Effect of adding a Chinese herbal preparation to acupuncture for seasonal allergic rhinitis: randomised double-blind controlled trial

ABSTRACT

Hong Kong Med J 2003;9:427-34 | Number 6, December 2003
ORIGINAL ARTICLE
Effect of adding a Chinese herbal preparation to acupuncture for seasonal allergic rhinitis: randomised double-blind controlled trial
CCL Xue, FCK Thien, JJS zhang, W Yang, C Da Costa, CG Li
RMIT Chinese Medicine Research Group, RMIT University, Bundoora West Campus, Bundoora, Victoria 3083, Australia
 
 
OBJECTIVE. To assess whether the addition of a Chinese herbal medicine formula to acupuncture affects the severity of symptoms and quality-of-life scores among patients with seasonal allergic rhinitis.
 
DESIGN. Randomised double-blind placebo-controlled trial.
 
SETTING. University teaching and research clinic, Australia.
 
PARTICIPANTS. Sixty-five patients with seasonal allergic rhinitis, who were recruited through public media.
 
INTERVENTION. Between July and December 1999, patients received acupuncture twice a week for 8 weeks plus either a Chinese herbal drug formula (n=33) or placebo (n=32) at a dosage of four capsules, three times daily.
 
MAIN OUTCOME MEASURES. The severity of nasal and non-nasal symptoms on a five-point scale, as assessed by both patients and an ear, nose, and throat specialist, and quality-of-life scores as measured by the Rhinoconjunctivitis and Rhinitis Quality of Life Questionnaire.
 
RESULTS. Sixty-one patients completed the study (31 in the intervention group and 30 in the control group). After 8 weeks, no significant difference was found between the two groups in the severity of nasal and non-nasal symptoms and in the Rhinoconjunctivitis and Rhinitis Quality of Life Questionnaire scores. Intention-to-treat analysis of categorical variables showed moderate-to-marked improvement rates of 72.7% and 81.2% for intervention and control groups, respectively. Six patients reported mild adverse events––three from each of the study groups.
 
CONCLUSION. The Chinese herbal formulation under investigation did not provide additional symptomatic relief or improvement in quality-of-life scores among patients with seasonal allergic rhinitis who were receiving acupuncture.
 
Key words: Acupuncture; Clinical trials; Hay fever; Medicine, traditinal; Treatment outcome
 
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Suicide in Hong Kong: epidemiological profile and burden analysis, 1981 to 2001

ABSTRACT

Hong Kong Med J 2003;9:419-26 | Number 6, December 2003
ORIGINAL ARTICLE
Suicide in Hong Kong: epidemiological profile and burden analysis, 1981 to 2001
PSF Yip, CK Law, YW Law
The Hong Kong Jockey Club Centre for Suicide Research and Prevention, The University of Hong Kong, Pokfulam, Hong Kong
 
 
OBJECTIVE. To describe changes of the epidemiological profile of suicides in Hong Kong, and the burden of suicides in terms of years of life lost between 1981 and 2001.
 
DESIGN. Retrospective study.
 
SETTING. Hong Kong.
 
PARTICIPANTS. Data on registered deaths of the Hong Kong population from 1981 to 2001 were retrieved from records of the Census and Statistics Department of the Government of the Hong Kong Special Administrative Region.
 
MAIN OUTCOME MEASURES. Crude, standardised, age- and sex-standardised suicide rates; years of life lost; suicide method used; and rank among leading causes of death.
 
RESULTS. Suicide ranked sixth in the leading cause of deaths and represented about 3% of all deaths each year. The suicide rate has increased from 9.6 per 100 000 to 15 per 100 000 between 1981 and 2001. The total years of life lost due to suicide increased by 96.0%, from about 9900 years in 1981 to 19 400 years in 2001, whereas the figure for all causes of death decreased by 14.0%, from 274 600 years to 236 700 years. The total share of years of life lost attributable to suicide deaths has increased from 3.6% to 8.1% and is still increasing, especially among in the middle age-groups (30-59 years). The use of charcoal burning as a suicide method has increased from 6.0% before 1998 to more than 28.0% in 2001.
 
CONCLUSION. The burden on the years of life lost due to suicide is underestimated and overlooked. The increase of suicides in recent years has had a significant impact on the years of life lost and can be used as a useful indicator of performance in Hong Kong.
 
Key words: Hong Kong; Suicide
 
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Penicillin and vancomycin tolerance among clinical isolates of Streptococcus pneumoniae in Hong Kong

ABSTRACT

Hong Kong Med J 2003;9:415-8 | Number 6, December 2003
ORIGINAL ARTICLE
Penicillin and vancomycin tolerance among clinical isolates of Streptococcus pneumoniae in Hong Kong
MV Boost, WM Ko, M O'donoghue
School of Nursing, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong
 
 
OBJECTIVE. To determine the prevalence of penicillin and vancomycin tolerance in clinical isolates of Streptococcus pneumoniae.
 
DESIGN. Laboratory testing of 50 consecutive clinical isolates.
 
SETTING. District hospital, Hong Kong.
 
PATIENTS. Fifty patients with pneumonia or meningitis who were admitted to a district hospital in Hong Kong between August and October 2002.
 
MAIN OUTCOME MEASURES. Lysis, as assessed by loss of optical density at 4 hours at 540 nm, and reduction in viable count expressed as the log of the number killed ('log kill') after exposure of cultures to 10 times the minimum inhibitory concentration of penicillin and vancomycin.
 
RESULTS. Of the 50 isolates, five (10%) were tolerant to penicillin and one (2%) was tolerant to vancomycin.
 
CONCLUSION. This is the first report of vancomycin tolerance in Streptococcus pneumoniae in Hong Kong. Because vancomycin tolerance is associated with clinical failure in the treatment of pneumococcal meningitis, increased monitoring for resistant strains of organisms is suggested.
 
Key words: Streptococcus pneumoniae; Drug tolerance; Vancomycin
 
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Status of obstetric epidural analgesia services in Hong Kong public hospitals: postal questionnaire survey

ABSTRACT

Hong Kong Med J 2003;9:407-14 | Number 6, December 2003
ORIGINAL ARTICLE
Status of obstetric epidural analgesia services in Hong Kong public hospitals: postal questionnaire survey
BB Lee, PP Chen, WD Ngan
Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
OBJECTIVE. To examine the status of obstetric epidural analgesia services in Hong Kong public hospitals in 2001, and to compare findings with those from a similar survey conducted in 1995.
 
DESIGN. Postal questionnaire survey.
 
SETTING. Hospital Authority hospitals in Hong Kong offering an obstetric and delivery service.
 
PARTICIPANTS. Chiefs of Service of departments of anaesthesia and coordinators of obstetric anaesthesia and analgesia service.
 
MAIN OUTCOME MEASURES. The availability of an obstetric epidural analgesia service, specialist staff allocation to the service, existence of clinical protocols, rate of epidural analgesia, techniques of epidural administration, obstetric outcome or mode of delivery, and the incidence of adverse events associated with the use of epidural analgesia.
 
RESULTS. Between 1 January and 31 December 2001, all eight Hospital Authority hospitals with an obstetric service provided epidural analgesia for labour pain relief, but only six (75%) offered a 24-hour service. A dedicated anaesthetist provided obstetric anaesthesia and analgesia during office hours in all units, but after hours in only three. This level of service provision compared favourably with that available in 1995, when only 82% of public maternity units provided epidural analgesia and only 36% offered a 24-hour service. The median epidural analgesia rate was 15% (range, 8%-20%) compared with 10% in 1995. The incidence of adverse events and complications was very low. Formal written protocols for the conduct of epidural analgesia for labour were used in six units. All units used mixtures of local anaesthetic combined with opioid, administered as intermittent boluses, continuous epidural infusion, or patient-controlled epidural analgesia.
 
CONCLUSIONS. Although there has been progress and improvement in the provision of obstetric epidural analgesia services in our public hospitals, the rate is still relatively low and the provision of services after hours is limited. Further progress will likely be hindered by current or future cutbacks in public hospital budgets.
 
Key words: Analgesia, epidural; Analgesia, obstetric; Health care survey; Hong Kong
 
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Treatment of severe acute respiratory syndrome with lopinavir/ritonavir: a multicentre retrospective matched cohort study

ABSTRACT

Hong Kong Med J 2003;9:399-406 | Number 6, December 2003
ORIGINAL ARTICLE
Treatment of severe acute respiratory syndrome with lopinavir/ritonavir: a multicentre retrospective matched cohort study
KS Chan, ST Lai, CM Chu, E Tsui, CY Tam, MML Wong, MW Tse, TL Que, JSM Peiris, J Sung, VCW Wong, KY Yuen
Department of Medicine and Geriatrics, United Christian Hospital, 130 Hip Wo Street, Kwun Tong, Hong Kong
 
 
OBJECTIVES. To investigate the possible benefits and adverse effects of the addition of lopinavir/ritonavir to a standard treatment protocol for the treatment of severe acute respiratory syndrome.
 
DESIGN. Retrospective matched cohort study. SETTING. Four acute regional hospitals in Hong Kong.
 
PATIENTS AND METHODS. Seventy-five patients with severe acute respiratory syndrome treated with lopinavir/ritonavir in addition to a standard treatment protocol adopted by the Hospital Authority were matched with controls retrieved from the Hospital Authority severe acute respiratory syndrome central database. Matching was done with respect to age, sex, the presence of co-morbidities, lactate dehydrogenase level and the use of pulse steroid therapy. The 75 patients treated with lopinavir/ritonavir were divided into two subgroups for analysis: lopinavir/ritonavir as initial treatment, and lopinavir/ritonavir as rescue therapy. These groups were compared with matched cohorts of 634 and 343 patients, respectively. Outcomes including overall death rate, oxygen desaturation, intubation rate, and use of pulse methylprednisolone were reviewed.
 
RESULTS. The addition of lopinavir/ritonavir as initial treatment was associated with a reduction in the overall death rate (2.3%) and intubation rate (0%), when compared with a matched cohort who received standard treatment (15.6% and 11.0% respectively, P<0.05) and a lower rate of use of methylprednisolone at a lower mean dose. The subgroup who had received lopinavir/ritonavir as rescue therapy, showed no difference in overall death rate and rates of oxygen desaturation and intubation compared with the matched cohort, and received a higher mean dose of methylprednisolone.
 
CONCLUSION. The addition of lopinavir/ritonavir to a standard treatment protocol as an initial treatment for severe acute respiratory syndrome appeared to be associated with improved clinical outcome. A randomised double-blind placebocontrolled trial is recommended during future epidemics to further evaluate this treatment.
 
Key words: Coronavirus; Protease inhibitors; SARS virus; Treatment outcome
 
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Sleeping energy expenditure in paediatric patients with obstructive sleep apnoea syndrome

ABSTRACT

Hong Kong Med J 2003;9:353-6 | Number 5, October 2003
ORIGINAL ARTICLE
Sleeping energy expenditure in paediatric patients with obstructive sleep apnoea syndrome
AM Li, J Yin, D Chan, S Hui, TF Fok
Department of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
OBJECTIVE. To investigate sleeping energy expenditure in paediatric patients with obstructive sleep apnoea syndrome.
 
DESIGN. Retrospective study.
 
SETTING. University teaching hospital, Hong Kong. PATIENTS AND METHODS. A retrospective analysis comparing sleeping energy expenditure in patients with confirmed obstructive sleep apnoea syndrome and control subjects matched for age, sex, and ideal weight for body height. Subjects were recruited from the Paediatric Chest Clinic and all had undergone overnight polysomnography and sleeping energy expenditure measurement by open-circuit indirect calorimetry using a metabolic cart and canopy system. The measurements were taken during slow-wave sleep.
 
RESULTS. Twenty-four cases with obstructive sleep apnoea syndrome (apnoea hypopnoea index >5) and 23 control subjects were studied. Mean age and ideal weight for body height were 9.4 (standard deviation, 3.9) years and 152.5% (27.2%), respectively. Mean sleeping energy expenditure corrected for body weight for the cases and the control group were 44.83 (standard deviation, 10.49) Kcal/day and 40.71 (10.60) Kcal/day, respectively. Sleeping energy expenditure was not found to be associated with the severity of obstructive sleep apnoea syndrome (r=0.34, P=0.27).
 
CONCLUSION. A trend towards greater sleeping energy expenditure was found in patients with obstructive sleep apnoea syndrome. Further studies on the metabolic aspects of this condition are required.
 
Key words: Energy expenditure; Sleep apnea, obstructive
 
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Clinical significance and management of cervical atypical glandular cells of undetermined significance

ABSTRACT

Hong Kong Med J 2003;9:346-51 | Number 5, October 2003
ORIGINAL ARTICLE
Clinical significance and management of cervical atypical glandular cells of undetermined significance
CW Chan, KB Cheung
Department of Obstetrics and Gynaecology, Tuen Mun Hospital, Tsing Chung Koon Road, Tuen Mun, Hong Kong
 
 
OBJECTIVES. To assess the clinical significance of a cervical cytological diagnosis of atypical glandular cells of undetermined significance and to formulate the most appropriate management guidelines for patients with such a diagnosis.
 
DESIGN. Retrospective study. SETTING. Regional hospital, Hong Kong.
 
PATIENTS. Seventy-two patients with diagnoses of atypical glandular cells of undetermined significance who were managed in a colposcopy clinic between January 1998 and December 1999.
 
MAIN OUTCOME MEASURES. Age, cytological diagnoses of atypical glandular cells of undetermined significance and its subtypes, method of evaluation, final diagnosis, and outcome after 2 years.
 
RESULTS. Atypical glandular cells of undetermined significance were diagnosed in 83 (0.4%) of 21 854 cervical smear samples taken during the 2-year study period. Follow-up data were available from 72 patients, whose mean age was 43 years (range, 22-69 years). Forty-three percent of these patients had significant diseases of the genital tract. Patients with the subtype diagnosis of atypical glandular cells of undetermined significance–favour neoplasia had the worst outcome, with 90% of patients having significant disease, followed by patients with atypical glandular cells of undetermined significance 'not otherwise specified' (43%), and atypical glandular cells of undetermined significancefavour reactive (8%).
 
CONCLUSION. Patients with atypical glandular cells of undetermined significance should be investigated early and thoroughly, because many of them will have premalignant or malignant disease.
 
Key words: Atypical glandular cell of undetermined significance; Vaginal smears
 
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Prognostic factors for successful outcome in patients undergoing controlled ovarian stimulation and intrauterine insemination

ABSTRACT

Hong Kong Med J 2003;9:341-5 | Number 5, October 2003
ORIGINAL ARTICLE
Prognostic factors for successful outcome in patients undergoing controlled ovarian stimulation and intrauterine insemination
G Makkar, EHY Ng, WSB Yeung, PC Ho
Department of Obstetrics and Gynaecology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
OBJECTIVE. To determine the prognostic factors associated with successful outcome following controlled ovarian stimulation and intrauterine insemination.
 
DESIGN. Retrospective analysis.
 
SETTING. University-based assisted reproductive technology centre, Hong Kong.
 
PATIENTS AND METHODS. Patients included 292 couples undergoing 600 treatment cycles, following a standard protocol of human menopausal gonadotrophin injections. Multiple logistic regression analysis was performed to determine which demographic and sperm parameters gave the maximum discrimination to predict pregnancy.
 
RESULTS. One hundred and eleven pregnancies resulted from treatment. The pregnancy rates were 18.5% per cycle and 37.9% per couple. The age of the women was significantly lower for pregnant cycles, and the serum oestradiol levels and number of follicles greater than 16 mm in diameter were significantly higher, compared with non-pregnant cycles. The sperm concentration and number of motile spermatozoa were also significantly increased in pregnant cycles. Pregnancy rate was significantly increased when the raw semen sample contained 20 million/mL or more spermatozoa, normal forms comprised 7% or more, and when the number of motile spermatozoa in inseminated samples was 1 million or greater.
 
CONCLUSION. Using multiple logistic regression analysis, age of the women and serum oestradiol level had the maximum power to predict pregnancy following ovarian stimulation and intrauterine insemination.
 
Key words: Insenmination; Ovarian stimulation; Prognosis; Semen
 
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Outcome analysis of intraventricular thrombolytic therapy for intraventricular haemorrhage

ABSTRACT

Hong Kong Med J 2003;9:335-40 | Number 5, October 2003
ORIGINAL ARTICLE
Outcome analysis of intraventricular thrombolytic therapy for intraventricular haemorrhage
MWY Lee, KY Pang, WWS Ho, CK Wong
Department of Neurosurgery, Pamela Youde Nethersole Eastern Hospital, 3 Lok Man Road, Chai Wan, Hong Kong
 
 
OBJECTIVES. To evaluate the outcome of intraventricular thrombolytic therapy for intraventricular haemorrhage and to formulate a safe and effective regimen.
 
DESIGN. Retrospective study.
 
SETTING. Regional neurosurgical centre, Hong Kong.
 
PATIENTS. Twenty-nine consecutive adult patients who presented from November 1995 to November 1998 with non-traumatic intraventricular haemorrhage (Graeb score, >=7) with no active rebleeding risks from vascular abnormalities.
 
INTERVENTIONS. Fourteen consecutive patients received intraventricular streptokinase via the external ventricular drainage, and 15 consecutive patients received intraventricular urokinase treatment.
 
MAIN OUTCOME MEASURES. Patient demographics, Glasgow coma scale score, Graeb score, mortality rate, shunt rate, fever response, infection rate, catheter blockage rate, and local and systemic bleeding tendency. RESULT. The mean age of the 16 men and 13 women was 59 years (range, 14-76 years). The median Graeb score for cases of intraventricular haemorrhage was 10 (range, 7-12). There was no significant difference in terms of the Graeb score distribution, total dosage, and duration of treatment between the streptokinase and urokinase groups. More cases of fever were observed in the streptokinase group, which could be due to its antigenicity. The infection rate of the central nervous system was 3%, and the shunt rate was 24%. The overall 1-month postoperative mortality was 10%, which was related to a low preoperative Glasgow coma scale score (<=4). No local rebleeding, systemic coagulopathy, or catheter blockage occurred.
 
CONCLUSIONS. Intraventricular thrombolytic therapy is a safe and effective method of managing intraventricular haemorrhage. We suggest instilling 20 000 units urokinase intra-operatively, followed by 20 000 units daily for about 3 days, except in cases of vascular abnormality, bleeding tendency, and trauma.
 
Key words: Cerebral ventricles; Drainage; Intracranial hemorrhages; Thrombolytic therapy; Tomography, X-ray computed
 
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Large-scale mercury exposure due to a cream cosmetic: community-wide case series

ABSTRACT

Hong Kong Med J 2003;9:329-34 | Number 5, October 2003
ORIGINAL ARTICLE
Large-scale mercury exposure due to a cream cosmetic: community-wide case series
KW Sin, HS Tsang
Disease Prevention and Control Division, Department of Health, 18/F, Wu Chung House, 213 Queen's Road East, Wanchai, Hong Kong
 
 
OBJECTIVE. To describe demographic characteristics, patterns of use, reported symptoms, and laboratory results associated with mercury exposure among people who used a beauty cream containing mercury.
 
DESIGN. Descriptive study of a case series.
 
SETTING. The Hong Kong community.
 
PARTICIPANTS. Users of a cream cosmetic who contacted the Department of Health following a public announcement.
 
MAIN OUTCOME MEASURES. Urine and blood mercury concentrations, cream mercury content, self-reported symptoms, duration of cream use, and duration since last cream use.
 
RESULTS. We interviewed 314 cream users, 99% of whom were women. The mean urine and blood mercury concentrations of 286 users, who submitted a urine or blood sample, were 45.2 µg/L (reference level, <20µg/L) and 17.1 µg/L (reference level, <10 µg/L), respectively; 65% of these participants had elevated mercury concentrations. The mercury content of the cream cosmetic ranged from 660 to 57 000 ppm. Seventy-eight percent of all cream users reported no symptoms, but absence of symptoms was not predictive of low urine and blood mercury concentrations. Urine mercury concentrations were significantly higher among people who last used the cream within 45 days. Blood mercury concentrations were elevated following cream use for as short as 2 days.
 
CONCLUSIONS. The majority of cream users had increased urine or blood mercury concentrations but remained asymptomatic, implying that the incidence of overt symptomatic mercury poisoning resulting from dermal application of creams with mercury content lower than 57 000 ppm is low. Doctors should take a history of the use of cosmetics if patients have clinical or laboratory evidence of mercury exposure; such cases should be reported to public health authorities.
 
Key words: Cosmetics/adverse effects; Female; Mercury poisoning
 
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