Latent class analysis permits unbiased estimates of the validity of DAT for the diagnosis of visceral leishmaniasis

被引:23
作者
Boelaert, M
El Safi, S
Goetghebeur, E
Gomes-Pereira, S
Le Ray, D
Van der Stuyft, P
机构
[1] Inst Trop Med Prince Leopold, Epidemiol Unit, B-2000 Antwerp, Belgium
[2] Univ Khartoum, Dept Med Microbiol & Parasitol, Khartoum, Sudan
[3] Univ Ghent, Dept Appl Math & Informat, Ghent, Belgium
[4] Univ Nova Lisboa, Int Higiene & Med Trop, Unidad Leishmanioses, P-1200 Lisbon, Portugal
[5] Inst Trop Med Prince Leopold, Protozool Unit, B-2000 Antwerp, Belgium
关键词
visceral leishmaniasis; direct agglutination test; sensitivity; specificity; latent class analysis;
D O I
10.1046/j.1365-3156.1999.00421.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
BACKGROUND Substantial uncertainty surrounds the specificity of the Direct Agglutination Test (DAT) for visceral leishmaniasis (VL) in clinical suspects, since no good gold standard exists for unequivocally identifying diseased subjects. We explored the Latent Class Analysis (LCA) modelling technique to circumvent this problem. PATIENTS AND METHODS Data on 149 clinical suspects recruited in 1993-96 during a multicentre study in Sudan were re-examined. Clinical data, lymph node and bone marrow aspirate and DAT results were available. IFAT was performed in 1997 on stored filter paper blood of 80 individuals. Classical Validity Analysis (CVA) in a 2 x 2 contingency table with parasitology as a gold standard was compared with the parameter estimates produced by the best fitting LCA model. RESULTS The sensitivity estimates of DAT produced by CVA (98% (89%-100%)) were almost exactly reproduced by LCA. The specificity estimates by LCA were substantially higher than those obtained in CVA. Specificity of DAT depended, however, on whether the subject was treated for VL before. In subjects without prior treatment, CVA estimated DAT specificity at 68% (56%-79%), whereas LCA estimated it at 85% (63%-100%). CONCLUSION LCA modelling proved a useful tool, as it gave consistent estimates of test characteristics and allowed for control of confounding factors and interaction effects. Since VL is a life-threatening disease for which expensive but effective and safe treatment exists, a clinical suspect in an endemic area should be treated on the basis of a positive DAT result.
引用
收藏
页码:395 / 401
页数:7
相关论文
共 31 条
[1]  
ABRANCHES P, 1984, THESIS U NOVA LISBOA
[2]   FACTOR-ANALYSIS AND AIC [J].
AKAIKE, H .
PSYCHOMETRIKA, 1987, 52 (03) :317-332
[3]   EPIDEMIC VISCERAL LEISHMANIASIS IN SOUTHERN SUDAN - IDENTITY AND SYSTEMATIC POSITION OF THE PARATIES FROM PATIENTS AND VECTORS [J].
ASHFORD, RW ;
SEAMAN, J ;
SCHORSCHER, J ;
PRATLONG, F .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1992, 86 (04) :379-380
[4]   BIASES IN THE ASSESSMENT OF DIAGNOSTIC-TESTS [J].
BEGG, CB .
STATISTICS IN MEDICINE, 1987, 6 (04) :411-423
[5]   Operational validation of the direct agglutination test for diagnosis of visceral leishmaniasis [J].
Boelaert, M ;
El Safi, S ;
Jacquet, D ;
De Muynck, A ;
Van der Stuyft, P ;
Le Ray, D .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1999, 60 (01) :129-134
[6]   Multi-centre evaluation of repeatability and reproducibility of the direct agglutination test for visceral leishmaniasis [J].
Boelaert, M ;
El Safi, S ;
Mousa, H ;
Githure, J ;
Mbati, P ;
Gurubacharya, VL ;
Shrestha, J ;
Jacquet, D ;
De Muynck, A ;
Le Ray, D ;
Van der Stuyft, P .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 1999, 4 (01) :31-37
[7]  
Bryceson A. D. M., 1996, Manson's tropical diseases., P1213
[8]   INDIRECT FLUORESCENT IMMUNOASSAY IN THE DIAGNOSIS OF INFANTILE AND ADULT KALA-AZAR [J].
CAMPINO, L ;
ABRANCHES, P .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1991, 85 (04) :476-476
[9]  
Campino L, 1997, ANN TROP MED PARASIT, V91, P433, DOI 10.1080/00034989761067
[10]   IMPROVEMENT OF A DIRECT AGGLUTINATION-TEST FOR FIELD STUDIES OF VISCERAL LEISHMANIASIS [J].
ELHARITH, A ;
KOLK, AHJ ;
LEEUWENBURG, J ;
MUIGAI, R ;
HUIGEN, E ;
JELSMA, T ;
KAGER, PA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (07) :1321-1325