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Safety of biologics in severe asthmatic patients with SARS-CoV-2 infection: A prospective study.
Manti, Sara; Giallongo, Alessandro; Pecora, Giulia; Parisi, Giuseppe F; Papale, Maria; Mulè, Enza; Aloisio, Donatella; Rotolo, Novella; Leonardi, Salvatore.
  • Manti S; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Giallongo A; Department of Human Pathology of Adult and Childhood Gaetano Barresi, Pediatric Unit, University of Messina, Messina, Italy.
  • Pecora G; Pediaric Unit, Maggiore Hospital, Modica, Italy.
  • Parisi GF; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Papale M; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Mulè E; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Aloisio D; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Rotolo N; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Leonardi S; Pediatric Respiratory Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Pediatr Pulmonol ; 58(4): 1085-1091, 2023 04.
Article in English | MEDLINE | ID: covidwho-2173398
ABSTRACT

BACKGROUND:

Asthma guidelines have recommended continuing treatment with biologics during coronavirus disease 2019 (COVID-19) pandemic. However, a continuation of treatment with biologics in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been little investigated.

OBJECTIVE:

To assess the safety of biologics in patients with SARS-CoV-2 infection.

METHODS:

A pilot, monocentric, prospective study. Patients aged 6 years old and older with severe asthma on treatment with biologics and confirmed SARS-CoV-2 infection were enrolled. Patients were followed-up with periodic calls at different time points up to 3 months to detect any adverse effect and its relationship with biologic treatment according to the Naranjo Adverse Probability Scale (NAPS). The severity of SARS-CoV-2 infection and clinical outcome were also assessed.

RESULTS:

Overall, we included 21 patients (10 on therapy with omalizumab, 9 with dupilumab, and 2 with mepolizumab). Only a patient-reported two local adverse events. No other adverse event was reported. Twenty out of 21 patients had a mild COVID-19 course, and no adverse outcome was observed.

CONCLUSION:

We showed that the scheduled dose of the biologic therapy can be administered safely on time in patients with SARS-CoV-2 infection, as the treatment did not result in adverse events or outcomes.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Asthma / Biological Products / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Limits: Child / Humans Language: English Journal: Pediatr Pulmonol Journal subject: Pediatrics Year: 2023 Document Type: Article Affiliation country: Ppul.26298

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Asthma / Biological Products / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Limits: Child / Humans Language: English Journal: Pediatr Pulmonol Journal subject: Pediatrics Year: 2023 Document Type: Article Affiliation country: Ppul.26298