PMID- 35584831 OWN - NLM STAT- MEDLINE DCOM- 20220520 LR - 20240426 IS - 1473-4893 (Electronic) IS - 1470-2118 (Print) IS - 1470-2118 (Linking) VI - 22 IP - 3 DP - 2022 May TI - The clinical course of pneumomediastinum in patients with SARS-CoV-2 before invasive mechanical ventilation. PG - 271-275 LID - 10.7861/clinmed.2021-0441 [doi] AB - Pneumomediastinum and pneumothorax are recognised complications encountered in COVID-19 before or during invasive mechanical ventilation (IMV). The clinical course of patients developing pneumomediastinum before IMV is yet to be evaluated.Four-thousand, one-hundred and thirty-one patients hospitalised with COVID-19 over a 12-month period were retrospectively reviewed to evaluate for incidence, clinical characteristics and outcomes. A subgroup analysis was done to identify any clinical traits between survivors and non-survivors. The overall incidence of pneumomediastinum prior to IMV was 0.92% (n=38) and was seen at admission or during non-invasive respiratory support. Thirty-seven per cent had associated pneumothorax most commonly unilateral (right side). The median (interquartile range (IQR)) duration from admission to developing pneumomediastinum was 7 days (3-11) and complete resolution was seen in 53% of patients; median (IQR) duration to resolution was 8 days (4-17). The in-hospital mortality associated with pneumomediastinum in patients with SARS-CoV-2 (PneumoCoV) was 55%. Increasing age (68 +/- 12 years vs 56 +/- 14 years; p=0.01), higher body mass index (31 +/- 5 kg/m(2) vs 28 +/- 5 kg/m(2); p=0.04), lack of resolution of pneumomediastinum (67% vs 24%; p=0.01; odds ratio (OR) 6.5; 95% confidence interval (CI) 1.5-27.5), presence of concurrent pneumothorax (65% vs 14%; p=0.002; OR 11; 95% CI 2.2-53.1) and elevated procalcitonin levels (>0.5 ng/mL; 81% vs 41%; p=0.01; OR 6; 95% CI 1.4-26) were significant features in those who did not survive.The incidence of PneumoCoV, despite being low, is associated with increased mortality. It is a hallmark of moderate to severe disease with multifaceted contributory factors. Both demographic and clinical factors predict survival. CI - (c) Royal College of Physicians 2022. All rights reserved. FAU - Dwarakanath, Akshay AU - Dwarakanath A AD - The Mid Yorkshire Hospitals NHS Trust, Wakefield, UK akshay.dwarakanath@nhs.net. FAU - Horgan, Laura AU - Horgan L AD - The Mid Yorkshire Hospitals NHS Trust, Wakefield, UK. FAU - Jayawardena, Manika AU - Jayawardena M AD - The Mid Yorkshire Hospitals NHS Trust, Wakefield, UK. FAU - Thirumaran, Muthu AU - Thirumaran M AD - The Mid Yorkshire Hospitals NHS Trust, Wakefield, UK. FAU - Johnson, Owen AU - Johnson O AD - The Mid Yorkshire Hospitals NHS Trust, Wakefield, UK. LA - eng PT - Journal Article PL - England TA - Clin Med (Lond) JT - Clinical medicine (London, England) JID - 101092853 SB - IM MH - Aged MH - Aged, 80 and over MH - *COVID-19/complications/therapy MH - Humans MH - *Mediastinal Emphysema/epidemiology/etiology/therapy MH - Middle Aged MH - *Pneumothorax/epidemiology/etiology/therapy MH - Respiration, Artificial/adverse effects MH - Retrospective Studies MH - SARS-CoV-2 PMC - PMC9135094 OTO - NOTNLM OT - SARS-CoV-2 OT - pneumomediastinum OT - pneumothorax OT - pulmonary complication OT - respiratory failure EDAT- 2022/05/19 06:00 MHDA- 2022/05/21 06:00 PMCR- 2022/05/01 CRDT- 2022/05/18 20:33 PHST- 2022/05/18 20:33 [entrez] PHST- 2022/05/19 06:00 [pubmed] PHST- 2022/05/21 06:00 [medline] PHST- 2022/05/01 00:00 [pmc-release] AID - S1470-2118(24)02966-X [pii] AID - clinmedicine [pii] AID - 10.7861/clinmed.2021-0441 [doi] PST - ppublish SO - Clin Med (Lond). 2022 May;22(3):271-275. doi: 10.7861/clinmed.2021-0441.