TY - JOUR
T1 - Clinical spectrum of pulmonary involvement in leptospirosis in a region of endemicity, with quantification of leptospiral burden
AU - Segura, Eddy R.
AU - Ganoza, Christian A.
AU - Campos, Kalina
AU - Ricaldi, Jessica N.
AU - Torres, Sonia
AU - Silva, Hermann
AU - Céspedes, Manuel J.
AU - Matthias, Michael A.
AU - Swancutt, Mark A.
AU - Liñán, Renzo López
AU - Gotuzzo, Eduardo
AU - Guerra, Humberto
AU - Gilman, Robert H.
AU - Vinetz, Joseph M.
N1 - Funding Information:
Financial support. Funding was received from the Fogarty International Center, US National Institutes of Health/US National Institute of Environmental Health Sciences (grant R01TW05860); Tutorial in Tropical Health at JHU/Peru Overseas Sites TG-35 (grant T35AI07646); US National Institutes of Health/Fogarty International Center (grants D43TW00910, D43TW006581, and D43TW007120) and the RG-ER anonymous Tropical Medicine Research Fund.
PY - 2005/2/1
Y1 - 2005/2/1
N2 - Background. Pulmonary involvement in leptospirosis remains poorly recognized in regions where it is endemic, despite reports of recent outbreaks and epidemic disease. Methods. A prospective, population-based study was carried out to identify febrile patients exposed to Leptospira in urban and rural contexts in Iquitos, Peru. Evidence of exposure to Leptospira was obtained by serologic testing, and diagnosis of leptospirosis was confirmed in pulmonary cases by culture or quantitative real-time PCR assay. Results. Of 633 consecutively enrolled febrile patients, 321 (50.7%) had antileptospiral IgM antibodies or high titers of antileptospiral antibodies. Seven patients with histories of only urban exposure to leptospires had severe pulmonary manifestations; of these, 5 patients died; 4 of the deaths were caused by pulmonary hemorrhage, and 1 was caused by acute respiratory distress syndrome and multiorgan failure. Real-time, quantitative PCR assay showed high levels of leptospiremia (≥104 leptospires/mL) in most fatal cases; 1 patient, from whom tissue specimens were obtained at autopsy, had ≥10 5 leptospires/g of lung, kidney, and muscle tissue. Discussion. This study demonstrates the underdiagnosis of leptospirosis in a region of high endemicity and the underrecognition of grave pulmonary complications. Pulmonary involvement in leptospirosis was present in urban but not rural areas. Presumptive treatment for leptospirosis should be initiated immediately in the appropriate epidemiological and clinical context.
AB - Background. Pulmonary involvement in leptospirosis remains poorly recognized in regions where it is endemic, despite reports of recent outbreaks and epidemic disease. Methods. A prospective, population-based study was carried out to identify febrile patients exposed to Leptospira in urban and rural contexts in Iquitos, Peru. Evidence of exposure to Leptospira was obtained by serologic testing, and diagnosis of leptospirosis was confirmed in pulmonary cases by culture or quantitative real-time PCR assay. Results. Of 633 consecutively enrolled febrile patients, 321 (50.7%) had antileptospiral IgM antibodies or high titers of antileptospiral antibodies. Seven patients with histories of only urban exposure to leptospires had severe pulmonary manifestations; of these, 5 patients died; 4 of the deaths were caused by pulmonary hemorrhage, and 1 was caused by acute respiratory distress syndrome and multiorgan failure. Real-time, quantitative PCR assay showed high levels of leptospiremia (≥104 leptospires/mL) in most fatal cases; 1 patient, from whom tissue specimens were obtained at autopsy, had ≥10 5 leptospires/g of lung, kidney, and muscle tissue. Discussion. This study demonstrates the underdiagnosis of leptospirosis in a region of high endemicity and the underrecognition of grave pulmonary complications. Pulmonary involvement in leptospirosis was present in urban but not rural areas. Presumptive treatment for leptospirosis should be initiated immediately in the appropriate epidemiological and clinical context.
UR - http://www.scopus.com/inward/record.url?scp=13444306150&partnerID=8YFLogxK
U2 - 10.1086/427110
DO - 10.1086/427110
M3 - Artículo
C2 - 15668855
AN - SCOPUS:13444306150
SN - 1058-4838
VL - 40
SP - 343
EP - 351
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 3
ER -