Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey

Introduction: “Long COVID” is a multisystem disease that lasts for 4 or more weeks following initial symptoms of COVID-19. In the UK, at least 10% of patient report symptoms at 12 weeks following a positive COVID-19 test. The aims of this quality improvement survey were to explore patients’ acute an...

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Main Authors: Mohammad Sharif Razai, Roaa Al-Bedaery, Laxmi Anand, Katherine Fitch, Hannah Okechukwu, Teniola M. Saraki, Pippa Oakeshott
Format: Article
Language:English
Published: SAGE Publishing 2021-09-01
Series:Journal of Primary Care & Community Health
Online Access:https://doi.org/10.1177/21501327211041846
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spelling doaj-fa8cf64e67eb4f969a1cb4a26e8137f62021-09-07T22:03:47ZengSAGE PublishingJournal of Primary Care & Community Health2150-13272021-09-011210.1177/21501327211041846Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement SurveyMohammad Sharif Razai0Roaa Al-Bedaery1Laxmi Anand2Katherine Fitch3Hannah Okechukwu4Teniola M. Saraki5Pippa Oakeshott6Wandsworth Primary Care Network, Chatfield Health Care, London, UKPopulation Health Research Institute, St George’s University of London, London, UKWandsworth Primary Care Network, Chatfield Health Care, London, UKWandsworth Primary Care Network, Chatfield Health Care, London, UKImperial College London, London, UKImperial College London, London, UKPopulation Health Research Institute, St George’s University of London, London, UKIntroduction: “Long COVID” is a multisystem disease that lasts for 4 or more weeks following initial symptoms of COVID-19. In the UK, at least 10% of patient report symptoms at 12 weeks following a positive COVID-19 test. The aims of this quality improvement survey were to explore patients’ acute and post-acute “long” COVID-19 symptoms, their experiences of community services and their recommendations for improving these services. Methods: Seventy patients diagnosed with COVID were randomly selected from 2 large socially and ethnically diverse primary care practices. Of those contactable by telephone, 85% (41/48) agreed to participate in the quality improvement survey. They were interviewed by telephone using a semi-structured questionnaire about community services for COVID-19 patients. Interviews lasted 10 to 15 minutes. Results: Forty-nine percent of patients reported at least 1 post-acute COVID-19 symptom. The most common were severe fatigue (45%), breathlessness (30%), neurocognitive difficulties (such as poor memory), poor concentration and “brain fog” (30%), headaches (20%), and joint pain (20%). Many patients felt isolated and fearful, with scant information about community resources and little safety netting advice. Patients also expected more from primary care with over half (56%) recommending regular phone calls and follow up from healthcare staff as the most important approach in their recovery. Conclusions: In line with patients’ requests for more support, the practices now routinely refer patients with long COVID to an on-site social prescriber who explores how they are getting on, refers them to the GP or practice nurse when required, and sign posts them to support services in the community.https://doi.org/10.1177/21501327211041846
collection DOAJ
language English
format Article
sources DOAJ
author Mohammad Sharif Razai
Roaa Al-Bedaery
Laxmi Anand
Katherine Fitch
Hannah Okechukwu
Teniola M. Saraki
Pippa Oakeshott
spellingShingle Mohammad Sharif Razai
Roaa Al-Bedaery
Laxmi Anand
Katherine Fitch
Hannah Okechukwu
Teniola M. Saraki
Pippa Oakeshott
Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey
Journal of Primary Care & Community Health
author_facet Mohammad Sharif Razai
Roaa Al-Bedaery
Laxmi Anand
Katherine Fitch
Hannah Okechukwu
Teniola M. Saraki
Pippa Oakeshott
author_sort Mohammad Sharif Razai
title Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey
title_short Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey
title_full Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey
title_fullStr Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey
title_full_unstemmed Patients’ Experiences of “Long COVID” in the Community and Recommendations for Improving Services: A Quality Improvement Survey
title_sort patients’ experiences of “long covid” in the community and recommendations for improving services: a quality improvement survey
publisher SAGE Publishing
series Journal of Primary Care & Community Health
issn 2150-1327
publishDate 2021-09-01
description Introduction: “Long COVID” is a multisystem disease that lasts for 4 or more weeks following initial symptoms of COVID-19. In the UK, at least 10% of patient report symptoms at 12 weeks following a positive COVID-19 test. The aims of this quality improvement survey were to explore patients’ acute and post-acute “long” COVID-19 symptoms, their experiences of community services and their recommendations for improving these services. Methods: Seventy patients diagnosed with COVID were randomly selected from 2 large socially and ethnically diverse primary care practices. Of those contactable by telephone, 85% (41/48) agreed to participate in the quality improvement survey. They were interviewed by telephone using a semi-structured questionnaire about community services for COVID-19 patients. Interviews lasted 10 to 15 minutes. Results: Forty-nine percent of patients reported at least 1 post-acute COVID-19 symptom. The most common were severe fatigue (45%), breathlessness (30%), neurocognitive difficulties (such as poor memory), poor concentration and “brain fog” (30%), headaches (20%), and joint pain (20%). Many patients felt isolated and fearful, with scant information about community resources and little safety netting advice. Patients also expected more from primary care with over half (56%) recommending regular phone calls and follow up from healthcare staff as the most important approach in their recovery. Conclusions: In line with patients’ requests for more support, the practices now routinely refer patients with long COVID to an on-site social prescriber who explores how they are getting on, refers them to the GP or practice nurse when required, and sign posts them to support services in the community.
url https://doi.org/10.1177/21501327211041846
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