Card agglutination test for trypanosomiasis (CATT) end-dilution titer and cerebrospinal fluid cell count as predictors of human African trypanosomiasis (Trypanosoma brucei gambiense) among serologically suspected individuals in southern Sudan

被引:33
作者
Chappuis, F
Stivanello, E
Adams, K
Kidane, S
Pittet, A
Bovier, PA
机构
[1] Univ Hosp Geneva, Dept Community Med, Travel & Migrat Med Unit, CH-1211 Geneva, Switzerland
[2] Med Grontieres, Swiss Sect, CH-1203 Geneva, Switzerland
关键词
D O I
10.4269/ajtmh.2004.71.313
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The diagnosis of human African tryparbosomiasis (HAT) due to Trypanosoma brucei gambiense relies on an initial serologic screening with the card agglutination test for trypanosomiasis (CATT) for T. b. gambiense, followed by parasitologic confirmation in most endemic areas. Unfortunately, field parasitologic methods lack sensitivity and the management of serologically suspected individuals (i.e., individuals with a positive CATT result but negative parasitology) remains controversial. In Kajo-Keji County in southern Sudan, we prospectively collected sociodemographic and laboratory data of a cohort of 2,274 serologically suspected individuals. Thirty-three percent (n = 749) attended at least one follow-up visit and HAT was confirmed in 64 (9%) cases. Individuals with lower initial CATT-plasma (CATT-P) end-dilution titers had lowest risks (10.4 and 13.8/100 person-years for 1:4 and 1:8 titers, respectively) that significantly increased for higher dilutions: relative risks = 5.1 (95% confidence interval [CI] = 2.6-9.5) and 4.6 (95% CI = 2.8-9.8) for 1:16 and 1:32 titers, respectively. The cumulative yearly risk was also high (76%) in individuals found with 1.1-20 cells in the cerebrospinal fluid, but this involved only eight patients. Adjustment for potential confounders did not affect the results. In conclusion, treatment with pentamicline should be considered for all serologically suspected individuals with a CATT-P end-dilution titer greater than or equal to 1:16 in areas of a moderate to high prevalence of HAT.
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页码:313 / 317
页数:5
相关论文
共 11 条
[1]  
Ancelle T, 1997, Med Trop (Mars), V57, P245
[2]   Field evaluation of the CATT/Trypanosoma brucei gambiense on blood-impregnated filter papers for diagnosis of human African trypanosomiasis in southern Sudan [J].
Chappuis, F ;
Pittet, A ;
Bovier, PA ;
Adams, K ;
Godineau, V ;
Hwang, SY ;
Magnus, E ;
Büscher, P .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2002, 7 (11) :942-948
[3]   The efficacy of pentamidine in the treatment of early-late stage Trypanosoma brucei gambiense trypanosomiasis [J].
Doua, F ;
Miezan, TW ;
Singaro, JRS ;
Yapo, FB ;
Baltz, T .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1996, 55 (06) :586-588
[4]   Follow-up of Card Agglutination Trypanosomiasis Test (CATT) positive but apparently aparasitaemic individuals in Cote d'Ivoire:: evidence for a complex and heterogeneous population [J].
Garcia, A ;
Jamonneau, V ;
Magnus, E ;
Laveissière, C ;
Lejon, V ;
N'Guessan, P ;
N'Dri, L ;
Van Meirvenne, N ;
Büscher, P .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2000, 5 (11) :786-793
[5]   Preliminary evaluation of LATEX/T-b. gambiense and alternative versions of CATT/T-b. gambiense for the serodiagnosis of Human African Trypanosomiasis of a population at risk in Cote d'Ivoire:: considerations for mass-screening [J].
Jamonneau, V ;
Truc, P ;
Garcia, A ;
Magnus, E ;
Büscher, P .
ACTA TROPICA, 2000, 76 (02) :175-183
[6]   Neuro-inflammatory risk factors for treatment failure in "early second stage" sleeping sickness patients treated with Pentamidine [J].
Lejon, V ;
Legros, D ;
Savignoni, A ;
Etchegorry, MG ;
Mbulamberi, D ;
Büscher, P .
JOURNAL OF NEUROIMMUNOLOGY, 2003, 144 (1-2) :132-138
[7]  
MAGNUS E, 1978, ANN SOC BELG MED TR, V58, P169
[8]   Attitude towards CATT-positive individuals without parasitological confirmation in the African Trypanosomiasis (T.b. gambiense) focus of Quicama (Angola) [J].
Simarro, PP ;
Ruiz, JA ;
Franco, JR ;
Josenando, T .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 1999, 4 (12) :858-861
[9]  
Truc P, 2002, B WORLD HEALTH ORGAN, V80, P882
[10]  
VANMEIRVENNE N, 1999, PROGR HUMAN AFRICAN, P235