embryo transfer after fertilisation. Historically, multiple embryos were transferred to compensate for low rates of implantation for individual embryos as well as to achieve higher pregnancy rates. Consequently, IVF carried a high risk of multiple pregnancy and its associated adverse effects on mothers and children.1 In 2003 the Chairman of the European Society of Human Reproduction and Embryology (ESHRE) commented that assisted reproduction techniques should result in the birth of one healthy child and that a twin pregnancy should be regarded as a complication.2
 
In January 2013, the “Code of Practice on Reproductive Technology & Embryo Research” issued by the Council on Human Reproductive Technology of Hong Kong stipulated that no more than three embryos should be placed in a woman in any one cycle.3 In August 2001, the Human Fertilisation and Embryology Authority in the UK recommended reducing the number of embryos that should be transferred in a single IVF treatment cycle from three to two.4
 
In 2001, ESHRE recommended elective single embryo transfer (eSET) for women aged under 34 years at the time of their first attempt, as soon as they had obtained a top-quality embryo.5 In 2008, the British Fertility Society, in conjunction with the Association of Clinical Embryologists, introduced guidelines for eSET in the UK that aimed to reduce IVF multiple pregnancy rates to less than 10%.6 Meta-analyses have shown that in a selected population, compared with double embryo transfer (DET), eSET could reduce multiple pregnancy rates significantly, without compromising cumulative pregnancy rates.7 8
 
Our centre offered eSET to eligible women in order to reduce the multiple pregnancy rate. The aim of this study was to compare the live birth rate, multiple pregnancy rate, and obstetric outcomes after eSET and DET in mothers having their first IVF/intra-cytoplasmic sperm injection (ICSI) attempt.
 
Methods
This was a retrospective study carried out at the Centre of Assisted Reproduction and Embryology, Queen Mary Hospital, The University of Hong Kong, Hong Kong. Clinical details of all treatment cycles were prospectively entered into a computerised database, and checked for correctness and completeness on a regular basis. For this study, data were retrieved for analysis and ethics committee approval was deemed not necessary for retrospective analysis of data.
 
Patients
In our programme, a maximum of two embryos were replaced, irrespective of the woman’s age. Women were eligible for eSET if they were ≤35 years of age at the time of the embryo transfer, were undergoing their first IVF cycle, had an endometrial thickness of ≥8 mm, and had at least two good-quality embryos available for transfer or freezing. Good-quality embryos were defined by their morphological features and cleavage rate, and included embryos with less than 25% fragmentation and four cells at day 2. Eligible patients were individually counselled about eSET. Women who opted for eSET would have one embryo replaced (eSET group), while those who opted for DET had two embryos transferred (DET group).
 
Ovarian stimulation and in-vitro fertilisation/intra-cytoplasmic sperm injection procedures
All women were treated either with the long gonadotropin-releasing hormone (GnRH) agonist protocol or the GnRH antagonist protocol for pituitary down-regulation. The details of the long protocol for the ovarian stimulation regimen, handling of gametes, as well as standard insemination and ICSI were as previously described.9 In short, women received buserelin (Suprecur; Hoechst, Frankfurt, Germany) nasal spray 150 μg 4 times a day starting from the mid-luteal phase of the cycle preceding the treatment cycle, followed by human menopausal gonadotropins (hMG) or recombinant follicle-stimulating hormone (FSH) for ovarian stimulation after return of a period. In the GnRH antagonist protocol, after confirming a basal serum oestradiol level, ovarian stimulation was started with either hMG or recombinant FSH. Ganirelix (NV Organon; Swords Co, Dublin, Ireland) 250 μg was started from the sixth day of stimulation. The starting dose of gonadotropin was based on the baseline antral follicle count.
 
Transvaginal ultrasonography was used to monitor the ovarian response. When the mean diameter of the leading follicle reached 18 mm and there were at least three follicles reaching a mean diameter of 16 mm or more, human chorionic gonadotropin (hCG; Pregnyl; Organon, Oss, The Netherlands) 5000 or 10 000 units or Ovidrel (Merck Serono, Modugno, Italy) 250 μg was given and oocytes were collected about 36 hours later. Fertilisation was carried out in vitro either by conventional insemination or ICSI depending on semen parameters. Women were allowed to have replacement of at most two embryos 2 days after oocyte retrieval. A progesterone pessary (Endometrin 100 mg twice per day; Ferring Pharmaceuticals, Parsippany [NJ], US) was administered from the day of embryo transfer for 2 weeks to enable luteal support. Pregnancies were confirmed by positive urine hCG tests and transvaginal ultrasonographic evidence of a gestational sac.
 
Collection of clinical information
Clinical information including age, body mass index, basal serum levels of FSH, and baseline antral follicle counts were collected. During IVF treatment, such data included days of stimulation, total dosage of gonadotropin, oestradiol level on day of hCG, number of oocytes retrieved, number of available embryos, number of good-quality embryos, as well as pregnancy and miscarriage rates.
 
Clinically, pregnancy was defined as the presence of a gestational sac by ultrasonography, whereas the miscarriage rate per clinical pregnancy was defined as the proportion of patients whose pregnancy failed to develop before 20 weeks of gestation. Pregnancy outcome was collected from all pregnant women by a postal questionnaire or by phone. Live birth was defined as the delivery of a fetus with signs of life after 24 completed weeks of gestational age, and the multiple pregnancy rate was calculated as the number of multiple pregnancies divided by the number of clinical pregnancies, expressed as a percentage. Obstetric outcomes including antenatal complications, gestational age at delivery, mode of delivery, and birth weight were also recorded.
 
Statistical analysis
The primary outcome measure was the live birth rate and secondary outcomes included the multiple pregnancy rate and obstetric outcomes. Statistical analysis for the comparison of mean values was performed using Mann-Whitney and Student’s t tests, as appropriate. The Chi squared and Fisher’s exact tests were used to compare categorical variables. Statistical analysis was carried out using the Statistical Package for the Social Sciences (Windows version 20.0; SPSS Inc, Chicago [IL], US). A two-tailed P value of <0.05 was considered statistically significant.
 
Results
In all, 206 women undergoing their first IVF cycle from October 2009 to December 2011 met the inclusion criteria. A total of 74 women chose eSET and 132 chose DET. Patient and cycle characteristics are shown in Tables 1 and 2, respectively. Women who opted for eSET were significantly younger than those opting for DET, and had a significantly higher proportion of good-quality embryos than those in the DET group.
 

Table 1. Demographic and clinical characteristics of the patients referred for sperm cryopreservation (n=130)*
 

Table 2. Cycle characteristics*
 
The IVF and obstetric outcomes are shown in Table 3. Among women with eSET, 40 (54.1%) had a positive pregnancy test; two were biochemical pregnancies, eight miscarried, and one was an ectopic pregnancy. There was one pair of monozygotic and one pair of dizygotic twins in the eSET group. In women having DET, the positive pregnancy test rate was 58.3% (n=77/132); there were nine biochemical pregnancies, seven miscarriages, and four ectopic pregnancies. In the DET group, the multiple pregnancy rate was 40.4%, which was significantly higher than that in the eSET group (P<0.001). There were two sets of triplets, of which one underwent fetal reduction to a singleton and the other had fetal reduction to twins. One woman in the eSET group and four in the DET group were lost to follow-up for their obstetric outcomes. Overall, the live birth rate was comparable in the eSET and DET groups (39.2% vs 43.2%, respectively).
 

Table 3. In-vitro fertilisation and obstetric outcomes*
 
The mean gestational age at birth and the median birth weight were not significantly different in the eSET group compared with the DET group (38.6 ± 2.2 vs 37.9 ± 2.3 weeks and 2950 [interquartile range, 2830-3157] g vs 2785 [2475-3200] g, respectively). The preterm delivery rate (defined as delivery at <37 weeks) and the frequencies of antenatal complications (including gestational diabetes, gestational hypertension, pre-eclampsia, and placenta praevia) were higher in the DET group, although the difference did not reach statistical significance.
 
Discussion
The risk of multiple pregnancy has been a concern in IVF/ICSI as it is associated with adverse maternal and neonatal outcomes.1 This is the first study reporting live birth rates and obstetric outcomes after eSET and DET in a selected population in Hong Kong. Our study confirms recent literature findings,7 8 by showing that eSET can significantly reduce the multiple pregnancy rate without adversely affecting the live birth rate in young women with good ovarian function. No triplets were observed in the eSET group, but rather unexpectedly it did contain two pairs of twins; one was monozygotic and one dizygotic. Dizygotic twin pregnancy following a single embryo transfer was a rare event, and suggestive of a spontaneous pregnancy occurring concurrently with one due to IVF.10 The multiple pregnancy rate of 40.4% in the DET group and the live birth rates in our study (39.2% and 43.2% in the eSET and DET groups, respectively) were similar to or higher than those previously reported.7 11 12 13 14
 
Our study showed that the obstetric outcomes were not significantly different in the two groups. Antenatal complications were more common in the DET group (43.9% vs 27.6% in eSET group), although the difference did not reach statistical significance (P=0.142). Regrettably, data on the Apgar score, neonatal intensive care unit admissions, and perinatal mortality were not available. A recent meta-analysis by Grady et al15 showed that eSET babies were associated with decreased risks of preterm birth and low birth weight than those involving DET. Moreover, eSET singletons had a higher birth weight and lower preterm birth rate than DET singletons, which was postulated to be related to the vanishing twin.16 Our study failed to demonstrate the difference but this could be attributed to the small sample size.
 
Our study was limited by its retrospective nature and small sample size. Also, women having eSET were significantly younger than those having DET, which might lead to possible confounding. The younger mean age in the eSET group could explain the higher number of good-quality embryos available for transfer, which might have an impact on the cumulative pregnancy rate. The cumulative pregnancy rate was not always included as many women still had frozen embryos, but this would be an important aspect to look into in the future. Another bias was that women were allowed to choose between one or two embryos to transfer, instead of allocation by randomisation. Nonetheless, it reflected the actual situation in our centre. Blastocyst transfer is not routinely performed in out unit, because of the possible increased risk of congenital abnormalities and preterm labour,17 18 although the pregnancy and live birth rates of the fresh cycle may be higher than those following early cleavage stage transfer.19
 
The eSET policy is increasingly being applied and in a country like Belgium, the law requires eSET for all patients aged under 36 years during their first two IVF attempts.20 In Hong Kong, eSET is not imposed and suitable women were given the choice of eSET and DET with detailed counselling. From our data, only a third of the women chose eSET, which suggests that such women are still resistant to eSET. Child et al21 found that 41% of women having assisted reproductive technology were actually inclined to prefer a twin pregnancy, and some women waiting for IVF treatment viewed severe child disability outcomes more desirable than having no child at all.22 This barrier might be overcome by providing educational material to women so as to improve their knowledge on outcomes and risks of multiple pregnancies.23 The feasibility of eSET also relies on improving outcomes with cryopreserved embryos and the technique on vitrification. Information from the present study may also improve the uptake of eSET in the unit.
 
Our study confirms that when compared with DET, eSET can reduce the rate of multiple pregnancies without compromising the live birth rate in the fresh cycle. Elective SET should be offered to patients with a good prognosis and IVF centres should promote it, whenever appropriate, through provider and patient education.
 
Acknowledgements
The authors would like to thank Mr TM Cheung for data collection.
 
Declaration
No conflicts of interest were declared by the authors.
 
References
1. Pinborg A. IVF/ICSI twin pregnancies: risks and prevention. Hum Reprod Update 2005;11:575-93. CrossRef
2. Land JA, Evers JL. Risks and complications in assisted reproduction techniques: report of an ESHRE consensus meeting. Hum Reprod 2003;18:455-7. CrossRef
3. Council on Human Reproductive Technology, Hong Kong. Code of Practice on Reproductive Technology & Embryo Research. Available from: http://www.chrt.org.hk/english/service/service_cod.html. Accessed Apr 2013.
4. HFEA reduces maximum number of embryos transferred in single IVF treatment from three to two [press release]. Human Fertilisation and Embryology Authority; 2001 Aug 8.
5. Prevention of twin pregnancies after IVF/ICSI by single embryo transfer. ESHRE Campus Course Report. Hum Reprod 2001;16:790-800.
6. Cutting R, Morroll D, Roberts SA, Pickering S, Rutherford A; BFS and ACE. Elective single embryo transfer: guidelines for practice British Fertility Society and Association of Clinical Embryologists. Hum Fertil (Camb) 2008;11:131-46. CrossRef
7. McLernon DJ, Harrild K, Bergh C, et al. Clinical effectiveness of elective single versus double embryo transfer: meta-analysis of individual patient data from randomised trials. BMJ 2010;341:c6945. CrossRef
8. Pandian Z, Bhattacharya S, Ozturk O. Number of embryos for transfer following in vitro fertilization or intracytoplasmic sperm injection. Cochrane Database Syst Rev 2009:CD003416.
9. Ng EH, Yeung WS, Lau EY, So WW, Ho PC. High serum oestradiol levels in fresh IVF cycles do not impair implantation and pregnancy rates in subsequent FET cycles. Hum Reprod 2000;15:250-5. CrossRef
10. Van der Hoorn ML, Helmerhorst F, Claas F, Scherjon S. Dizygotic twin pregnancy after transfer of one embryo. Fertil Steril 2011;95:805.e1-3.
11. Gremeau AS, Brugnon F, Bouraoui Z, Pekrishvili R, Janny L, Pouly JL. Outcome and feasibility of elective single embryo transfer (eSET) policy for the first and second IVF/ICSI attempts. Eur J Obstet Gynecol Reprod Biol 2012;160:45-50. CrossRef
12. Fauque P, Jouannet P, Davy C, et al. Cumulative results including obstetrical and neonatal outcome of fresh and frozen-thawed cycles in elective single versus double fresh embryo transfers. Fertil Steril 2010;94:927-35. CrossRef
13. Thurin A, Hausken J, Hillensjo T, et al. Elective single-embryo transfer versus double-embryo transfer in in vitro fertilization. N Engl J Med 2004;351:2392-402. CrossRef
14. Council on Human Reproductive Technology, Hong Kong. Reports and statistics. CHRT website: www.chrt.org.hk/english/publications/publications_rep.html. Accessed Apr 2013.
15. Grady R, Alavi N, Vale R, et al. Elective single embryo transfer and perinatal outcomes: a systematic review and meta-analysis. Fertil Steril 2012;97:324-31. CrossRef
16. De Sutter P, Delbaere I, Gerris J, et al. Birthweight of singletons after assisted reproduction is higher after single- than after double-embryo transfer. Hum Reprod 2006;21:2633-7. CrossRef
17. Källén B, Finnström O, Lindam A, Nilsson E, Nygren KG, Olausson PO. Blastocyst versus cleavage stage transfer in in vitro fertilization: differences in neonatal outcome? Fertil Steril 2010;94:1680-3. CrossRef
18. Dar S, Librach CL, Gunby J, et al. Increased risk of preterm birth in singleton pregnancies after blastocyst versus Day 3 embryo transfer: Canadian ART Register (CARTR) analysis. Hum Reprod 2013;28:924-8. CrossRef
19. Glujovsky D, Blake D, Farquhar C, Bardach A. Cleavage stage versus blastocyst stag embryo transfer in assisted reproductive technology. Cochrane Database Syst Rev 2012;7:CD002118.
20. Debrock S, Spiessens C, Meuleman C, et al. New Belgian legislation regarding the limitation of transferable embryos in in vitro fertilization cycles does not significantly influence the pregnancy rate but reduces the multiple pregnancy rate in a threefold way in the Leuven University Fertility Center. Fertil Steril 2005;83:1572-4. CrossRef
21. Child TJ, Henderson AM, Tan SL. The desire for multiple pregnancy in male and female infertility patients. Hum Reprod 2004;19:558-61. CrossRef
22. Scotland GS, McNamee P, Peddie VL, Bhattacharya S. Safety versus success in elective single embryo transfer: women’s preferences for outcomes of in vitro fertilization. BJOG 2007;114:977-83. CrossRef
23. Hope N, Rombauts L. Can an educational DVD improve the acceptability of elective single embryo transfer? A randomized controlled study. Fertil Steril 2010;94:489-95. CrossRef

Ultrasound-guided plugged percutaneous biopsy of solid organs in patients with bleeding tendencies

Hong Kong Med J 2014;20:107–12 | Number 2, April 2014 | Epub 22 Jul 2013
DOI: 10.12809/hkmj133972
© Hong Kong Academy of Medicine. CC BY-NC-ND 4.0
 
ORIGINAL ARTICLE
Ultrasound-guided plugged percutaneous biopsy of solid organs in patients with bleeding tendencies
WK Tsang, MB, ChB, FRCR1; WH Luk, FRCR, FHKAM (Radiology)2; Adrian XN Lo, FRCR, FHKAM (Radiology)2
1 Department of Radiology and Nuclear Medicine, Tuen Mun Hospital, Tuen Mun, Hong Kong
2 Department of Radiology and Organ Imaging, United Christian Hospital, Kwun Tong, Hong Kong
 
Corresponding author: Dr WK Tsang (tsang_k@yahoo.com.hk)
Abstract
Objective: To establish and verify the utility of plugging biopsy tracts, using a combination of Gelfoam slurry and torpedo in the prevention of post-biopsy bleeding in patients at high risk of post-procedure haemorrhage following ultrasound-guided percutaneous biopsy of solid organs.
 
Design: Case series.
 
Setting: Radiology Department of a regional hospital in Hong Kong.
 
Patients: In our unit, all patients considered to be at high risk of post-biopsy haemorrhage of a solid organ underwent ultrasound-guided plugged percutaneous biopsy from year 2005 to 2012.
 
Interventions: All the included patients had undergone real-time ultrasound-guided biopsy of solid organs (liver in 10 and spleen in one patient). In all cases, a combination of a coaxial introducer needle and Temno needle were used. After adequate specimens were obtained, Gelfoam slurry (for distal embolisation) followed by Gelfoam torpedo (for proximal embolisation) were used to plug the biopsy tract.
 
Main outcome measures: Technical success, any post-biopsy haemorrhage treated by transfusion or other intervention, and plugging-related complications were reviewed for each patient.
 
Results: Technical success was achieved in all patients and none experienced post-biopsy haemorrhage treated by blood transfusion or any other intervention.
 
Conclusion: Plugging of the biopsy tract with Gelfoam slurry followed by Gelfoam torpedo is a direct and simple procedure that can safely and effectively prevent haemorrhage in patients at high risk of post-biopsy haemorrhage.
 
 
New knowledge added by this study
  • Plugging of the biopsy tract using a combination of Gelfoam slurry followed by Gelfoam torpedo is a new technique that has not been previously described.
Implications for clinical practice or policy
  • Plugging of the biopsy tract using a combination of Gelfoam slurry and torpedo is safe and easy to undertake and should be used in patients at high risk of post-biopsy haemorrhage.
 
Introduction
Ultrasound-guided percutaneous biopsy is a well-established means for diagnosis of focal or diffuse disease in solid organs. It is generally safe and confers minimal risk of complications. However, it is contra-indicated in patients with bleeding tendencies, which means that histological diagnosis may be lacking and sometimes life-saving treatment cannot be commenced. Plugging of the biopsy tract is a promising technique to decrease the risk of post-biopsy haemorrhage, for which Gelfoam is the most commonly used agent. In this article, we share our experience in performing this procedure using Gelfoam slurry followed by Gelfoam torpedo in patients at high risk of post-procedure haemorrhage in our institution.
 
Methods
The Department of Radiology and Organ Imaging, United Christian Hospital, is the main radiology training centre of the Kowloon East Cluster, Hong Kong. Apart from diagnostic imaging, we provide both emergency and elective interventional radiology services. In the form of a retrospective study approved by our local ethics committee, since 2005, it has been our standard practice to plug the biopsy tract in all patients considered at risk of haemorrhage after having ultrasound-guided percutaneous biopsy of a solid organ. Our departmental registry recorded all the cases receiving plugged percutaneous biopsy (PPB) of solid organs performed from 1 January 2005 to 30 September 2012. There was no reported refusal of the procedure by any patient. Demographic data, indication for the biopsy and for plugging of the biopsy tract, details of the biopsy technique, biopsy results, and any episodes of post-biopsy haemorrhage treated by transfusion or any other type of intervention were reviewed for each patient. Relevant details are listed in Table 1.
 

Table 1. Details of patient demographic data, indication for plugged biopsy, biopsy site and technique, and pathological results
 
Technique
All PPBs were performed under strict aseptic conditions with instruments as shown in Figure 1. A biopsy path avoiding critical structures and major vessels was selected under ultrasound guidance. The length of the biopsy path starting from the organ capsule to the target region was measured (Fig 2a). A strip of Gelfoam of the same length and with a width of approximately 2 mm was cut from a sheet of Gelfoam. Before being cut, the sheet of Gelfoam was compressed manually to expel all air bubbles. A Gelfoam torpedo was formed by rolling the strip of Gelfoam into a rod-like structure (Fig 2b). The remaining Gelfoam sheet was then cut into tiny pledgets of around 2 mm x 2 mm in size. A syringe filled with Gelfoam pledgets and another syringe filled with saline were both connected to a 3-way stopcock. Macerating the suspension with two syringes and a 3-way stopcock allowed further decreases in size of the pledgets into a slurry (Fig 2c). After the Gelfoam torpedo and slurry were ready, the puncture site was injected with local anaesthetic (5-10 mL of 1-2% lignocaine) and a small skin incision was created. Patients were then instructed to hold their breath while a coaxial introducer needle (17G or 19G, CareFusion; Waukegan [IL], US) was advanced to the target region. The stylet of the coaxial introducer needle was removed, with the outer sheath held firmly in place. A Temno biopsy needle (18G or 20G, CareFusion) was then inserted through the sheath under ultrasound guidance. Biopsy specimens were obtained in a standard manner. After removal of the Temno needle between passes, the stylet of the coaxial introducer needle was reinserted into the sheath to decrease the chance of haemorrhage. After adequate specimens were obtained by inspection, 1 to 2 mL of Gelfoam slurry was injected into the sheath of the coaxial introducer needle (Fig 3). The Gelfoam torpedo was then placed at the hub of the sheath of the coaxial introducer needle (Fig 4a) and pushed by the stylet until the echogenic tip of the stylet was advanced to the organ capsule (Fig 4b). The outer sheath was then withdrawn while keeping the stylet still (Fig 4c), so that the Gelfoam torpedo could be deployed along it and therefore sealing the biopsy tract. Finally, the entire coaxial introducer needle was removed.
 

Figure 1. Instruments needed in plugged percutaneous biopsy
 

Figure 2. (a) The length of the biopsy path starting from the organ capsule to the target region is measured on ultrasonography. (b) A strip of Gelform of the same length with a width of 2 mm is cut from a sheet of Gelfoam. It is then rolled into a rod-like structure (torpedo). (c) Macerating the suspension of Gelfoam with two syringes and a 3-way stopcock allows further decrease in size of the pledgets
 

Figure 3. After adequate specimens are taken, 1-2 mL of Gelfoam slurry is injected to the sheath of coaxial introducer needle
 

Figure 4. (a) Gelfoam torpedo (arrow) is placed at the hub of the coaxial introducer needle. (b) Gelfoam torpedo is then pushed by the stylet of the coaxial introducer needle (arrowheads). (c) The outer sheath of the coaxial introducer needle is withdrawn with the stylet stays still so that the Gelfoam torpedo can be deployed and seals the biopsy tract
 
Results
During a 7-year period, we performed 11 cases of plugged percutaneous solid organ biopsy in 11 patients, all of whom were considered at high risk of post-biopsy bleeding due to the reasons listed in Table 1. The mean patient age was 58 (standard deviation [SD], 14) years. Three patients were male and eight were female. The target organ was the liver in 10 cases and the spleen in one. The indications for biopsy were to achieve a diagnosis of a focal mass in five cases, and characterisation of diffuse hepatic diseases in six (Table 1). The number of needle passes ranged from one to four, with a mean of 2.5 (SD, 0.9). In all cases, the combination of a coaxial introducer needle and Temno needle (both by CareFusion) were used. The combination of a 17G coaxial introducer needle and 18G Temno needle was used in eight biopsies, while the combination of a 19G coaxial introducer needle and 20G Temno needle was used thrice. All the biopsies were technically successful in obtaining adequate specimens for a histological diagnosis. None of the patients experienced post-biopsy haemorrhage treated by transfusion or any other form of intervention.
 
Discussion
Ultrasound-guided percutaneous solid organ biopsy is a well-established means of diagnosing focal or diffuse disease in solid organs. In general, it is safe and confers minimal risk of complications. Major and minor complication (mainly bleeding) rates of 0.8% and 2-3.8%, respectively, have been reported.1 2 Many factors increase the risk of post-biopsy haemorrhage, which can be divided into lesional, technical, and patient-related. Lesional factors consist of peripheral subcapsular location, close proximity to major vessels, hypervascularity, and hypervascular biopsy sites (such as the spleen). Technical factors include increased numbers of needle passes, large needle sizes, use of cutting needles, blind biopsies, and less-experienced operators.3 Patient factors include coagulopathy, platelet dysfunction or thrombocytopenia, medications (eg antiplatelet agents and anticoagulants), chronic liver disease, haematological malignancy, presence of moderate-to- severe ascites, and uncooperative patients.2 4 5 Some studies showed that peripheral blood coagulation indices have a poor correlation with liver bleeding time following laparoscopic biopsy, which might be caused by low regional platelet counts, clotting factor deficiencies in the liver parenchyma, and the lack of mechanical compression of the biopsy tract by inelastic tissue (eg cirrhotic liver).6 Therefore operators should always be prepared for the possibility of significant post-biopsy haemorrhage, even in patients with normal clotting profiles and platelet counts.
 
Obviously, the main contra-indication to image-guided percutaneous solid organ biopsy is a bleeding diathesis.2 However, histological diagnosis is critical and even lifesaving, by means of achieving correct treatment. In the past, transjugular liver biopsy had been advocated in patients with bleeding diathesis, massive ascites, and poor respiratory control.7 8 However, this has multiple disadvantages. In particular, it is not feasible for liver lesions far from the major hepatic veins. Moreover, it is technically demanding and associated with a high rate of insufficient specimen retrieval for satisfactory histological examination (11.2-29%).7 9 10 11 12 It can also give rise to complications at the puncture site (jugular vein) and induce arrhythmias during right atrial passage. Haemoperitoneum is possible if the liver capsule is perforated, which can sometimes be fatal.
 
Plugged percutaneous biopsy is an alternative to transjugular liver biopsy in patients at high risk of bleeding.2 8 13 It was first described by Riley et al in 1984.13 In plugged biopsy, the tract is embolised (plugged) after the percutaneous biopsy, thus decreasing the risk of haemorrhage. Multiple studies on PPB have demonstrated at least a 95% success rate in obtaining adequate specimens for histological diagnoses. It is also a safe procedure with a complication rate of less than 2% (Table 27 8 9 14 15 16). It has the obvious advantages of being direct and can be used to biopsy focal hepatic lesions away from major hepatic veins and in other organs. Also, a larger biopsy needle can be used, which increases the chance of obtaining adequate specimens. Finally, it does not involve the vascular system or passage through the right atrium and thus the relevant complications can be avoided.
 

Table 2. Comparison of the results of various plugged biopsy studies
 
The most commonly used embolic agent is Gelfoam, which is an absorbable compressed gelatin sponge prepared from purified porcine skin.3 7 It is capable of absorbing up to 45 times its weight of whole blood, and induces haemostasis by speeding up thrombus formation and providing structural support for the clot. Gelfoam is a temporary embolic agent, which is usually completely absorbed within a few days or weeks, depending on the amount used, the degree of saturation with blood, and the application site. It is widely used in tract plugging as it is relatively inexpensive and readily available. It is easy to use and can be prepared in different forms, depending on the site of application. In our centre, Gelfoam was prepared in the form of torpedo and slurry. The Gelfoam torpedo was made from tight rolling of a small strip and used at the site of active bleeding. Due to their larger size, Gelfoam torpedoes can remain at the site of deployment instead of being flushed away by blood. The drawback of the torpedo is that distal embolisation cannot be achieved. In contrast, Gelfoam slurry is suitable for distal embolisation. It can be prepared by mixing tiny Gelfoam pledgets with contrast or saline. Further decrease in size of the pledgets can be created by macerating the suspension with two syringes and a 3-way stopcock. The syringe should be held nose up as Gelfoam floats in fluid. The disadvantage of slurry is that it is difficult to deploy at sites of active bleeding, as the suspension can be flushed away by blood. In our centre, we injected Gelfoam slurry first for distal embolisation and then filled up the rest of the biopsy tract with a torpedo. To the best of our knowledge, plugging of the biopsy tract using a combination of Gelfoam slurry followed by Gelfoam torpedo is a new technique that has not been previously described. Gelfoam is safe to use most of the time, although there is a minute risk of non-targeted embolisation of the biliary or vascular systems and of becoming a nidus for microbial growth.3
 
Apart from plugging of the biopsy tract, there are other measures to decrease the risk of bleeding in patients undergoing solid organ biopsy. First, as appropriate, we should try to correct any coagulopathy by administration of fresh frozen plasma, platelets, coagulation factors, and vitamin K, whilst also withholding antiplatelet or anticoagulant medications if at all feasible. Although not related to the bleeding risk, red cell or whole blood transfusion should be given before the biopsy to significantly anaemic patients. Next, careful planning of the method of biopsy is important. A safe biopsy path not traversing vessels or critical structures should be sought. Leaving adequate distance of normal parenchyma from the organ capsule and the biopsy site can also help mechanical compression of the biopsy tract by virtue of tissue elasticity, after the needle is removed. We have to strike a balance between the tissue yield and the use of smaller needles. The use of a coaxial system allows multiple needle passes with just a single puncture. Reducing ascites, if present with diuretics or paracentesis, can also decrease the risk of haemorrhage.
 
One limitation of our study was the small sample size. Second, it was a retrospective observational study without a control group. A large-scale prospective randomised controlled study may be ideal to validate the efficacy and safety of PPB. We share our experience in this small-scale study to raise the awareness of this procedure (especially for those not specialised in interventional radiology), as it shows that PPB is a simple and safe method with a high technical success rate that can help prevent post-biopsy haemorrhage.
 
Conclusion
Plugging of the biopsy tract with Gelfoam slurry followed by a Gelfoam torpedo is a direct, simple, safe, and effective means of preventing haemorrhage in patients at high risk of post-biopsy haemorrhage.
 
References
1. Hatfield MK, Beres RA, Sane SS, Zaleski GX. Percutaneous imaging-guided solid organ core needle biopsy: coaxial versus non coaxial method. AJR Am J Roentgenol 2008;190:413-7. CrossRef
2. Albeniz Arbizu E, Lopez San Roman A, Garcia Gonzalez M, et al. Fibrin-glue sealed liver biopsy in patients with a liver transplantation or in liver transplantation waiting list: preliminary results. Transplant Proc 2003;35:1911-2. CrossRef
3. Azar N, Delman T, Nakamoto D. Transcutaneous management of bleeding after solid organ biopsy what the radiologist needs to know and use. US Radiology 2011;3:53-6.
4. Chuah SY. Liver biopsy-past, present and future. Singapore Med J 1996;37:86-90.
5. Sherlock S, Dick R, Van Leeuwen DJ. Liver biopsy today. The Royal Free Hospital Experience. J Hepatol 1984;1:75-85. CrossRef
6. Ewe K. Bleeding after liver biopsy does not correlate with indices of peripheral coagulation. Dig Dis Sci 1981;26:388-93. CrossRef
7. Zins M, Vilgrain V, Gayno S, et al. US-guided percutaneous liver biopsy with plugging of the needle track: a prospective study in 72 high-risk patients. Radiology 1992;184:841-3.
8. Atar E, Ben Ari Z, Bachar GN, et al. A comparison of transjugular and plugged-percutaneous liver biopsy in patients with contraindications to ordinary percutaneous liver biopsy and an "in-house" protocol for selecting the procedure of choice. Cardiovasc Intervent Radiol 2010;33:560-4. CrossRef
9. Kamphuisen PW, Wiersma TG, Mulder CJ, de Vries RA. Plugged-percutaneous liver biopsy in patients with impaired coagulation and ascites. Pathophysiol Haemost Thromb 2002;32:190-3. CrossRef
10. Lebrec D, Goldfarb G, Degott C, Rueff B, Benhamou JP. Transvenous liver biopsy: an experience based on 1000 hepatic tissue samplings with this procedure. Gastroenterology 1982;83:338-40.
11. Velt PM, Choy OG, Shimkin PM, Link RJ. Transjugular liver biopsy in high-risk patients with hepatic disease. Radiology 1984;153:91-3.
12. Wolska-Krawczyk M, Krawczyk M, Katoh M, et al. Liver fibrosis: how many samples in transjugular liver biopsy are sufficient? Histological vs. clinical value. Abdom Imaging 2013;38:461-4. CrossRef
13. Riley SA, Ellis WR, Irving HC, Lintott DJ, Axon AT, Losowsky MS. Percutaneous liver biopsy with plugging of needle track: a safe method for use in patients with impaired coagulation. Lancet 1984;2:436. CrossRef
14. Tobin MV, Gilmore IT. Plugged liver biopsy in patients with impaired coagulation. Dig Dis Sci 1989;34:13-5. CrossRef
15. Sawyerr AM, McCormick PA, Tennyson GS, et al. A comparison of transjugular and plugged-percutaneous liver biopsy in patients with impaired coagulation. J Hepatol 1993;17:81-5. CrossRef
16. Smith TP, McDermott VG, Ayoub DM, Suhocki PV, Stackhouse DJ. Percutaneous transhepatic liver biopsy with tract embolization. Radiology 1996;198:769-74.

Uterine compression sutures for management of severe postpartum haemorrhage: five-year audit

Hong Kong Med J 2014;20:113–20 | Number 2, April 2014 | Epub 21 Oct 2013
DOI: 10.12809/hkmj134023
© Hong Kong Academy of Medicine. CC BY-NC-ND 4.0
 
ORIGINAL ARTICLE
Uterine compression sutures for management of severe postpartum haemorrhage: five-year audit
Victoria YK Chai, MB, BS, MRCOG; William WK To, MD, FRCOG
Department of Obstetrics and Gynaecology, United Christian Hospital, Kwun Tong, Hong Kong
 
Corresponding author: Dr WWK To (towkw@ha.org.hk)
Abstract
Objectives: To audit the use of compression sutures for the management of massive postpartum haemorrhage and compare outcomes to those documented in the literature.
 
Design: Retrospective study.
 
Setting: A regional obstetric unit in Hong Kong.
 
Patients: Patients with severe postpartum haemorrhage encountered over a 5-year period from January 2008 to December 2012, in which compression sutures were used for management.
 
Main outcome measures: Successful management with prevention of hysterectomy.
 
Results: In all, 35 patients with massive postpartum haemorrhage with failed medical treatment, for whom compression sutures were used in the management, were identified. The overall success rate for the use of B-Lynch compression sutures alone to prevent hysterectomy was 23/35 (66%), and the success rate of compression sutures in conjunction with other surgical procedures was 26/35 (74%). This reported success rate appeared lower than that reported in the literature.
 
Conclusion: Uterine compression was an effective method for the management of massive postpartum haemorrhage in approximately 70% of cases, and could be used in conjunction with other interventions to increase its success rate in terms of avoiding hysterectomy.
 
 
New knowledge added by this study
  • Compression sutures are effective in the management of postpartum haemorrhage arising from uterine atony as well as placenta praevia.
  • In an unselected case series audit in a regional obstetric training unit, the efficacy of uterine compression sutures appeared to be lower than that reported in the literature.
Implications for clinical practice or policy
  • Uterine compression sutures should be adopted as part of the management of severe postpartum haemorrhage in local obstetric units. Contingent treatment protocols for further interventions should be available if compression sutures fail.
 
Introduction
Postpartum haemorrhage (PPH) is a serious and life-threatening obstetric complication. It is usually defined as an estimated blood loss of more than 500 mL after delivery and occurs in around 5% of all deliveries.1 As increased maternal morbidity and morbidity are associated with further blood loss, alternative definitions for severe PPH, such as estimated blood loss exceeding 1000 mL, are commonly used in various guidelines.2 Conventionally, the first-line treatment options for PPH include conservative management with uterotonic drugs (oxytocin or prostaglandins), while second-line therapy includes uterine packing, external compression with uterine sutures, selective devascularisation by ligation, or embolisation of the uterine artery.3 4 5 6 7 These various treatment modalities have been included as an integral part of the HEMOSTASIS management algorithm widely advocated in the UK.8 The use of such measures should reduce the need for hysterectomy, which is associated with further blood loss and additional morbidity.9
 
The B-Lynch suture has been the most wellestablished compression suture technique since reporting of the first published series in 1997, and described oversewing of the uterus with a continuous suture to apply ongoing compression.4 Since then, the technique has been adopted for control of bleeding in severe PPH due to uterine atony as well as placenta praevia/accreta.10 11 Modifications of the original technique, as well as various other suturing techniques, have since been advocated.5 12 13 14 The current case series described the use of compression sutures in the management of massive PPH that failed to respond to medical therapy over a review period of 60 months encountered in a single obstetric training and service unit of the Hong Kong Hospital Authority. The compression suture techniques employed in this series were the basic B-Lynch or the slightly modified Bhal technique.15 Various associated prognostic factors were assessed and compared to evaluate whether they could predict success or failure.
 
Methods
A retrospective review of all patients having a severe PPH over a 60-month period (January 2008 to December 2012 inclusive) was performed, based on details logged in a comprehensive obstetric database currently used in all Hospital Authority obstetric units. Specific codings for “primary PPH”, “compression sutures of uterus”, “caesarean section with hysterectomy”, and “peripartum hysterectomy” were searched for and identified from the clinical management system of the hospital. Cases of severe PPH with blood loss exceeding 1 L were also identified from the Labour Ward registry. The case notes or operative records of each of these patients were also reviewed to verify whether management entailed use of compression suturing techniques. All identified cases where compression sutures had been used or their use attempted were then reviewed in detail for the mode of delivery, intrapartum complications, cause of the PPH, sequence of treatment modalities used, estimated total blood loss, any complications resulting from the different manoeuvres, and clinical outcome.
 
The application of the B-Lynch suture was in accordance with the original description with the hysterectomy wound still open, using either Monocryl or Vicryl No.1 sutures in accordance with the surgeon’s preference. In some cases, two separate sutures were applied instead of one continuous suture as described by Bhal et al.15 All patients had an indwelling Foley catheter to monitor urine output, and broad-spectrum antibiotics were used for prophylaxis. All patients who had severe haemorrhage treated by intra-operative transfusions and all who had evidence of coagulopathy were admitted to the intensive care unit after their operation.
 
Results
There were a total of 26 029 deliveries over the review period. The point prevalence of primary PPH with estimated blood loss exceeding 500 mL was 3.2% (n=825), and that exceeding 1 L (severe PPH) was 105/26 029 (0.4%). Among the latter, 33 had vaginal delivery and 72 caesarean sections; 25 of these patients were managed by medical treatment alone. Regarding the remaining 80 patients with severe PPH, their management is shown in the Figure.
 

Figure. Summary of secondary procedures for severe postpartum haemorrhage (PPH) after failed medical treatment and hysterectomy rates
 
Within this study period, there were 24 peripartum hysterectomies, of which nine involved attempted use of compression sutures and were included in this case series. The other 15 cases included the 10 who had an a priori hysterectomy (6 for placenta praevia/accreta, 4 for intractable uterine atony) without resort to other more conservative procedures, two for uterine atony with failed treatment following radiological uterine arterial embolisation, and three who had hysterectomy when attempted intrauterine balloon tamponade failed to control the bleeding. Cases that did not entail recourse to uterine compression sutures were not analysed any further.
 
All the identified cases of PPH that involved the use of compression sutures had failed initial medical management with oxytoxics, including bolus syntometrine, syntocinon bolus or infusion, intramuscular carboprost injections, and in nine cases, additional intramyometrial carboprost injections. The most common aetiology of PPH was uterine atony (28/35), followed by major placenta praevia (7/35), and the total estimated intra-operative blood losses of 1000 to 9300 mL. Approximately 80% (28/35) of the patients were deemed to require intra-operative blood product transfusion, and disseminated intravascular coagulopathy was documented in at least 13 (37%) of them. In one patient (No. 3), attempted Bhal sutures failed to arrest the bleeding from uterine atony, and subtotal hysterectomy was performed. She had a stump haematoma and massive stump bleeding 3 days later, for which the cervical stump was removed. The bladder was perforated and despite immediate repair at operation, she subsequently developed a vesico-vaginal fistula that was surgically repaired 2 months after the hysterectomy. This was the only patient in our series with major organ trauma. There was no maternal mortality (Table: left, right).
 

Table. Clinical data and variables in patients with use of compression sutures (cases are listed in chronological order)
 
One patient (No. 16) had a normal vaginal delivery followed by massive PPH despite oxytoxics. Examination under anaesthesia was performed, and vaginal tears were repaired. Laparotomy and B-Lynch sutures were applied because of concurrent uterine atony, but hysterectomy was finally performed. This patient had the highest estimated blood loss (9.3 L) in our case series and was the only one given Factor VIIa for coagulopathy management.
 
Compression sutures were attempted together with intrauterine balloon tamponade in five cases. In one patient (No. 5) with uterine atony after caesarean section for twin pregnancy, abdominal placement of a Bakri balloon (for tamponade) was attempted but failed to arrest the bleeding. The balloon was removed and compression sutures were applied but to no avail, and so a hysterectomy was performed. In another patient with uterine atony following caesarean section for fetal distress (No. 29), when balloon tamponade failed to arrest bleeding, an attempt to add on B-Lynch sutures in the form of a “sandwich”16 led to puncturing of the balloon, and so a hysterectomy was performed. In two others with uterine atony after caesarean section, abdominal placement of a Bakri balloon failed to control bleeding, but a B-Lynch suture was effective (Nos. 25 and 26). In a third patient (No. 27) with major placenta praevia, B-Lynch sutures failed to arrest haemorrhage. The sutures were therefore removed and a Bakri balloon inserted via the hysterotomy wound, and successfully controlled bleeding into the lower uterine placental bed.
 
In two patients with uterine atony after caesarean section (Nos. 14 and 17), continuous bleeding from the vagina was observed after application of B-Lynch sutures, and thus ligation of the internal iliac arteries/uterine arteries was performed with effective outcome. In a third patient (No. 34), internal iliac artery ligation failed to control the haemorrhage, and so a hysterectomy was performed. Four other patients (Nos. 2, 6, 13, and 35) failed to have their bleeding controlled by compression sutures and underwent hysterectomies.
 
Thus, in our series the overall success rate of compression sutures alone as the primary second-line (n=21) or rescue procedure (n=2) to prevent hysterectomy was 23/35 (66%). The success rate of compression sutures in conjunction with other second-line procedures (two with iliac artery ligation and one with intrauterine balloon tamponade) was 26/35 (74%). Specifically, when the aetiology of the PPH was taken into consideration, the success rate for B-Lynch compression sutures in patients with uterine atony was 17/28 (61%) and that for placenta praevia cases it was 6/7 (86%). The Bhal suture was used in four cases only (Nos. 3, 13, 22, and 32) and its success rate of 50% was not statistically significantly different from that of B-Lynch sutures.
 
Particular putative patient risk factors that could reliably predict the success of compression sutures as a means of avoiding hysterectomy included age, parity, mode of delivery, operator experience, aetiology of the PPH, and the extent of blood loss at that time. Based on a multivariate stepwise regression analysis, no significant risk factors for the success of compression sutures could be identified in the current data set.
 
Discussion
In this series, we were able to avoid hysterectomy with the use of uterine compression sutures, either alone or in combination with other surgical interventions, in only around 70% of patients with severe PPH. This success rate was lower than that reported in many other reported case series.4 5 11 12 13 14 17 18 19 20 21
 
The first description of uterine compression sutures was published in 1996 as a single case report from Zurich,22 which was followed by the famous report of five consecutive cases utilising the B-Lynch suture in 1997.4 Various modifications of the B-Lynch suture, and various other compression suture techniques have been reported since then. In 2000, Cho et al13 described a haemostatic multiple square suture to approximate the anterior and posterior uterine wall. In 2002, Hayman et al5 proposed a uterine compression suture that involved two vertical apposition sutures together with two transverse horizontal cervico-isthmic sutures. In 2005, Hwu et al14 described the use of two parallel vertical compression sutures placed in the lower segment to control bleeding from placenta praevia. These sutures compressed the anterior and posterior uterine wall without penetrating the full thickness of the posterior wall. Another modification was the Pereira suture reported in 2005, which consisted of longitudinal and transverse sutures applied with superficial intramyometrial bites only.17 In the current case series, the only modification to the B-Lynch suture utilised was the Bhal technique.15 This entailed two sutures instead of one, with the knots tied in the anterior-inferior margin of the lower uterine segment, without any difference in the compression effects compared to the original B-Lynch suture. It can be seen that the principle, namely, compression of the uterine body, remains basically the same for all types of compression sutures. The main differences being the figure at which the suture is applied, the numbers of longitudinal and/or transverse sutures used, and whether or not the uterine cavity is penetrated.23
 
In the literature, some series have described compression sutures solely used for placenta praevia/accreta,11 14 18 24 while others detailed their use exclusively for atonic uteruses,19 20 and still others referred to application of the technique to all aetiologies.4 21 Apart from compressing the uterine body in uterine atony, the original paper on the B-Lynch suture also advocated its use for placenta praevia. It was proposed that the sutures would exert longitudinal compression and achieve evenly distributed tension over the uterus, including the lower segment.25 In addition, for cases of major placenta praevia, B-Lynch also described the use of additional independent figure-of-eight sutures placed either anteriorly, posteriorly, or both on the lower segment prior to suture application.4 Our results from this series confirm the effectiveness of the B-Lynch suture for patients with uterine atony and placenta praevia.
 
Very high success rates with compression sutures, usually in the range of 90﹪ to 100%, have been reported since the first paper by B-Lynch in 1997.4 However, many of these reports had very small sample sizes (single case reports or cohorts of 15-20 patients).13 26 In recent years, larger case series started to be reported. One of the largest published series described experience from India, and reported a success rate of 94% (45 out of 48 patients) using Hayman sutures for PPH due to uterine atony.19 That series did not include cases with placenta praevia/ accreta.19 Another interesting case series consisted of a single surgeon’s experience in Argentina over a 20-year period, and involved 539 cases of excessive obstetric bleeding from a variety of causes, including uterine atony, placenta praevia/accreta, cervical scar pregnancies as well as uterine/vaginal/cervical tears.21 Various surgical methods (often in combination) were utilised to treat these cases, and the overall success rate in those having the B-Lynch suture was 94% (81/86), while for Hayman sutures, Cho sutures, and Pereira sutures, the rates were 92% (34/37), 100% (37/37), and 100% (11/11), respectively.21 The very high success rates reported in this personal series could be ascribed to excellent surgical skills, optimal patient selection, and choice of procedures by a super-specialist, but may be difficult to reproduce elsewhere.
 
An earlier systematic review published in 2007 reported a success rate for uterine compression sutures ranging from 68﹪ to 100% with an overall success rate of 92%.6 Another review in 2010 compared success rates of 95﹪ to 100% with eight different types of compression sutures.27 However, both reviews were based on case series with relatively small patient numbers, which might indicate a reporting bias and probably exaggerated the proportions with positive outcomes. Interestingly, another review published in 2010 that focused on the long-term complications of compression sutures and attempted to sum outcomes with B-Lynch sutures from 32 separate case series.23 This reported an overall hysterectomy (failure) rate of 70/174 (40%), which was higher than most individual case series.23
 
In this series, the mode of delivery was vaginal in only one case (3%), the rest being delivered by caesarean section (97%). This was likely due to a bias in case selection in our practice. In patients with severe PPH not delivered by caesarean section, compression sutures were probably not the first-choice surgical treatment due to consideration for laparotomy and opening a hysterotomy wound. Apparently, methods such as balloon tamponade28 were more common and convenient. The original intrauterine Bakri balloon was designed to control bleeding in patients with PPH caused by low-lying placenta praevia/accreta.29 It could be inserted easily and rapidly, without the need for laparotomy, and under minimal anaesthesia. It can also be used as a ‘tamponade test’ to aid decisions regarding proceeding to laparotomy.3 Of the 27 cases of severe PPH with balloon tamponade as the first- or second-line procedure within our review period (Fig), 10 (37%) had vaginal delivery. Our experience with the use of balloon tamponade has recently been published in another case series.30
 
We were unable to identify any reliable factors that would predict the success or failure of compression sutures in this case series, possibly due to the small size of our sample. Nor could we offer any coherent hypothesis to explain our lower success rate compared with that reported in the literature. As an obstetric specialist is available on-site in our hospital 24 hours a day, specialist involvement was initiated promptly in the management of all our cases. The 35 compression suture procedures were performed by a total of eight surgeons with very similar training and experiences in compression suture techniques. They all used a relatively standard technique with standard suture materials, and with standard anaesthetic and transfusion support in accordance with our hospital protocol. As compression sutures placed for prophylactic purposes were not included in this cohort, and all sutures were applied only in the presence of severe PPH, the unselected nature of our cases could have contributed to the lower success rate. We believe that a success rate of around 70% would likely reflect the practical experience in a general regional obstetric training unit locally.
 
Major complications of B-Lynch and other compression sutures have been repeatedly described in the literature. Cases of uterine necrosis presenting several weeks post-delivery finally culminating in total or subtotal hysterectomy have been reported.31 32 Uterine necrosis was apparently the result of ischaemia produced by compression sutures. Haematometra might present with amenorrhoea33 and pyometria coupled with abdominal pain and fever, weeks or months postpartum.34 The occurrence of uterine cavity synechiae causing uterine outflow obstruction has also been reported after compression sutures, though infrequently.35 The combination of compression sutures and additional vessel ligation appeared more likely to cause complications such as ischaemia and inflammation, but so far no deaths have been reported in association with compression sutures.23
 
Apart from compression suture and balloon tamponade techniques, various fertility-preserving methods had been employed for patients with PPH, including pelvic devascularisation and radiological arterial embolisation. Pelvic devascularisation includes ligation of uterine artery and internal iliac artery, but such techniques require surgical expertise to apply and may be time-consuming. Complications such as broad-ligament haematoma, peripheral nerve ischaemia, and inadvertent ligation of the lower limb arteries have been reported.36 37 Radiological embolisation of the uterine artery warrants facilities and expertise in interventional radiology, which may not be readily available in some obstetric units. In addition, in cases of massive ongoing PPH, it may be difficult to transfer patients to such radiological facilities. Infrequently, complications such as ischaemia of the bladder and uterus have also been reported.38 A systematic review estimated a success (avoidance of hysterectomy) rate of around 92% with uterine compression sutures, 91% after arterial embolisation, 84% after balloon tamponade, and 85% after iliac artery ligation or uterine devascularisation.6 Randomised controlled trials of these treatment options would be difficult to perform in such life-threatening emergencies. To date, there is no good evidence to suggest that one method is superior to another. As illustrated in several of the cases in our series, the sequential or concomitant use of these different interventions may help to increase the success rate. The patient’s condition, cause of the PPH, expertise of the surgeon, and facilities available should all be considered when choosing the most suitable treatment option.
 
Conclusion
In our experience, the use of compression sutures for the management of massive PPH was effective in preventing hysterectomy in around two thirds of the cases. In this unselected cohort of patients with severe PPH, our success rate appeared to be lower than that reported in the literature. Other contingent protocols should be available, should compression sutures fail to control the haemorrhage. The combined or sequential use of compression sutures with other treatment modalities, such as balloon tamponade, pelvic devascularisation or radiological embolisation, may help to increase the success rate, and should be explored further.
 
References
1. American College of Obstetricians and Gynecologists. ACOG Practice Bulletin. Clinical Management Guidelines for Obstetricians-Gynecologists. Number 76, October 2006: postpartum hemorrhage. Obstet Gynecol 2006;108:1039-47.
2. Chandraharan E, Arulkumaran S. Surgical aspects of postpartum haemorrhage. Best Pract Res Clin Obstet Gynaecol 2008;22:1089-102. CrossRef
3. Condous GS, Arulkumaran S. Medical and conservative surgical management of postpartum hemorrhage. J Obstet Gynaecol Can 2003;25:931-6.
4. B-Lynch C, Coker A, Lawal AH, Abu J, Cowen MJ. The B-Lynch surgical technique for the control of massive postpartum haemorrhage: an alternative to hysterectomy? Five cases reported. Br J Obstet Gynaecol 1997;104:372-5. CrossRef
5. Hayman RG, Arulkumaran S, Steer PJ. Uterine compression sutures: surgical management of postpartum hemorrhage. Obstet Gynecol 2002;99:502-6. CrossRef
6. Doumouchtsis SK, Papageorghiou AT, Arulkumaran S. Systematic review of conservative management of postpartum hemorrhage: what to do when medical treatment fails. Obstet Gynecol Surv 2007;62:540-7. CrossRef
7. Royal College of Obstetricians and Gynaecologists. RCOG Green-top guideline No 52. Prevention and management of postpartum haemorrhage; May 2009.
8. Varatharajan L, Chandraharan E, Sutton J, Lowe V, Arulkumaran S. Outcome of management of massive postpartum haemorrhage using the algorithm "HEMOSTASIS". Int J Gynecol Obstet 2011;113:152-4. CrossRef
9. Knight M; UKOSS. Peripartum hysterectomy in the UK: management and outcomes of the associated haemorrhage. BJOG 2007;114:1380-7. CrossRef
10. Allam MS, B-Lynch C. The B-Lynch and other uterine compression suture techniques. Int J Gynaecol Obstet 2005;89:236-41. CrossRef
11. Arduini M, Epicoco G, Clerici G, Bottaccioli E, Arena S, Affronti G. B-Lynch suture, intrauterine balloon, and endouterine hemostatic suture for the management of postpartum hemorrhage due to placenta previa accreta. Int J Gynaecol Obstet 2010;108:191-3. CrossRef
12. Ghezzi F, Cromi A, Uccella S, Raio L, Bolis P, Surbek D. The Hayman technique: a simple method to treat postpartum haemorrhage. BJOG 2007;114:362-5. CrossRef
13. Cho JH, Jun HS, Lee CN. Hemostatic suturing technique for uterine bleeding during cesarean delivery. Obstet Gynecol 2000;96:129-31. CrossRef
14. Hwu YM, Chen CP, Chen HS, Su TH. Parallel vertical compression sutures: a technique to control bleeding from placenta praevia or accreta during caesarean section. BJOG 2005;112:1420-3. CrossRef
15. Bhal K, Bhal N. Mulik V, Shankar L. The uterine compression suture—a valuable approach to control major haemorrhage at lower segment caesarean section. J Obstet Gynaecol 2005;25:10-4. CrossRef
16. Nelson WL, O'Brien JM. The uterine sandwich for persistent uterine atony: combining the B-Lynch compression suture and an intrauterine Bakri balloon. Am J Obstet Gynecol 2007;196:e9-10. CrossRef
17. Pereira A, Nunes F, Pedroso S, Saraiva J, Retto H, Meirinho M. Compressive uterine sutures to treat postpartum bleeding secondary to uterine atony. Obstet Gynecol 2005;106:569-72. CrossRef
18. Shazly SA, Badee AY, Ali MK. The use of multiple 8 compression suturing as a novel procedure to preserve fertility in patients with placenta accreta: case series. Aust NZ J Obstet Gynaecol 2012;52:395-9. CrossRef
19. Nanda S, Singhal SR. Hayman uterine compression stitch for arresting atonic postpartum hemorrhage: 5 years experience. Taiwan J Obstet Gynecol 2011;50:179-81. CrossRef
20. Zheng J, Xiong X, Ma Q, Zhang X, Li M. A new uterine compression suture for postpartum haemorrhage with atony. BJOG 2011;118:370-4. CrossRef
21. Palacios-Jaraquemada JM. Efficacy of surgical techniques to control obstetric haemorrhage: analysis of 539 cases. Acta Obstet Gynecol Scand 2011;90:1036-42. CrossRef
22. Schnarwyler B, Passweg D, von Castelberg B. Successful treatment of drug refractory uterine atony by fundal compression sutures [in German]. Geburtshilfe Frauenheilkd 1996;56:151-3. CrossRef
23. Fotopoulou C, Dudenhausen JW. Uterine compression sutures for preserving fertility in severe postpartum haemorrhage: an overview 13 years after the first description. J Obstet Gynaecol 2010;30:339-49. CrossRef
24. Makino S, Tanaka T, Yorifuji T, Koshiishi T, Sugimura M, Takeda S. Double vertical compression sutures: a novel conservative approach to managing post-partum haemorrhage due to placenta praevia and atonic bleeding. Aust NZ J Obstet Gynaecol 2012;52:290-2. CrossRef
25. B-Lynch C. Partial ischemic necrosis of the uterus following a uterine brace compression suture. BJOG 2005;112:126-7. CrossRef
26. Quahba J, Piketty M, Huel C, et al. Uterine compression sutures for postpartum bleeding with uterine atony. BJOG 2007;114:619-22. CrossRef
27. Mallappa Saroja CS, Nankani A, El-Hamamy E. Uterine compression sutures, an update: review of efficacy, safety and complications of B-Lynch suture and other uterine compression techniques for postpartum haemorrhage. Arch Gynecol Obstet 2010;281:581-8. CrossRef
28. Georgiou C. Balloon tamponade in the management of postpartum haemorrhage: a review. BJOG 2009;116:748-57. CrossRef
29. Bakri YN, Amri A, Abdul Jabbar F. Tamponade-balloon for obstetrical bleeding. Int J Gynaecol Obstet 2001;74:139-42. CrossRef
30. Kong MC, To WW. Balloon tamponade for postpartum haemorrhage: case series and literature review. Hong Kong Med J 2013;19:484-90.
31. Treloar EJ, Anderson RS, Andrews HS, Bailey JL. Uterine necrosis following B-Lynch suture for primary postpartum haemorrhage. BJOG 2006;113:486-8. CrossRef
32. Joshi VM, Shrivastava M. Partial ischemic necrosis of the uterus following a uterine brace compression suture. BJOG 2004;111:279-80. CrossRef
33. Dadhwal V, Sumana G, Mittal S. Hematometra following uterine compression sutures. Int J Gynaecol Obstet 2007;99:255-6. CrossRef
34. Ochoa M, Allaire AD, Stitely ML. Pyometria after hemostatic square suture technique. Obstet Gynecol 2002;99:506-9. CrossRef
35. Wu HH, Yeh GP. Uterine cavity synechiae after hemostatic square suturing technique. Obstet Gynecol 2005;105:1176-8. CrossRef
36. O'Leary JA. Uterine artery ligation in the control of postcesarean hemorrhage. J Reprod Med 1995;40:189-93.
37. Shin RK, Stecker MM, Imbesi SG. Peripheral nerve ischaemia after internal iliac artery ligation. J Neurol Neurosurg Psychiatry 2001;70:411-2. CrossRef
38. Porcu G, Roger V, Jacquier A, et al. Uterus and bladder necrosis after uterine artery embolisation for postpartum haemorrhage. BJOG 2005;112:122-3. CrossRef

Pages