Snakebites in Cameroon: Tolerance of a Snake Antivenom (Inoserp™ PAN-AFRICA) in Africa in Real-Life Conditions

Author:

Benhammou David1,Chippaux Jean-Philippe2ORCID,Ntone Rodrigue3,Madec Yoann1,Amta Pierre4,Noel Gaëlle5,Karl Fai Njuwa3ORCID,Perilhou Anaïs6,Matchim Lucrece3ORCID,Sanchez Marie7,Ndifon Mark3,Clauteaux Pedro5,Eteki Lucrèce3,Boum Yap389,Nkwescheu Armand Seraphin10,Taieb Fabien11ORCID

Affiliation:

1. Emerging Diseases Epidemiology Unit, Institut Pasteur, Paris Cité University, F-75015 Paris, France

2. MERIT Unit, Institut de Recherche pour le Développement, Paris Cité University, F-75006 Paris, France

3. Epicentre Yaounde, Yaounde BP 12069, Cameroon

4. Tokombere Hospital, Tokombere, Mora BP 74, Cameroon

5. Institut Pasteur, Translational Research Center, Paris Cité University, F-75015 Paris, France

6. Institut Pasteur, Clinical Research Coordination Center, Paris Cité University, F-75015 Paris, France

7. Institut Pasteur, Data Management Core Facility, Paris Cité University, F-75015 Paris, France

8. Institut Pasteur de Bangui, Bangui BP 923, Central African Republic

9. Faculté de Médecine et de Sciences Biomédicales, Yaounde I University, Yaounde BP 1364, Cameroon

10. Cameroon Society of Epidemiology, Yaounde BP 1411, Cameroon

11. Institut Pasteur Medical Center, Paris Cité University, F-75015 Paris, France

Abstract

Snakebite envenomation (SBE) is a public health issue in sub-Saharan countries. Antivenom is the only etiological treatment. Excellent tolerance is essential in managing SBE successfully. This study aimed to evaluate tolerance of InoserpTM PAN-AFRICA (IPA). It was conducted on fourteen sites across Cameroon. IPA was administered intravenously and repeated at the same dose every two hours if needed. Early and late tolerance was assessed by the onset of clinical signs within two hours and at a visit two weeks or more after the first IPA administration, respectively. Over 20 months, 447 patients presenting with a snakebite were included. One dose of IPA was administered to 361 patients and repeated at least once in 106 patients. No significant difference was shown between the proportion of adverse events in patients who received IPA (266/361, 73.7%) and those who did not (69/85, 81.2%) (p = 0.95). Adverse reactions, probably attributable to IPA, were identified in four (1.1%) patients, including one severe (angioedema) and three mild. All these reactions resolved favorably. None of the serious adverse events observed in twelve patients were attributed to IPA. No signs of late intolerance were observed in 302 patients. Tolerance appears to be satisfactory. The availability of effective and well-tolerated antivenoms would reduce the duration of treatment and prevent most disabilities and/or deaths.

Funder

Institut Pasteur

Inosan Biopharma

Publisher

MDPI AG

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