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A risk-stratified approach toward safely resuming OnabotulinumtoxinA injections based on dosing and ambulatory status in pediatric patients with cerebral palsy during the Coronavirus pandemic of 2019 (COVID-19).
McLaughlin, Matthew J; Fisher, Mark T; Vadivelu, Sathya; Ramsey, Justin; Ratnasingam, Denesh; McGhee, Emily; Hartman, Kim.
  • McLaughlin MJ; Children's Mercy Hospital Kansas City, MO, USA.
  • Fisher MT; Children's Mercy Hospital Kansas City, MO, USA.
  • Vadivelu S; Children's Mercy Hospital Kansas City, MO, USA.
  • Ramsey J; Children's Mercy Hospital Kansas City, MO, USA.
  • Ratnasingam D; Rehabilitation Institute of Michigan, Detroit Medical Center, Wayne State University, Detroit, MI, USA.
  • McGhee E; University of Missouri, Columbia, MO, USA.
  • Hartman K; Children's Mercy Hospital Kansas City, MO, USA.
J Pediatr Rehabil Med ; 13(3): 273-279, 2020.
Article in English | MEDLINE | ID: covidwho-949027
ABSTRACT

PURPOSE:

After the onset of the Coronavirus pandemic of 2019-2020 (COVID-19), physicians who inject OnabotulinumtoxinA (BoNT-A) were left with determining risks and benefits in pediatric patients with cerebral palsy. Many of these patients have pre-existing conditions that make them more prone to COVID-19 symptoms, and this susceptibility potentially increases after BoNT-A injections.

METHODS:

A retrospective chart review of 500 patients identified 256 pediatric patients with cerebral palsy who received an intramuscular BoNT-A injection to determine relative doses used for each Gross Motor Functional Classification Score (GMFCS). Data regarding age, weight, GMFCS, BoNT-A total body dosage, and inpatient hospitalizations for 6 months post-injection were collected. Differences between GMFCS levels were analyzed using one-way analysis of variance testing. Inpatient hospitalizations were recorded and assessed using relative risk to determine the population risk of hospitalization in the setting of initiating injections during the COVID-19 pandemic.

RESULTS:

Based on GMFCS level, patients who were GMFCS I or II received fewer units of BoNT-A medication per kilogram of body weight compared to GMFCS III-V (p< 0.0005, F= 25.38). There was no statistically significant difference in frequency or time to hospitalization when comparing patients receiving BoNT-A compared to a control group.

CONCLUSIONS:

Resumption of BoNT-A injections during the time of COVID-19 requires a systematic approach based on risks and potential benefits. Data from this analysis does not show increased risk for patients who received injections historically; however, recommendations for resumption of injections has not previously been proposed in the setting of a pandemic. In this manuscript, a tiered approach to considerations for injections was proposed. Botulinum toxin type A injections have a history of improving spasticity in the pediatric patient with cerebral palsy. Ensuring appropriate selection of patients for injection with BoNT-A during this pandemic is increasingly important.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Cerebral Palsy / Botulinum Toxins, Type A / Pandemics / COVID-19 / Neuromuscular Agents Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials / Systematic review/Meta Analysis Limits: Child / Humans Country/Region as subject: North America Language: English Journal: J Pediatr Rehabil Med Year: 2020 Document Type: Article Affiliation country: PRM-200756

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Cerebral Palsy / Botulinum Toxins, Type A / Pandemics / COVID-19 / Neuromuscular Agents Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials / Systematic review/Meta Analysis Limits: Child / Humans Country/Region as subject: North America Language: English Journal: J Pediatr Rehabil Med Year: 2020 Document Type: Article Affiliation country: PRM-200756