Your browser doesn't support javascript.
loading
Safety and clinical efficacy of human rabies immunoglobulin in post exposure prophylaxis for category III animal exposures.
Haradanhalli, Ravish S; Fotedar, Nidhi; Kumari, Nitu; Narayana, D H Ashwath.
Afiliação
  • Haradanhalli RS; Department of Community Medicine, Kempegowda Institute of Medical Sciences, Bangalore, India.
  • Fotedar N; Department of Community Medicine, Kempegowda Institute of Medical Sciences, Bangalore, India.
  • Kumari N; Department of Community Medicine, Bangalore Medical College & Research Institute, Bangalore, India.
  • Narayana DHA; Department of Community Medicine, Kempegowda Institute of Medical Sciences, Bangalore, India.
Hum Vaccin Immunother ; 18(5): 2081024, 2022 11 30.
Article em En | MEDLINE | ID: mdl-35687876
ABSTRACT
The human rabies immunoglobulin (HRIG) is a life-saving immune biological essential for all category III animal exposures. It provides neutralizing antibodies at the site of exposure until the body can produce vaccine-mediated antibodies. We conducted this study to determine the safety and clinical efficacy of an HRIG being used presently for post-exposure prophylaxis (PEP) and to strengthen the existing evidence for its further usage. We conducted a prospective cohort study in 123 subjects with category III animal exposures at the KIMS Hospital and Research Center, Bangalore, India. Post-exposure prophylaxis (PEP) with wound toilet, a single application of HRIG, and a full course of anti-rabies vaccination were provided to all the study subjects. The volume of HRIG was calculated according to the body weight, and all the wounds were infiltrated as was anatomically feasible. All the study subjects were followed up for immediate and delayed adverse events (AE), both local and systemic. Subsequently, all the subjects were followed up for 6 months to demonstrate the clinical efficacy of PEP. The incidence of AEs was 11.4% including local pain, erythema, itching, headache, body ache, fever, and malaise. All AEs were mild and subsided without any complications. All the study subjects were healthy and alive after 6 months following the administration of HRIG, along with a full course of anti-rabies vaccine. Our study provides evidence of safety and clinical efficacy of HRIG for category III animal exposures and supports its continued usage.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacina Antirrábica / Profilaxia Pós-Exposição Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Animals / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacina Antirrábica / Profilaxia Pós-Exposição Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Animals / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article