Treatment of early rectal tumours by transanal endoscopic microsurgery in Hong Kong: prospective study

ABSTRACT

Hong Kong Med J 2004;10:239-43 | Number 4, August 2004
ORIGINAL ARTICLE
Treatment of early rectal tumours by transanal endoscopic microsurgery in Hong Kong: prospective study
WCS Meng, PYY Lau, AWC Yip
Department of Surgery, Kwong Wah Hospital, 25 Waterloo Road, Kowloon, Hong Kong
 
 
OBJECTIVE. To summarise the results of transanal endoscopic microsurgery for the treatment of rectal villous adenoma and early rectal tumours.
 
DESIGN. Prospective study.
 
SETTING. Regional hospital, Hong Kong.
 
PATIENTS. Consecutive patients between November 1995 and January 2003.
 
INTERVENTION. Transanal endoscopic microsurgery.
 
MAIN OUTCOME MEASURES. Intra-operative morbidity and mortality, complication rate, operating time, postoperative morbidity and mortality, recurrence rate and correlation between preoperative ultrasonography staging and postoperative pathological staging.
 
RESULTS. Thirty-two patients with rectal villous adenoma and early rectal carcinoma were registered, 31 of whom (14 men and 17 women) were included in the study. The median tumour size was 2.5 (range, 1-8) cm and the median operating time was 95 (45-220) minutes. The median follow-up period was 23 (2-92) months, and there was no local recurrence. There was no operation-related mortality and the resection margins were all clear. Complications included temporary flatus incontinence (n=2), acute retention of urine (n=1), exacerbation of chronic obstructive airway disease (n=1), and secondary haemorrhage in a patient on aspirin.
 
CONCLUSIONS. Transanal endoscopic microsurgery is a safe procedure and can achieve good local tumour control. It is ideal in the management of rectal villous adenomas at stages pT0 and pTis. Its application is now extended to the treatment of early rectal carcinoma at stage pT1 with curative intent. For tumours at stage pT2 or later, it can also serve as a good option for local palliation.
 
Key words: Adenoma; Microsurgery; Proctoscopy; Rectal neoplasms; Treatment outcome
 
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Chronic benign neutropenia among Chinese children

ABSTRACT

Hong Kong Med J 2004;10:231-6 | Number 4, August 2004
ORIGINAL ARTICLE
Chronic benign neutropenia among Chinese children
BHY Chung, GCF Chan, TL Lee, JSY Kwok, AKS Chiang, HK Ho, SY Ha, YL Lau
Department of Paediatrics and Adolescent Medicine,The University of Hong Kong, Queen Mary Hospital, Pokfulam Road, Hong Kong
 
 
OBJECTIVE. To delineate the clinical behaviour of chronic benign neutropenia in Chinese children in Hong Kong.
 
DESIGN. Retrospective study.
 
SETTING. University teaching hospital, Hong Kong.
 
PATIENTS. All infants and children with absolute neutrophil count of 1.5 x 109 /L or lower for more than 3 months.
 
MAIN OUTCOME MEASURES. Development of significant infection, and achievement of remission.
 
RESULTS. Twenty-four children with chronic benign neutropenia were identified between 1992 and 2001. Their median age of diagnosis was 9 months. The mean (standard deviation) initial absolute neutrophil count was 0.28 x 109 /L (0.24 x 109 /L). Twenty-three patients presented with infection. Of the 19 patients tested, four (21%) were positive for anti-neutrophil antibodies. Bone marrow examination was performed in 17 patients: nine had normal results, but six showed evidence of peripheral consumption, one showed late maturation arrest at band stage, and one showed phagocytosis of myeloid cells by histiocytes. The overall hospitalised infection rate was 51.6 episodes per 1000 patient months. Ten percent of cases were considered ‘significant’ infections and required hospital admission with either surgical intervention or intravenous therapy (antibiotics or fluid replacement). In the first year of diagnosis, more than 80% of patients had their lowest absolute neutrophil count (mean, 0.16 x 109 /L; standard deviation, 0.11 x 109 /L). Granulocyte-colony stimulating factor was used to treat three patients and induced transient elevation of absolute neutrophil count in all three. The projected remission rate was 55.4% at 3 years. Even for those with persistent disease, there was significant recovery in absolute neutrophil count to a mean of 0.5 x 109 /L (P<0.01).
 
CONCLUSIONS. Patients with chronic benign neutropenia experienced a relatively benign clinical course regardless of their remission status. Only a small proportion of patients developed significant infections. A multi-centre prospective study may help identify predictive factors of remission.
 
Key words: Autoimmune diseases; Chinese; Immunoglobulins; Neutropenia
 
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Wireless capsule endoscopy in Chinese patients with suspected small bowel diseases

ABSTRACT

Hong Kong Med J 2004;10:179-83 | Number 3, June 2004
ORIGINAL ARTICLE
Wireless capsule endoscopy in Chinese patients with suspected small bowel diseases
WK Leung, SSL Fung, MY Wong, JJY Sung
Endoscopy Centre, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
OBJECTIVE. To evaluate the use of wireless capsule endoscopy in Chinese patients.
 
DESIGN. Retrospective analysis.
 
SETTING. University teaching hospital, Hong Kong.
 
PATIENTS. Twenty-eight patients who had undergone wireless capsule endoscopy between December 2002 and December 2003.
 
MAIN OUTCOME MEASURES. Diagnoses according to findings of capsule endoscopy and complications from the procedure.
 
RESULTS. The mean age of the 28 patients (15 men and 13 women) was 60.0 (standard deviation, 18.3) years. The indications for capsule endoscopy were obscure gastro-intestinal bleeding (n=16), unexplained iron-deficiency anaemia (n=9), and recurrent abdominal pain (n=3). Half of the patients had abnormal endoscopy findings that may account for their presenting symptoms. The most common abnormality was angioectasia of the small bowel. Small bowel ulcers and erosions were also noted in three patients with obscure bleeding. In contrast, none of the patients with recurrent abdominal pain had abnormal capsule endoscopy. No complications arose from the procedure.
 
CONCLUSIONS. Wireless capsule endoscopy is a safe and useful mode of investigation for the diagnosis of obscure gastro-intestinal bleeding in Chinese patients.
 
Key words: Chinese; Endoscopy, gastrointestinal; Equipment design; Gastrointestinal hemorrhage
 
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Reliability of Hong Kong Chinese version of the Patient-rated Forearm
Evaluation Questionnaire for lateral epicondylitis

ABSTRACT

Hong Kong Med J 2004;10:172-7 | Number 3, June 2004
ORIGINAL ARTICLE
Reliability of Hong Kong Chinese version of the Patient-rated Forearm Evaluation Questionnaire for lateral epicondylitis
HB Leung, CH Yen, PYT Tse
Department of Orthopaedics and Traumatology, Kwong Wah Hospital, Waterloo Road, Kowloon, Hong Kong
 
 
OBJECTIVE. To determine the reliability and validity of a dedicated assessment tool for lateral epicondylitis after translation into Hong Kong Chinese.
 
DESIGN. Cross-sectional study.
 
SETTING. District hospital, Hong Kong.
 
PATIENTS. Seventy-four patients, 12 of whom were bilingual, were recruited (total of 82 elbows).
 
MAIN OUTCOME MEASURES. Translation equivalence and reliability were measured with the test-retest method. Validity was measured against the Roles and Maudsley outcome score and mean maximal grip strength.
 
RESULT. The Patient-rated Forearm Evaluation Questionnaire had high English-Chinese equivalence (Spearman’s rho correlation coefficient=0.926; P<0.001). It was also very reliable (intraclass correlation coefficient=0.99; P<0.001). Validity according to the Roles and Maudsley outcome score and mean of maximal grip strength was significant (P<0.01).
 
CONCLUSION. The Hong Kong Chinese version of Patient-rated Forearm Evaluation Questionnaire is a reliable and valid assessment tool for chronic lateral epicondylitis. Its equivalence to the original English version makes outcome assessment across cultural barrier feasible.
 
Key words: Outcome assessment; Questionnaires; Tennis elbow
 
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Use of an electronic barcode system for patient identification during blood transfusion: 3-year experience in a regional hospital

ABSTRACT

Hong Kong Med J 2004;10:166-71 | Number 3, June 2004
ORIGINAL ARTICLE
Use of an electronic barcode system for patient identification during blood transfusion: 3-year experience in a regional hospital
JCW Chan, RW Chu, BWY Young, F Chan, CC Chow, WC Pang, C Chan, SH Yeung, PK Chow, J Lau, PMK Leung
Department of Medicine, Pamela Youde Nethersole Eastern Hospital, 3 Lok Man Road, Chai Wan, Hong Kong
 
 
OBJECTIVE. To evaluate the use of an electronic barcode system for patient identification during blood transfusion.
 
DESIGN. Retrospective study.
 
SETTING. Regional hospital, Hong Kong.
 
PATIENTS. For all patients requiring blood transfusion between May 1999 and April 2002, with the exception of patients in the psychiatric wards and the accident and emergency department, a portable, hand-held scan-and-print electronic device was used to verify and document patients’ identity at two critical points of transfusion: blood sampling for the compatibility test and blood administration.
 
MAIN OUTCOME MEASURES. Scope of use of the electronic device, cost, effectiveness, staff compliance, problems and solution for improvement.
 
RESULTS. In the first 3 years of hospital-wide use of the new device, no incidents of blood transfusion to wrong patients, or wrong labelling of blood samples, occurred with 41 000 blood sampling procedures and administration of 27 000 units of blood. Blood sampling took 6 minutes to complete with the use of the electronic device—similar to that taken by the conventional second-checker system. Among hospital staff, the compliance rate of using the new device approached 90%. Battery problems occurred in 12% of episodes of use of the device.
 
CONCLUSIONS. The electronic barcode system was effective in reducing human error related to bedside transfusion procedures. The future goal is to tailor-make a more efficient device with additional functions.
 
Key words: Blood transfusion; Patient identification systems
 
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Pain and disability in a group of Chinese elderly out-patients in Hong Kong

ABSTRACT

Hong Kong Med J 2004;10:160-5 | Number 3, June 2004
ORIGINAL ARTICLE
Pain and disability in a group of Chinese elderly out-patients in Hong Kong
DKY Miu, TY Chan, MH Chan
Department of Medicine and Geriatrics, Kwong Wah Hospital, 25 Waterloo Road, Hong Kong
 
 
OBJECTIVE. To investigate the relationship between musculoskeletal pain and disability among a group of geriatric out-patients.
 
DESIGN. Consecutive case series.
 
SETTING. Regional hospital, Hong Kong.
 
PARTICIPANTS. Attendees at a geriatric specialist out-patient clinic from October 2002 to February 2003.
 
MAIN OUTCOME MEASURES. Pain duration, location, intensity, and frequency; use of analgesics; ability to identify the cause of pain; disability (Barthel index) and Lawton Instrumental Activities of Daily Living scale score; depressive symptoms (Geriatric Depression Scale score); and self-reported sleep quality.
 
RESULTS. Of the 749 respondents, 461 (61.5%) had experienced pain in the previous 2 weeks. Among these patients, 51.3% had received a pain-relieving drug. Compared with men, women reported a higher pain intensity (5.87 versus 5.26; P=0.001), had a lower Barthel index (96.0 versus 97.9; P=0.005), and had a lower score on the Lawton Instrumental Activities of Daily Living scale (42.19 versus 44.52; P=0.008). Multivariate logistic regression showed that the presence of pain was associated with female sex (odds ratio=2.25), poor self-rated health (0.69), and depression (1.54).
 
CONCLUSION. Pain is a common problem among the elderly population, but it is not associated with physical disability, and only half of the patients received analgesics. The study provides information for health care workers to develop strategies to better assess and manage pain problems among elderly people.
 
Key words: Aged; Disability evaluation; Musculoskeletal diseases; Pain; Sex factors
 
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Features predicting adverse outcomes of status epilepticus in childhood

ABSTRACT

Hong Kong Med J 2004;10:156-9 | Number 3, June 2004
ORIGINAL ARTICLE
Features predicting adverse outcomes of status epilepticus in childhood
KL Kwong, K Chang, SY Lam
Department of Paediatrics, Tuen Mun Hospital, Tuen Mun, Hong Kong
 
 
OBJECTIVE. To examine variables that might predict abnormal outcome of status epilepticus among children.
 
DESIGN. Retrospective study.
 
SETTING. Regional hospital, Hong Kong.
 
PATIENTS. All children younger than 15 years who were admitted to the paediatric intensive care unit with status epilepticus between 1997 and 2002.
 
MAIN OUTCOME MEASURES. Neurodevelopmental outcomes.
 
RESULTS. Two of the 25 patients died, resulting in a mortality rate of 8%. No deaths were due to status epilepticus itself. No patient with febrile or idiopathic status epilepticus developed epilepsy. Neurological deterioration was observed in a quarter (six of 23) of the survivors. Symptomatic aetiology (acute or remote) and refractory status epilepticus were associated with adverse outcomes (P<0.05). Young age at status epilepticus (<12 months) and duration of status epilepticus (>60 minutes) tended to be more frequent among those who developed adverse outcome. Rectal diazepam was given before hospital arrival in only four patients.
 
CONCLUSIONS. Paediatric patients with status epilepticus who had normal neurodevelopmental status before the onset of an attack and who did not sustain an acute insult to the central nervous system or have progressive encephalopathy, had favourable outcomes. Prompt use of rectal diazepam or buccal midazolam administered by caretakers or paramedics should be encouraged.
 
Key words: Child; Infant; Status epilepticus
 
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Out-patient chronic pain service in Hong Kong: prospective study

ABSTRACT

Hong Kong Med J 2004;10:150-5 | Number 3, June 2004
ORIGINAL ARTICLE
Out-patient chronic pain service in Hong Kong: prospective study
PP Chen, J Chen, T Gin, M Ma, KC Fung, KH Woo, PY Wong
Division of Pain Medicine, Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
OBJECTIVE. To examine the profile and referral pattern of patients attending an out-patient pain management service in Hong Kong.
 
DESIGN. Prospective cross-sectional survey.
 
SETTING. Regional public hospitals, Hong Kong.
 
PATIENTS. All patients attending out-patient pain management clinics in the New Territories East public hospitals between 1 September and 31 December 2002.
 
MAIN OUTCOME MEASURES. Demographic profiles, referring specialty, pain diagnosis, pain sites, duration and severity of pain, treatment modality, litigation, compensation, and social welfare status. Data were collected using a standardised questionnaire.
 
RESULTS. Two hundred and forty-eight patients were interviewed. Most patients (70%) were middle-aged, with 21% over 60 years. Seventy-nine percent of patients were referred to the clinics either from orthopaedic surgeons (64.1%), general and other surgeons (14.9%), or general practitioners (3.6%). The median (range) duration of pain was 2.3 (0.08-26.7) years. The most common pain diagnoses were musculoskeletal back pain (46.4%) and neuropathic pain (27.8%). A total of 11.3% of the patients had two pain diagnoses, while 40.7% complained of pain in more than one location. Pain in the limbs was the most frequent complaint followed by the head, neck, and back. Approximately 38% of patients had tried four or more treatment modalities. Oral medication was the most common method (86.7%) of pain-relief treatment. More than half of the patients had also tried physiotherapy and traditional Chinese medicine. Approximately 37% of the patients were unemployed, while 31% were receiving social security subsidy. Eighty-six patients had pain associated with a work-related injury, and of these patients, 80% were involved in compensation claims.
 
CONCLUSIONS. The profile of patients referred to the pain management clinics was complex. Patients were mainly referred from specialists. The economic implication in this group of patients is likely to be significant as many patients utilised multiple treatment modalities, were unemployed and on social welfare benefits, and were involved in compensation and litigation proceedings.
 
Key words: Health care surveys; Pain; Pain clinics
 
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Oseltamivir prophylaxis during the influenza season in a paediatric cancer centre: prospective observational study

ABSTRACT

Hong Kong Med J 2004;10:103-6 | Number 2, April 2004
ORIGINAL ARTICLE
Oseltamivir prophylaxis during the influenza season in a paediatric cancer centre: prospective observational study
KW Chik, CK Li, PKS Chan, MMK Shing, V Lee, JSL Tam, PMP Yuen
Department of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
OBJECTIVES. To determine the role of oseltamivir prophylaxis for immunocompromised patients.
 
DESIGN. Prospective, non-blinded, non-controlled observational study.
 
SETTING. A paediatric cancer centre, Hong Kong.
 
PARTICIPANTS. Thirty-two patients, immunocompromised by chemotherapy or bone marrow transplantation during an influenza season in 2001.
 
INTERVENTION. Oral oseltamivir prophylaxis 75 mg/d for 8 weeks.
 
MAIN OUTCOME MEASURES. Laboratory-confirmed influenza infection, symptoms of influenza, drug compliance, and any side-effects from oseltamivir treatment. Laboratory monitoring included virological surveillance for influenza A and B, blood counts, and renal and liver function tests.
 
RESULTS. Patients' median age was 14.3 years (range, 6.3-23.4 years). Underlying conditions included malignancy (n=29) and other haematological diseases (n=3). No documented influenza infection according to serological tests was present throughout the study period. Five patients with symptoms of upper respiratory tract infection did not have any influenza infection detected by rapid virological assay and viral culture. For 16% of patients, the main side-effect in the study was gastro-intestinal upset.
 
CONCLUSIONS. Oral oseltamivir 75 mg once daily for 8 weeks may be useful in the prevention of influenza infection in patients immunocompromised by chemoradiotherapy; side-effects are few and acceptable.
 
Key words: Acetamides; Antiviral agents; Influenza; Neuraminidase/antagonists & inhibitors
 
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Precipitating factors for systolic and diastolic heart failure: a four-year follow-up of 192 patients

ABSTRACT

Hong Kong Med J 2004;10:97-101 | Number 2, April 2004
ORIGINAL ARTICLE
Precipitating factors for systolic and diastolic heart failure: a four-year follow-up of 192 patients
O Erk
Department of Emergency Medicine, Istanbul Faculty of Medicine, Istanbul University, Istanbul 34390, Turkey
 
 
OBJECTIVES. To investigate precipitating factors for systolic and diastolic heart failure.
 
DESIGN. Prospective study.
 
PATIENTS AND METHODS. The study population consisted of 192 patients with heart failure treated for 536 episodes of acute decompensation of heart failure from 1998 to 2002. The patients were classified as having systolic or diastolic heart failure, and grouped according to aetiology and precipitating factors.
 
RESULTS. Coronary heart disease was the most common cause of systolic heart failure, whereas rheumatic heart disease was the most frequent cause of diastolic heart failure. The most important precipitating factors in systolic heart failure were infections (38%), arrhythmias (35%), and vascular causes (24%), whereas the precipitating factors in diastolic heart failure were infections (50%), arrhythmias (46%), and uncontrolled hypertension (26%). Avoidable precipitating factors in systolic and diastolic heart failure were noted in 34% and 68% of cases, respectively.
 
CONCLUSIONS. Better patient education and better follow-up of patients by physicians according to the most recent guidelines may decrease the frequency of heart failure events and consequent morbidity and mortality.
 
Key words: Heart failure, congestive; Precipitating factors; Ventricular dysfunction, left; Ventricular dysfunction, right
 
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