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Assessing causality by means of the Naranjo scale in a paediatric patient with life threatening respiratory failure after alemtuzumab administration: a case report.
Smeets, Nori J L; Eijk, Ruud J R; de Wildt, Saskia N; Bootsma-Robroeks, Charlotte M H H T.
Afiliación
  • Smeets NJL; Department of Pharmacology and Toxicology, Radboud Institute of Health Sciences, Radboud University Medical Center, 6525 EZ, Nijmegen, The Netherlands. Nori.smeets@radboudumc.nl.
  • Eijk RJR; Department of Intensive Care and Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, 3015 GJ, Rotterdam, The Netherlands. Nori.smeets@radboudumc.nl.
  • de Wildt SN; Department of Pediatric Intensive Care, Radboud University Medical Centre, 6500 HB, Nijmegen, The Netherlands.
  • Bootsma-Robroeks CMHHT; Department of Pharmacology and Toxicology, Radboud Institute of Health Sciences, Radboud University Medical Center, 6525 EZ, Nijmegen, The Netherlands.
BMC Pediatr ; 21(1): 229, 2021 05 12.
Article en En | MEDLINE | ID: mdl-33980211
ABSTRACT

BACKGROUND:

Alemtuzumab is a T cell depleting antibody agent used as induction immunosuppressant therapy in solid organ transplant recipients. In addition, it is being increasingly used to treat severe or glucocorticoid-resistant graft rejection. Despite the effectiveness of the treatment, severe adverse events have been reported related to alemtuzumab administration. We present a similar event illustrating the severity of this adverse drug reaction (ADR) and we highlight the structure causality assessment provides in approaching such a case. CASE PRESENTATION We report a case of life-threatening respiratory failure after alemtuzumab administration in a 17 year old paediatric kidney transplant recipient. He developed near fatal severe respiratory and circulatory failure based on acute respiratory distress syndrome (ARDS) with diffuse alveolar oedema and haemoptysis hours after his second alemtuzumab administration. As it was questionable whether alemtuzumab could be regarded as the origin of his reaction and in order to assess the causality of this reaction as well as to structure clinical reasoning, we applied a widely used ADR probability scale to systematically review our case. DISCUSSION AND

CONCLUSIONS:

Our case shows a severe ADR after alemtuzumab administration. It illustrates the importance of proper causality assessment, the structure it provides and the benefit of a clinical pharmacology consultation when a severe reaction is suspected to be an ADR. By taking our case as an example, we demonstrate the added value of structured causality assessment to clinical reasoning and in generating differential diagnoses.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Insuficiencia Respiratoria / Anticuerpos Monoclonales Humanizados Tipo de estudio: Diagnostic_studies / Etiology_studies / Qualitative_research Límite: Adolescent / Child / Humans / Male Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Insuficiencia Respiratoria / Anticuerpos Monoclonales Humanizados Tipo de estudio: Diagnostic_studies / Etiology_studies / Qualitative_research Límite: Adolescent / Child / Humans / Male Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos