Outcomes Among Patients Referred to Outpatient Rehabilitation Clinics After COVID-19 diagnosis — United States, January 2020–March 2021
Weekly / July 9, 2021 / 70(27);967–971
Please note: This report has been corrected. An erratum has been published.
Jessica S. Rogers-Brown, PhD1,2; Valentine Wanga, PhD1,3; Catherine Okoro, PhD4; Diane Brozowsky, MBA5; Alan Evans, DPT5; David Hopwood, MSHI5; Jennifer R. Cope, MD1; Brendan R. Jackson, MD1; Dena Bushman, MSN, MPH1,3; Alfonso C. Hernandez-Romieu, MD1,3; Robert A. Bonacci, MD1,3; Tim McLeod, MPH1; Jennifer R. Chevinsky, MD1,3; Alyson B. Goodman, MD1; Meredith start highlightG. Dixonend highlight, MD1; Caitlyn start highlightLutfyend highlight, MPH1; Julie Rushmore, PhD, DVM1; Emily Koumans, MD1; Sapna Bamrah Morris, MD1; William Thompson, PhD2 (View author affiliations)View suggested citation
What is already known about this topic?
COVID-19 patients might experience symptoms that persist months after initial infection.
What is added by this report?
Compared with control patients enrolled in a cancer rehabilitation program, adult post–COVID-19 patients referred for rehabilitation services reported poorer physical health and being less able to engage in physical activities and activities of daily living. Patients recovering from COVID-19 also had significantly higher health care use than control patients.
What are the implications for public health practice?
Patients recovering from COVID-19 might require tailored physical and mental health rehabilitation services.
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As of June 30, 2021, 33.5 million persons in the United States had received a diagnosis of COVID-19 (1). Although most patients infected with SARS-CoV-2, the virus that causes COVID-19, recover within a few weeks, some experience post–COVID-19 conditions. These range from new or returning to ongoing health problems that can continue beyond 4 weeks. Persons who were asymptomatic at the time of infection can also experience post–COVID-19 conditions. Data on post–COVID-19 conditions are emerging and information on rehabilitation needs among persons recovering from COVID-19 is limited. Using data acquired during January 2020–March 2021 from Select Medical* outpatient rehabilitation clinics, CDC compared patient-reported measures of health, physical endurance, and health care use between patients who had recovered from COVID-19 (post–COVID-19 patients) and patients needing rehabilitation because of a current or previous diagnosis of a neoplasm (cancer) who had not experienced COVID-19 (control patients). All patients had been referred to outpatient rehabilitation. Compared with control patients, post–COVID-19 patients had higher age- and sex-adjusted odds of reporting worse physical health (adjusted odds ratio [aOR] = 1.8), pain (aOR = 2.3), and difficulty with physical activities (aOR = 1.6). Post–COVID-19 patients also had worse physical endurance, measured by the 6-minute walk test† (6MWT) (p<0.001) compared with control patients. Among patients referred to outpatient rehabilitation, those recovering from COVID-19 had poorer physical health and functional status than those who had cancer, or were recovering from cancer but not COVID-19. Patients recovering from COVID-19 might need additional clinical support, including tailored physical and mental health rehabilitation services.
Data were obtained from electronic health records (EHRs) of patients referred to Select Medical’s outpatient rehabilitation clinics during January 2020–March 2021. Epidemiologic, clinical, and functional data from 1,295 post–COVID-19 patients and 2,395 control patients were examined. Post-COVID-19 patients were defined as those who were referred to a Select Medical facility for post–COVID-19 physical rehabilitation. Control patients, defined as those needing rehabilitation for a current or previous diagnosis of cancer with no history of an International Classification of Diseases, Tenth Revision (ICD-10) COVID-19 diagnosis code,§ were referred to a Select Medical cancer rehabilitation program. This control population was chosen because patients in this group completed the same initial evaluations as patients referred for post–COVID-19 rehabilitation. Information on type of cancer or interval since diagnosis was not available. Patient data were collected from EHRs and initial clinical evaluation, which included self-reported health measures and a 6MWT. At intake, self-reported measures and clinical evaluations were administered for health, physical endurance, and health care use.
Using validated scales, CDC assessed patients’ mental and physical health, functional health, social participation ability, applied cognition, and physical endurance with Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health (version 1.2; National Institutes of Health), PROMIS Physical Function, PROMIS Ability,¶ Quality of Life in Neurologic Disorders (Neuro-QoL),** and the 6MWT,†† respectively. For self-reported item-level data, five-point Likert scales were recoded to proportions. T-scores were computed for composite measures of physical and mental health, social participation ability, and applied cognition, where the summed raw scores were converted to T-scores based on standardized scoring tables; T-scores were designed to have a mean of 50 and a standard deviation (SD) of 10 for the general adult population Logistic regression analysis, adjusted for age and sex, was used to examine differences in patient-reported measures of health, physical endurance, and health care use between post–COVID-19 and control patients.§§ All analyses were conducted using SAS (version 9.4; SAS Institute). This activity was reviewed by CDC and was conducted consistent with applicable federal law and CDC policy.¶¶
Post–COVID-19 patients referred for rehabilitation services differed from control patients by several characteristics, including sex, age, race, ethnicity, employment status, health insurance coverage, and U.S. Census region (Table 1). Compared with control patients, post–COVID-19 patients were more likely to be male, younger, in the labor force, insured by a commercial plan or a worker’s compensation plan, and less likely to be covered by Medicaid or Medicare (Table 1). Post–COVID-19 patients were more likely to have received a diagnosis of generalized muscle weakness or fatigue (72.7% versus 42.3%) and patient-reported symptoms of generalized muscle weakness, malaise, and fatigue (69.0% versus 59.7%) (Table 2).
Compared with control patients, post–COVID-19 patients had higher prevalences of reported fair or poor general health (32.9% versus 25.4%), poorer physical health (44.1% versus 32.6%), pain level ≥7 (on a scale of 0–10) (40.4% versus 24.8%), and difficulty with physical activities (32.3% versus 24.2%) (Table 3). Post–COVID-19 patients also reported a higher prevalence of fair or poor overall mental health than control patients (19.1% versus 15.3%). Post–COVID-19 patients and control patients reported more challenges with applied cognition as indicated by T-scores (42.2 versus 41.2), both approximately one SD below the normative sample with which the scale was developed. Post–COVID-19 patients also demonstrated reduced physical endurance on the 6MWT compared with control patients (distance of 303 m versus 377 m; p<0.001) and reported increased difficulty completing chores (38.2% versus 25.2%), navigating stairs (40.2% versus 18.3%), running errands or shopping (34.3% versus 16.0%), and walking for 15 minutes (38.2% versus 16.6%). Compared with control patients, post–COVID-19 patients also reported more difficulty doing usual work or work at home (37.2% versus 20.4%) and challenges in ability to participate in activities with friends (33.0% versus 18.8%). For measures of health care use, post–COVID-19 patients required significantly more visits (median = 9, interquartile range [IQR] = 4–20) than control patients (median = 5, IQR 1–11; p<0.001) and longer therapy duration (median = 35 days, IQR = 15–71 days versus median = 27 days, IQR = 0–57 days; p<0.001).
Among patients referred to Select Medical’s outpatient rehabilitation clinics during January 2020–March 2021 (during the COVID-19 pandemic), patients who previously had COVID-19 reported poorer general, mental, and physical health (i.e., overall physical health, physical activities, and pain), and functioning (i.e., physical and social, such as ability to do chores, usual work, or activities with friends) compared with patients with no previous diagnosis of COVID-19 referred for cancer rehabilitation. Also, post–COVID-19 patients did not perform as well as control patients on a measured assessment of physical functioning (6MWT). Finally, post–COVID-19 patients used more rehabilitative services than control patients. These findings indicate that among patients referred to outpatient rehabilitation, those recovering from COVID-19 might have poorer physical health and functional status than do patients with cancer but not COVID-19 and could benefit from additional clinical support, including tailored physical and mental health rehabilitation services.
The identification of poorer physical health among post–COVID-19 patients is consistent with a previous study that found that 92% of post–COVID-19 patients had diagnoses potentially related to post–COVID-19 conditions, including weakness, malaise, fatigue, respiratory failure with hypoxia, and gait abnormalities (2,3). Poorer self-reported physical and mental health is associated with long-term negative health outcomes including chronic diseases (e.g., diabetes and cardiovascular disease), functional decline (4), and mortality (5). The lower scores on applied cognitive ability tasks suggest more subtle deficits in cognitive functioning, which might indicate the need for further evaluation and additional need for health care resources and services (6). Further, physical function, as measured by the 6MWT, has been shown to be an important outcome for assessing impact of COVID-19 (4). Additional studies have shown that patients recovering from COVID-19 have higher incidences of negative health outcomes, including poorer physical health and functional status, and might need additional clinical support such as tailored physical and mental health rehabilitation services (7,8). These findings have implications for health care systems during and after the COVID-19 pandemic (9). Postacute sequalae associated with COVID-19 have not been comprehensively described, and data from studies of long-term follow-up to provide reliable estimates of the long-term sequelae associated with COVID-19 are still emerging (6–8). Continued assessments of self-reported health data are important to characterize the sequelae of novel infectious diseases and are critical for developing cost-effectiveness estimates for lifesaving interventions, such as vaccines and other potentially important rehabilitation therapies and interventions, including physical therapy, occupational therapy, and services and therapies associated with cognitive and functional decline (9,10).
The findings in this report are subject to at least six limitations. First, date of infection was not available; therefore, time-varying effects associated with infection date could not be examined. Second, data on severity of illness, including hospitalization status, were not available, precluding assessment of the impact of illness severity on post–COVID-19 conditions. Third, given the large amount of missing data (>50%) for many demographic variables (e.g., race, ethnicity, employment status, and occupation), which are common limitations in large EHR data sets, it was not possible to control for additional demographic differences. Fourth, the absence of pre–COVID-19 assessments did not permit controlling for premorbid function. Fifth, the types of cancer diagnoses and treatments were not available, which is an important consideration given heterogeneity of cancer sequelae. Similarly, assessing other comorbidities was not possible; post–COVID-19 patients might have had more underlying medical conditions (e.g., diabetes or obesity) than did control patients, which could explain poorer physical and mental health measures. However, given that patients in the post–COVID-19 group were younger and more commonly employed than were those in the control group, it is likely that these two populations are different with regard to demographic factors and the prevalence of comorbid chronic conditions. Finally, referral to physical rehabilitation depended on nonstandardized clinical judgment, which might have led to differences in patient population by group. Therefore, these results should not be interpreted to mean that post–COVID-19 patients overall had poorer physical and mental health than patients with cancer. Instead, results indicate that post–COVID-19 patients specifically referred to a large physical rehabilitation network had poorer health measures than those referred for cancer, which indicates that some patients recovering from COVID-19 had substantial rehabilitation needs.
Patients recovering from COVID-19 might experience continued poor health and could benefit from additional support and tailored physical and mental health rehabilitation services. Health care systems and providers should be prepared to recognize and meet the ongoing needs of this patient population. Efforts to increase COVID-19 vaccination could include messaging that states that preventing COVID-19 also prevents post–COVID-19 conditions with potential effects on long-term health.
Corresponding author: Jessica S. Rogers-Brown, email@example.com.
1CDC COVID-19 Response Team; 2Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, CDC; 3Epidemic Intelligence Service, CDC; 4Division of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities, CDC; 5Select Medical, Mechanicsburg, Pennsylvania.
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.
* Data used were from Select Medical, a network of rehabilitation clinics in 36 states and the District of Columbia. https://www.selectmedical.com/external icon
† https://www.thoracic.org/statements/resources/pfet/sixminute.pdfpdf iconexternal icon
§ International Classification of Diseases, Tenth Revision codes used to examine potential post-COVID condition were J96.01, M62.81, R.26.2, R26.89 R53, R53.1, and R53.83.
¶ PROMIS items use a Likert-type response scale (https://commonfund.nih.gov/promis/indexexternal icon). The 10 PROMIS items used in this analysis included overall self-rated health; overall quality of life; overall physical health; overall mental health; and individual items on fatigue, pain, emotional distress, and social activities and roles. Most questions asked about a person’s experience “in general,” with items on fatigue, pain, and emotional problems experienced during the past 7 days. Psychometric evaluation of the PROMIS global health items were based on two global physical health (GPH) and global mental health (GMH) scales. The PROMIS GPH scale included four items that rated overall physical health (physical functioning, physical activities, pain, and fatigue). GPH and GMH total raw scores were computed by summing item scores that ranged from 1 to 5, such that higher scores reflected better functioning and are then rescaled to a mean of 50 and an SD of 10 using nationally normative data from the U.S. general population. The estimated correlation between the GPH and GMH was 0.63.
** Neuro-QoL is a set of self-report measures that assesses the health-related quality of life of adults with neurologic disorders. Neuro-QoL AC-GC assesses perceived difficulties in everyday cognitive abilities, such as memory, attention, and decision-making. https://www.healthmeasures.net/explore-measurement-systems/neuro-qolexternal icon
†† Physical endurance was assessed using the 6-minute walk test. A poor 6-minute walk distance (e.g., <300 m) might have prognostic value (i.e., usually associated with an increased risk of mortality), and a change of 14.0 to 30.5 m might be clinically relevant.
§§ Other demographic variables besides sex and age had substantial proportions of missing data (26%–75%); therefore, these variables were not included in the analysis.
¶¶ 45 C.F.R. part 46, 21 C.F.R. part 56; 42 U.S.C. Sect. 241(d); 5 U.S.C. Sect. 552a; 44 U.S.C. Sect. 3501 et seq.
- CDC. COVID data tracker. Atlanta, GA: US Department of Health and Human Services, CDC. Accessed April 30, 2021. https://covid.cdc.gov/covid-data-tracker/#demographics.
- National Opinion Research Center. General social surveys, 1972–2018: cumulative codebook. Chicago, Illinois: University of Chicago, National Opinion Research Center; 2019. https://gss.norc.org/documents/codebook/gss_codebook.pdfpdf iconexternal icon
- Hernandez-Romieu AC, Leung S, Mbanya A, et al. Health care utilization and clinical characteristics of nonhospitalized adults in an integrated health care system 28–180 days after COVID-19 diagnosis—Georgia, May 2020–March 2021. MMWR Morb Mortal Wkly Rep 2021;70:644–50. https://doi.org/10.15585/mmwr.mm7017e3external icon PMID:33914727external icon
- Idler EL, Benyamini Y. Self-rated health and mortality: a review of twenty-seven community studies. J Health Soc Behav 1997;38:21–37. https://doi.org/10.2307/2955359external icon PMID:9097506external icon
- Simpson R, Robinson L. Rehabilitation after critical illness in people with COVID-19 infection. Am J Phys Med Rehabil 2020;99:470–4. https://doi.org/10.1097/PHM.0000000000001443external icon PMID:32282359external icon
- Taquet M, Geddes JR, Husain M, Luciano S, Harrison PJ. 6-month neurological and psychiatric outcomes in 236 379 survivors of COVID-19: a retrospective cohort study using electronic health records. Lancet Psychiatry 2021;8:416–27. https://doi.org/10.1016/S2215-0366(21)00084-5external icon PMID:33836148external icon
- Al-Aly Z, Xie Y, Bowe B. High-dimensional characterization of post-acute sequelae of COVID-19. Nature 2021;594:259–64. https://doi.org/10.1038/s41586-021-03553-9external icon PMID:33887749external icon
- Writing Committee for the COMEBAC Study Group, Morin L, Savale L, et al. Four-month clinical status of a cohort of patients after hospitalization for COVID-19. JAMA 2021;325:1525–34. https://doi.org/10.1001/jama.2021.3331external icon PMID:33729425external icon
- Williams I, Essue B, Nouvet E, et al. Priority setting during the COVID-19 pandemic: going beyond vaccines. BMJ Glob Health 2021;6:e004686. https://doi.org/10.1136/bmjgh-2020-004686external icon PMID:33461979external icon
- Du Z, Pandey A, Bai Y, et al. Comparative cost-effectiveness of SARS-CoV-2 testing strategies in the USA: a modelling study. Lancet Public Health 2021;6:e184–91. https://doi.org/10.1016/S2468-2667(21)00002-5external icon PMID:33549196external icon
Suggested citation for this article: Rogers-Brown JS, Wanga V, Okoro C, et al. Outcomes Among Patients Referred to Outpatient Rehabilitation Clinics After COVID-19 diagnosis — United States, January 2020–March 2021. MMWR Morb Mortal Wkly Rep 2021;70:967–971. DOI: http://dx.doi.org/10.15585/mmwr.mm7027a2external icon.
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