Neuroleptics used in critical COVID associated with moderate-severe dyspnea after hospital discharge.
Summary
In a prospective cohort of 100 severe COVID-19 survivors, limiting dyspnea (mMRC >1) affected 57% at 1 month and 34% at 12 months. The total inpatient neuroleptic dose and baseline comorbidities independently predicted 1-month dyspnea; dyspnea at 1 month predicted persistence at 12 months, which correlated with worse mental health, frailty, and quality of life.
Key Findings
- Limiting dyspnea (mMRC >1) occurred in 56.6% at 1 month and 33.9% at 12 months post-discharge.
- Total inpatient neuroleptic dose and pre-existing comorbidities independently predicted 1-month dyspnea.
- Dyspnea at 1 month predicted persistent dyspnea at 12 months, associated with higher depression, anxiety, frailty, and lower quality of life.
Clinical Implications
Minimize neuroleptic exposure when feasible in critically ill COVID-19 patients; screen those with early dyspnea for targeted rehabilitation and mental health support.
Why It Matters
Identifies a modifiable inpatient exposure—neuroleptics—linked to long-term dyspnea, informing ICU pharmacologic stewardship and post-COVID rehabilitation priorities.
Limitations
- Single-center study with modest sample size and 37% loss to 12-month follow-up
- Potential confounding by indication regarding neuroleptic use
Future Directions
Interventional studies to reduce neuroleptic exposure in ICU and randomized rehabilitation strategies for patients with early post-discharge dyspnea.
Study Information
- Study Type
- Cohort
- Research Domain
- Prognosis
- Evidence Level
- III - Prospective cohort with multivariable analysis of risk factors
- Study Design
- OTHER