Methotrexate exposure and risk of strongyloidiasis

被引:4
作者
Richards, Ceri [1 ]
Penner, Justin [2 ,3 ]
Colmegna, Ines [4 ]
Loewen, Hal [5 ]
Melaku, Zenebe [6 ,7 ]
Melkie, Addisu [7 ]
Meltzer, Michele [8 ]
Scuccimarri, Rosie [9 ]
Mengistu, Yewondwossen [7 ]
Hitchon, Carol A. [1 ]
机构
[1] Univ Manitoba, Dept Internal Med, RR149 800 Sherbrook St, Winnipeg, MB R3A 1M4, Canada
[2] Univ British Columbia, Dept Paediat, Trail, BC, Canada
[3] Imperial Coll London, Dept Paediat Infect Dis, London, England
[4] McGill Univ, Dept Med, Montreal, PQ, Canada
[5] Univ Manitoba, Neil John Mclean Lib, Winnipeg, MB, Canada
[6] Columbia Univ, Mailman Sch Publ Hlth, ICAP, New York, NY USA
[7] Addis Ababa Univ, Dept Internal Med, Addis Ababa, Ethiopia
[8] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[9] McGill Univ, Dept Pediat, Montreal, PQ, Canada
关键词
Strongyloides; methotrexate; systematic review; rheumatologic disease; RHEUMATOID-ARTHRITIS; DISEASE PATIENTS; STERCORALIS; HYPERINFECTION; INFECTIONS; SERIES;
D O I
10.1111/tmi.13288
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective Rheumatologic disease patients receiving immunomodulating drugs such as methotrexate (MTX) have increased infection rates. Strongyloides, a global endemic intestinal parasite, can cause significant or fatal disease in immunocompromised patients. The risk of serious Strongyloides infection with MTX dosed for rheumatologic disease is unknown. Methods We performed a systematic literature review searching EMBASE, Medline and Web of Science databases. All studies reporting humans exposed to MTX and tested for Strongyloides were reviewed. Exclusion criteria were bone marrow transplantation, intrathecal route and MTX exposure completed >1 year prior to clinically apparent Strongyloides disease. Results After excluding duplicates, 294 articles were reviewed. Of these, 29 cases were described in 27 papers. Twenty cases (69%) had an underlying rheumatologic or dermatologic disease, the rest had a haematologic disease. Hyperinfection or dissemination was found in 59% of cases (52% low-dose MTX; 75% high-dose MTX). Death occurred in 34% of cases (19% low-dose MTX; 75% high-dose MTX, P < 0.01). All eight patients on high-dose MTX received other immunosuppressants. Corticosteroids were taken in 18/21 patients on low-dose MTX. One of the three patients on MTX monotherapy had hyperinfection syndrome. None had disseminated Strongyloides. Conclusions Serious Strongyloides infection can occur with low-dose MTX particularly when given with other immunosuppression. Global travel and greater awareness of rheumatologic conditions in low- to middle-income countries will increase the exposure of individuals prescribed MTX (with or without corticosteroids) to Strongyloides. Strongyloides screening and treatment should be considered for individuals receiving low-dose MTX therapy, particularly if combined with additional immunosuppression.
引用
收藏
页码:1032 / 1041
页数:10
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