Rapid accurate field diagnosis of Indian visceral leishmaniasis

被引:201
作者
Sundar, S
Reed, SG
Singh, VP
Kumar, PCK
Murray, HW
机构
[1] Banaras Hindu Univ, Inst Med Sci, Kala Azar Med Res Ctr, Varanasi 221005, Uttar Pradesh, India
[2] Corixa Corp, Seattle, WA USA
[3] Cornell Univ, Coll Med, Dept Med, New York, NY USA
关键词
D O I
10.1016/S0140-6736(97)04350-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background A firm diagnosis of visceral leishmaniasis (kalaazar) requires demonstration of the parasite in organ aspirates or tissue biopsy samples. The aim of this prospective study was to assess the diagnostic usefulness of non-invasive testing for antibody to the leishmanial antigen K39 by means of antigen-impregnated nitrocellulose paper strips adapted for use under field conditions. Methods One drop of peripheral blood is applied to the nitrocellulose strip. Three drops of test buffer (phosphate-buffered saline plus bovine serum albumin) are added to the dried blood. The development of two visible bands indicates presence of IgG anti-K39. 323 consecutive patients with suspected kala-azar referred to two specialist units in India, and 25 healthy controls, provided fingerstick blood samples for the test. Spleen aspirates were taken from 250 patients. Findings Kala-azar was confirmed by microscopy of spleen-aspirate smears in 127 patients. The K39 strip test was positive in all 127; the estimated sensitivity was therefore 100% (95% CI 98-100). Four patients had positive strip tests but negative aspirate smears; all four responded to treatment for leishmaniasis. 217 individuals, including the 25 healthy controls, 73 patients with malaria or tuberculosis, and 119 spleen-aspirate-negative patients who had presumed malaria or cirrhosis (79) or no final diagnosis (40), had negative strip-test results. None of the 119 aspirate-negative patients developed evidence of kala-azar during 3-6 months of follow-up. The estimated specificity of the strip test was 98% (95-100; 217/221). Interpretation Detection of anti-K39 by immunochromatographic strip testing is a rapid and non-invasive method of diagnosing kala-azar, which has good sensitivity and specificity and is well suited for use in field conditions.
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页码:563 / 565
页数:3
相关论文
共 22 条
[1]  
ACHORD D, 1991, PRINCIPLES PRACTICE, P584
[2]   ESTIMATION OF POPULATION AT RISK OF INFECTION AND NUMBER OF CASES OF LEISHMANIASIS [J].
ASHFORD, RW ;
DESJEUX, P ;
DERAADT, P .
PARASITOLOGY TODAY, 1992, 8 (03) :104-105
[3]   NEW PERSPECTIVES ON A SUBCLINICAL FORM OF VISCERAL LEISHMANIASIS [J].
BADARO, R ;
JONES, TC ;
CARVALHO, EM ;
SAMPAIO, D ;
REED, SG ;
BARRAL, A ;
TEIXEIRA, R ;
JOHNSON, WD .
JOURNAL OF INFECTIOUS DISEASES, 1986, 154 (06) :1003-1011
[4]  
BARDARO R, 1996, J INFECT DIS, V173, P758
[5]   MOLECULAR CHARACTERIZATION OF A KINESIN-RELATED ANTIGEN OF LEISHMANIA-CHAGASI THAT DETECTS SPECIFIC ANTIBODY IN AFRICAN AND AMERICAN VISCERAL LEISHMANIASIS [J].
BURNS, JM ;
SHREFFLER, WG ;
BENSON, DR ;
GHALIB, HW ;
BADARO, R ;
REED, SG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :775-779
[6]  
GALVIN JP, 1987, RAPID METHODS AUTOMA, P558
[7]   PREVALENCE AND DISEASE SPECTRUM IN A NEW FOCUS OF VISCERAL LEISHMANIASIS IN KENYA [J].
HO, M ;
SIONGOK, TK ;
LYERLY, WH ;
SMITH, DH .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1982, 76 (06) :741-746
[8]   USE OF THE LEISHMANIN SKIN-TEST AND WESTERN-BLOT-ANALYSIS FOR EPIDEMIOLOGIC STUDIES IN VISCERAL LEISHMANIASIS AREAS - EXPERIENCE IN A HIGHLY ENDEMIC FOCUS IN ALPES-MARITIMES (FRANCE) [J].
MARTY, P ;
LELIEVRE, A ;
QUARANTA, JF ;
RAHAL, A ;
GARITOUSSAINT, M ;
LEFICHOUX, Y .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1994, 88 (06) :658-659
[9]   DIAGNOSIS OF SYMPTOMATIC VISCERAL LEISHMANIASIS BY USE OF THE POLYMERASE CHAIN-REACTION ON PATIENT BLOOD [J].
NUZUM, E ;
WHITE, F ;
THAKUR, C ;
DIETZE, R ;
WAGES, J ;
GROGL, M ;
BERMAN, J .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (03) :751-754
[10]   Clinical spectrum of Leishmaniasis [J].
Pearson, RD ;
Sousa, AD .
CLINICAL INFECTIOUS DISEASES, 1996, 22 (01) :1-11