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26 result(s)
Journal Article > ResearchFull Text

Snakebites in Cameroon by species whose effects are poorly described

Trop Med Infect Dis. 6 December 2024; Volume 9 (Issue 12); 300.; DOI: 10.3390/tropicalmed9120300
Chippaux JP, Madec Y, Amta P, Ntone R, Noël G,  et al.
Trop Med Infect Dis. 6 December 2024; Volume 9 (Issue 12); 300.; DOI: 10.3390/tropicalmed9120300

Snakes responsible for bites are rarely identified, resulting in a loss of information about snakebites from venomous species whose venom effects are poorly understood. A prospective clinical study including patients bitten by a snake was conducted in Cameroon between 2019 and 2021 to evaluate the efficacy and tolerability of a marketed polyvalent antivenom. Clinical presentation during the first 3 days of hospitalization was recorded following a standardized protocol. This ancillary study aimed to assess the frequency of bites by the different species encountered in Cameroon and to describe the symptoms of bites by formally identified species. Of the 447 patients included in the study, 159 (35.6%) brought the snake that caused the bite that was identified by a specialist. Out of these, 8 specimens could not be identified due to poor condition, 19 were non-venomous species, and 95 belonged to Echis romani—formerly E. ocellatus—species. The remaining 37 specimens included 2 Atheris squamigera, 12 Atractaspis spp., 2 Bitis arietans, 11 Causus maculatus, 1 Dendroaspis jamesoni, 1 Naja haje, 1 N. katiensis, 5 N. melanoleuca complex, and 2 N. nigricollis. Symptoms, severity of envenomation, and post-treatment course are described. Symptoms and severity of bites are consistent with cases described in the literature, but some specific features are highlighted.

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Journal Article > CommentaryFull Text

Debate-Pro: manufacturers should assess the long-term stability of their antivenoms

Emerg Med J. 21 August 2024; Volume 41 (Issue 9); 560.; DOI:10.1136/emermed-2024-214173
Potet J
Emerg Med J. 21 August 2024; Volume 41 (Issue 9); 560.; DOI:10.1136/emermed-2024-214173
Conference Material > Poster

Characteristics of children affected by snake bite and snake envenomation in Abs Hospital, Yemen

de Bartolome Gisbert F, Awad Alhatec MH, Hajaji A, Hindi A, Salem S,  et al.
MSF Paediatric Days 2024. 3 May 2024; DOI:10.57740/SN6Tcc
Journal Article > ResearchFull Text

Snakebites in Cameroon: Tolerance of a snake antivenom (Inoserp™ PAN-AFRICA) in Africa in real-life conditions

Toxins. 22 March 2024; Volume 16 (Issue 4); 165.; DOI:10.3390/toxins16040165
Benhammou D, Chippaux JP, Ntone R, Madec Y, Amta P,  et al.
Toxins. 22 March 2024; Volume 16 (Issue 4); 165.; DOI:10.3390/toxins16040165
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.More
Journal Article > ResearchFull Text

Real life condition evaluation of Inoserp PAN-AFRICA antivenom effectiveness in Cameroon

PLoS Negl Trop Dis. 8 November 2023; Volume 17 (Issue 11); e0011707.; DOI:10.1371/journal.pntd.0011707
Chippaux JP, Ntone R, Benhammou D, Madec Y, Noël G,  et al.
PLoS Negl Trop Dis. 8 November 2023; Volume 17 (Issue 11); e0011707.; DOI:10.1371/journal.pntd.0011707
BACKGROUND
Snakebites is a serious public health issue but remains a neglected tropical disease. Data on antivenom effectiveness are urgently needed in Africa. We assessed effectiveness of Inoserp PAN-AFRICA (IPA), the recommended antivenom available in Cameroon.

METHODOLOGY/PRINCIPAL FINDINGS
We enrolled 447 patients presenting with snakebite in 14 health facilities across Cameroon. At presentation, cytotoxicity, coagulation troubles and neurotoxicity were graded. We administered two to four vials of antivenom to patients based on hemotoxic or neurotoxic signs. We renewed antivenom administration to patients with persistence of bleedings or neurotoxicity 2 hours after each injection. We defined early improvement as a reduction of the grade of envenomation symptoms 2 hours after first injection. Medium-term effectiveness was investigated looking at disappearance of symptoms during hospitalization. After hospital discharge, a home visit was planned to assess long-term outcomes.

Between October 2019 and May 2021, we enrolled 447 (93.7%), including 72% from the savannah regions. The median [IQR] age was 25 [14–40]. Envenomation was diagnosed in 369 (82.6%) participants. The antivenom was administered to 356 patients (96.5%) of whom 256 (71.9%) received one administration. Among these patients, cytotoxic symptoms were observed in 336 (94.4%) participants, coagulation disorders in 234 (65.7%) participants and neurotoxicity in 23 (6.5%) participants. Two hours after the first administration of antivenom, we observed a decrease in coagulation disorders or neurotoxicity in 75.2% and 39.1% of patients, respectively. Complete cessation of bleedings and neurotoxicity occurred in 96% and 93% of patients within 24 hours, respectively. Sequelae have been observed in 9 (3%) patients at the home visit 15 days after hospital admission and 11 (3%) died including one before antivenom injection.

CONCLUSIONS/SIGNIFICANCE
We confirmed good effectiveness of the IPA and highlighted the rapid improvement in bleeding or neurotoxicity after the first administration. Sequential administrations of low doses of antivenom, rigorously assessed at short intervals for an eventual renewal, can preserve patient safety and save antivenom.
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Journal Article > CommentaryFull Text

Availability, accessibility and use of antivenom for snakebite envenomation in Africa with proposed strategies to overcome the limitations

Toxicon: X. 26 February 2023; Volume 18; 100152.; DOI:10.1016/j.toxcx.2023.100152
Dalhat MM, Potet J, Mohammed A, Chotun N, Tesfahunei HA,  et al.
Toxicon: X. 26 February 2023; Volume 18; 100152.; DOI:10.1016/j.toxcx.2023.100152
Africa remains one of the regions with the highest incident and burden of snakebite. The goal of the World Health Organization to halve the global burden of snakebite by 2030 can only be achieved if sub-optimal access to antivenoms in the most affected regions is addressed. We identified upstream, midstream, and downstream factors along the antivenom value chain that prevent access to antivenoms in the African region. We identified windows of opportunities that could be utilized to ensure availability, accessibility, and affordability for snakebite endemic populations in Africa. These include implementation of multicomponent strategies such as intensified advocacy, community engagement, healthcare worker trainings, and leveraging the institutional and governance structure provided by African governments to address the challenges identified.More
Journal Article > ResearchFull Text

A global core outcome measurement set for snakebite clinical trials

Lancet Global Health. 1 February 2023; Volume 11 (Issue 2); e296-e300.; DOI:10.1016/S2214-109X(22)00479-X
Abouyannis M, Esmail H, Hamaluba M, Ngama M, Mwangudzah H,  et al.
Lancet Global Health. 1 February 2023; Volume 11 (Issue 2); e296-e300.; DOI:10.1016/S2214-109X(22)00479-X
Snakebite clinical trials have often used heterogeneous outcome measures and there is an urgent need for standardisation. A globally representative group of key stakeholders came together to reach consensus on a globally relevant set of core outcome measurements. Outcome domains and outcome measurement instruments were identified through searching the literature and a systematic review of snakebite clinical trials. Outcome domains were shortlisted by use of a questionnaire and consensus was reached among stakeholders and the patient group through facilitated discussions and voting. Five universal core outcome measures should be included in all future snakebite clinical trials-mortality, WHO disability assessment scale, patient-specific functional scale, acute allergic reaction by Brown criteria, and serum sickness by formal criteria. Additional syndrome-specific core outcome measures should be used depending on the biting species. This core outcome measurement set provides global standardisation, supports the priorities of patients and clinicians, enables meta-analysis, and is appropriate for use in low-income and middle-income settings.More
Journal Article > ResearchFull Text

Définition d'un jeu universel de critères de décision de base pour les essais cliniques sur les morsures de serpent

Med Trop Sante Int MTSI MTSI bulletin MTSI magazine MTSI-Revue Médecine tropicale et santé internationale. Bulletin Médecine tropicale et santé internationale. Magazine MTSI, la revue de la Société francophone de médecine tropicale et santé internationale. 1 February 2023; Volume 3 (Issue 3); DOI:10.48327/mtsi.v3i3.2023.421
Abouyannis M, Esmail H, Hamaluba M, Ngama M, Mwangudzah H,  et al.
Med Trop Sante Int MTSI MTSI bulletin MTSI magazine MTSI-Revue Médecine tropicale et santé internationale. Bulletin Médecine tropicale et santé internationale. Magazine MTSI, la revue de la Société francophone de médecine tropicale et santé internationale. 1 February 2023; Volume 3 (Issue 3); DOI:10.48327/mtsi.v3i3.2023.421
English
Français
CONTEXTE
Les essais cliniques sur les morsures de serpent ont souvent utilisé des critères de décision hétérogènes qui demandent à être standardisés.

MÉTHODE
Un groupe d'acteurs clés mondialement représentatifs s'est réuni pour parvenir à un consensus sur un jeu universel de critères de décision de base. Les domaines d'intérêt et les instruments d'évaluation des critères de décision ont été identifiés à partir d'une recherche documentaire et d'un examen systématique des essais cliniques concernant les envenimations par morsure de serpent. Les domaines d'intérêt ont été présélectionnés à l'aide d'un questionnaire et un consensus a été obtenu entre le groupe d'acteurs et un groupe représentatif de patients à la suite de discussions orientées et d'un vote.

RÉSULTATS
Cinq critères de décision de base universels devraient être inclus dans tous les futurs essais cliniques sur les morsures de serpent : la mortalité, l'échelle d'évaluation du handicap de l'OMS, l'échelle fonctionnelle propre à chaque patient, la réaction allergique immédiate selon les critères de Brown et la maladie sérique en fonction de critères formels. D'autres critères de décision spécifiques aux différents syndromes observés lors des envenimations par morsure de serpent doivent être utilisés en fonction de l'espèce responsable de la morsure.

CONCLUSION
Ce jeu universel de critères de décision de base permet une standardisation mondiale, répond aux priorités des patients et des cliniciens, favorise des méta-analyses et est compatible avec une utilisation dans les pays à revenu faible ou intermédiaire.
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Journal Article > CommentaryFull Text

Snakebite envenoming at MSF: A decade of clinical challenges and antivenom access issues

Toxicon: X. 21 December 2022; Volume 17; 100146.; DOI:10.1016/j.toxcx.2022.100146
Potet J, Singh SN, Ritmeijer KKD, Sisay K, Alcoba G,  et al.
Toxicon: X. 21 December 2022; Volume 17; 100146.; DOI:10.1016/j.toxcx.2022.100146
The medical humanitarian organization Médecins Sans Frontières (MSF) provides medical care in more than 70 countries and admits more than 7000 cases of snakebite in its facilities each year.

We describe our activities against snakebite in three African countries: Central African Republic, South Sudan and Ethiopia, in which different models of care have been developed. A standard protocol using two different antivenoms depending on the patient's syndrome has been introduced, and a simple blood coagulation test is performed to detect venom-induced coagulopathy. Other services, including surgery for necrotizing wounds, are offered in the facilities where MSF admits a large number of snakebite patients. All services, including provision of antivenom, are offered free-of-charge in MSF-supported facilities. Community-based activities focusing on preventive measures and prompt transport to hospital have been developed in a few MSF projects.

The provision of quality care and treatment, including effective antivenoms, without out-of-pocket payments by the patients, probably explains why MSF has admitted an increasing number of snakebite victims over the last years. This model requires significant resources and monitoring, including regular training of healthcare workers on treatment protocols and a considerable budget for antivenom procurement.
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Journal Article > CommentaryFull Text

Understanding and tackling snakebite envenoming with transdisciplinary research

PLoS Negl Trop Dis. 17 November 2022; Volume 16 (Issue 11); e0010897.; DOI:10.1371/journal.pntd.0010897
Gutiérrez JM, Borri J, Giles-Vernick T, Duda R, Habib AG,  et al.
PLoS Negl Trop Dis. 17 November 2022; Volume 16 (Issue 11); e0010897.; DOI:10.1371/journal.pntd.0010897