# Trajectory, healthcare utilisation and recovery in 3590 individuals with long covid: a 4-year prospective cohort analysis

**Authors:** Jai Prashar, Toby Hillman, Emma C Wall, Amanpreet Sarna, Emma Mi, Robert Bell, Jagdeep Sahota, Michael Zandi, Patricia McNamara, Rebecca Livingston, Rebecca Gore, Catherine Lunken, Elena Bax, Rachel Nyam, Amir Masood Rafie Manzelat, Lyth Hishmeh, Emily Attree, Stephen Cone, Amitava Banerjee, Melissa Heightman

PMC · DOI: 10.1136/bmjopen-2025-103884 · 2026-01-14

## TL;DR

This study tracks recovery in 3590 long covid patients over 4 years, finding that only a third recover to 75% of their best health, with vaccination and fatigue levels influencing recovery.

## Contribution

The study provides the largest single-center analysis of long covid recovery trajectories and identifies key predictors of recovery.

## Key findings

- Only 33.4% of individuals recovered to >75% of their best health within 4 years.
- Vaccinated individuals had faster recovery rates compared to unvaccinated individuals.
- Fatigue severity, myalgia, and dysautonomic symptoms were inversely associated with recovery.

## Abstract

To characterise long-term trajectory of recovery in individuals with long covid.

Prospective cohort.

Single-centre, specialist post-COVID service (London, UK).

Individuals aged ≥18 years with long covid (hospitalised and non-hospitalised) from April 2020 to March 2024.

Routine, prospectively collected data on symptoms, quality of life (including Fatigue Assessment Scale (FAS) and EuroQol 5 Dimensions (EQ-5D), return to work status and healthcare utilisation (investigations, outpatient and emergency attendances). The primary outcome was recovery by self-reported >75% of ‘best health’ (EQ-5D Visual Analogue Scale) and was assessed using Cox proportional hazards regression models over 4 years. Linked National Health Service England registry data provided secondary care healthcare utilisation and expenditure.

We included 3590 individuals (63.3% female, 73.5% non-hospitalised, median age 50.0 years, 71.9% with ≥2 doses of COVID-19 vaccination), who were followed up for a median of 136 (0–346) days since first assessment and 502 (251–825) days since symptom onset. At first assessment, 33.2% of employed individuals were unable to work. Dominant symptoms were fatigue (78.7%), breathlessness (68.1%) and brain fog (53.5%). 33.4% of individuals recovered to >75% of best health prior to clinic discharge (recovery occurred median 202 (94–468) days from symptom onset). Vaccinated individuals were more likely to recover faster (pre: HR 2.93 (2.00–4.28) and post: HR 1.34 (1.05–1.71) COVID-19 infection), whereas recovery hazard was inversely associated with FAS (HR 0.37 (0.33–0.42)), myalgia (HR 0.59 (0.45–0.76)) and dysautonomic symptoms (HR 0.46 (0.34–0.62)). There was high secondary care healthcare utilisation (both emergency and outpatient care). Annual inpatient and outpatient expenditure was significantly lower in hospitalised individuals while under the service. When compared with the prereferral period, emergency department attendances were reduced in non-hospitalised patients with long covid, but outpatient costs increased.

In the largest long covid cohort from a single specialist post-COVID service to date, only one-third of individuals under follow-up achieved satisfactory recovery. Fatigue severity and COVID-19 vaccination at presentation, even after initial COVID-19 infection, was associated with long covid recovery. Ongoing service provision for this and other post-viral conditions is necessary to support care, progress treatment options and provide capacity for future pandemic preparedness. Research and clinical services should emphasise these factors as the strongest predictors of non-recovery.

## Full-text entities

- **Genes:** FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}
- **Diseases:** breathlessness (MESH:D004417), myalgia (MESH:D063806), Fatigue (MESH:D005221), dysautonomic symptoms (MESH:D012791), COVID-19 (MESH:D000086382), brain fog (MESH:D005222), long covid (MESH:D000094024)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12815175/full.md

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Source: https://tomesphere.com/paper/PMC12815175