Host, parasite and drug determinants of clinical outcomes following treatment of visceral leishmaniasis: a protocol for individual participant data meta-analysis

被引:2
|
作者
Kumar, Rishikesh [1 ]
Dahal, Prabin [2 ,3 ]
Singh-Phulgenda, Sauman [2 ,3 ]
Siddiqui, Niyamat Ali [1 ]
Munir, Abdalla [2 ,3 ]
Naylor, Caitlin [2 ,3 ]
Wilson, James [2 ,3 ]
Buck, Gemma [2 ,3 ]
Rahi, Manju [4 ]
Malaviya, Paritosh [5 ]
Alves, Fabiana [6 ]
Sundar, Shyam [5 ]
Ritmeijer, Koert [7 ]
Stepniewska, Kasia [2 ,3 ]
Guerin, Philippe J. [2 ,3 ]
Pandey, Krishna [1 ]
机构
[1] Indian Council Med Res ICMR, Rajendra Mem Res Inst Med Sci RMRIMS, Patna, India
[2] Univ Oxford, Infect Dis Data Observ IDDO, Oxford, England
[3] Univ Oxford, Ctr Trop Med & Global Hlth, Nuffield Dept Med, Oxford, England
[4] Indian Council Med Res ICMR, Epidemiol & Communicable Dis, Delhi, India
[5] Banaras Hindu Univ, Inst Med Sci, Dept Med, Infect Dis Res Lab, Varanasi, India
[6] Drugs Neglected Dis Initiat, Geneva, Switzerland
[7] Med Sans Frontieres, Amsterdam, Netherlands
来源
BMJ OPEN | 2023年 / 13卷 / 10期
关键词
Neglected Diseases; INFECTIOUS DISEASES; PUBLIC HEALTH; Tropical medicine; Epidemiology; LIPOSOMAL AMPHOTERICIN-B; KALA-AZAR; MILTEFOSINE; RESISTANCE; FAILURE;
D O I
10.1136/bmjopen-2023-074679
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionVisceral leishmaniasis (VL) is a parasitic disease with an estimated 30 000 new cases occurring annually. There is an observed variation in the efficacy of the current first-line therapies across different regions. Such heterogeneity could be a function of host, parasite and drug factors. An individual participant data meta-analysis (IPD-MA) is planned to explore the determinants of treatment outcomes.Methods and analysisThe Infectious Diseases Data Observatory (IDDO) VL living systematic review (IDDO VL LSR) library is an open-access resource of all published therapeutic studies in VL since 1980. For this current review, the search includes all clinical trials published between 1 January 1980 and 2 May 2021. Studies indexed in the IDDO VL LSR library were screened for eligibility for inclusion in this IPD-MA. Corresponding authors and principal investigators of the studies meeting the eligibility criteria for inclusion were invited to be part of the collaborative IPD-MA. Authors agreeing to participate in this collaborative research were requested to share the IPD using the IDDO VL data platform. The IDDO VL data platform currently holds data sets from clinical trials standardised to a common data format and provides a unique opportunity to identify host, parasite and drug determinants of treatment outcomes. Multivariable regression models will be constructed to identify determinants of therapeutic outcomes using generalised linear mixed-effects models accounting for within-study site clustering.Ethics and disseminationThis IPD-MA meets the criteria for waiver of ethical review as defined by the Oxford Tropical Research Ethics Committee (OxTREC) granted to IDDO, as the research consists of secondary analysis of existing anonymised data (Exempt granted on 29 March 2023, OxTREC REF: IDDO) Ethics approval was granted by the ICMR-Rajendra Memorial Research Institute of Medical Sciences ethics committee (Letter no: RMRI/EC/30/2022) on 04-07-2022. The results of this IPD-MA will be disseminated at conferences, IDDO website and any peer-reviewed publications. All publications will be open source. Findings of this research will be critically important for the control programmes at regional/global levels, policy makers and groups developing new VL treatments.PROSPERO registrationCRD42021284622.
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页数:7
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