Long-Term Effects of COVID-19

Abstract

Coronavirus disease 2019 (COVID-19) is the third deadly coronavirus infection of the 21st century that has proven to be significantly more lethal than its predecessors, with the number of infected patients and deaths still increasing daily. From December 2019 to July 2021, this virus has infected nearly 200 million people and led to more than 4 million deaths. Our understanding of COVID-19 is constantly progressing, giving better insight into the heterogeneous nature of its acute and long-term effects. Recent literature on the long-term health consequences of COVID-19 discusses the need for a comprehensive understanding of the multisystemic pathophysiology, clinical predictors, and epidemiology to develop and inform an evidence-based, multidisciplinary management approach. A PubMed search was completed using variations on the term post-acute COVID-19. Only peer-reviewed studies in English published by July 17, 2021 were considered for inclusion. All studies discussed in this text are from adult populations unless specified (as with multisystem inflammatory syndrome in children). The preliminary evidence on the pulmonary, cardiovascular, neurological, hematological, multisystem inflammatory, renal, endocrine, gastrointestinal, and integumentary sequelae show that COVID-19 continues after acute infection. Interdisciplinary monitoring with holistic management that considers nutrition, physical therapy, psychological management, meditation, and mindfulness in addition to medication will allow for the early detection of post-acute COVID-19 sequelae symptoms and prevent long-term systemic damage. This review serves as a guideline for effective management based on current evidence, but clinicians should modify recommendations to reflect each patient's unique needs and the most up-to-date evidence. The presence of long-term effects presents another reason for vaccination against COVID-19.

Coronavirus disease 2019 (COVID-19) is the third deadly coronavirus infection of the 21^st century and has proven to be significantly more deadly than its predecessors, with the number of infections and deaths still increasing daily.¹ Since its emergence in December 2019, this virus has spread across the globe infecting nearly 200 million people and leading to more than 4 million deaths as of July 17, 2021.²

Knowledge of COVID-19, which is caused by severe acute respiratory coronavirus 2 (SARS-CoV-2), is constantly progressing with the discovery of new scientific and clinical evidence. Comparison between the timeline, common symptoms, systematic effects, and risk factors for adverse events of acute versus chronic COVID-19 symptoms can be found in Table 1 .

Table 1.

Comparison Between the Timeline, Common Symptoms, Systematic Effects, and Risk Factors for Adverse Events of Acute Versus Chronic COVID-19 Symptoms^a

Features	Acute COVID-19	Post-acute COVID-19
Initiation of symptoms 3, 4, 5, 6, 7, 8	2 to 14 days after exposure	4 weeks after initial response
Pathophysiology9, 10, 11, 12, 13, 14, 15	Direct viral toxicity via ACE2/TMPRSS2 expressing cells (alveolar epithelial type II cells, heart, kidneys, gastrointestinal tract, lung tissue, and nasal olfactory cells) Immune-mediated dysregulation of RAAS pathway Microvascular dysfunction via endothelial damage Dysregulation of the innate immune system with lymphopenia Prolonged activation of type 1 interferons and endothelial cell damage lead to thromboembolic events Decrease in lymphocytes may allow for viral particles to persist, resulting in excessive inflammation that can increase symptom severity and need for ICU admission	Presence of autoreactive antibodies Inflammatory and metabolic changes to parenchyma, and supporting structures during initial infection Sequelae mediated by hospitalization interventions
Common symptoms3, 4, 5, 6, 7,16, 17, 18, 19, 20	Fever, dry cough, and shortness of breath >50% of patients	Fatigue, pneumonia, myalgias, headache, thromboembolic conditions, and MIS
Systems commonly involved16,17,19,21	Respiratory, renal (AKI), hematological (thromboembolism)	Respiratory, cardiovascular, neurologic, MIS, hematological Less frequently involved: renal, endocrine, gastrointestinal, or integumentary
Laboratory markers and clinical indications of severe disease16,20,22,23	Progressive elevation of cardiac troponins, hepatic enzymes, and serum creatinine, along with advanced lymphocytopenia and increased neutrophils ARDS development for severe cases	See Table 2 for systematic breakdown of lab markers and risk factors
Risk factors for adverse consequences4,16,23, 24, 25	Hypertension, diabetes, mechanical ventilation, ICU admission, advanced age, frailty, immune response	Ages 40-49 (OR, 15.3) years Hospitalization during acute infection (OR, 2.9) Clinical findings from the initial infection (variable)
Risk factors for death26	Hospitalization, 85+ years old (OR, 11.36 years), pneumonia, diabetes, heart failure, CKD	Not yet determined

ACE2, angiotensin-converting enzyme 2; AKI, acute kidney injury; ARDS, acute respiratory distress syndrome; CKD, chronic kidney disease; COVID-19, coronavirus disease 2019; ICU, intensive care unit; MIS, multisystem inflammatory syndrome; OR, odds ratio; RAAS, renin-angiotensin aldosterone system; TMPRSS2, transmembrane serine protease 2.

The long-term sequelae of COVID-19 (referred to as long-COVID, post-acute COVID-19, post-COVID condition, and post-COVID sequelae interchangeably) are defined as an inflammatory or host response towards virus that occurs approximately 4 weeks after initial infection and continues for a yet uncharacterized duration (Supplemental Table, available online at http://www.mayoclinicproceedings.org).⁸ This review aims to report the up-to-date epidemiology, pathophysiology, clinical predictors, management recommendations, and the unanswered questions and future directions for the systematic effects of long-term COVID-19 infections that clinicians can refer to when managing COVID-19 long-haulers (Table 2 ).

Table 2.

Summary of Important Findings in the Systemic Sequelae of Post-Acute COVID-19^a,b

System	Clinical findings or diagnostic criteria 17,19	Risk factors 27, 28, 29	Management recommendations 30, 31, 32, 33, 34, 35, 36, 37	Clinical trial based pharmacology 30,38, 39, 40, 41, 42, 43, 44
Pulmonary	Fatigue, dyspnea CT: ground-glass opacities and fibrotic changes	Severe disease, ICU admission, or severe hospital stay Lower limit 6MWT, higher CT severity score, increased D-dimer or urea nitrogen Advanced age, male, history of cigarette smoking	Initial evaluation 4-6 weeks with pulmonary function testing and 6MWT Follow-up imaging at 12 wks Dyspnea: pulmonary and cardiac workup	Maximum initial dose 0.5 mg/kg oral prednisolone: FVC, radiological and symptomatic improvement 2403 mg daily pirfenidone: FVC, 6WMT, and disease progression improvement 150 mg of twice daily nintedanib: FVC improvement Pulmonary rehabilitation: pulmonary function improvements Ongoing clinical trials to determine potential pharmacological candidates, use current recommended guidelines for most likely differential diagnosis
Cardiovascular	Chest pain, heart palpitations CMR: myocardial inflammation, myocarditis, pericarditis, cardiac fibrosis Echocardiogram: impaired LVEF, pericarditis, myocarditis, other cardiac anomalies Increased troponin level	Severe disease, high viral load, pneumonia during hospitalization Increased troponin levels, decrease in LVEF Hydroxychloroquine with or without ritonavir/lopinavir and azithromycin use in acute COVID-19	Initial evaluation with noninvasive technology (point-of-care ECG, transthoracic echocardiogram, laboratory tests for CRP, and troponin-T) Escalate to invasive testing and referral if abnormalities are detected in the initial evaluation	Ongoing clinical trials to determine potential pharmacological candidates, use current recommended guidelines for most likely differential diagnosis Continue RAAS modifying drug use (ACE-inhibitors, ARBs, etc) Avoid amiodarone as it may exacerbate pulmonary fibrosis
Neurological	Neuropsychiatric: anxiety, depression, PTSD, OCD, insomnia Cognitive: headaches, brain fog, memory loss, nonrestorative sleep Peripheral: anosmia, ageusia, fatigue, malaise, POTS	Severity of illness, ICU admission, MIS-C Medications such as lopinavir-ritonavir and corticosteroid use (rare)	Standard screening tools be used for neuropsychiatric conditions by primary care providers to evaluate for disorders such as anxiety, depression, PTSD, and OCD No specific published guidelines on screening protocols for neurological disorders	Standard therapies with referral to neurological specialists for refractory conditions or imaging abnormalities Beta-blockers, diet, and exercise: beneficial in reducing POTS symptoms
Hematological	Pulmonary embolism, VTE, ATE	Disease severity, length of acute infection, and ICU admission Low fibrinogen and higher D-dimer on admission, and DI ≥1.5-fold Increased age, cancer, and corticosteroid use (critically ill)	In-patient (all): CBC, coagulation studies PT and aPTT, fibrinogen and D-Dimer Outpatient (symptomatic or at-risk): same as in-patient Proceed to further invasive testing and imaging studies under standard protocols recommended for the suspected differential diagnosis if abnormalities are present	Thromboprophylaxis in those with high clot burden or at risk of thromboembolic events if there is no bleeding risk Ongoing clinical trials to determine potential pharmacological candidates, use current recommended guidelines for most likely differential diagnosis
Renal	AKI, wide spectrum of glomerular and tubular diseases	Same as hematological system High-risk APOL1 variant (collapsed glomerulopathy)	Refer to a nephrologist if AKI is persistent or there is severe dysfunction	Standard therapies with referral to specialists as needed
Endocrine	New-onset diabetes, worsening pre-existing diabetes, DKA, subacute thyroiditis, Graves thyrotoxicosis	High viral loads, severe disease	Initial evaluation for new-onset diabetes should include testing for antibodies to beta-islet cells and CRP and rule out risk factors for type 2 diabetes Monitor labs to rule out new-onset thyroid autoimmune diseases (Graves and Hashimoto thyroiditis) vs COVID-19 thyroiditis Refer to an endocrine specialist as necessary	Standard therapies with referral to specialists as needed
Gastrointestinal	Loss of appetite, nausea, acid reflux, diarrhea, abdominal distension, belching, vomiting, and bloody stools	High viral loads, severe disease	Fecal cultures to check for gut dysbiosis, refer to a gastrointestinal specialist as necessary	Dietary changes or fecal transplantation Standard therapies with referral to specialists as needed
Integumentary	Hair loss, skin rash, urticarial lesions, angioedema	Unknown	Standard protocols with referral to specialists as needed	Standard therapies with referral to specialists as needed
MIS-C	(Age ≤ 21 y): fever ≥ 38.0°C or subjective fever for ≥24 h, laboratory inflammation evidence, severe illness requiring hospitalization with ≥ 2 organ involvement	Presenting to the emergency department or admitted to the general ward Increased D-dimer, troponin, BNP, pro-BNP,CRP, and ferritin In patients ≥5 y old, identify as Black	Tier 1: CBC, CMP, ESR, CRP and SARS-CoV-2 PCR/serology If tier 1 results reach the diagnostic threshold then tier 2: cardiac enzymes (BNP, troponin T, etc), hematological/coagulation factors (D-dimer, fibrinogen, PTT, blood smear, etc), cardiac studies (ECG and echocardiogram), LDH, triglycerides, urinalysis, and cytokine panel In shock without clear etiology: tiers 1 and 2	1st line in shock: IVIG 2 gm/kg and MPIV at 1-2 mg/kg per day Refractory disease with shock: MPIV 10-30 mg/kg per day or high dose anakinra No shock: IVIG 2 gm/kg per day Refractory Disease, No shock: MPIV 1-2 mg/kg per day or high-dose anakinra

^a6MWT, 6-minute walk test; ACE, angiotensin-converting enzyme; AKI, acute kidney injury; APOL1, apolipoprotein L1; aPTT, activated partial prothrombin time; ARB, angiotensin receptor blocker; ATE, arterial thromboembolism; BNP, brain natriuretic peptide; CBC, complete blood count; CMP, complete metabolic panel; CMR, cardiac magnetic resonance; COVID-19, coronavirus disease 2019; CRP, C-reactive protein; CT, computed tomography; DI, D-dimer increment; DKA, diabetic ketoacidosis; ECG, electrocardiogram; ESR, erythrocyte sedimentation rate; FVC, forced vital capacity; ICU, intensive care unit; IVIG, intravenous immunoglobulin; LDH, lactate dehydrogenase; LVEF, left ventricular ejection fraction; MIS-C, multisystem inflammatory syndrome in children; MPIV, methylprednisone intravenous; OCD, obsessive compulsive disorder; PCR, polymerase chain reaction; POTS, postural orthostatic tachycardia syndrome; PT, prothrombin time; PTSD, post-traumatic stress disorder; RAAS, renin angiotensin-aldosterone system; SARS-CoV-2, severe acute respiratory syndrome; VTE, venous thromboembolism.

^bHigh-risk or symptomatic individuals are the priority for screening.

A PubMed search was completed using the terms “long-COVID,” “post-acute COVID-19,” “post-COVID condition,” “post-COVID sequelae,” or “long-term sequelae of COVID-19.” Only peer-reviewed studies in English published by July 17, 2021, were considered for inclusion. All studies discussed in this text are from adult populations unless specified (as with multisystemic inflammatory syndrome in children [MIS-C]).

Pulmonary System

Epidemiology

The evidence of the epidemiology of post–COVID-19 pulmonary sequelae comes from primary studies that look at persistent symptomology, acute manifestations of COVID-19, as well as extrapolations from follow-up from previous coronaviruses. Overall, the most common symptoms of long-term pulmonary sequelae experienced by those with COVID-19 include fatigue, dyspnea, and/or cough. The prevalence of these symptoms and the severity of abnormalities on imaging depend on the severity of acute illness and intensive care unit (ICU) admission status. A breakdown of the major studies looking at post-acute COVID-19 pulmonary effects can be found in Table 3 .

Table 3.

Epidemiological Studies of Post-Acute COVID-19 Broken Down by System

Author	Study type	Key findings	Key takeaways
Pulmonary
Ahmed et al45	Meta-analysis on SARS/MERS 6 months post-discharge	DLCO, FVC, TLC abnormalities more prevalent than abnormalities in FEV1 TLC and FVC abnormalities resolve with time, but DLCO impairment remained in 24.35% for >6 months	1.Restrictive pattern of lung pathology may occur. 2.Consider taking serial DLCO measurements, D-dimer and urea nitrogen to serve as a proxy for lung function and risk of disease. 3.ICU admission and severe disease are risk factors. 4.Symptoms decrease with time.
Carvalho-Schneider et al46	Prospective follow-up study of 150 patients after 60 days	Instances of grade 2-4 dyspnea decrease with time (at the onset-42.2%, Day 30-10.7% vs. Day 60- 7.7% post-infection) Increased odds of persistent symptoms in those between ages 40 and 60 y, admitted to hospitals, and abnormal auscultation
Halpin et al47	Prospective study of 100 subjects in the United Kingdom after 4 weeks	Fatigue (72% ICU vs 60.3% non-ICU) and dyspnea (65.6% ICU vs 42.6% non-ICU)
Huang et al17	Ambidirectional cohort study of 1733 patients after 6 months	Severe disease: 4.6 times more likely to have lung diffusion impairments and 2.69 times more likely to report fatigue 1+ major lung abnormality in 50% of patients after 6 months; most common is ground-glass opacities
Zhao et al48	39 patients after 3 months	Persistent fibrotic changes on CT in 25% of mild to moderate and 65% of severe COVID-19 patients Increases in urea nitrogen and D-dimer levels at admission were prognostic indicators of impaired lung diffusion
Cardiovascular
Carfi et al19	Italian study with 143 patients after 2 months	22% experience chest pain	1.Studies have a small sample size, therefore need more data to know prevalence. 2.Similar coronaviruses have shown cardiac sequelae therefore it is possible. 3.Chest pain, palpitations and IHCA/OHCAs are major symptoms. 4.Severe disease is a risk factor. 5.Athletes need to be evaluated before return to play.
Huang et al17	Ambidirectional cohort study of 1733 patients after 6 months	Chest pain and palpitations to be <5%
Sultanian et al49	Observational study of 3026 patients in Sweden	COVID-19 was also involved in at least 16% of IHCAs and 10% of all OHCAs, 2.3-fold increase in 30-day mortality due to IHCA and 3.4-fold in OHCA
Wu et al50	12-year follow-up study of SARS patients	40% continued to have cardiovascular complications
Puntmann et al51	Cohort study of 100 patients 60 days post COVID-19 infection	60% of participants had ongoing myocardial inflammation on CMR and 78% had some cardiac involvement independent of pre-existing conditions or illness severity Endomyocardial biopsy in severe patients revealed active lymphocytic infiltration without viral genome presence
Rajpal et al52	26 college athletes after 11-53 days	Myocarditis and pericarditis in 4 of 26 and 2 of 26 participants, respectively
Neurological
Taquet et al53	Retrospective cohort study with 236,371 patients after 6 months	23% to 37% had 1+ neuropsychiatric disorders Rates of neuropsychiatric disorder varied dependent on disease severity: Encephalopathy > ICU > hospitalized/nonhospitalized Patients with COVID-19 are 5.28-4.52x more likely to develop myoneural junction diseases than other respiratory infections	1.Severity of disease is a risk factor for neuropsychiatric effects not cognitive effects. 2.Peripheral nervous system effects need increased data to determine prevalence. 3.Prolonged anosmia may be an indicator of mild forms of COVID-19.
Mazza et al54	Self-rating among patients at a 1-mo follow-up	Anxiety (42%), insomnia (40%), depression (31%), PTSD (28%), and obsessive compulsive disorders (20%)
Garrigues et al55	120 patients, 100 d after an initial infection	Memory loss was the third most common persistent symptom at 34% Cognitive symptom manifestation did not differ between ICU and hospitalized patients
National Institute of Neurological Disorders and Stroke56	Retrospective study, 20 patients, with persistent neurological and cardiovascular complaints	15 had POTS, 3 neurocardiogenic syncope, and 2 orthostatic hypotension 85% had persistent residual autonomic symptoms, and 12 could not return to work after 6-8 mo 1.Severity of disease is a risk factor for neuropsychiatric effects nut not cognitive effects 2.Peripheral nervous system effects need increased data to determine prevalence Prolonged anosmia may be an indicator of mild forms of COVID-19
Lechien et al57	Multicenter European study of 1363 subjects after 6 months	5% of patients had prolonged anosmia with the highest prevalence in those with mild COVID 19
Hematological
Guan et al3	Retrospective study of 1099 people in China	Lymphocytopenia 83.2%, thrombocytopenia in 36.2%, and leukopenia in 33.7% on admission Elevated C-reactive protein (60.7%) and D-dimer (46.7%) Severe disease had more pronounced laboratory anomalies	1.Pulmonary emboli are of concern in severe illness patients, but rates of other thromboembolic events remain low. 2.D-Dimer values can be prognostic but should be taken in context with other clinical findings.
Roncon et al58	Systematic review	23.4% incidence of pulmonary embolism in ICU vs 14.7% in general ward Segmental/subsegmental arteries more frequently involved than main/lobar arteries
Rashidi et al59	Multicenter prospective study of 1529 participants	Venous thromboembolism is at 0.2%
Fan et al60	Case reports 40-90 d after positive serology	Arterial thromboembolic events have been seen in young, asymptomatic COVID-19 subjects
Townsend et al61	Prospective study of 150 participants in Ireland	Increased D-Dimer levels in 25.3% of patients up to 4 months More common in hospitalized patients and 50+ y old; also seen in 29% of patients exclusively managed in outpatient settings
Renal
Nugent et al62	Cohort study of 1612 patients in the United States	eGFR declined faster with COVID-19–associated AKI vs other causes (adjusted hazard ratio, 0.57; 95% CI, 0.35-0.92)	1.Majority recover renal function. 2.APOL1 gene variant may increase susceptibility towards lasting kidney damage.
Gupta et al63	Multicenter cohort study with 2215 adults, 60 days post-discharge	56% of patients discharged RRT (35% with COVID-19 AKI) unable to get off of it
Stevens et al64	Cohort study of 115 patients	84% with RRT during acute infection recovered kidney function
Kudose et al65	Kidney biopsies done at Columbia University	15 (88%) AKI, 9 (53%) nephrotic-range proteinuria, 5 (29%) collapsing glomerulopathy, 4 (24%) isolated acute tubular injury, 2 (12%) membranous glomerulopathy, 1 (6%) anti-GBM nephritis, 1 crescentic transformation of lupus nephritis, and 1 minimal change disease Collapsing glomerulopathy and minimal change disease showed the presence of the APOL1 gene variant
Endocrine
Zhou et al66	Retrospective study from China	6.4% of COVID-19 patients with DKA, but only 35.7% had diabetes	1.Insufficient evidence to determine prevalence of new thyroid conditions due to COVID-19.
Multiple studies67, 68, 69, 70, 71	Various case reports	Subacute thyroiditis and Graves thyrotoxicosis, and new diagnoses of DM diagnosed in COVID-19 patients
Gastrointestinal
Weng et al72	Follow-up study of 117 patients after 90 days	Loss of appetite (24%), nausea (18%), acid reflux (18%), diarrhea (15%), and abdominal distension (14%) with <10% of patients reporting belching, vomiting, and bloody stools	1.More studies needed for accurate prevalence.
Integumentary
Huang et al17	Ambidirectional cohort study of 1733 patients after 6 months	Hair loss (20% of patients) and skin rash which resolved in 97% of patients	1.More studies needed for accurate prevalence. 2.Hair loss, skin rash, urticarial lesions, and angioedema are reported.
Galván Casas et al73	Prospective study of 375 cases in Spain	Urticarial lesions made up 19% of COVID-19 cutaneous manifestations
Argolo et al74	Retrospective studies in Argentina	30% of patients reported worsening chronic urticaria during the pandemic
Multiple studies75, 76, 77	Case reports	Oral angioedema with or without urticaria on the tongue and/or lips 1-2 weeks into the acute disease course

AKI, acute kidney injury; APOL1, apolipoprotein L1; CMR, cardiac magnetic resonance; COVID-19, coronavirus disease 2019; CT, computed tomography; DKA, diabetic ketoacidosis; DLCO, diffusing capacity of the lung for carbon monoxide; DM, diabetes mellitus; eGFR, estimated glomerular filtration rate; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; GBM, glomerular basement membrane ; ICU, intensive care unit; IHCA, in-hospital cardiac arrest; MERS, Middle East respiratory syndrome; OHCA, out-of-hospital cardiac arrest; POTS, postural orthostatic tachycardia syndrome; PTSD, post-traumatic stress syndrome; RRT, renal replacement therapy; SARS, severe acute respiratory syndrome; TLC, total lung capacity.

Pathophysiology

A summary of the pathophysiology of pulmonary sequelae due to post-acute COVID-19 can be found in Figure 1 . An analysis of 41 post-mortem samples in Italy found extensive alveolar damage in 100% of subjects, lung macro- and microvasculature thrombosis in 71% of individuals, and thrombi stage of the organization consistent with local origin. Pneumocytes and endothelial cells contained viral ribonucleic acid even in the later stages of the disease, but viral infection was not detected in other organs.⁹⁵ The mechanism for thrombotic changes in this disease can also be found in Figure 1.

Figure 1.

Pathophysiology of pulmonary, cardiac, neurological, hematological, renal, gastrointestinal, integumentary, and endocrine effects of post-acute coronavirus disease 2019 and its subsequent clinical manifestations.^{15,17,28,29,48,}78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94 BBB = blood brain barrier; ACE = angiotensin-converting enzyme; ACE2 = angiotensin-converting enzyme 2; AKI = acute kidney injury; APOL1 = apolipoprotein L1; COVID-19 = coronavirus disease 2019; DAMP = damage-associated molecular patterns; DKA = diabetic ketoacidosis; ECM = extracellular matrix; HIF-1 = hypoxia-inducible factor 1; HPA = hypothalamic-pituitary-adrenal; IL = interleukin; PAMP = pathogen-associated molecular pattern; PNS = peripheral nervous system; TGF = tumor growth factor; TMPSSR2 = type 2 transmembrane protein; TNF = tumor necrosis factor.

Clinical Predictors

A comprehensive list of risk factors for the development of pulmonary manifestations for post-acute COVID-19 can be found in Table 2. In a study of 1733 patients from China, patients categorized as having a more severe hospital stay were more likely to have diffusion impairments (4.6 times) and report fatigue (2.69 times) than less severe counterparts (Supplemental Figure 1, available online at http://www.mayoclinicproceedings.org).¹⁷ There is also an increased prevalence of fatigue and dyspnea in ICU patients than non-ICU groups 4 weeks after acute infection resolution.⁴⁷ Six-minute walk testing (6MWT) results can provide prognostic factors for illness severity as those with more severe disease had a higher proportion of subjects below the lower limit of the normal range (Supplemental Figure 1).¹⁷ The odds for developing pulmonary fibrosis were significantly increased in subjects with increased urea nitrogen (odds ratio [OR], 7.149) and D-dimer levels (OR, 1.066) at admission.⁴⁸

Management Recommendations

Priority for prognostic screening for pulmonary sequelae of post-acute COVID-19 should be given to those who are symptomatic or show appropriate clinical predictors. Management recommendations for those that meet these criteria can be found in Table 2.

For high-risk patients (see Table 2), the British Thoracic Society recommends an initial evaluation at 4 to 6 weeks post-discharge and in-person visit/follow-up imaging within 12 weeks.³¹ Radiological imaging is recommended for all COVID-19 patients 12 weeks after discharge regardless of symptom status. However, the study from Liu et al.⁹⁶ of 150 patients from China shows that radiological resolution of pulmonary abnormalities occurs in greater than or equal to 50% of patients within 3 weeks of discharge; therefore, imaging of nonsymptomatic patients may be unnecessary.

Steroid use in the setting of post-acute COVID-19 has mixed results; therefore, steroid-sparing therapies should be considered when possible.¹⁷ An observational study in the United Kingdom has shown some rapid functional improvements with corticosteroid therapy.³⁸ Of the 837 patients assessed by telephone at 4 weeks after infection resolution, 35 (4.8%) were initially diagnosed with interstitial lung disease and significant functional deficits. These 35 patients were brought in for outpatient evaluation where 30 were diagnosed with persistent interstitial lung changes and were offered steroid treatment with a maximum dose of 0.5 mg/kg oral prednisolone for 3 weeks. Improvements were noted in transfer factor (31.6%±27.6%, P<0.001) and forced vital capacity (9.6%±13.0%, P=0.014) with treatment, and significant symptomatic and radiological improvement.

Unanswered Questions and Future Directions

Questions that remain include whether patients with significant lung involvement ever go back to pre–COVID-19 baseline, both symptomatically and by objective measures of lung function. In addition, we also do not know how long it takes for symptoms to resolve completely or for lung function to fully recover. Future studies involving medications that can help decrease permanent lung damage such as pulmonary fibrosis would be beneficial.

Cardiovascular System

Epidemiology

A breakdown of the major studies looking at post-acute COVID-19 cardiac effects can be found in Table 3. Increases in cardiac troponin levels may indicate underlying cardiovascular pathology and is correlated with increased severity of acute illness and use of mechanical ventilation during hospitalization, cardiac dysfunction, arrhythmias, and death.⁹⁷

Pathophysiology

The pathophysiology behind the cardiovascular sequelae of post-acute COVID-19 can be found in Figure 1. These findings indicate immune-mediated pathogenesis in the cardiovascular sequelae of post-acute COVID-19 instead of viral pathogenesis that leads to cardiac fibrosis. Imbalances in electrolytes can also interfere with electrical conduction in myocytes resulting in fatal rhythmic abnormalities. Hydroxychloroquine and azithromycin may cause QT prolongation which can lead to torsade de pointes and fatal arrhythmias.⁹⁸ In patients at risk of cardiovascular symptoms of COVID-19, medication lists and electrolyte levels should be closely monitored to reduce instances of arrhythmias.

Clinical Predictors

History of increased troponin, disease severity, higher viral load, and pneumonia increase the risk of cardiovascular sequelae in patients who have had COVID-19. Patients with elevated troponin levels are also at an increased risk due to higher white blood cell counts and longer prothrombin times.⁹⁷ In a meta-analysis of 591 patients with severe acute respiratory syndrome (SARS), Corrales-Medina et al⁹⁹ found that hospitalization with pneumonia increases the risk of cardiovascular disease 2.1 times within the first year and 1.86 times in 10 years. Hospitalization records in COVID-19 patients should be evaluated for pneumonia during active infection and flagged for cardiac follow-up. A cytokine response panel consisting of 6 pro-inflammatory cytokines (tumor necrosis factor [TNF]-alpha, interferon-gamma, C-C motif chemokine ligand 5, interleukin 6 [IL-6], IL-8, and IL-18) were elevated in 16 patients with viral loads greater than 1000 copies per real-time polymerase chain reaction (rt-PCR) and cardiac fibrosis.¹⁰⁰ These lab markers may serve as prognostic indicators of post–COVID-19 patients that may have cardiac sequelae due to fibrosis. Cardiac fibrosis is central to the pathophysiology of heart failure (HF), which explains the increased incidence of acute HF in COVID-19 and acute decompensation in patients with chronic-HF in this study of 3080 patients in Spain.⁴³

Prolonged corticosteroid use may increase viral shedding, thus increasing the odds of developing cardiovascular and other systemic sequelae. A multicenter randomized control trial of 86 patients with COVID-19 found that early use of corticosteroids (methylprednisolone) prolongs viral shedding in patients with COVID-19 pneumonia by suppressing immune cells.¹⁰¹ In this single-blind prospective trial, patients were either given 1 mg/kg per day of methylprednisolone in 100 mL 0.9% saline or 100 mL 0.9% normal saline for 7 days within 72 hours of being admitted to the hospital. Viral RNA was detectable in the methylprednisolone group (11 days; interquartile range, 6 to 16 days), which was significantly longer than that in the control group (8 days; interquartile range, 2 to 12 days; P=0.030) with throat cultures. CD3+ T cells and CD8+ T cells in the methylprednisolone group were also lower than the control group (P<0.05). However, this study also found no significant differences in other secondary outcomes or incidence of clinical deterioration.

Corticosteroid use was beneficial in reducing patient mortality in patients with acute respiratory distress syndrome (ARDS) (HR, 0.38).¹⁰² A landmark Randomised Evaluation of COVID-19 Therapy (RECOVERY) open-label trial with 6425 hospitalized COVID-19 patients who were assigned to either take dexamethasone 6 mg once a day for 10 days or have “usual” care. Reduction in mortality with glucocorticoid therapy varied greatly depending on the level of respiratory support at the time of randomization. Mortality was lower in treatment groups in patients receiving invasive mechanical ventilation (29.3% vs 41.4%; rate ratio [RR], 0.64) or oxygen without invasive mechanical ventilation (23.3% vs 26.2%; RR, 0.82) but not in subjects receiving no respiratory support (17.8% vs 14.0%; RR, 1.19).¹⁰³ Although corticosteroids may cause systemic sequelae issues in the long term, it would not be reasonable to delay treatment given the mortality benefits in patients who need respiratory support or who have ARDS.

Management Recommendations

Major concerns in the cardiovascular sequelae of COVID-19 are acute coronary syndrome, myocarditis, arrhythmias, cardiogenic shock, and medication-induced heart conditions. Full cardiac workup should be limited to patients with active symptoms or at increased risk. Point-of-care electrocardiogram (ECG), transthoracic echocardiogram, laboratory tests for C-reactive protein (CRP) and troponin-T, and pro-inflammatory markers (TNF-alpha, C-C motif chemokine ligand 5, IL-6, IL-8, IL-18, and interferon-gamma) should be measured in symptomatic patients. Decreases in left ventricular ejection fraction, abnormal increases in the aforementioned laboratory tests, and any electrical abnormalities warrant invasive measures such as cardiac catheterization, transesophageal echocardiography, and cardiac magnetic resonance if they are of clinical benefit.¹⁰⁴ Athletes presenting with clinical findings of myocarditis at the onset of illness (disproportionate dyspnea on exertion, chest pain, unexpected elevations in serum troponins, arrhythmias/atrioventricular block, etc) should stop aerobic activity and athletic participation and undergo an echocardiogram, 24-hour Holter monitoring, and exercise ECG within 3 to 6 months after initial illness. They can resume training if cardiac and inflammatory biomarkers, electrical activity, and ventricular systolic function have returned to normal.¹⁰⁵

The current clinical trial–based pharmacology for management of cardiac sequelae in post-acute COVID-19 can be found in Table 2. Corticosteroids may improve cardiac function in viral-induced myocarditis if viral RNA is undetectable due to concerns of prolonged viral shedding.¹⁰⁶

Unanswered Questions and Future Directions

There are many unanswered questions on the long-term cardiovascular effects of COVID-19. This is an evolving question due to the novelty of COVID-19. We do not know if post–COVID-19 arrhythmias are permanent or temporary. We do not know how long patients will need to avoid proarrhythmic drugs. We also do not know if post–COVID-19–associated myocarditis or cardiomyopathy and related congestive HF will fully recover. The duration of treatment with angiotensin-converting enzymes or beta blockers in these patients is also unknown. Another unknown is how long should limitations on strenuous activity remain. Future studies should focus on determining risk factors for long-term cardiovascular side effects and the development of mitigation measures to prevent these sequelae.

Neurological System

Epidemiology

Survivors of COVID-19 report prolonged anosmia/ageusia, headaches, “brain fog”/memory loss, fatigue, malaise, and nonrestorative sleep.^{16 , 17 , 19 , 47} A breakdown of the major studies of post-acute COVID-19 neurological effects can be found in Table 3. The prevalence of brain fog lacks significant scientific validity due to the lack of objective evidence.

Pathophysiology

A summary of the pathophysiology of neurological effects of post-acute COVID-19 can be found in Figure 1.

Clinical Predictors

The severity of illness, ICU admission, MIS-C, and certain medication during acute infection all increase risk of neurological sequelae in the post-acute COVID-19 period. A retrospective cohort study with 236,371 patients found substantial neurological and psychiatric morbidity among patients with severe illness.⁵³ Intensive care unit admissions are also associated with increased neuropsychiatric symptom manifestation (depression, anxiety, etc) but not cognitive symptoms (memory loss and headache). Instances of neuropsychiatric diseases increase with encephalopathy during the acute phase of illness (Supplemental Figure 1).⁵³ Case reports of children with MIS-C show unexpectedly high instances of neurological involvement (40%) as well.¹⁰⁷ Persistent anosmia after infection resolution may be a prognostic sign of a milder disease because it is prevalent in people with less severe COVID-19. Increased production of immunoglobulin A limits viral spread in those with mild COVID-19, but it escalates local inflammatory reactions in the olfactory system.⁵⁷

Medications used in acute COVID-19 such as lopinavir-ritonavir and corticosteroids have neurological side effects that can manifest and persist during the acute or post-acute phase of illness. Ototoxicity-mediated sensorineural hearing loss is associated with lopinavir-ritonavir treatment, although this effect is rare and resolves approximately 20 weeks after discontinuation.¹⁰⁸ A multicenter cohort study in France unrelated to COVID-19 with 88 patients showed prednisone use greater than 20 mg/day caused delirium and manic mood changes in 52% of patients.¹⁰⁹ A controlled, open-label trial of 6425 patients that looked at dexamethasone (6 mg once a day for 10 days) as a potential treatment for patients hospitalized with COVID-19 had four adverse reactions, one of which included psychosis.¹⁰³ The neurological side effects of corticosteroids are infrequent but can still cause significant neuropsychological and peripheral symptoms. Corticosteroids are frequently used in hospital and outpatient settings during acute COVID-19 infection, so clinicians must consider the neurological effects of these medications when monitoring patients in the outpatient setting.

Management Recommendations

There are no specific published guidelines on screening protocols for neurological disorders caused by COVID-19 other than for postural orthostatic tachycardia syndrome (POTS). Primary care providers should use standard screening tools to evaluate for common disorders such as anxiety, depression, post-traumatic stress disorder (PTSD), and obsessive compulsive disorder (OCD).⁵⁴ Standard therapies should be implemented for all conditions with referral to neurological specialists for refractory conditions or imaging abnormalities. Diagnostic criteria for POTS are light-headedness or fainting accompanied by an increase in heart rate greater than 30 beats/min or heart rate greater than or equal to 120 beats/min after 10 minutes of rising.⁵⁶ Beta blockers are effective in managing this condition in combination with diet and exercise.⁴¹

Unanswered Questions and Future Directions

As in the case of pulmonary and cardiovascular manifestations, the duration of symptoms is still unknown. The effectiveness of rehabilitation exercises in recovering function is not clear. Depression post–COVID-19 must be distinguished from depression due to pandemic-related secondary issues, including work, school, and economic factors. Olfactory rehabilitation exercises have been shown to improve identification, discrimination, and threshold for odor detection.¹¹⁰ However, it is unclear how effective olfactory rehabilitation exercises are for people who have not spontaneously regained sense of smell after COVID-19 infection.

Hematological System

Epidemiology

A breakdown of the major studies looking at post-acute COVID-19 hematological effects can be found in Table 3. Common hematological findings of an acute COVID-19 infection are lymphocytopenia, neutrophilia, eosinopenia, and thrombocytopenia.^{111 , 112} Lymphocytopenia, thrombocytopenia, elevated CRP, and elevated procalcitonin have also been identified as markers of severe disease in other studies, which increases the risk of thromboembolic events.^{113 , 114} However, the analysis from Zuin et al¹¹³ of post-acute thromboembolic events shows that the rate of thrombotic events is lower post-discharge than during the acute infection; therefore, it is a rarer complication of COVID-19.

Pathophysiology

A summary of the pathophysiology of hematological effects of post-acute COVID-19 can be found in Figure 1.

Thromboembolic events observed after infection resolution are immune-mediated rather than true thromboembolic events.¹¹³ The increase in thrombotic risk due to SARS-CoV-2 is limited to acute illness even in those with severe disease that require admission.⁵⁹ The multicenter prospective study from Rashidi et al⁵⁹ of 1529 patients did not find a high rate of symptomatic venous thromboembolism (VTE) after hospital discharge. Of the 3.3% of patients who died after discharge, only 0.2% deaths could be attributed to VTE. Severely ill patients may have an increased risk for bleeding due to thrombocytopenia and depletion of coagulation factors, but it has been shown that thromboembolic events occur at higher rates than bleeding complications in acute COVID-19.⁸⁸ Consequently, extended thromboprophylaxis after discharge may not provide any net benefit clinically, but randomized clinical trials are needed for additional verification.

Clinical Predictors

Acute illness severity and ICU admissions are risk factors for coagulation abnormality–induced thromboembolisms. Severe disease is associated with an increased risk of VTE and arterial thromboembolic events, which increases short-term morbidity and mortality.^{113 , 114} Intensive care unit admission associated with increased pulmonary embolism as compared with non-ICU patients and independent factors include age, cancer, length of acute infection phase, low fibrinogen and higher D-dimer on admission, and D-dimer increment (DI) greater than or equal to 1.5-fold. Fibrinogen, D-dimer, and DI predicted instances of VTE in the acute phase with a 93% sensitivity and 0.71% specificity.^{58 , 115} Patients with any of the mentioned clinical factors should be monitored for coagulation abnormalities that can present in any system and prioritized for post-illness follow-up when clinical indications are present.

Management Recommendations

Guidelines for management of thromboembolic conditions due to COVID-19 can be found in Table 2. These are based on recommendations from the American College of Cardiology and American Society of Hematology on care for patients in the hospital; in out-patient cases, post-hospital thromboprophylaxis should also be given to at-risk patients and those that have undergone prolonged corticosteroid therapy who do not have an active bleeding risk to reduce risk of VTE. Extended use of thromboprophylaxis or use in all patients is not recommended at this time.⁵⁹

Unanswered Questions and Future Directions

Unanswered questions include the mechanisms by which COVID-19 leads to long-term lipid abnormalities which can lead to atherogenesis. The role of statins in the maintenance of vascular health and integrity is unknown with regard to COVID-19.

Multisystem Inflammatory Syndromes

Epidemiology

Multi-inflammatory syndrome (MIS) sequelae are rare but severe complications following acute COVID-19 infection in previously symptomatic and asymptomatic individuals that present a few weeks after initial infection.¹¹⁶ Although this syndrome was first documented in children younger than 21 years old (MIS-C), there is an increasing number of case reports that show adults (21 to 50 years old) may also develop these sequelae (MIS-A).¹¹⁷

The diagnostic criteria for MIS-C can be found in Table 2. Similarities have been observed between MIS-C, Kawasaki disease (KD), and toxic shock syndrome with common clinical features such as persistent fever, systemic hyperinflammation, multiorgan involvement with prominent and severe gastrointestinal (GI) symptoms, erythematous rashes, conjunctivitis, and inflammatory changes in the oral mucosa.¹¹⁸ As a result, the pathophysiology of COVID-19 MIS-C may be revealed from studying these diseases. Critical differences between KD and MIS-C include ethnicities of those predominantly affected, organ systems attacked, and laboratory findings.118, 119, 120 Sixty-two percent of MIS-C patients are Hispanic, Latino, or Black as of June 2021, whereas most KD patients are of Asian heritage.^{116 , 118} Patients with MIS-C are also characterized by myocardial dysfunction, neuropsychological/central nervous system findings, and severe GI symptoms compared with the mild GI symptoms of KD and lack of neurological and cardiovascular shock clinical characteristics.¹¹⁸ Patients with MIS-C also show increased D-dimer and troponin levels, lymphocytopenia, and thrombocytopenia.^{119 , 120} In contrast, toxic shock syndrome has nearly identical symptom presentation, laboratory findings, and drug response and only differs in ethnicity, affecting those of White descent more, and does not show increased troponin levels.^{119 , 120}

Epidemiological information and subdivisions of the three distinct classes of MIS-C compiled from the Centers for Disease Control and Prevention (CDC) database for 4018 reported cases of MIS-C as of June 2, 2021, can be found in Figure 2 .^{121 , 122} Diagnosis of MIS-A still lacks clear criteria, but has been described by the CDC using case reports from 16 patients between the ages of 21 and 50 years.¹²³ This criteria includes age 21 years and older, being hospitalized for 24 hours or longer, fever greater than or equal to 38.0°C or a subjective fever for 24 hours or longer or within the first 3 days of hospitalization, meeting at least one primary clinical criteria (severe cardiac illness, rash, and nonpurulent conjunctivitis), and may have secondary criteria (new-onset neurological symptoms, shock/hypotension that is not from medical therapy such as medications or dialysis, abdominal symptoms, and thrombocytopenia).¹²⁴ They must also have laboratory evidence of SARS-CoV-2 infection either by rt-PCR or serology and evidence of inflammation.¹²⁴ Little epidemiological data is currently available about MIS-A, and there are no registered Cochrane trials ongoing to study MIS-A specifically.

Figure 2.

Multisystem inflammatory syndrome in children (MIS-C) by the numbers. Epidemiological images derived from the Centers for Disease Control and Prevention data on 4018 reported cases of MIS-C as of June 2, 2021.¹²¹ Disease classifications from 570 MIS-C case reports from March 2 to July 18, 2020.¹²² Percentages by race and ethnicity may exceed 100%. Multiple race identities could be selected. Race/ethnicity data were not reported for 276 of 4018 cases. Percentages of Asian, NH/OPI, and AI/NA were rounded up to 1%. AI = American Indian; ARDS = acute respiratory distress syndrome; NA = Native Alaskan; NH = Native Hawaiian; OPI = Other Pacific Islander; rt-PCR = real-time polymerase chain reaction; SOB = shortness of breath.

Pathophysiology

The pathophysiology behind the sequelae remains relatively unknown due to the small sample sizes of MIS-C and MIS-A. Reports show abnormalities in the coagulation cascade similar to adults at increased thrombosis risk after COVID-19.³⁰ In addition, most patients with MIS symptoms are antibody-positive but do not have an active viral infection.³⁰ Pediatric hospitalizations due to COVID-19 are on the rise again in unvaccinated children due to the increased transmission rates of the delta variant.¹¹⁷ More data should be available soon and the mechanism of MIS can be further explored.

Clinical Predictors

Symptoms of MIS have been reported in both the pediatric (MIS-C) and adult (MIS-A) populations, but clinical predictors for MIS-C are currently more reliable due to their earlier characterization. Clinical predictors for MIS-C can be found in Table 2.

Management Recommendations

The American College of Rheumatology updated information regarding MIS-C diagnosis, and treatment guidelines were released in December 2020 and are continually being revised as more information becomes available.³⁰ Treatment guidelines for MIS-C can be found in Table 2.

Unanswered Questions and Future Directions

Little epidemiological data are currently available for MIS-A, and there are no registered Cochrane trials ongoing to study MIS-A specifically. Therefore, more case studies must be identified to develop an accurate epidemiological picture before analyzing the pathophysiology and management recommendations. For MIS-C, there is a greater database of cases, but this too must be expanded to further characterize pathophysiology and management recommendations.

Other Long-Term Systematic Effects

Other rare long-term systemic effects of COVID-19 involve the renal, endocrine, integumentary, and GI systems. Pertinent information about the pathophysiology, clinical predictors, and management recommendations can be found in Figure 1 and Table 2, respectively. A breakdown of the major studies looking at post-acute COVID-19 effects of these systems can be found in Table 3. As of June 2021, 683 trials are registered with the Cochrane COVID-19 study registrar which should further clarify the prevalence of these infrequent systemic complications (available at https://covid-19.cochrane.org).

Unanswered Questions and Future Directions

Endocrine

Elevated blood sugar levels have been observed in many patients during acute COVID-19 infection. How long does this hyperglycemic effect last? Should all at-risk patients be placed on low-sugar diets? Other questions include the duration of thyroid function monitoring and whether or not fertility is affected post–COVID-19 infection.

Gastrointestinal

Fecal microbiota alterations have been associated with prolonged persistent fecal levels of SARS-CoV-2 and increased COVID-19 severity through modulation of host immune responses.^{125 , 126} How aggressive we should be in restoring gut microbiome post–COVID-19 is unclear and is a candidate for future studies.

Skin

Increased cases of urticaria have been reported after COVID-19. Urticaria is observed after many other viral infections. Is COVID-19 different in this regard, or does it lead to longer duration of chronic urticaria, such as that seen in autoimmune or chronic idiopathic urticaria?

Effective Multidisciplinary Management of Long-Term Effects of Covid-19

Patients with severe disease, increased risk factors, as well as symptomatic and/or hospitalized individuals should be prioritized for in-person or telemedicine visits (Supplemental Figure 2, available online at http://www.mayoclinicproceedings.org). Long-term management should focus on a holistic approach that involves physical therapy, nutrition, and psychological interventions in addition to medication-based methods.

Rehabilitation in post-acute COVID-19 involves appropriate management of the consequences of ventilatory support, prolonged immobilization, and bed rest. These include impaired lung function, physical deconditioning that leads to impaired muscle function, and cognitive impairments.¹²⁷ Patients should resume regular activities 6 to 8 weeks post-discharge, but this may be more challenging in patients who have severe disease, extended hospital stays, or prolonged symptoms.^{19 , 128} Even if a formal exercise and exertional desaturation assessment cannot be conducted in patients with COVID-19, they should perform low- or moderate-intensity exercise to reduce muscle deterioration and improve pulmonary function.¹²⁸ A randomized control trial of 150 participants showed an increased rate of 6MWT results in participants with critical illness who participated in outpatient physiotherapy after ICU discharge.¹²⁹ A 6-week respiratory rehabilitation program in elderly COVID-19 patients shows significant improvements in forced expiratory volume-1 (FEV1), forced vital capacity (FVC), FEV1/FVC percentage, diffusing capacity for carbon monoxide percentage, and 6MWT.¹³⁰ Neurological rehabilitation may also be beneficial in patients with residual COVID-19 neurological dysfunction, but research on this is minimal. Clinicians should schedule a 6- to 8-week follow-up appointment for hospitalized patients to measure lung function, exercise capacity, and cognitive function.¹²⁸ For nonsevere patients, a comprehensive physical should be performed if symptomatic, but a mental-health assessment should be conducted for all.

Nutrition after COVID-19 infections plays a vital role in aiding recovery. Studies show that 50% or more of elderly in-patient participants with COVID-19 are malnourished with an additional 25.7% at risk of malnourishment.¹³¹ Inflammation, ageusia, decreased appetite, prolonged bed rest, and gut-microbiome disturbances during acute and post-acute COVID-19 leave patients deficient in key micro- and macronutrients necessary for physical reconditioning and recovery. Nutrition evaluations and consultations with registered dieticians should be considered in muscle loss, GI abnormalities, and/or vitamin deficiencies.

With all the challenges of the pandemic that patients may face, mental health becomes a significant concern. The physical effects of long-term COVID-19 sequelae can often be intertwined with the psychological outlook of patients and efforts should be made to ensure that mental health is preserved. To this end, complementary therapies such as acupuncture, massage, low-impact yoga, and Tai Chi may be of benefit.

Conclusion

The findings in this review show that the effects of COVID-19 do not end with acute infection resolution. In all patients, interdisciplinary monitoring is required to detect post-acute COVID-19 symptoms before long-term systemic damage occurs. Patients post–COVID-19 may visit many different providers because of multisystem involvement and multiple symptoms. Integrated health care settings are crucial to facilitate communication between providers about health care plans and progress and avoid unnecessary duplicate tests, thus saving patients time and health care costs. Health care systems have already begun establishing dedicated COVID-19 care clinics that facilitate multidisciplinary care. Policy and practices also need to be established to effectively harness and optimize collaboration between medical specialties, multiple health care professionals, and patients.

This review discusses the most up-to-date evidence-based knowledge on management of common systemic sequelae of post-acute COVID-19. More information about post-acute COVID-19 continues to be discovered as the pandemic continues. This will help develop a detailed explanation of the mechanisms behind symptoms and classify the risk factors that predispose patients to adverse outcomes. Guidelines will need to be continuously updated to reflect the most up-to-date body of knowledge. Every patient, symptom, and circumstance is unique; thus, the guidelines recommended in this article should be modified according to each patient’s needs and the clinicians’ discretion.

The clear association between COVID-19 and long lasting sequelae that has the potential to affect multiple organ systems is another reason why everyone should be vaccinated. No longer can any demographic be confident that their illness may be mild and that they will completely recover from it. The best way to prevent the acute illness and long-term effects of COVID-19 is not to get the infection in the first place. Social distancing measures, masking, and vaccines are effective ways of lowering the risk of infection.