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1.
Singapore Med J ; 41(4): 179-81, 2000 Apr.
Article in English | MEDLINE | ID: mdl-11063184

ABSTRACT

Cutaneous leishmaniasis (CL) is not common in South-East Asia and often presents as a granulomatous plaque on the exposed areas, with a high index of suspicion required for diagnosis. Two such cases were seen at the National Skin Centre recently, and both were Gurkha men with a history of travel to Belize. They were treated with intravenous sodium stibogluconate with success. A discussion on CL and its management follows.


Subject(s)
Antimony Sodium Gluconate/administration & dosage , Antiprotozoal Agents/administration & dosage , Leishmaniasis, Cutaneous/diagnosis , Leishmaniasis, Cutaneous/drug therapy , Adult , Belize , Biopsy, Needle , Ear, External , Hospitalization , Hospitals, Urban , Humans , Injections, Intravenous , Male , Singapore , Travel
2.
J Pediatr ; 133(6): 795-8, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9842048

ABSTRACT

During an outbreak of hand-foot-mouth disease caused by enterovirus 71 (EV-71) in 1997, 4 children presented with sudden cardiopulmonary collapse and minimal neurologic features. All children received cardiopulmonary resuscitation but died within a few hours of admission. Postmortem studies showed infection by EV-71 with extensive damage to the medulla and pons. We postulate an etiologic link between EV-71 and brainstem encephalomyelitis as the cause of pulmonary edema and death.


Subject(s)
Encephalomyelitis/virology , Enterovirus Infections , Child, Preschool , Encephalomyelitis/pathology , Enterovirus Infections/pathology , Fatal Outcome , Female , Humans , Infant , Male , Medulla Oblongata/pathology , Pulmonary Edema/virology
3.
J Pediatr ; 120(4 Pt 1): 634-8, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1552406

ABSTRACT

We compared a new coated-particle formulation of valproate (Depakote Sprinkle) capsules with valproic acid (Depakene) syrup for bioavailability, side effects, and patient and parent preference. Twelve children with epilepsy, aged 5 to 16 years, participated in this randomized, two-period, crossover study. They were assigned to a 7-day regimen with one formulation and then crossed over to the other; the drug was given every 12 hours. On day 7, blood samples collected during a 12-hour period were analyzed for the presence of valproate. At the study's end, parents and children were asked structured questions regarding formulation preference and adverse events. The extent of absorption from sprinkle equaled that from syrup (relative bioavailability = 1.02), but absorption was slower (time to maximum concentration = 4.2 vs 0.9 hour; p less than 0.01). Fluctuations in serum concentrations were less with sprinkle (34.8% vs 62.3%; p less than 0.01). Sprinkle was preferred by 9 of the 12 parents because of east of administration, and by nine of the children because of improved palatability. We conclude that sprinkle may be substituted for syrup without changing the daily dose. Furthermore, sprinkle, because of its prolonged absorption, may be given every 12 hours to children receiving monotherapy. Compliance may be enhanced because of the more convenient dosing schedules and the high degree of patient and parent acceptance.


Subject(s)
Epilepsy/drug therapy , Valproic Acid/administration & dosage , Valproic Acid/pharmacokinetics , Absorption , Adolescent , Biological Availability , Chemistry, Pharmaceutical , Child , Child, Preschool , Drug Administration Schedule , Epilepsy/metabolism , Female , Humans , Male , Patient Compliance , Valproic Acid/adverse effects , Valproic Acid/chemistry
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