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Use of the Postacute Sequelae of COVID-19 Diagnosis Code in Routine Clinical Practice in the US

Educational Objective
To identify the key insights or developments described in this article
1 Credit CME
Key Points

Question  How is the International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code for postacute sequelae of COVID-19 being used in clinical practice?

Findings  In this cohort study, 56 143 patients had an ICD-10-CM code for post–COVID-19 conditions; among patients with 3 months of preindex continuous enrollment, 1080 (8.6%) were children. Only 698 patients (5.5%) had at least 1 of the 5 codes listed as possible concurrent conditions in the coding guidance.

Meaning  These findings suggest the diagnosis code is being used to identify patients of all ages with continuing illness following the acute phase of disease; however, the clinical presentation of postacute COVID-19 spans a range of conditions.

Abstract

Importance  A new International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) diagnosis code (U09.9 Post COVID-19 condition, unspecified) was introduced by the Centers for Disease Control and Prevention on October 1, 2021.

Objective  To examine the use of the U09.9 code and describe concurrently diagnosed conditions to understand physician use of this code in clinical practice.

Design, Setting, and Participants  This cohort study of US patients with an ICD-10-CM code for post–COVID-19 condition used deidentified patient-level claims data aggregated by HealthVerity. Children and adolescents (aged 0-17 years) and adults (aged 18-64 and ≥65 years) with a post–COVID-19 condition code were identified between October 1, 2021, and January 31, 2022. To identify a prior COVID-19 diagnosis, 3 months of continuous enrollment (CE) before the post–COVID-19 diagnosis date was required.

Main Outcomes and Measures  Presence of the ICD-10-CM U09.9 code.

Results  There were 56 143 patients (7723 female patients [61.2%]; mean [SD] age, 47.6 [19.2] years) with a post–COVID-19 diagnosis code, with cases increasing in mid-December 2021 following the trajectory of the Omicron case wave by 3 to 4 weeks. The analysis cohort included 12 622 patients after the 3-month preindex CE criteria was applied. Among this cohort, the median (IQR) age was 49 (35-61) years; however, 1080 (8.6%) were pediatric patients. The U09.9 code was used most often in the outpatient setting, although 305 older adults (14.0%) were inpatients. Only 698 patients (5.5%) had at least 1 of the 5 codes listed as possible concurrent conditions in the coding guidance. Only 8879 patients (70.4%) had a documented acute COVID-19 diagnosis code (569 [52.7%] among children), and the median (IQR) time between acute COVID-19 and post–COVID-19 diagnosis codes was 56 (21-200) days. The most common concurrently coded conditions varied by age; children experienced COVID-19–like symptoms (eg, 207 [19.2%] had cough and 115 [10.6%] had breathing abnormalities), while 459 older adults aged 65 years or older (21.1%) experienced respiratory failure and 189 (8.7%) experienced viral pneumonia.

Conclusions and Relevance  This retrospective cohort study found patients with a post–COVID-19 ICD-10-CM diagnosis code following the acute phase of COVID-19 disease among patients of all ages in clinical practice in the US. The use of the U09.9 code encompassed a wide range of conditions. It will be important to monitor how the use of this code changes as the pandemic continues to evolve.

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CME Disclosure Statement: Unless noted, all individuals in control of content reported no relevant financial relationships. If applicable, all relevant financial relationships have been mitigated.

Article Information

Accepted for Publication: August 11, 2022.

Published: October 6, 2022. doi:10.1001/jamanetworkopen.2022.35089

Open Access: This is an open access article distributed under the terms of the CC-BY-NC-ND License. © 2022 McGrath LJ et al. JAMA Network Open.

Corresponding Author: Leah J. McGrath, PhD, Real World Evidence Center of Excellence, Pfizer Inc, 235 E 42nd St, New York, NY 10017 (leah.mcgrath@pfizer.com).

Author Contributions: Dr McGrath and Mr Surinach had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: McGrath, Scott, Surinach, Malhotra.

Acquisition, analysis, or interpretation of data: McGrath, Scott, Surinach, Chambers, Benigno.

Drafting of the manuscript: McGrath, Scott, Surinach.

Critical revision of the manuscript for important intellectual content: Scott, Surinach, Chambers, Benigno, Malhotra.

Statistical analysis: McGrath, Surinach, Chambers, Benigno.

Obtained funding: McGrath.

Supervision: Benigno, Malhotra.

Conflict of Interest Disclosures: Dr McGrath reported being employed by and holding stock in Pfizer, Inc. Ms Scott reported being employed by and holding stock and stock options in Pfizer, Inc. Mr Surinach reported receiving consulting fees from Pfizer, Inc. Mr Chambers being employed by Pfizer, Inc. Mr Benigno reported being employed by and owning stock in Pfizer, Inc. Ms Malhotra reported being employed by and holding stock in Pfizer, Inc. No other disclosures were reported.

Funding/Support: This study was funded by Pfizer, Inc.

Role of the Funder/Sponsor: All authors participated, as employees of Pfizer, Inc, in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Additional Contributions: Amanda Miles, MPH (Pfizer, Inc), provided quality review of this manuscript and figures. Sina Noshad, MD (Genesis Research, Inc), provided writing assistance. Phoenix Riley, PharmD, MSc, and Amy Guisinger, PharmD, MPH (both from AESARA, Inc), provided assistance with revisions and were funded by Pfizer Inc.

References
1.
Bellan  M , Soddu  D , Balbo  P , Baricich  A , Zeppegno  P , Avanzi  G .  Respiratory and psychophysical sequelae among patients with COVID-19 four months after hospital discharge.   JAMA Netw Open. 2021;4(1):e2036142. doi:10.1001/jamanetworkopen.2020.36142PubMedGoogle ScholarCrossref
2.
Crook  H , Raza  S , Nowell  J , Young  M , Edison  P.   Long covid—mechanisms, risk factors, and management.   BMJ. 2021;374:n1648. doi:10.1136/bmj.n1648PubMedGoogle ScholarCrossref
3.
Tabacof  L , Tosto-Mancuso  J , Wood  J ,  et al.  Post-acute COVID-19 syndrome negatively impacts health and wellbeing despite less severe acute infection.   MedRxiv. Preprint posted online November 6, 2020. doi:10.1101/2020.11.04.20226126Google Scholar
4.
Nalbandian  A , Sehgal  K , Gupta  A ,  et al.  Post-acute COVID-19 syndrome.   Nat Med. 2021;27(4):601-615. doi:10.1038/s41591-021-01283-zPubMedGoogle ScholarCrossref
5.
Centers for Disease Control and Prevention. New ICD-10-CM code for post-COVID conditions, following the 2019 novel coronavirus (COVID-19). Accessed September 1, 2022. https://www.cdc.gov/nchs/data/icd/announcement-new-icd-code-for-post-covid-condition-april-2022-final.pdf
6.
Kadri  SS , Gundrum  J , Warner  S ,  et al.  Uptake and accuracy of the diagnosis code for COVID-19 among US hospitalizations.   JAMA. 2020;324(24):2553-2554. doi:10.1001/jama.2020.20323PubMedGoogle ScholarCrossref
7.
Centers for Disease Control and Prevention. ICD-10-CM tabular list of diseases: U09.9. 2022. Accessed September 1, 2022. https://icd10cmtool.cdc.gov/
8.
Xie  Y , Bowe  B , Al-Aly  Z .  Burdens of post-acute sequelae of COVID-19 by severity of acute infection, demographics and health status.   Nat Commun. 2021;12(1):6571. doi:10.1038/s41467-021-26513-3PubMedGoogle ScholarCrossref
9.
Say  D , Crawford  N , McNab  S , Wurzel  D , Steer  A , Tosif  S .  Post-acute COVID-19 outcomes in children with mild and asymptomatic disease.   Lancet Child Adolesc Health. 2021;5(6):e22-e23. doi:10.1016/S2352-4642(21)00124-3PubMedGoogle ScholarCrossref
10.
Borch  L , Holm  M , Knudsen  M , Ellermann-Eriksen  S , Hagstroem  S .  Long COVID symptoms and duration in SARS-CoV-2 positive children—a nationwide cohort study.   Eur J Pediatr. 2022;181(4):1597-1607. doi:10.1007/s00431-021-04345-zPubMedGoogle ScholarCrossref
11.
Buonsenso  D , Munblit  D , De Rose  C ,  et al.  Preliminary evidence on long COVID in children.   Acta Paediatr. 2021;110(7):2208-2211. doi:10.1111/apa.15870Google ScholarCrossref
12.
Fontana  LM , Villamagna  AH , Sikka  MK , McGregor  JC .  Understanding viral shedding of severe acute respiratory coronavirus virus 2 (SARS-CoV-2): review of current literature.   Infect Control Hosp Epidemiol. 2021;42(6):659-668. doi:10.1017/ice.2020.1273PubMedGoogle ScholarCrossref
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