# Assessment of long COVID symptom burden in patients testing positive for SARS-CoV-2 at a nationwide retail pharmacy

**Authors:** Xiaowu Sun, Joseph C. Cappelleri, Laura L. Lupton, Mary M. Moran, Santiago M. C. Lopez, Laura Puzniak, Alon Yehoshua, Manuela Di Fusco

PMC · DOI: 10.1371/journal.pone.0345639 · PLOS One · 2026-03-25

## TL;DR

This study evaluated how many long COVID symptoms patients experience and found that symptom count is a reliable way to measure symptom burden.

## Contribution

The study proposes a valid and internally consistent method for categorizing long COVID symptom burden using symptom count.

## Key findings

- Number of long COVID symptoms correlated strongly with validated patient-reported outcome measures like fatigue and activity impairment.
- Patients with more symptoms showed significantly worse outcomes in all five EQ-5D domains.
- Symptom count can classify patients into low, medium, and high long COVID burden categories.

## Abstract

Numerous grouping and scoring methodologies have been proposed to assess long COVID symptomatology. One approach is to use symptom count as a simple, quantifiable measure of long COVID symptom burden.

This was a secondary analysis of a nationwide patient-reported outcomes (PRO) study that recruited symptomatic adults testing positive for SARS-CoV-2 at a Retail Pharmacy in the spring of 2023. EQ-5D-5LTM, work productivity and impairment (WPAI), the Patient-Reported Outcomes Measurement Information System (PROMIS®) fatigue, and a long COVID symptom questionnaire were administered at Week 4, Month 3, and Month 6 after testing. Pre-infection EQ-5D-5L, WPAI, PROMIS fatigue were collected via recall. Cronbach’s α assessed internal consistency of symptoms. Scree plots determined number of significant factors (symptoms) to retain for analysis. Spearman correlation coefficients were calculated between number of symptoms and EQ-5D-5L, WPAI, PROMIS fatigue scores and their changes from pre-COVID baseline. Categorization of long COVID burden using number of symptoms was proposed based on scores via equipercentile linking.

Of 505 patients, mean age was 46.3 years, 70.7% were female. Cronbach’s α was 0.865, denoting good internal consistency of the symptom survey instrument. The scree plot supported use of one factor for the composite 30-symptom list. Number of symptoms correlated strongly with EuroQol Utility Index (r = −0.53), presenteeism (r = 0.51), activity impairment (r = 0.51) and fatigue (r = 0.56). Statistically significant differences in mean number of symptoms were found between patients with versus those without problems in any of the 5 domains of the EQ-5-dimensional descriptive system. Based on linked PRO scores, subjects could be classified into low (≤2), medium (3–9), and high (≥10) symptom burden.

Number of long COVID symptoms correlated with validated PRO measures and identified three symptom-based categories of long COVID burden. Number of symptoms is a valid and internally consistent measure to assess long COVID burden in outpatient settings.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, HPS1 (HPS1 biogenesis of lysosomal organelles complex 3 subunit 1) [NCBI Gene 3257] {aka BLOC3S1, HPS}
- **Diseases:** symptomatic (MESH:D010302), cough (MESH:D003371), AD (MESH:D000544), Fatigue (MESH:D005221), brain fog (MESH:D005222), Long COVID (MESH:D000094024), neurologic symptoms (MESH:D009461), productivity loss (MESH:D007787), COVID (MESH:D000086382), NEW (OMIM:181405), anxiety (MESH:D001007), Impairment (MESH:D060825), infection (MESH:D007239), COVID (MESH:D018352), WPAI (MESH:D000073397), depression (MESH:D003866), cardiac and respiratory symptoms (MESH:D012818), digestive (MESH:D004828), activity impairment (MESH:D001523), PD (MESH:D010300), sleep problems (MESH:D012893), pain (MESH:D010146), immune system (MESH:D007154), microvascular damage (MESH:D017566)
- **Chemicals:** EQ-5D (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13016359/full.md

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Source: https://tomesphere.com/paper/PMC13016359