Differences in Clinical Presentation With Long COVID After Community and Hospital Infection and Associations With All-Cause Mortality: English Sentinel Network Database Study.

BACKGROUND: Most studies of long COVID (symptoms of COVID-19 infection beyond 4 weeks) have focused on people hospitalized in their initial illness. Long COVID is thought to be underrecorded in UK primary care electronic records.
OBJECTIVE: We sought to determine which symptoms people present to primary care after COVID-19 infection and whether presentation differs in people who were not hospitalized, as well as post-long COVID mortality rates.
METHODS: We used routine data from the nationally representative primary care sentinel cohort of the Oxford-Royal College of General Practitioners Research and Surveillance Centre (N=7,396,702), applying a predefined long COVID phenotype and grouped by whether the index infection occurred in hospital or in the community. We included COVID-19 infection cases from March 1, 2020, to April 1, 2021. We conducted a before-and-after analysis of long COVID symptoms prespecified by the Office of National Statistics, comparing symptoms presented between 1 and 6 months after the index infection matched with the same months 1 year previously. We conducted logistic regression analysis, quoting odds ratios (ORs) with 95% CIs.
RESULTS: In total, 5.63% (416,505/7,396,702) and 1.83% (7623/416,505) of the patients had received a coded diagnosis of COVID-19 infection and diagnosis of, or referral for, long COVID, respectively. People with diagnosis or referral of long COVID had higher odds of presenting the prespecified symptoms after versus before COVID-19 infection (OR 2.66, 95% CI 2.46-2.88, for those with index community infection and OR 2.42, 95% CI 2.03-2.89, for those hospitalized). After an index community infection, patients were more likely to present with nonspecific symptoms (OR 3.44, 95% CI 3.00-3.95; P<.001) compared with after a hospital admission (OR 2.09, 95% CI 1.56-2.80; P<.001). Mental health sequelae were more strongly associated with index hospital infections (OR 2.21, 95% CI 1.64-2.96) than with index community infections (OR 1.36, 95% CI 1.21-1.53; P<.001). People presenting to primary care after hospital infection were more likely to be men (OR 1.43, 95% CI 1.25-1.64; P<.001), more socioeconomically deprived (OR 1.42, 95% CI 1.24-1.63; P<.001), and with higher multimorbidity scores (OR 1.41, 95% CI 1.26-1.57; P<.001) than those presenting after an index community infection. All-cause mortality in people with long COVID was associated with increasing age, male sex (OR 3.32, 95% CI 1.34-9.24; P=.01), and higher multimorbidity score (OR 2.11, 95% CI 1.34-3.29; P<.001). Vaccination was associated with reduced odds of mortality (OR 0.10, 95% CI 0.03-0.35; P<.001).
CONCLUSIONS: The low percentage of people recorded as having long COVID after COVID-19 infection reflects either low prevalence or underrecording. The characteristics and comorbidities of those presenting with long COVID after a community infection are different from those hospitalized. This study provides insights into the presentation of long COVID in primary care and implications for workload. ©Bernardo Meza-Torres, Gayathri Delanerolle, Cecilia Okusi, Nikhil Mayor, Sneha Anand, Jack Macartney, Piers Gatenby, Ben Glampson, Martin Chapman, Vasa Curcin, Erik Mayer, Mark Joy, Trisha Greenhalgh, Brendan Delaney, Simon de Lusignan. Originally published in JMIR Public Health and Surveillance (https://publichealth.jmir.org), 16.08.2022.

Introduction

Background

Long COVID (LC) is defined as fatigue, breathlessness, cognitive dysfunction, and a variety of other symptoms occurring after COVID-19 infection [1,2]. More than 1 million people in the United Kingdom are estimated to have prolonged symptoms after COVID-19 infection, with 60% of the patients with long COVID reporting extended symptoms lasting months and 240,000 people reporting symptoms that limit day-to-day activity [3,4]. The spectrum of symptoms implies widespread involvement of organs, and there is a recognizable pattern of long COVID disease resulting from autonomic dysfunction and mast cell disorder [5]. The Office for National Statistics (ONS) suggests that the prevalence of long COVID is greater in women, middle-aged people, those from the most deprived areas, and those with an activity-limiting health condition or disability [4]. Symptoms are wide ranging, but fatigue, shortness of breath, and cognitive difficulties (termed brain fog by patients) are most commonly reported [6-8]. In late 2020, there was a release of International Classification of Disease and Systematized Nomenclature of Medicine Clinical Terms (SNOMED CT) to support long COVID coding (termed post–COVID-19 condition) but recording in primary care electronic records varied [9,10]. However, primary care data remain the most useful source of epidemiological data outside hospital records and bespoke surveys to understand the symptoms that patients with long COVID present to primary care after documented COVID-19 infection [6]. There is a need to characterize the prevalence, risk factors, and symptom patterns in patients with long COVID using routine clinical data to understand the symptoms that people present with at primary care facilities after COVID-19 infection and whether presentation and postacute mortality differ in people who were not hospitalized.

This Study

This study reports the symptoms, sociodemographic profile, and outcomes of people identified as having long COVID in English primary care. Our study has four components: (1) a comparison of clinical symptoms of people with long COVID before and after COVID-19 infection, (2) a description of the characteristics of people with long COVID compared with those without long COVID, (3) a comparison of those with long COVID who were hospitalized with COVID-19 infection versus those who were not, and (4) an analysis of all-cause mortality in people with long COVID.

Methods

Overview

This study was conducted as part of the Predicting Risk of Hospital Admission in Patients With Suspected COVID-19 in a Community Setting (Remote COVID-19 Assessment in Primary Care) project [11-13]. The project included creating a phenotype for LC through an observational study. The population characteristics, baseline data, and our LC phenotype were published in the study protocol [14]. The protocol also set out the details of the comparisons undertaken in this study. These were as follows: (1) undertaking a before-and-after comparison of the number of symptoms identified by the ONS as more common in LC; (2) comparing sociodemographic, comorbid, and exposure characteristics of people who had received a coded diagnosis of LC from their general practitioner (GP) with those of people who had not; (3) comparing characteristics of people with LC who had contracted their index infection in hospital with those of people who had contracted a community infection; and (4) an analysis of all-cause mortality in people with LC. The study period included COVID-19 infection cases between March 1, 2020, and April 1, 2021, with a follow-up period of a further 6 months, up to September 30, 2021.

Study Population

We used pseudonymized data extracted from the primary care sentinel cohort (PCSC) of the Oxford–Royal College of General Practitioners Research and Surveillance Centre [15]. The PCSC includes 743 practices (N=7,396,702) that were recruited to be nationally representative of the English population, and it is one of Europe’s oldest sentinel systems [11]. PCSC data have been widely used in COVID-19 research [16]. Practices are encouraged to have high-quality records and to record cases of LC [10]. Key diagnoses in primary care in England are recorded in computerized medical records (CMRs) using SNOMED CT [17]. This includes COVID-19 test results and vaccination. Over the period of the study, all community COVID-19 test and vaccination data were posted electronically back into patients’ CMRs. We have previously found that 7.81% (58/743) of the practices did not have any LC cases recorded in their CMR systems, and these practices were excluded from the study. The registered population of the PCSC was 7,396,702 patients at the time of the study; after exclusions, approximately 6.9 million patients were included, and 6.15% (428,588/6,968,114) had COVID-19 infection recorded in their CMR (Figure 1).

Figure 1

CONSORT (Consolidated Standards of Reporting Trials) diagram of the English primary care sentinel cohort population, the people with COVID-19 infection, those with long COVID, and the numbers of people with index community infection and those hospitalized for treatment for their index infection. Oxford–RCGP RSC: Oxford–Royal College of General Practitioners Research and Surveillance Centre.

Long COVID Cases

LC cases were defined using our phenotype, with LC cases being defined by a clinical term for a case, referral to an LC service, or a symptom score suggestive of LC based on the ONS set of possible LC symptoms. The phenotype also differentiated community cases from hospital cases. Using this phenotype, 1.83% (7623/416,505) of the population who had been exposed to COVID-19 infection were recorded in the GP CMR as having LC; 82.85% (6316/7623) were index community COVID-19 infection cases, and 17.15% (1307/7623) had been hospitalized for treatment for their primary COVID-19 infection; and 0.3% (23/7623) of the people with a prior record of LC diagnosis had died. Most (7347/7623, 96.38%) of our LC cases had not received a vaccination dose before their diagnosis, 3.49% (266/7623) had received a single vaccine dose, and 0.13% (10/7623) had received 2 doses. We have set out how the PCSC population was subdivided to identify people with LC in Figure 1. Sociodemographic details included age, sex, use of the Index of Multiple Deprivation as a measure of deprivation, ethnicity, population density, obesity, and smoking. The Index of Multiple Deprivation score was dichotomized into the top 3 (least) and bottom 2 (most) deprived quintiles. Ethnicity was also dichotomized into White and non-White. Population density categories were based on the ONS national figures and categorized into conurbation (highest density), town and city (medium density), and rural (lowest density). Obesity was reported based on BMI>30 kg/m2 or a term for obesity from SNOMED CT. Symptoms associated with LC were those present >28 days after the index infection.

Before-and-After Study

We compared the recording of symptoms associated with LC in the period between 1 and 6 months after the index COVID-19 infection. We made a historical comparison matched by month in the year before the index COVID-19 infection. We did this to make allowance for seasonality in symptom presentations in primary care.

Reporting frequencies and underreporting are likely to be similar to unrecorded cases of patients with LC. The comparisons between before-and-after symptoms reported among patients with LC before the pandemic were matched by month, provided that an acute COVID-19 infection code was present; for example, patients with a COVID-19 infection code entered on January 1, 2021, would have a follow-up period beginning from February 1, 2021, to July 31, 2021, with a historic comparator period from February 1, 2019, to July 31, 2019. This comparative method demonstrated the clinical phenotype variation.

Comparing LC and Uncomplicated COVID-19 Infection

We compared people with LC with those with COVID-19 infection uncomplicated by subsequent LC. We made this comparison across all variables of interest, identified through a literature review reported in our protocol [14]. In addition, we included the Cambridge Multimorbidity Score (CMS) as an overall measure of comorbidity; although CMS was initially developed using the Read clinical terminology, we have subsequently validated it using SNOMED CT [17]. An increasing CMS is associated with greater levels of comorbidity and associated with increased risk of mortality [18]. We conducted a multivariate logistic regression analysis to characterize people with LC.

Comparison of Hospitalized and Community Initial Infections

We used the same variables to make comparisons between patients who were hospitalized with their index COVID-19 infection and those who were not. We compared people with posthospitalization LC with those who had index community COVID-19 infection followed by LC.

All-Cause Mortality as an Outcome for LC

We measured all-cause mortality as an outcome for all patients with LC drawn from the hospitalized and community groups. We conducted a multivariate analysis using age, sex, geographical location, CMS, and whether the patients had received their vaccination doses before or after their COVID-19 infection diagnosis.

Statistical Methods

We conducted this secondary analysis of routine data from the PCSC, and full details are available in our protocol [18]. We reported descriptive statistics of mean, median, and proportion, with measures of dispersion such as SD and IQR for normally distributed data and nonparametric data, respectively. We conducted a univariate analysis reporting odds ratios (ORs) and 95% CIs. We used the Bonferroni correction to correct for multiple testing in our before-and-after study of symptoms associated with LC. The probability of an observed difference happening by chance (P values) were reported for categorical variables using chi-square tests. ANOVA was used for continuous variables.

Multivariate logistic regression modelling was used to identify comorbidities, demographics, and exposure covariates associated with (1) LC diagnosis, (2) hospitalization, and (3) all-cause mortality as binary outcomes in separate models. For each model, relevant risk factors identified in the literature underwent univariate analysis, and all covariates were then included in a 3-step backward elimination using thresholds of α levels of .20, .10, and .05 in each step respectively, where a 2-sided α value of .05 was considered statistically significant. Age and sex were forced into the model at each step. Results were presented through forest plots.

Ethics Approval

Retrospective pseudonymized routine data were used for this study. These data are held at the Oxford–Royal College of General Practitioners Clinical Informatics Digital Hub, a trusted research environment [19] that meets the NHS Digital Data Security and Protection standards [20]. Ethics approval was granted by the North West–Greater Manchester East Research Ethics Committee and Health Research Authority on May 27, 2021 (Integrated Research Application System number: 283024; Research Ethics Committee reference number: 20/NW/0266).

Results

Cohort Summary

A total of 416,505 people had a record of acute COVID-19 infection between March 1, 2020, and April 1, 2021. Baseline characteristics of the population are reported in Table 1. The mean age of the patients was 44.5 (SD 21.7) years, with a majority being women (232,775/416,505, 55.89%). The most common comorbid conditions were obesity, anxiety, depression, eczema, hypertension, and asthma. The all-cause mortality rate within the study population was 4.08% (16,993/416,505). Only 1.81% (7531/416,505) of the deaths were attributable to complications related to COVID-19 infection.

Table 1

Frequencies of baseline characteristics and univariate odds ratios for people with COVID-19 infection stratified by long COVID status in the primary care sentinel cohort in England (March 1, 2020, to April 1, 2021; N=416,505).

Variable and category						COVID-19 infection, n=408,882			Long COVID, n=7623		Unadjusted odds ratio (95% CI)		P value
Sociodemographic characteristics
	Age (years), mean (SD)
				Continuous		44.5 (21.77)			47.7 (14.82)		1.01 (1.01-1.01)		<.001
	Sex, n (%)
				Female (reference)		227,849 (55.7)			4926 (64.6)		1.00 (N/Aa)		N/A
				Male		181,033 (44.3)			2697 (35.4)		0.69 (0.66-0.72)		<.001
	Deprivation, n (%)
				Least deprived (reference)		164,001 (40.1)			3048 (40)		1.00 (N/A)		N/A
				Most deprived		244,881 (59.9)			4575 (60)		1.01 (0.96-1.05)		.83
	Ethnicity, n (%)
				White (reference)		268,624 (65.7)			5529 (72.5)		1.00 (N/A)		N/A
				Non-White		56,645 (13.9)			1094 (14.4)		0.94 (0.88-1.00)		.06
				Missing		83,613 (20.4)			1000 (13.1)		0.58 (0.54-0.62)		<.001
	Population density, n (%)
				City (reference)		205,159 (50.2)			3191 (41.9)		1.00 (N/A)		N/A
				Conurbation		137,378 (33.6)			3196 (41.9)		1.50 (1.42-1.57)		<.001
				Rural		66,345 (16.2)			1236 (16.2)		1.20 (1.12-1.28)		<.001
	BMI, n (%)
				Nonobese (reference)		252,114 (61.7)			4522 (59.3)		1.00 (N/A)		N/A
				Obese		101,386 (24.8)			2575 (33.8)		1.42 (1.35-1.49)		<.001
				Missing		55,382 (13.5)			526 (6.9)		0.53 (0.48-0.58)		<.001
	Smoker, n (%)
				Nonsmoker (reference)		210,505 (51.5)			4458 (58.5)		1.00 (N/A)		N/A
				Smoker or former smoker		149,583 (36.6)			2945 (38.6)		0.93 (0.89-0.97)		<.001
				Missing		48,794 (11.9)			220 (2.9)		0.21 (0.19-0.24)		<.001
Comorbidities
	Depression, n (%)
				No (reference)		315,510 (77.2)			4862 (63.8)		1.00 (N/A)		N/A
				Yes		93,372 (22.8)			2761 (36.2)		1.92 (1.83-2.01)		<.001
	Anxiety, n (%)
				No (reference)		313,782 (76.7)			4969 (65.2)		1.00 (N/A)		N/A
				Yes		95,100 (23.3)			2654 (34.8)		1.76 (1.68-1.85)		<.001
	Asthma, n (%)
				No (reference)		333,083 (81.5)			5821 (76.4)		1.00 (N/A)		N/A
				Yes		75,799 (18.5)			1802 (23.6)		1.36 (1.29-1.43)		<.001
	Chronic lung disease, n (%)
				No (reference)		394,414 (96.5)			7429 (97.5)		1.00 (N/A)		N/A
				Yes		14,468 (3.5)			194 (2.5)		0.71 (0.62-0.82)		<.001
	COPDb, n (%)
			No (reference)		396,024 (96.9)			7473 (98)		1.00 (N/A)		N/A
			Yes		12,858 (3.1)			150 (2)		0.62 (0.53-0.73)		<.001
		Hypertension, n (%)
			No (reference)		328,025 (80.2)			6001 (78.7)		1.00 (N/A)		N/A
			Yes		80,857 (19.8)			1622 (21.3)		1.10 (1.04-1.16)		<.001
		Ischemic heart disease
			No (reference)		387,015 (94.7)			7283 (95.5)		1.00 (N/A)		N/A
			Yes		21,867 (5.3)			340 (4.5)		0.83 (0.74-0.92)		<.001
		Atrial fibrillation, n (%)
			No (reference)		395,170 (96.6)			7490 (98.3)		1.00 (N/A)		N/A
			Yes		13,712 (3.4)			133 (1.7)		0.51 (0.43-0.61)		<.001
		Congestive heart failure, n (%)
			No (reference)		400,573 (98)			7558 (99.1)		1.00 (N/A)		N/A
			Yes		8309 (2)			65 (0.9)		0.41 (0.32-0.53)		<.001
		CKDc, n (%)
			No (reference)		385,985 (94.4)			7350 (96.4)		1.00 (N/A)		N/A
			Yes		22,897 (5.6)			273 (3.6)		0.63 (0.55-0.71)		<.001
		Type 2 diabetes, n (%)
			No (reference)		378,258 (92.5)			7042 (92.4)		1.00 (N/A)		N/A
			Yes		30,624 (7.5)			581 (7.6)		1.02 (0.94-1.11)		.67
		Type 1 diabetes, n (%)
			No (reference)		406,311 (99.4)			7581 (99.4)		1.00 (N/A)		N/A
			Yes		2571 (0.6)			42 (0.6)		0.88 (0.64-1.19)		.38
		Cirrhosis, n (%)
			No (reference)		407,827 (99.7)			7607 (99.8)		1.00 (N/A)		N/A
			Yes		1055 (0.3)			16 (0.2)		0.81 (0.50-1.33)		.40
		Eczema, n (%)
			No (reference)		318,124 (77.8)			5891 (77.3)		1.00 (N/A)		N/A
			Yes		90,758 (22.2)			1732 (22.7)		1.03 (0.98-1.09)		.28
		CMSd, mean (SD)
			Continuous		0.45 (1.59)			0.29 (1.12)		0.94 (0.92-0.95)		<.001
Exposures
		ICUe admission, n (%)
			No (reference)		406,302 (99.4)			7351 (96.4)		1.00 (N/A)		N/A
			Yes		2580 (0.6)			272 (3.6)		5.83 (5.13-6.62)		<.001
		Vaccination at any time, n (%)
			No vaccine (reference)		84,094 (20.6)			872 (11.4)		1.00 (N/A)		N/A
			One dose		25,571 (6.3)			371 (4.9)		1.40 (1.24-1.58)		<.001
			Two doses		299,217 (73.2)			6380 (83.7)		2.06 (1.92-2.21)		<.001
		Pre– long COVID vaccination, n (%)
			No vaccine (reference)		392,324 (96)			7347 (96.4)		1.00 (N/A)		N/A
			One dose		15,832 (3.9)			266 (3.5)		0.90 (0.79-1.01)		.08
			Two doses		726 (0.2)			10 (0.1)		0.74 (0.39-1.37)		.31
Outcomes
		All-cause mortality, n (%)
			No (reference)		391,912 (95.8)			7600 (99.7)		1.00 (N/A)		N/A
			Yes		16,970 (4.2)			23 (0.3)		0.07 (0.05-0.11)		<.001

aN/A: not applicable.

bCOPD: chronic obstructive pulmonary disease.

cCKD: chronic kidney disease.

dCMS: Cambridge Multimorbidity Score.

eICU: intensive care unit.

Overall, symptomatic presentations to primary care increased in people after their diagnosis compared with a matched historic period. The odds of presenting with these symptoms more than doubled. The increased ORs were 2.66 (95% CI 2.46-2.88) and 2.42 (95% CI 2.03-2.89) for community and hospitalized patients, respectively (Figure 2).

Figure 2

Change in long COVID symptom presentation by symptom category for people who contracted a posthospitalization and index community COVID-19 infection. Univariate odds ratios (ORs) and 95% CIs are presented for COVID-19 infection cases in the primary care sentinel cohort in England between March 1, 2020, and April 1, 2021. ONS: Office for National Statistics.

There were no differences between people who had been hospitalized with COVID-19 infection and those who had contracted community infections by category, other than the differences in general and mental health symptoms. Patients presented with more general symptoms after an index community infection (OR 3.44, 95% CI 3.00-3.95) than after an index hospital infection (OR 2.09, 95% CI 1.56-2.80; P<.001). Presentations with mental health sequelae were associated more with index hospital infections (OR 2.21, 95% CI 1.64-2.96) than with index community infections (OR 1.36, 95% CI 1.21-1.53).

There was an overall increase in reporting individual symptoms for 95% (20/21) of the symptoms monitored in both the index hospital and community infection groups. Among those hospitalized, shortness of breath (OR 15.8, 95% CI 9.5-26.4), loss of taste (OR 6.0, 95% CI 0.73-50.0), and memory loss and confusion (OR 5.0, 95% CI 0.58-43.32) were the symptoms that showed a higher increase after LC. For the community group, difficulty concentrating (OR 11.7, 95% CI 3.6-38.0), loss of taste (OR 8.7, 95% CI 3.4-21.7), and loss of smell (OR 7.5, 95% CI 4.2-13.2) showed a higher increase after LC. Only abdominal pain in the hospitalized group saw a decrease after LC versus before LC (Table 2).

Table 2

Change in symptoms in the hospitalized and community groups before and after developing long COVID for people presenting with COVID-19 infection in the primary care sentinel cohort in England between March 1, 2020, and April 1, 2021 (N=7609).

ONSa symptom variables			Long COVID: hospitalized (n=1294)							Unadjusted ORb (95% CI)			Pvalue			Long COVID: community (n=6315)							Unadjusted OR (95% CI)			Pvalue
			Before, n (%)		After, n (%)		Difference, %								Before, n (%)			After, n (%)		Difference, %
Overall, one or more ONS symptomc			315 (24.34)		567 (43.82)		19.48		2.42 (2.03-2.89)			<.001			1326 (21)			2616 (41.43)		20.43		2.66 (2.46-2.88)			<.001
Central nervous systemc			65 (5.02)		103 (7.96)		2.94		1.64 (1.2-2.24)			.004			250 (3.96)			578 (9.15)		5.19		2.44 (2.09-2.86)			<.001
	Memory loss and confusion	1 (0.08)		5 (0.39)		0.31		5.02 (0.58-43.32)			.22			4 (0.06)			14 (0.22)		0.16		3.51 (1.15-10.71)			.03
	Difficulty concentrating	0		6 (0.46)		0.46		Infd			.04			3 (0.23)			35 (0.55)		0.32		11.73 (3.62-38.01)			<.001
	Loss of smell	3 (0.23)		6 (0.46)		0.23		2 (0.5-8.06)			.50			14 (0.22)			103 (1.63)		1.41		7.46 (4.23-13.17)			<.001
	Trouble sleeping	9 (0.7)		21 (1.62)		0.92		2.36 (1.08-5.16)			.05			19 (0.3)			46 (0.73)		0.43		2.43 (1.43-4.13)			<.001
	Headache	37 (2.86)		48 (3.71)		0.85		1.31 (0.85-2.01)			.28			158 (2.5)			306 (4.85)		2.35		1.98 (1.63-2.41)			<.001
	Loss of taste	1 (0.08)		6 (0.46)		0.38		6.02 (0.73-50.02)			.12			5 (0.08)			43 (0.68)		0.6		8.65 (3.44-21.74)			<.001
	Vertigo and dizziness	16 (1.24)		30 (2.32)		1.08		1.9 (1.03-3.48)			.05			66 (1)			137 (2.17)		1.17		2.1 (1.56-2.82)			<.001
Respiratoryc			118 (9.12)		294 (22.72)		13.6		2.93 (2.32-3.71)			<.001			416 (6.59)			1088 (17.24)		10.65		2.95 (2.62-3.32)			<.001
	Sore throat	16 (1.24)		18 (1.39)		0.15		0.36 (0.21-0.62)			.86			83 (1.31)			77 (1.22)		–0.09		0.93 (0.68-1.27)			.71
	Shortness of breath	49 (3.79)		214 (16.54)		12.75		15.83 (9.51-26.35)			<.001			150 (2.38)			714 (11.31)		8.93		5.24 (4.39-6.25)			<.001
	Cough	70 (5.41)		114 (8.81)		3.4		1.69 (1.23-2.31)			.002			250 (3.96)			544 (8.61)		4.65		2.29 (1.96-2.68)			<.001
Cardiovascularc			46 (3.55)		113 (8.73)		5.18		2.6 (1.82-3.69)			<.001			171 (2.71)			468 (7.41)		4.7		2.88 (2.41-3.43)			<.001
	Palpitations	9 (0.7)		26 (2)		1.3		2.93 (1.36-6.29)			.007			38 (0.6)			128 (2.01)		1.41		3.42 (2.35-4.96)			<.001
	Chest pain	38 (2.94)		97 (7.5)		4.6		2.68 (1.81-3.96)			.001			143 (2.26)			371 (5.87)		3.61		2.69 (2.21-3.28)			<.001
Generalc			78 (6.03)		153 (11.82)		5.79		2.09 (1.56-2.8)			<.001			341 (5.4)			1037 (16.42)		11.02		3.44 (3-3.95)			<.001
	Weakness and tiredness	26 (2.01)		95 (7.34)		5.33		3.86 (2.51-5.95)			.001			123 (1.95)			786 (12.45)		10.5		7.16 (5.88-8.71)			<.001
	Fever	11 (0.85)		20 (1.55)		0.7		1.83 (0.87-3.86)			.16			48 (0.76)			105 (1.66)		0.9		2.21 (1.55-3.14)			<.001
	Muscle aches	8 (0.62)		24 (1.85)		1.23		3.04 (1.36-6.79)			.004			33 (0.52)			121 (1.92)		1.4		3.72 (2.51-5.5)			<.001
	Abdominal pain	40 (3.09)		37 (2.86)		–0.23		0.92 (0.59-1.45)			.83			158 (2.5)			178 (2.82)		0.32		1.13 (0.91-1.4)			.30
Gastrointestinalc			23 (1.78)		45 (3.48)		1.7		1.99 (1.2-3.31)			.01			64 (1.01)			167 (2.64)		1.63		2.65 (1.98-3.56)			<.001
	Nausea and vomiting	7 (0.54)		23 (1.78)		1.24		3.33 (1.43-7.73)			.006			27 (0.43)			72 (1.14)		0.71		2.69 (1.71-4.22)			<.001
	Loss of appetite	2 (0.15)		6 (0.46)		0.31		3.01 (0.6-15.01)			.29			9 (0.14)			35 (0.55)		0.41		3.9 (1.89-8.06)			<.001
	Diarrhea	16 (1.24)		25 (1.93)		0.69		1.57 (0.84-2.95)			.21			34 (0.54)			79 (1.25)		0.71		2.34 (1.55-3.53)			<.001
Mental healthc			70 (5.41)		145 (11.21)		5.8		2.21 (1.64-2.96)			<.001			457 (7.24)			607 (9.61)		2.37		1.36 (1.21-1.53)			<.001
	Worry and anxiety	33 (2.55)		82 (6.34)		3.79		2.59 (1.71-3.9)			<.001			274 (4.34)			407 (6.44)		2.1		1.52 (1.3-1.78)			<.001
	Low mood and not enjoying anything	57 (4.4)		97 (7.5)		3.1		1.76 (1.26-2.45)			.002			292 (4.62)			389 (6.16)		1.54		1.35 (1.16-1.58)			<.001

aONS: Office for National Statistics.

bOR: odds ratio.

cThe P values by category of symptoms have had the Bonferroni correction applied for multiple testing.

dInf: infinite.

Comparison of People With COVID-19 Infection Without LC and Those With LC

The frequencies of baseline characteristics and univariate ORs for people with COVID-19 infection stratified by LC status are shown in Table 1 (n=416,505). The mean age was 44.5 (SD 21.77) years for the COVID-19 infection group and 47.7 (SD 14.8) years for the LC group. A higher proportion of those with LC was found among women (4926/7623, 64.62%), and male sex was associated with a lower odds of an LC diagnosis (OR 0.69, 95% CI 0.66-0.72). The proportion of those with a record of intensive care unit (ICU) admission was 0.63% (2580/408,882) in people with COVID-19 infection and 3.57% (272/7623) in people with LC, and a record of ICU admission was associated with a higher odds of an LC diagnosis (OR 5.83, 95% CI 5.13-6.62). A moderate association with LC was found for history of depression, anxiety, living in a conurbation, and COVID-19 vaccination at any time. A lower association was found for people with obesity, asthma, and hypertension.

The multivariate logistic regression analysis using LC as an outcome (Figure 3) showed that a greater odds of having LC was associated with increasing age, higher population density (conurbation), mental health problems (anxiety and depression), and ICU admission. By contrast, male sex, being more deprived, chronic kidney disease (CKD), and a higher comorbidity score (measured using the CMS) were not.

Figure 3

Multivariate logistic regression analysis showing associations with long COVID among people with COVID-19 infection diagnosed in the primary care sentinel cohort in England (March 1, 2020, to April 1, 2021). Results are shown as odds ratios (ORs) with 95% CIs. CKD: chronic kidney disease; CMS: Cambridge Multimorbidity Score; ICU: intensive care unit; Q: quintiles.

An additional year of age was associated with a 5% increase in odds of an LC diagnosis (OR 1.05, 95% CI 1.04-1.05). After adjusting for confounders, the demographic factors associated with a decreased odds of an LC diagnosis among people with COVID-19 infection included male sex (OR 0.9, 95% CI 0.85-0.94) and higher deprivation (OR 0.94, 95% CI 0.9-0.99). However, residing in a conurbation was associated with increased odds of an LC diagnosis (OR 1.46, 95% CI 1.39-1.53). Among the history of comorbidities and exposures, depression (OR 1.55, 95% CI 1.47-1.64), anxiety (OR 1.35, 95% CI 1.28-1.35), asthma (OR 1.28, 95% CI 1.21-1.35), type 2 diabetes (OR 1.18, 95% CI 1.07-1.29), eczema (OR 1.06, 95% CI 1-1.12), and a record of ICU admission (OR 5.74, 95% CI 5.02-6.53) were associated with increased odds of an LC diagnosis. By contrast, history of CKD (OR 0.76, 95% CI 0.67-0.87) and a higher CMS (OR 0.54, 95% CI 0.52-0.56) were associated with lower odds of an LC diagnosis (Figure 3).

Comparison of Posthospitalization- and Postcommunity Infection With LC

The frequencies of baseline characteristics and univariate ORs for people with LC stratified by community versus hospital index infection are shown in Table 3 (n=7623). Among baseline characteristics, the mean age was 54.8 (SD 14.3) years for the posthospitalization-infection LC group and 46.2 (SD 14.5) years for the postcommunity-infection LC group, whereas the proportion of female patients was 53.94% (705/1307) in the posthospitalization-infection LC group and 66.83% (4221/6316) in the postcommunity-infection LC group. Demographic factors associated with higher odds of hospitalization included male sex, higher deprivation, and non-White ethnicity. Among comorbidities, congestive heart failure, type 2 diabetes, CKD, ischemic heart disease, hypertension, chronic lung disease, obesity, and atrial fibrillation were all significantly associated with higher odds of a posthospitalization LC diagnosis.

Table 3

Frequencies of baseline characteristics and univariate odds ratios (ORs) for people with long COVID stratified by community versus hospital index infection in the primary care sentinel cohort in England (March 1, 2020, to April 1, 2021; N=7623).

Variable and category			Community, n=6316	Hospitalized, n=1307	Unadjusted odds ratio (95% CI)	P value
Sociodemographic characteristics
	Age (years), mean (SD)
		Continuous	46.2 (14.49)	54.8 (14.3)	1.04 (1.04-1.05)	<.001
	Sex, n (%)
		Female (reference)	4221 (66.83)	705 (53.94)	1.00 (N/Aa)	N/A
		Male	2095 (33.17)	602 (46.06)	1.72 (1.52-1.94)	<.001
	Deprivation, n (%)
		Least deprived (reference)	2639 (41.78)	409 (31.29)	1.00 (N/A)	N/A
		Most deprived	3677 (58.22)	898 (68.71)	1.58 (1.39-1.79)	<.001
	Ethnicity, n (%)
		White (reference)	4619 (73.13)	910 (69.63)	1.00 (N/A)	N/A
		Non-White	844 (13.36)	250 (19.13)	1.50 (1.28-1.76)	<.001
		Missing	853 (13.51)	147 (11.25)	0.87 (0.72-1.06)	.16
	Population density, n (%)
		City (reference)	2639 (41.78)	552 (42.23)	1.00 (N/A)	N/A
		Conurbation	2621 (41.5)	575 (43.99)	1.05 (0.92-1.19)	.47
		Rural	1056 (16.72)	180 (13.77)	0.81 (0.68-0.98)	.03
	BMI, n (%)
		Nonobese (reference)	3957 (62.65)	565 (43.23)	1.00 (N/A)	N/A
		Obese	1882 (29.8)	693 (53.02)	2.58 (2.28-2.92)	<.001
		Missing	477 (7.55)	49 (3.75)	0.72 (0.53-0.98)	.03
	Smoker, n (%)
		Nonsmoker (reference)	3696 (58.52)	762 (58.3)	1.00 (N/A)	N/A
		Smoker or former smoker	2411 (38.17)	534 (40.86)	1.07 (0.95-1.21)	.25
		Missing	209 (3.31)	11 (0.84)	0.26 (0.14-0.47)	<.001
Comorbidities
	Depression, n (%)
		No (reference)	4029 (63.79)	833 (63.73)	1.00 (N/A)	N/A
		Yes	2287 (36.21)	474 (36.27)	1.00 (0.89-1.13)	.97
	Anxiety, n (%)
		No (reference)	4094 (64.82)	875 (66.95)	1.00 (N/A)	N/A
		Yes	2222 (35.18)	432 (33.05)	0.91 (0.80-1.03)	.14
	Asthma, n (%)
		No (reference)	4869 (77.09)	952 (72.84)	1.00 (N/A)	N/A
		Yes	1447 (22.91)	355 (27.16)	1.25 (1.10-1.44)	<.001
	Chronic lung disease, n (%)
		No (reference)	6185 (97.93)	1244 (95.18)	1.00 (N/A)	N/A
		Yes	131 (2.07)	63 (4.82)	2.39 (1.76-3.25)	<.001
	COPDb, n (%)
		No (reference)	6218 (98.45)	1255 (96.02)	1.00 (N/A)	N/A
		Yes	98 (1.55)	52 (3.98)	2.63 (1.87-3.70)	<.001
	Hypertension, n (%)
		No (reference)	5168 (81.82)	833 (63.73)	1.00 (N/A)	N/A
		Yes	1148 (18.18)	474 (36.27)	2.56 (2.25-2.92)	<.001
	Ischemic heart disease, n (%)
		No (reference)	6102 (96.61)	1181 (90.36)	1.00 (N/A)	N/A
		Yes	214 (3.39)	126 (9.64)	3.04 (2.42-3.82)	<.001
	Atrial fibrillation, n (%)
		No (reference)	6228 (98.61)	1262 (96.56)	1.00 (N/A)	N/A
		Yes	88 (1.39)	45 (3.44)	2.52 (1.75-3.63)	<.001
	Congestive heart failure, n (%)
		No (reference)	6283 (99.48)	1275 (97.55)	1.00 (N/A)	N/A
		Yes	33 (0.52)	32 (2.45)	4.78 (2.93-7.80)	<.001
	CKDc, n (%)
		No (reference)	6155 (97.45)	1195 (91.43)	1.00 (N/A)	N/A
		Yes	161 (2.55)	112 (8.57)	3.58 (2.79-4.60)	<.001
	Type 2 diabetes, n (%)
		No (reference)	5982 (94.71)	1060 (81.1)	1.00 (N/A)	N/A
		Yes	334 (5.29)	247 (18.9)	4.17 (3.50-4.98)	<.001
	Type 1 diabetes, n (%)
		No (reference)	6282 (99.46)	1299 (99.39)	1.00 (N/A)	N/A
		Yes	34 (0.54)	8 (0.61)	1.14 (0.53-2.46)	.75
	Cirrhosis, n (%)
		No (reference)	6305 (99.83)	1302 (99.62)	1.00 (N/A)	N/A
		Yes	11 (0.17)	5 (0.38)	2.20 (0.76-6.35)	.17
	Eczema, n (%)
		No (reference)	4871 (77.12)	1020 (78.04)	1.00 (N/A)	N/A
		Yes	1445 (22.88)	287 (21.96)	0.95 (0.82-1.09)	.47
	CMSd, mean (SD)
		Continuous	0.16 (1.03)	0.95 (1.33)	1.75 (1.66-1.84)	<.001
Exposures
	ICUe admission, n (%)
		No (reference)	6316 (100)	1035 (79.19)	1.00 (N/A)	N/A
		Yes	0 (0)	272 (20.81)	Inff	<.001
	Vaccination at any time, n (%)
		No vaccine (reference)	743 (11.76)	129 (9.87)	1.00 (N/A)	N/A
		One dose	326 (5.16)	45 (3.44)	0.80 (0.55-1.14)	.21
		Two doses	5247 (83.07)	1133 (86.69)	1.24 (1.02-1.52)	.03
	Pre–long COVID vaccination, n (%)
		No vaccine (reference)	6108 (96.71)	1239 (94.8)	1.00 (N/A)	N/A
		One dose	199 (3.15)	67 (5.13)	1.66 (1.25-2.20)	<.001
		Two doses	9 (0.14)	1 (0.08)	0.55 (0.07-4.33)	.54
Outcomes
	All-cause mortality, n (%)
		No (reference)	6310 (99.91)	1290 (98.7)	1.00 (N/A)	N/A
		Yes	6 (0.09)	17 (1.3)	13.9 (5.5-35.2)	<.001

aN/A: not applicable.

bCOPD: chronic obstructive pulmonary disease.

cCKD: chronic kidney disease.

dCMS: Cambridge Multimorbidity Score.

eICU: intensive care unit.

fInf: infinite.

The multivariate logistic regression analysis using posthospitalization LC as an outcome produced results (Figure 4) that contrasted with the previous analysis. Although increasing age, asthma, and type 2 diabetes remained associated with LC after both index community infection and hospitalization for the index COVID-19 infection, people who had received a diagnosis of LC after hospitalization were more likely to be men, more deprived, of non-White ethnicity, and have CKD and higher comorbidity scores (Figure 4).

Figure 4

Multivariate logistic regression analysis showing associations with long COVID acquired after hospitalization. Results are shown as odds ratios (ORs) with 95% CIs. CKD: chronic kidney disease; CMS: Cambridge Multimorbidity Score; Q: quintiles.

An additional year of age was associated with a 1% increase in odds of having been hospitalized for COVID-19 infection (OR 1.01, 95% CI 1-1.02). After adjusting for confounders, the demographic factors associated with an increased odds of an LC diagnosis after hospitalization for COVID-19 infection included male sex (OR 1.43, 95% CI 1.25-1.64), higher deprivation (OR 1.42, 95% CI 1.24-1.63), non-White ethnicity (OR 1.78, 95% CI 1.5-2.12), and obesity (OR 2.18, 95% CI 1.9-2.5). Asthma (OR 1.27, 95% CI 1.1-1.47), CKD (OR 1.44, 95% CI 1.08-1.09), and type 2 diabetes (OR 1.66, 95% CI 1.35-2.02) were also associated with LC after hospitalization for COVID-19 infection. An increase in CMS was also associated with a 41% increase in odds of a posthospitalization LC diagnosis (OR 1.41, 95% CI 1.26-1.57). Only history of depression was associated with lower odds (OR 0.84, 95% CI 0.73-0.96).

LC and All-Cause Mortality

The frequencies of baseline characteristics and univariate ORs for people with LC stratified by vital status are shown in Table 4 (n=7623). We paired data for people with LC who died (23/7623, 0.3%) and those who remained alive within the study period (7600/7623, 99.7%). Demographic factors associated with a higher risk of mortality include male sex (OR 4.19, 95% CI 1.72-10.21) and age, where the mean age was 75.7 (SD 8.23) years in the mortality group and 47.6 (SD 14.75) years in the living group. Every additional year of age was associated with a 10% increased risk of death (OR 1.15, 95% CI 1.11-1.19). Among comorbidities, all cardiovascular comorbidities were associated with a higher risk of mortality, particularly congestive heart failure (OR 26, 95% CI 8.60-78.74) and atrial fibrillation (OR 20.8, 95% CI 8.06-53.54). Pulmonary conditions, including chronic obstructive pulmonary disease (OR 14.3, 95% CI 5.23-38.99) and chronic lung disease (OR 13.9, 95% CI 5.43-35.69) were also associated with higher mortality. Among metabolic and inflammatory conditions, cirrhosis, type 1 diabetes, type 2 diabetes, and eczema were associated with all-cause mortality. Finally, ICU admission (OR 7.63, 95% CI 2.81-20.70) was associated with a higher risk of death.

Table 4

Frequencies of baseline characteristics and univariate odds ratios for people with LC stratified by vital status in the primary care sentinel cohort in England (March 1, 2020, to April 1, 2021; N=7623).

Variable and category						Alive, n=7600			All-cause mortality, n=23			Unadjusted odds ratio (95% CI)			P value
Sociodemographic characteristics
	Age (years), mean (SD)
		Continuous		47.6 (14.75)			75.7 (8.23)			1.15 (1.11-1.19)			<.001
	Sex, n (%)
		Female (reference)		4919 (64.72)			7 (30.43)			1.00 (N/Aa)			N/A
		Male		2681 (35.28)			16 (69.57)			4.19 (1.72-10.21)			<.001
	Deprivation, n (%)
		Least deprived (reference)		3042 (40.01)			6 (26.09)			1.00 (N/A)			N/A
		Most deprived		4558 (59.97)			17 (73.9)			1.89 (0.74-4.80)			.16
	Ethnicity, n (%)
		White (reference)		5509 (72.49)			20 (86.96)			1.00 (N/A)			N/A
		Non-White		1092 (14.37)			2 (8.7)			0.50 (0.12-2.16)			.31
		Missing		999 (13.14)			1 (4.35)			0.28 (0.04-2.06)			.12
	Population density, n (%)
		City (reference)		3179 (41.83)			12 (52.17)			1.00 (N/A)			N/A
		Conurbation		3191 (42)			5 (21.74)			0.42 (0.15-1.18)			.08
		Rural		1230 (16.18)			6 (26.09)			1.29 (0.48-3.45)			.61
	BMI, n (%)
		Nonobese (reference)		4506 (59.29)			16 (69.57)			1.00 (N/A)			N/A
		Obese		2568 (33.79)			7 (30.43)			0.77 (0.32-1.87)			.55
		Missing		526 (6.92)			0 (0)			0.26 (0.02-4.33)			.06
	Smoker, n (%)
		Nonsmoker (reference)		4447 (58.51)			11 (47.82)			1.00 (N/A)			N/A
		Smoker or former smoker		2933 (38.59)			12 (52.17)			1.65 (0.73- 3.75)			.23
		Missing		220 (2.89)			0 (0)			0.88 (0.05-14.93)			.30
Comorbidities
	Depression, n (%)
		No (reference)		4843 (63.72)			19 (82.61)			1.00 (N/A)			N/A
		Yes		2757 (36.28)			4 (17.39)			0.37 (0.13-1.09)			.05
	Anxiety, n (%)
		No (reference)		4952 (65.16)			17 (73.91)			1.00 (N/A)			N/A
		Yes		2648 (34.84)			6 (26.09)			0.66 (0.26-1.68)			.37
	Asthma, n (%)
		No (reference)		5802 (76.34)			19 (82.61)			1.00 (N/A)			N/A
		Yes		1798 (23.66)			4 (17.39)			0.68 (0.23-2.00)			.47
	Chronic lung disease, n (%)
		No (reference)		7412 (97.53)			17 (73.91)			1.00 (N/A)			N/A
		Yes		188 (2.47)			6 (26.09)			13.91 (5.43-35.69)			<.001
	COPDb , n (%)
		No (reference)		7455 (98.09)			18 (78.26)			1.00 (N/A)			N/A
		Yes		145 (1.91)			5 (21.74)			14.28 (5.23-38.99)			<.001
	Hypertension, n (%)
		No (reference)		5993 (78.86)			8 (34.78)			1.00 (N/A)			N/A
		Yes		1607 (21.14)			15 (65.22)			6.99 (2.96-16.52)			<.001
	Ischemic heart disease, n (%)
		No (reference)		7265 (95.59)			18 (78.26)			1.00 (N/A)			N/A
		Yes		335 (4.41)			5 (21.74)			6.02 (2.22-16.32)			<.001
	Atrial fibrillation, n (%)
		No (reference)		7473 (98.33)			17 (73.91)			1.00 (N/A)			N/A
		Yes		127 (1.67)			6 (26.09)			20.77 (8.06-53.54)			<.001
	Congestive heart failure, n (%)
		No (reference)		7539 (99.2)			19 (82.61)			1.00 (N/A)			N/A
		Yes		61 (0.8)			4 (17.39)			26.02 (8.60-78.74)			<.001
	CKDc, n (%)
		No (reference)		7332 (96.47)			18 (78.26)			1.00 (N/A)			N/A
		Yes		268 (3.53)			5 (21.74)			7.60 (2.80-20.62)			<.001
	Type 2 diabetes, n (%)
		No (reference)		7028 (92.47)			14 (60.87)			1.00 (N/A)			N/A
		Yes		572 (7.53)			9 (39.13)			7.90 (3.40-18.33)			<.001
	Type 1 diabetes, n (%)
		No (reference)		7559 (99.46)			22 (95.65)			1.00 (N/A)			N/A
		Yes		41 (0.54)			1 (4.35)			8.38 (1.10-63.64)			.12
	Cirrhosis, n (%)
		No (reference)		7585 (99.8)			22 (95.65)			1.00 (N/A)			N/A
		Yes		15 (0.2)			1 (4.35)			22.98 (2.91-181.62)			.04
	Eczema, n (%)
		No (reference)		5878 (77.34)			13 (56.52)			1.00 (N/A)			N/A
		Yes		1722 (22.66)			10 (43.48)			2.63 (1.15-6.00)			.03
	CMSd, mean (SD)
		Continuous		0.28 (1.11)			3.37 (1.1)			3.24 (2.55-4.11)			<.001
Exposures
	ICUe admission, n (%)
		No (reference)		7333 (96.49)			18 (78.26)			1.00 (N/A)			N/A
		Yes		267 (3.51)			5 (21.74)			7.63 (2.81-20.70)			<.001
	Vaccination at any time, n (%)
		No vaccine (reference)		867 (11.41)			5 (21.74)			1.00 (N/A)			N/A
		One dose		367 (4.83)			4 (17.39)			1.89 (0.50-7.08)			.35
		Two doses		6366 (83.76)			14 (60.87)			0.38 (0.14-1.06)			.09
	Pre– long COVID vaccination, n (%)
		No vaccine (reference)		7326 (96.39)			21 (91.3)			1.00 (N/A)			N/A
		One dose		264 (3.47)			2 (8.7)			2.64 (0.62- 11.33)			.25
		Two doses		10 (0.13)			0 (0)			Inff			N/A

aN/A: not applicable.

bCOPD: chronic obstructive pulmonary disease.

cCKD: chronic kidney disease.

dCMS: Cambridge Multimorbidity Score.

eICU: intensive care unit.

fInf: infinite.

The results for the multivariate logistic regression analysis for people with LC using all-cause mortality as an outcome are presented in Figure 5. Age (OR 1.08, 95% CI 1.02-1.14), male sex, and a higher CMS were all associated with higher odds of mortality. By contrast, COVID-19 vaccination at any time and living in a conurbation were associated with lower odds of mortality (Figure 5).

Figure 5

Multivariate logistic regression analysis of risk factors for all-cause mortality in people with long COVID. Results are shown as odds ratios (ORs) with 95% CIs. CMS: Cambridge Multimorbidity Score.

Discussion

Principal Findings

Although rates of recording of LC are low, an LC diagnosis was associated with an odds of more than twice as many consultations with ONS-defined LC-related symptoms in the 6 months after contracting the index infection compared with a historical control period. The increase in symptoms did not differ between those who had their initial COVID-19 infection managed in the hospital and those who were a community case. However, people with LC after hospitalization had greater odds of presenting with mental health problems, and those with LC after community infection had greater odds of presenting with general symptoms (weakness and tiredness, fever, myalgia, and abdominal pain).

There were some similarities, but there were marked contrasts between the characteristics of people who had been diagnosed with LC after a hospital infection and those who had been diagnosed with LC after a community infection. The similarities were associations with increasing age, asthma, and type 2 diabetes. The differences in the posthospitalization LC group were male sex, more deprivation, history of CKD, and higher multimorbidity scores, whereas those in the postcommunity LC group were female sex, less deprived, and more likely to have depression and anxiety as well as lower levels of comorbidities.

All-cause mortality in people with LC was higher in older men and those with higher multimorbidity scores, associations that were similar to those with hospitalized patients. COVID-19 vaccination was associated with lower odds of all-cause mortality in patients with LC.

Comparison With the Literature

Posthospitalization LC was associated with higher deprivation, non-White ethnicity, obesity, CKD, and type 2 diabetes compared with postcommunity LC. There are similarities between our study, Living Risk Prediction Algorithm (QCOVID) study [21], and other studies [6,7] that reported the same risk factors, although with different outcomes. Data from the UK Health Security Agency and ONS indicated economic disadvantage to the prevalence of sex, obesity, diabetes, hypertension, and cardiovascular disease. These disparities may have been exacerbated because of the COVID-19 pandemic, especially among ethnic groups. However, there remains uncertainty regarding the degree to which the risk of developing posthospitalization LC in more deprived segments is linked to the severity of the disease (COVID-19) and more comorbidities [22] or to the propensity to consult in primary care, as reported for other respiratory conditions [23]. Disentangling the relationship between LC and hospital versus community is confounded by the presence of post-ICU syndrome in patients admitted to the ICU, many of the features of which (anxiety, cognitive difficulties, and breathlessness) overlap with LC. It is possible that the differences in the 2 groups are due to this confounding.

There are similarities between our study, Living Risk Prediction Algorithm (QCOVID) study [21], and other reports [3,24] regarding sociodemographic and comorbidity variables associated with mortality. These include cardiometabolic conditions (eg, CKD, type 2 diabetes, ischemic heart disease, and atrial fibrillation), chronic obstructive pulmonary disease, and asthma. However, we additionally report on vaccination status and conurbation as associated with lower odds of death. A UK Health Security Agency report indicated twice the risk of death due to COVID-19 infection among people from Bangladesh in comparison with White British people. Caribbean, Indian, Pakistani, Chinese, and Black ethnic groups were identified to have a 10% to 50% higher risk of mortality in comparison with White British people. We do not report differences on mortality per ethnicity because the number of deaths in the LC group was too small to enable us to find differences across groups.

We identified a lower prevalence of LC compared with self-report population surveys (eg, ONS) [4], but the prevalence was higher than those reported by other studies using routine data [9]. The OpenSAFELY study found that 27% of practices had no LC recording compared with 7.8% in our sentinel cohort [9]. Low rates of clinical coding of LC and interpractice variation are a national problem. COVID-19 coding evolved over the course of the pandemic, and the United Kingdom also has a region-specific version of SNOMED CT, which further complicates the issue [19,25]. LC clinical codes were introduced to SNOMED CT in January 2021; therefore, primary care staff did not have access to these until February 2021 [9,10]. Levels recorded in GP CMRs are dependent both on patients consulting their GP (many do not) and the GP both recognizing LC and coding it; therefore, our estimate of 1.83% (7623/416,505) will be very conservative. In addition, vaccination has been shown to decrease the risk of developing LC by approximately half; therefore, risks will have fallen over time (ONS).

Strengths and Limitations

The data were sourced from a representative network (PCSC) where practices have received feedback throughout the pandemic. Data on COVID-19 infection diagnoses and comorbidity are likely to be of good quality [17,26]. Linkage to hospital and mortality data adds reliability compared with only using coded data. Clinicians may well be underrecording LC, either by not recognizing it or by coding it with a presenting symptom code. The ONS symptoms are the most well-validated set of LC symptoms available at present; however, a validation study is pending. In addition, LC may be diagnosed as other conditions and coded as such; for example, a patient with pre-existing anxiety may well have their LC-related tachycardia and breathlessness diagnosed as worsening anxiety. It is known that GPs tend not to record symptoms reliably in the record and tend to only record symptoms that support their working diagnosis, introducing bias [27]. As a result, vital data may not be coded and included in this study because of these being available as free text within CMRs. Considerable care needs to be taken in interpreting these very granular data from the CMR.

Implications of the Findings

It is very likely that LC was underrecorded, and clinicians should continue to be encouraged to record this condition in clinical records. LC is an important comorbidity that needs to be captured so that it can be taken into consideration in health service planning and assessment of vaccine benefit risk.

The differences between those presenting to community and hospital care may have represented the propensity of different groups to consult (eg, women more than men in primary care) and the possibility that some groups experienced more serious disease (eg, men and increasing age), as well as the potential for disparities in presentation.

As COVID-19 continues to circulate in the community, albeit with lower death and morbidity rates because of vaccines and a current less-virulent strain, learning to recognize groups of patients at greatest risk of acquiring LC and managing associated risk factors may affect presentations and disease impact. Comorbid conditions that increase the risk of acquiring LC, such as asthma, may shed light on possible etiological risk factors.

Call for Further Research

LC case identification within primary care requires improved data recording. Better case identification will enable successful interventions to be implemented. A range of incentives to improve case ascertainment and data quality have been successfully implemented in primary care. This would further aid in understanding communicable disease risk and to develop better controls in the future.

Conclusions

LC recording in primary care records was low, reflecting either low prevalence or underrecording. There are differences between the sociodemographic profiles and comorbidities of LC symptoms presented after an index community infection compared with those hospitalized with a COVID-19 infection. Factors associated with hospital presentation are also associated with higher all-cause mortality, although vaccination is protective. This suggests that the disparities flagged throughout the COVID-19 pandemic may also apply to LC, where better tools to identify and intervene are needed in those at greatest risk.