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Sex differences in sequelae from COVID-19 infection and in long COVID syndrome: a review.
Sylvester, Shirley V; Rusu, Rada; Chan, Biankha; Bellows, Martha; O'Keefe, Carly; Nicholson, Susan.
  • Sylvester SV; Johnson & Johnson, Women's Health, Office of the Chief Medical Officer, New Brunswick, NJ, USA.
  • Rusu R; Clinical Operations, Johnson & Johnson, Office of the Chief Medical Officer, Toronto, Canada.
  • Chan B; Clinical Operations, Johnson & Johnson, Office of the Chief Medical Officer, Toronto, Canada.
  • Bellows M; Johnson & Johnson, Healthcare Technology Center, Providence, RI, USA.
  • O'Keefe C; Johnson & Johnson, Healthcare Technology Center, Providence, RI, USA.
  • Nicholson S; Johnson & Johnson, Women's Health, Office of the Chief Medical Officer, New Brunswick, NJ, USA.
Curr Med Res Opin ; 38(8): 1391-1399, 2022 08.
Article in English | MEDLINE | ID: covidwho-1895655
ABSTRACT

OBJECTIVE:

We conducted literature reviews to uncover differential effects of sex on sequelae from coronavirus disease 2019 (COVID-19) and on long COVID syndrome.

METHODS:

Two authors independently searched OvidSP in Embase, Medline, Biosis, and Derwent Drug File. Publications reporting original, sex-disaggregated data for sequelae of COVID-19 (published before August 2020) and long COVID syndrome (published before June 2021) were included in the reviews. The association between COVID-19 sequelae (i.e. lasting <4 weeks after symptom onset) and sex, and between long COVID syndrome (i.e. lasting >4 weeks after symptom onset) and sex, was determined by odds ratio (OR) and 95% confidence interval (CI) (statistical significance defined by 95% CI not including 1).

RESULTS:

Of 4346 publications identified, 23 and 12 met eligibility criteria for COVID-19 sequelae and long COVID syndrome, respectively. COVID-19 sequelae in the categories of psychiatric/mood (OR = 1.80; 95% CI 1.35-2.41), ENT (OR = 1.42; 95% CI 1.39-1.46), musculoskeletal (OR = 1.15; 95% CI 1.14-1.16), and respiratory (OR = 1.09; 95% CI 1.08-1.11) were significantly more likely among females (vs. males), whereas renal sequelae (OR = 0.83; 95% CI 0.75-0.93) were significantly more likely among males. The likelihood of having long COVID syndrome was significantly greater among females (OR = 1.22; 95% CI 1.13-1.32), with the odds of ENT (OR = 2.28; 95% CI 1.94-2.67), GI (OR = 1.60; 95% CI 1.04-2.44), psychiatric/mood (OR = 1.58; 95% CI 1.37-1.82), neurological (OR = 1.30; 95% CI 1.03-1.63), dermatological (OR = 1.29; 95% CI 1.05-1.58), and other (OR = 1.36; 95% CI 1.25-1.49) disorders significantly higher among females and the odds of endocrine (OR = 0.75; 95% CI 0.69-0.81) and renal disorders (OR = 0.74; 95% CI 0.64-0.86) significantly higher among males.

CONCLUSIONS:

Sex-disaggregated differences for COVID-19 sequelae and long COVID syndrome were observed. Few COVID-19 studies report sex-disaggregated data, underscoring the need for further sex-based research/reporting of COVID-19 disease.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Observational study / Prognostic study / Reviews Topics: Long Covid Limits: Female / Humans / Male Language: English Journal: Curr Med Res Opin Year: 2022 Document Type: Article Affiliation country: 03007995.2022.2081454

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Observational study / Prognostic study / Reviews Topics: Long Covid Limits: Female / Humans / Male Language: English Journal: Curr Med Res Opin Year: 2022 Document Type: Article Affiliation country: 03007995.2022.2081454