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2.
Wilderness Environ Med ; 12(2): 155-7, 2001.
Article in English | MEDLINE | ID: mdl-11434493
6.
Clin Infect Dis ; 29(3): 613-6, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10530456

ABSTRACT

Although numerous studies have shown that diarrhea is the most common illness occurring during the first few weeks of travel, systematic studies of the incidence of diarrhea during long-term residence in developing countries have not been performed. We conducted a cohort study of the incidence and etiology of diarrhea among 77 expatriate adults who had lived in Nepal for <2 years. Persons were followed prospectively for up to 1 year (mean, 9 months). The incidence of diarrhea during the surveillance period was 3.3 episodes of diarrhea per person per year, or 0.27 episodes per person per month. The annual attack rate of specific pathogens was 42% for enterotoxigenic Escherichia coli, 32% for Cyclospora species, 16% for Giardia lamblia, 16% for Shigella species, 10% for Campylobacter species, > or =10% for rotavirus, and 6% for Entamoeba histolytica. This study suggests that adult persons from developed countries who move to developing countries such as Nepal remain at high risk for diarrhea during their first 2 years of residence.


Subject(s)
Diarrhea/epidemiology , Diarrhea/microbiology , Travel , Adolescent , Adult , Cohort Studies , Developing Countries , Female , Humans , Incidence , Male , Middle Aged , Nepal/epidemiology , Population Surveillance , Prospective Studies , Risk Factors
7.
Med Clin North Am ; 83(4): 1033-52, vii, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10453262

ABSTRACT

The persistence of gastrointestinal symptoms after travel to a developing country is one of the most common and troublesome post-travel illnesses. Few data exist to document the extent of this problem, but anecdotal examples abound among travel medicine practitioners, internists, and gastroenterologists. This article presents an approach to the patient with persistent gastrointestinal symptoms after travel.


Subject(s)
Diarrhea/etiology , Travel , Bacterial Infections/complications , Bacterial Infections/diagnosis , Chronic Disease , Diarrhea/epidemiology , Diarrhea/microbiology , Humans , Incidence , Military Personnel , Parasitic Diseases/complications , Parasitic Diseases/diagnosis
8.
N Engl J Med ; 340(1): 64; author reply 65, 1999 Jan 07.
Article in English | MEDLINE | ID: mdl-9882220
11.
J Clin Microbiol ; 35(6): 1639-41, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9163506

ABSTRACT

Enterotoxigenic Escherichia coli (ETEC) strains were isolated from travelers or military personnel who developed diarrhea after visiting Nepal or who were deployed to Thailand, Indonesia, or the Philippines. ETEC isolates were examined for colonization factor antigen (CFA). CFAs were identified on 59% (40 of 68) of the isolates examined. The lack of a detectable CFA on 41% (28 of 68) of the isolates is of concern for the development of an effective ETEC vaccine.


Subject(s)
Antigens, Bacterial/analysis , Bacterial Proteins/analysis , Diarrhea/microbiology , Escherichia coli Infections/microbiology , Escherichia coli/chemistry , Fimbriae Proteins , Travel , Antigens, Surface/analysis , Asia , Enterotoxins/analysis , Escherichia coli/genetics , Escherichia coli/immunology , Genes, Bacterial , Humans , Military Personnel , United States
12.
JAMA ; 275(7): 533-8, 1996 Feb 21.
Article in English | MEDLINE | ID: mdl-8606474

ABSTRACT

OBJECTIVE: To determine the etiology of diarrhea among expatriate residents living in a developing country and identify risk factors for travelers' diarrhea that are difficult to evaluate in tourist populations. DESIGN: Clinic based case-control study. SETTING: Primary care travel medicine clinic in Kathmandu, Nepal. PARTICIPANTS: A total of 69 expatriate residents with diarrhea, compared with 120 tourists with diarrhea, and 112 asymptomatic resident and tourist controls, selected systematically during a 1-year period. MAIN OUTCOME MEASURES: Risk factors for diarrhea assessed by questionnaire and pathogen prevalence assessed by microbiologic analysis of stool specimens. RESULTS: The dominant risk factors for diarrhea among expatriate residents included younger age (P = .003), shorter duration of stay in Nepal (P < .001), and eating out in restaurants (P = .01). Eating raw vegetables, salads, fresh fruit, or ice served in restaurants was not significantly associated with diarrhea. Longer duration of residence was linearly correlated with protection. Enteric pathogens were identified in 44 (64%) of 69 residents with diarrhea compared with 100 (83%) of 120 tourists with diarrhea, with enterotoxigenic Escherichia coli, Campylobacter, and Shigella predominant for both groups. Pathogens were also found in stools from 32 (37%) of 87 asymptomatic resident controls and 13 (52%) of 25 tourist controls. The attack rate of diarrhea among expatriates was estimated to be 49% (95% confidence interval, 37% to 61%) per month during the first 2 years of residence. The highest-risk months were April through July. CONCLUSIONS: Diarrhea among expatriates in a highly endemic environment is a persistent risk. The extremely high prevalence of enteric pathogens among asymptomatic persons reflects widespread exposure. The most important risk factors for travellers' diarrhea are difficult to modify, including younger age, duration of stay, eating in restaurants, and seasonality. Preventive dietary recommendations may not be fully protective, suggesting that pretravel advice should emphasize empiric treatment in addition to strategies to avoid exposure.


Subject(s)
Developing Countries , Diarrhea/epidemiology , Travel , Adult , Age Factors , Case-Control Studies , Diarrhea/microbiology , Disease Susceptibility , Emigration and Immigration , Environment , Feces/microbiology , Feeding Behavior , Female , Food , Humans , Incidence , Male , Nepal/epidemiology , Risk Factors , Seasons , Time Factors
14.
J Clin Microbiol ; 33(11): 3058-60, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8576377

ABSTRACT

Stools from 124 Nepalese children aged 6 to 60 months with diarrhea were examined for organisms of the coccidian genus Cyclospora and for other enteric pathogens. Enterotoxigenic Escherichia coli, Giardia Lamblia, Campylobacter species, Cyclospora species, and Cryptosporidium species were the most common pathogens identified. Cyclospora species were detected in none of 74 children < 18 months of age compared with 6 (12%) of 50 children > or = 18 months of age (P = 0.004).


Subject(s)
Coccidiosis/epidemiology , Diarrhea/diagnosis , Eucoccidiida , Intestinal Diseases, Parasitic/epidemiology , Intestinal Diseases/epidemiology , Animals , Bacterial Infections/epidemiology , Child, Preschool , Female , Humans , Infant , Male , Nepal/epidemiology , Rotavirus Infections/epidemiology , Strongyloidiasis/epidemiology
15.
16.
Clin Infect Dis ; 21(1): 97-101, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7578767

ABSTRACT

Although the pathogenicity of Blastocystis hominis has been extensively debated in the medical literature, controlled studies of the association between B. hominis and diarrhea are lacking. We conducted a case-control study among expatriates and tourists in Kathmandu, Nepal, in which we compared the prevalence of the organism among patients with diarrhea to that among a control group without diarrhea. B. hominis was detected in 56 (30%) of 189 patients with diarrhea, compared with 40 (36%) of 112 asymptomatic controls. Patients with diarrhea were significantly more likely to have > or = 10 B. hominis organisms per high-power (400x) field than were controls. However, among the 25 patients with this concentration of organisms, other enteric pathogens were detected in 17 (68%). Only 8 (4%) of 189 patients with diarrhea had > or = 10 B. hominis organisms per high-power field detected in the absence of other pathogens, compared with 5 (5%) of 112 asymptomatic controls. Thus, B. hominis in higher concentrations was not associated with diarrhea. There were no specific symptoms associated with B. hominis infection, and the presence of higher concentrations of the organism in stool was not associated with more-severe symptoms. Despite the high prevalence of the organism among travelers and expatriates in Nepal, the results of this study suggest that B. hominis does not cause diarrhea in this population.


Subject(s)
Blastocystis Infections/parasitology , Blastocystis hominis/pathogenicity , Diarrhea/parasitology , Adolescent , Adult , Animals , Bacteria/isolation & purification , Bacterial Infections/complications , Blastocystis Infections/epidemiology , Blastocystis hominis/isolation & purification , Case-Control Studies , Diarrhea/epidemiology , Diarrhea/microbiology , Feces/microbiology , Feces/parasitology , Female , Humans , Male , Nepal/epidemiology , Prevalence , Prospective Studies , Travel
17.
Wilderness Environ Med ; 6(2): 220-4, 1995 May.
Article in English | MEDLINE | ID: mdl-11995910

ABSTRACT

High-altitude pulmonary edema (HAPE) is a recognized risk of rapid ascent to high altitude. Since the recognition of this entity more than 30 years ago, most pulmonary deaths at high altitude have been attributed to HAPE. However, as the bodies can almost never be recovered for postmortem examination, rare diagnoses that appear clinically similar to HAPE will not be recognized. A 33-year-old woman climbing on Mt. Everest, and taking oral contraceptive pills, developed what seemed to be severe HAPE. Examination after she was evacuated from the mountain revealed a deep venous thrombosis in her left leg and multiple pulmonary emboli. We propose that multiple pulmonary emboli at high altitude can mimic HAPE, and fatal pulmonary embolism may be an explanation for some alleged victims of HAPE who died despite what should have been adequate descent.


Subject(s)
Altitude Sickness/diagnosis , Pulmonary Edema/diagnosis , Pulmonary Embolism/diagnosis , Adult , Altitude Sickness/complications , Anticoagulants/therapeutic use , Diagnosis, Differential , Female , Humans , Lung/diagnostic imaging , Pulmonary Edema/etiology , Pulmonary Embolism/drug therapy , Radiography
18.
Lancet ; 345(8951): 691-3, 1995 Mar 18.
Article in English | MEDLINE | ID: mdl-7885125

ABSTRACT

Cyclospora is a coccidian (previously referred to as cyanobacterium-like bodies) that has been implicated in cases of prolonged diarrhoea. The average duration of symptoms is more than three weeks, and no specific treatment has been shown to shorten the illness. A case report suggested that co-trimoxazole may be effective. Expatriate persons with gastrointestinal complaints and cyclospora detected on examination of faeces were recruited from two clinics in Kathmandu, Nepal, between May and August, 1994. Participants were assigned in a randomised, double-blinded manner to receive either cotrimoxazole (160 mg trimethoprim, 800 mg sulphamethoxazole) or placebo tablets twice daily for 7 days. Of 40 patients included in the study, 21 received cotrimoxazole and 19 placebo. There were no significant differences between these two groups in age, sex, time in Nepal, duration or severity of illness, or presence of other enteric pathogens. After 3 days, 71% of patients receiving co-trimoxazole still had cyclospora detected, compared with 100% of patients receiving placebo (p = 0.016). After 7 days, cyclospora was detected in 1 (6%) of 16 patients treated with co-trimoxazole who submitted stool specimens compared with 15 (88%) of 17 patients receiving placebo (p < 0.0001). Eradication of the organism was correlated with clinical improvement. There was no evidence of relapse of infection among treated patients followed for an additional 7 days. Treatment with co-trimoxazole for 7 days was effective in curing cyclospora infection among an expatriate population in Nepal.


Subject(s)
Coccidiosis/drug therapy , Diarrhea/drug therapy , Eucoccidiida/isolation & purification , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use , Adult , Animals , Coccidiosis/parasitology , Diarrhea/parasitology , Double-Blind Method , Feces/parasitology , Female , Humans , Male , Nepal , Placebos , Travel , Trimethoprim, Sulfamethoxazole Drug Combination/administration & dosage
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