Management of carbon monoxide poisoning using oxygen therapy

ABSTRACT

Hong Kong Med J 2000;6:113-5 | Number 1, March 2000
CASE REPORT
Management of carbon monoxide poisoning using oxygen therapy
TWL Mak, CW Kam, JPS Lai, CMC Tang
Department of Clinical Pathology, Tuen Mun Hospital, Tsing Chung Koon Road, Tuen Mun, Hong Kong
 
 
The management of carbon monoxide poisoning requires an accurate assessment of the extent of blood oxygenation. Measuring the fractional oxyhaemoglobin content by using co-oximetry gives a true picture of the oxygen-carrying capacity of blood in the presence of carboxhaemoglobin. The use of readings from pulse oximetry or a standard blood gas analyser is insufficient and can be misleading. We report on a case of carbon monoxide poisoning to illustrate this potential pitfall.
 
Key words: Carbon monoxide poisoning, Oxyhemoglobins/analysis, Oximetry
 
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Emergence of Streptococcus pneumoniae with high-level resistance to cefotaxime in Hong Kong

ABSTRACT

Hong Kong Med J 1999;5:406-9 | Number 4, December 1999
CASE REPORT
Emergence of Streptococcus pneumoniae with high-level resistance to cefotaxime in Hong Kong
SSY Wong, PCY Woo, PL Ho, VCC Cheng, KY Yuen
Division of Infectious Diseases, Department of Microbiology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
We report on two cases of pneumococcal infection caused by strains demonstrating high-level cefotaxime resistance (minimal inhibitory concentration, 4 microg/mL). One patient had acute community-acquired meningitis with bacteraemia and the other had bacteraemia probably as a result of nosocomial pneumonia. Both patients died despite treatment with third generation cephalosporins. This is the first report from Hong Kong of infection with Streptococcus pneumoniae with high-level cefotaxime resistance that resulted in death. The emergence of high-level resistance to third-generation cephalosporins will result in treatment failure when these agents or penicillin are used alone, especially in cases of severe infection, such as meningitis, in which drug penetration of the blood-brain barrier is critical. The treatment of severe infections due to these isolates is problematic. Indiscriminate use of life-saving third-generation cephalosporins as out-patient treatment of minor infections or as first-line therapy for uncomplicated community-acquired infections in the hospital and in the community should be discouraged.
 
Key words: Cefotaxime/adverse effects; Drug resistance, microbial; Microbial sensitivity tests; Pneumococcal infections/drug therapy; Streptococcus pneumoniae/drug effects
 
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Familial form of arrhythmogenic right ventricular dysplasia presenting with recurrent ventricular tachycardia

ABSTRACT

Hong Kong Med J 1999;5:402-5 | Number 4, December 1999
CASE REPORT
Familial form of arrhythmogenic right ventricular dysplasia presenting with recurrent ventricular tachycardia
NS Mok, HH Tsang, PO Lee, LS Ho, MT Chan, YC Choi
Department of Medicine, Princess Margaret Hospital, Laichikok, Kowloon, Hong Kong
 
 
We report on a 48-year-old man who presented with recurrent sustained monomorphic ventricular tachycardia, which resulted in syncope on one occasion. Subsequent investigation confirmed the diagnosis of arrhythmogenic right ventricular dysplasia. Familial screening for the disease was conducted using 12-lead electrocardiography, signal-averaged electrocardiography, and magnetic resonance imaging. Two of the four relatives who were screened showed evidence of the disease, thus confirming the familial form of arrhythmogenic right ventricular dysplasia in the patient. He underwent a subpectoral implantation of an implantable cardioverter defibrillator in view of the malignant nature of the ventricular tachycardia and his intolerance to drug treatment.
 
Key words: Arrhythmia/etiology; Heart ventricle/abnormalities; Magnetic resonance imaging; Myocardial diseases/diagnosis; Tachycardia, ventricular
 
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Vertebral artery dissection: a treatable cause of ischaemic stroke

ABSTRACT

Hong Kong Med J 1999;5:398-401 | Number 4, December 1999
CASE REPORT
Vertebral artery dissection: a treatable cause of ischaemic stroke
CS Lam, YK Yee, YK Tsui, ML Szeto
Department of Medicine, Tuen Mun Hospital, Tuen Mun, Hong Kong
 
 
Vertebral artery dissection used to be an uncommon diagnosis but it is now being diagnosed more frequently owing to the use of magnetic resonance imaging. We report on three patients with vertebral artery dissection to illustrate the importance of establishing this diagnosis by using magnetic resonance imaging in patients who present with cerebrovascular accident that involves the posterior territory. Treatment with heparin can help prevent recurrent embolic events and should be given in the absence of subarachnoid haemorrhage or other contra-indications.
 
Key words: Aneurism, dissecting/diagnosis; Cerebral infarction; Cerebral ischemia/diagnosis; Magnetic resonance imaging; Vertebral artery/pathology
 
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Antithyroid drug-induced agranulocytosis

ABSTRACT

Hong Kong Med J 1999;5:394-6 | Number 4, December 1999
CASE REPORT
Antithyroid drug-induced agranulocytosis
CH Lee, RHS Liang
Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
Thyrotoxicosis is a common endocrine disorder. Antithyroid drug therapy is the standard treatment for this disease, especially in young women of reproductive age. A serious side effect of antithyroid drug use, however, is agranulocytosis. We report on two patients with antithyroid drug-induced agranulocytosis. Both patients presented with fever and severe neutropenia. The administration of granulocyte colony-stimulating factor resulted in a dramatic improvement in the white blood cell count and symptoms. Antithyroid drug-induced agranulocytosis is a potentially lethal condition but is completely reversible when recognised early and when prompt treatment is offered.
 
Key words: Agranulocytosis; Antithyroid agents; Granulocyte colony-stimulating factor
 
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Carotid endarterectomy for non-hemispheric cerebrovascular symptoms: an unusual indication

ABSTRACT

Hong Kong Med J 1999;5:391-3 | Number 4, December 1999
CASE REPORT
Carotid endarterectomy for non-hemispheric cerebrovascular symptoms: an unusual indication
AK AhChong, CB Law, KM Chiu
Department of Surgery, Kwong Wah Hospital, Waterloo Road, Kowloon, Hong Kong
 
 
We report on an 80-year-old man who presented with non-hemispheric cerebrovascular symptoms in the form of daily multiple syncope. The left common carotid artery, its two main divisions, and the right vertebral artery were completely occluded. There was high-grade stenosis in the right carotid artery (82%) and left vertebral artery (60%). After excluding other causes of syncope such as postural hypotension, hypoglycaemia, cardiac arrhythymia, and epileptic seizure, a diagnosis of global ischaemia was made. The patient subsequently underwent carotid endarterectomy and the symptoms were relieved. This case represents an unusual indication for carotid endarterectomy.
 
Key words: Carotid arteries/surgery; Cerebrovascular disorders; Endarterectomy; Vertebrobasilar insufficiency; Syncope/etiology
 
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Use of intravenous immunoglobulin in a patient with refractory myasthenia gravis associated with malignant thymoma

ABSTRACT

Hong Kong Med J 1999;5:291-3 | Number 3, September 1999
CASE REPORT
Use of intravenous immunoglobulin in a patient with refractory myasthenia gravis associated with malignant thymoma
KK Lau, WC Ho
Department of Medicine, Princess Margaret Hospital, Princess Margaret Hospital Road, Kwai Chung, Hong Kong
 
 
We report on a case of refractory myasthenia gravis that was managed by using intravenous immunoglobulin. A 35-year-old Chinese woman with malignant thymoma-associated myasthenia gravis was treated by total thymectomy, followed by chemotherapy. Thirty months later, she developed respiratory failure and required mechanical ventilation for 2 months. A course of intravenous immunoglobulin was given and her condition improved significantly. Two weeks later, the patient became ambulatory, was prescribed oral pyridostigmine, and was discharged home.
 
Key words: Immunoglobulins, intravenous/therapeutic use; Myasthenia gravis/therapy; Thymoma/surgery
 
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Selective posterior rhizotomy: results of five pilot cases

ABSTRACT

Hong Kong Med J 1999;5:287-90 | Number 3, September 1999
CASE REPORT
Selective posterior rhizotomy: results of five pilot cases
KY Yam, D Fong, K Kwong, B Yiu
Department of Neurosurgery, Tuen Mun Hospital, Tsing Chung Koon Road, Tuen Mun, Hong Kong
 
 
We report on two patients with spastic quadriplegia and three patients with spastic diplegia who underwent selective posterior rhizotomy. The mean period of follow-up was 15 months (range, 12-21 months). The patients were assessed preoperatively and at 2 weeks, 3 months, 6 months, and 1 year after surgery. Tests included those for muscle tone (using a modified Ashworth scale), range of passive movement, functional status, and gait pattern. Muscle tone was reduced substantially after the procedure, and the range of passive movement was increased. Both the dependent and independent ambulators showed an increment in their walking velocity and stride length. There were no postoperative complications apart from mild fever and the treatment was well tolerated by both patients and parents. There was no return of spasticity in any of the patients during follow-up. The reduced spasticity resulted in better motor performance, and patients felt more comfortable with their daily activities. We conclude that selective posterior rhizotomy should be considered for those patients who have cerebral palsy and are disabled by spasticity.
 
Key words: Cerebral palsy; Muscle spasticity; Spinal nerve roots/surgery
 
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A case of Castlemans disease mimicking a multicystic ovarian tumour

ABSTRACT

Hong Kong Med J 1999;5:285-6 | Number 3, September 1999
CASE REPORT
A case of Castlemans disease mimicking a multicystic ovarian tumour
CY Leung, SY Ng, HM Ho
Department of Pathology, United Christian Hospital, Kwun Tong, Hong Kong
 
 
We report on a case of solitary Castleman's disease that had an unusual presentation. A 29-year-old Filipino woman who had a history of intermittent right lower abdominal pain for several years was admitted to the Princess Margaret Hospital because of a sudden exacerbation of the abdominal pain. Ultrasonography had previously detected a multilocular right ovarian cyst of approximately 6.5 cm in diameter. Intra-operative findings, however, revealed a retroperitoneal presacral cystic tumour of approximately 7 cm in diameter, which was unrelated to the ovaries. The tumour was removed and found to be well defined and measure 7 x 5 x 4 cm. The cut surface revealed homogenous light-brown tissue at the periphery. The central part showed cystic spaces of 1- to 3-cm diameter. Histological examination of the tumour led to the diagnosis of hyaline vascular-type Castleman's disease. Cystic spaces were visible within the infarcted tissue; extensive cystic changes in Castleman's disease are unusual and may have caused the diagnostic difficulty.
 
Key words: Diagnosis, differential; Giant lymph node hyperplasia; Retroperitoneal neoplasms
 
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Colchicine-induced myopathy and neuropathy

ABSTRACT

Hong Kong Med J 1999;5:204-7 | Number 2, June 1999
CASE REPORT
Colchicine-induced myopathy and neuropathy
SSL Choi, KF Chan, HK Ng, WP Mak
Department of Geriatrics, Caritas Medical Centre, 11 Wing Hong Street, Shamshuipo, Hong Kong
 
 
Myopathy and neuropathy that have been induced by colchicine have been described only occasionally, although colchicine is a widely used drug. We describe a case of colchicine-induced myopathy and neuropathy in an 84-year-old woman who had renal impairment. Results from a muscle biopsy showed characteristic vacuolar myopathy and autophagic vacuoles. The cessation of medication resulted in a marked improvement of myopathy.
 
Key words: Colchicine/adverse effects; Muscular diseases/chemically induced; Nervous system diseases/chemically induced
 
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