Change in CF care during COVID-19 pandemic: Single-center experience in a middle-income setting

Elpis Hatziagorou1, Ilektra Toulia1, Vasiliki Avramidou1

  • 1Paediatric Pulmonology and Cystic Fibrosis Unit, 3rd Paediatric Department, Hippokration Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.

Pediatric Pulmonology
|July 15, 2021
PubMed

Insights

During COVID-19, telephone monitoring improved cystic fibrosis (CF) patient care. Despite lockdowns, key health metrics like lung function and weight improved, showing the effectiveness of remote strategies for chronic disease management.

Area of Science:

  • Pulmonology
  • Infectious Diseases
  • Telemedicine

Background:

  • The COVID-19 pandemic necessitated changes in chronic disease care, particularly for cystic fibrosis (CF) patients at higher risk of severe SARS-CoV-2 infection.
  • Safer care delivery models were essential to mitigate transmission risks.

Discussion:

  • This study assessed the impact of lockdown and remote monitoring on CF patients in a middle-income setting.
  • Telephone visits replaced in-person clinic visits for monitoring health and therapy adherence over 10 weeks.
  • Pulmonary exacerbations affected 28.33% of patients, with most managed with oral antibiotics.

Key Insights:

  • Despite quarantine, mean forced expiratory volume in 1-second and body weight significantly increased post-lockdown.
  • Most patients maintained physiotherapy frequency, while 71% adapted their exercise routines.
  • Telephone monitoring proved crucial for maintaining CF patient care during the pandemic.

Outlook:

  • Implementing telephone contact is vital for CF patient care during pandemics.
  • Further research is needed to compare outcomes between traditional and telemedicine clinics for CF patients.
Abstract

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