# Health diagnosis associated with COVID-19 death in the United States: A retrospective cohort study using electronic health records

**Authors:** Mariam Joseph, Qiwei Li, Sunyoung Shin

PMC · DOI: 10.1371/journal.pone.0319585 · 2025-03-31

## TL;DR

This study identifies demographic factors and health conditions linked to higher risk of death from COVID-19 in the U.S.

## Contribution

The study highlights novel health diagnoses associated with increased risk of mortality from COVID-19.

## Key findings

- Patients from the West region of the U.S. had the highest odds ratio for COVID-19 mortality.
- Complications related to pregnancy showed the highest odds ratio for influencing COVID-19 death.
- Conditions like renal failure, influenza and pneumonia, and diabetes were significantly associated with increased mortality risk.

## Abstract

The United States has experienced high surge in COVID-19 cases since the dawn of 2020. Identifying the types of diagnoses that pose a risk in leading COVID-19 death casualties will enable our community to obtain a better perspective in identifying the most vulnerable populations and enable these populations to implement better precautionary measures.

To identify demographic factors and health diagnosis codes that pose a high or a low risk to COVID-19 death from individual health record data sourced from the United States.

We used logistic regression models to analyze the top 500 health diagnosis codes and demographics that have been identified as being associated with COVID-19 death.

Among 223,286 patients tested positive at least once, 218,831 (98%) patients were alive and 4,455 (2%) patients died during the duration of the study period. Through our logistic regression analysis, four demographic characteristics of patients; age, gender, race and region, were deemed to be associated with COVID-19 mortality. Patients from the West region of the United States: Alaska, Arizona, California, Colorado, Hawaii, Idaho, Montana, Nevada, New Mexico, Oregon, Utah, Washington, and Wyoming had the highest odds ratio of COVID-19 mortality across the United States. In terms of diagnoses, Complications mainly related to pregnancy (Adjusted Odds Ratio, OR:2.95; 95% Confidence Interval, CI:1.4 - 6.23) hold the highest odds ratio in influencing COVID-19 death followed by Other diseases of the respiratory system (OR:2.0; CI:1.84 – 2.18), Renal failure (OR:1.76; CI:1.61 – 1.93), Influenza and pneumonia (OR:1.53; CI:1.41 – 1.67), Other bacterial diseases (OR:1.45; CI:1.31 – 1.61), Coagulation defects, purpura and other hemorrhagic conditions(OR:1.37; CI:1.22 – 1.54), Injuries to the head (OR:1.27; CI:1.1 - 1.46), Mood [affective] disorders (OR:1.24; CI:1.12 – 1.36), Aplastic and other anemias (OR:1.22; CI:1.12 – 1.34), Chronic obstructive pulmonary disease and allied conditions (OR:1.18; CI:1.06 – 1.32), Other forms of heart disease (OR:1.18; CI:1.09 – 1.28), Infections of the skin and subcutaneous tissue (OR: 1.15; CI:1.04 – 1.27), Diabetes mellitus (OR:1.14; CI:1.03 – 1.26), and Other diseases of the urinary system (OR:1.12; CI:1.03 – 1.21).

We found demographic factors and medical conditions, including some novel ones which are associated with COVID-19 death. These findings can be used for clinical and public awareness and for future research purposes.

## Linked entities

- **Diseases:** Renal failure (MONDO:0001106), Diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Diseases:** purpura (MESH:D011693), Influenza and (MESH:D007251), Mood [affective] disorders (MESH:D019964), Renal failure (MESH:D051437), Coagulation defects (MESH:D001778), Injuries to the head (MESH:D006259), died (MESH:D003643), bacterial diseases (MESH:D001424), Chronic obstructive pulmonary disease (MESH:D029424), diseases of the respiratory system (MESH:D015619), hemorrhagic conditions (MESH:D006474), Aplastic and other anemias (MESH:D000741), pneumonia (MESH:D011014), COVID-19 (MESH:D000086382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11957315/full.md

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Source: https://tomesphere.com/paper/PMC11957315