The aim for this study is further to elucidate the presence of dysautonomia in post-covid-19 patients, by evaluating heart rate variability.
The COVID-19 pandemic is currently a serious global public health concern. This disease is
caused by a novel coronavirus which was first discovered in Wuhan, China in 2019 and later
spread rapidly throughout the world. Symptoms of the disease can manifest as fever, cough,
encephalitis, myalgia, fatigue, muscle weakness, arthralgia, anosmia, and impairment in other
bodily functions in the acute phase. In 17% to 67% of cases, COVID-19 patients will develop
acute respiratory distress syndrome (ARDS) and critical illness. Besides the impact on the
respiratory system, coronaviruses have an effect on other systems including the central
nervous system, cardiovascular system, musculoskeletal system, and gastrointestinal system.
Potential long-term secondary effects on the musculoskeletal system such as muscle weakness,
decreased muscle mass, and myopathies have been brought under attention. Persisting symptoms
in patients recovered from COVID-19 infection are frequently a complaint with at least 1
symptom, particularly fatigue and dyspnea. In recent papers, the authors commented on the
potential role of dysautonomia in the post-covid-19 entity related to microangiopathy and
endothelial injury. Such lesions were already reported in brain biopsy samples of severe
COVID-19.
Therefore, the aim of this study is further to elucidate the presence of dysautonomia in
post-covid-19 patients, by evaluating heart rate variability.
Other: Dysautonomia
Indicators of dysautonomia
Inclusion Criteria:
- Patients with a diagnosed covid-19 infection that took place 2-8 weeks before study
inclusion.
- Cognitive and language functioning enabling coherent communication between the
researcher and the participant.
- French-or Dutch speaking persons.
Exclusion Criteria:
- Covid-19 infection > 8 weeks ago.
- The presence of one or more coexisting conditions known to affect HRV analysis
(including but not limited to atrial fibrillation, numerous atrial or ventricular
extra beats, paced rhythm, left ventricular bundle branch block, cancer, kidney or
hepatic failure, and diabetes mellitus)
Universitair Ziekenhuis Brussel
Jette, Brussel, Belgium
Investigator: Marc Schiltz, MD
Contact: +32 2 477 60 20
marc.schiltz@uzbrussel.be
Investigator:
Marc Schiltz, MD
+32 2 477 60 20
marc.schiltz@uzbrussel.be