To the Editor
Long-term care facilities, particularly skilled nursing facilities (SNFs), have felt the impact of the COVID-19 pandemic, with high mortality rates observed in residents. SNF residents comprise less than 1% of the US population,1 however, this population accounted for over 31% of COVID-19 deaths in the United States through June 2021.2 Following the noted increased risk of venous thromboembolism observed in patients with COVID-19,3 , 4 investigations have demonstrated increased survival in noncritically ill hospitalized individuals treated with heparin.5 Professional societies and the National Institutes of Health have developed guidelines that encourage the use of anticoagulation in hospitalized individuals with COVID-19.6 , 7 Although studies support the use of heparin in hospitalized patients, no similar data have been published regarding the population that resides in SNFs.8 Our study aimed to evaluate the impact of underlying use of antithrombotics (ATs) on the 30-day mortality of individuals diagnosed with COVID-19 in SNFs. A secondary objective was to assess the relationship between age and sex with 30-day all-cause mortality in patients with COVID-19.
Methods
The study population included 6884 Institutional Special Needs Program enrollees initially diagnosed with COVID-19 between March 1, 2020, and May 31, 2020. The ISNP provides increased clinical resources at the SNF bedside to safely treat residents in their homes and avoid unnecessary transfers and hospital admissions. This subset of facility residents may have more on-site care and treatment than the broader SNF population. COVID-19 was determined from clinical documentation, the use of a International Classification of Diseases, Tenth Revision code for COVID-19 implemented by the Centers for Disease Control and Prevention on April 1, 2020, or an internally maintained COVID-19 registry. The registry also included location and date of death if applicable. Diagnoses were sourced from medical claims including hospital inpatient, skilled nursing inpatient, and outpatient claims. Age and sex were retrieved from medical claims and based on member age as of March 1, 2020. The project was determined to be exempt from institutional review board review under exemption category 4(ii).
Results
Some SNF residents are treated with ATs (defined as aspirin and other antiplatelets as well as anticoagulants such as warfarin or direct oral anticoagulants) because of pre-existing conditions such as venous thromboembolism, recent intravascular stent placement, and recent acute coronary syndromes. Most study members (81.8%) were not treated with ATs at the time of diagnosis. Use of ATs resulted in significantly lower odds of 30-day mortality compared with those without these medications (aOR 0.83, 95% CI 0.71-0.97) (Table 1 ). Thirty-day all-cause mortality for the study population was 23.2%. Mortality rates increased with age and were higher among male (26.1%) than female (21.6%) individuals. Older age groups had significantly higher odds of 30-day mortality compared with those less than 65 years old. Male individuals had significantly higher odds of 30-day mortality than female individuals (aOR 1.69, 95% CI 1.49-1.92). Limitations of this study include its focus on the first few months of the pandemic. Testing capacity was limited which likely contributed to underdiagnosis of asymptomatic SARS-CoV-2 infection during this period. In addition, prior to the development of the International Classification of Diseases, Tenth Revision code for COVID-19, positive diagnoses were identified for our database based on clinical documentation.
Table 1.
Features | Percent of Population | aOR | P Value | Confidence Low | Confidence High |
---|---|---|---|---|---|
Antithrombotic use | 18.2% | 0.83 | <.05 | 0.71 | 0.97 |
Age category: | |||||
65‒69 y | 10.7% | 1.41 | <.001 | 1.06 | 1.88 |
70‒74 y | 13.1% | 1.70 | <.001 | 1.30 | 2.23 |
75‒79 y | 14.9% | 1.79 | <.001 | 1.38 | 2.34 |
80‒84 y | 14.7% | 2.42 | <.001 | 1.87 | 3.15 |
85‒89 y | 15.5% | 3.03 | <.001 | 2.35 | 3.93 |
90 y and older | 19.1% | 3.71 | <.001 | 2.89 | 4.79 |
<65 y | 12.0% | Ref | |||
Sex: | |||||
Male | 35.6% | 1.69 | <.001 | 1.49 | 1.92 |
Female | 64.4% | Ref | |||
Medical conditions: | |||||
Cancer | 12.3% | 0.72 | <.001 | 0.60 | 0.87 |
CKD | 30.3% | 1.70 | <.001 | 1.50 | 1.93 |
COPD | 48.7% | 1.07 | .280 | 0.95 | 1.20 |
CAD CHF | 42.8% | 1.13 | <.05 | 1.00 | 1.28 |
Thrombosis | 4.0% | 0.76 | .086 | 0.54 | 1.04 |
CAD, coronary artery disease; CHF, congestive heart failure; CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease.
Discussion
Because of our limited sample size and the duration of the study, we were unable to determine if there was variability in the protective effect of one medication or class of medications over another. A separate review that includes more individuals followed over a longer period could help answer that question. Although we found coexistent AT use important in reducing 30-day mortality in COVID-19 positive nursing home residents, it is unclear whether ATs should be started in SNF residents newly infected with COVID-19 if they are not already using these medications. In addition, we must determine which patients are appropriate candidates for AT therapy in this context given the risk of bleeding posed by these medications in this population. Anticoagulant therapy has become a hallmark of medical care for COVID-19 in the hospital setting. It remains unclear whether other ATs would be effective, and questions remain about the indications and effectiveness of these therapies in the skilled nursing and outpatient settings. Additional areas of research include determining whether a specific class of AT medication is more effective at reducing 30-day mortality. The duration of the hypercoagulable period in this frail older population remains unclear, thus, recommendations regarding the duration of AT therapy warrant further study. Longer follow-up could provide additional insights into the risks and benefits of various therapies.
Acknowledgments
The authors wish to thank J. Michelle Graham PharmD, BCPS.
Footnotes
This research did not receive any funding from agencies in the public, commercial, or not-for-profit sectors. The authors declare no conflicts of interest.
References
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