TY - JOUR
T1 - The clinical impact of the Covid-19 pandemic first wave on patients with cystic fibrosis in New York
T2 - COVID-19 in Patients with Cystic Fibrosis in New York
AU - Simonson, Joseph L.
AU - Esposito, Christine
AU - Frantzen, Theresa
AU - Henthorne, Katherine
AU - Espinal, Aileen
AU - Romano, Serena
AU - Ramdeo, Ramona
AU - Trentacoste, Jessica
AU - Tsang, Donna
AU - LaVecchia, Geralyn
AU - Abdullah, Robert
AU - Berdella, Maria
AU - Bonitz, Lynn
AU - Condos, Rany
AU - Constantinescu, Andrei
AU - DeCelie-Germana, Joan K.
AU - DiMango, Emily
AU - Draine, Myah
AU - Gimeli, Tara
AU - Giusti, Robert
AU - Guzman, Jessenia
AU - Hammouda, Soumia
AU - Keating, Claire
AU - Kier, Catherine
AU - Lennox, Alison T.
AU - Liriano, Carmen
AU - Messer, Zachary
AU - Plachta, Amy
AU - Sadeghi, Hossein
AU - Schwind, Elinor
AU - Stables-Carney, Teresa
AU - Walker, Patricia
AU - Wang, Janice
N1 - Publisher Copyright: © 2022 European Cystic Fibrosis Society
PY - 2022/5
Y1 - 2022/5
N2 - Background: People with cystic fibrosis (pwCF) may be at risk of complications from COVID-19 but the impact of COVID-19 on pwCF remains unknown. Methods: We conducted a multicenter retrospective cohort study to assess the impact of the COVID-19 pandemic first wave on pwCF in the New York metropolitan area (NY) from March 1, 2020 to August 31, 2020. Objectives were to determine (1) the prevalence of COVID-19 by PCR and IgG antibody testing, (2) the clinical characteristics of COVID-19, (3) delay in routine outpatient care, and (4) the effect on anxiety and depression in pwCF. Results: There were 26 COVID-19 cases diagnosed by PCR or antibody testing among the study cohort of 810 pwCF. The prevalence of COVID-19 by PCR (1.6%) and IgG antibody (12.2%) testing was low. 58% of cases were asymptomatic and 82% were managed at home. 8% were hospitalized and 1 person died. 89% of pwCF experienced delay in care. The prevalence of anxiety increased from 43% baseline to 58% during the pandemic (P<0.01). In post-hoc analysis, the proportion of patients with diabetes (38% versus 16%, P<0.01) and pancreatic insufficiency (96% versus 66%, P<0.01) were higher while CFTR modulator use was lower (46% versus 65%, P = 0.05) in pwCF who tested positive for COVID-19. Conclusions: The prevalence of COVID-19 among pwCF in NY during the pandemic first wave was low and most cases were managed at home. CFTR modulators may be protective. PwCF experienced delay in routine care and increased anxiety.
AB - Background: People with cystic fibrosis (pwCF) may be at risk of complications from COVID-19 but the impact of COVID-19 on pwCF remains unknown. Methods: We conducted a multicenter retrospective cohort study to assess the impact of the COVID-19 pandemic first wave on pwCF in the New York metropolitan area (NY) from March 1, 2020 to August 31, 2020. Objectives were to determine (1) the prevalence of COVID-19 by PCR and IgG antibody testing, (2) the clinical characteristics of COVID-19, (3) delay in routine outpatient care, and (4) the effect on anxiety and depression in pwCF. Results: There were 26 COVID-19 cases diagnosed by PCR or antibody testing among the study cohort of 810 pwCF. The prevalence of COVID-19 by PCR (1.6%) and IgG antibody (12.2%) testing was low. 58% of cases were asymptomatic and 82% were managed at home. 8% were hospitalized and 1 person died. 89% of pwCF experienced delay in care. The prevalence of anxiety increased from 43% baseline to 58% during the pandemic (P<0.01). In post-hoc analysis, the proportion of patients with diabetes (38% versus 16%, P<0.01) and pancreatic insufficiency (96% versus 66%, P<0.01) were higher while CFTR modulator use was lower (46% versus 65%, P = 0.05) in pwCF who tested positive for COVID-19. Conclusions: The prevalence of COVID-19 among pwCF in NY during the pandemic first wave was low and most cases were managed at home. CFTR modulators may be protective. PwCF experienced delay in routine care and increased anxiety.
KW - Coronavirus
KW - Covid-19
KW - Cystic fibrosis
KW - SARS-CoV2
UR - https://www.scopus.com/pages/publications/85125816156
U2 - 10.1016/j.jcf.2022.02.012
DO - 10.1016/j.jcf.2022.02.012
M3 - Article
C2 - 35256307
SN - 1569-1993
VL - 21
SP - e176-e183
JO - Journal of Cystic Fibrosis
JF - Journal of Cystic Fibrosis
IS - 3
ER -