Heart failure in general and cardiac transplant patients with COVID-19

Abstract

Coronavirus disease 2019 (COVID-19) is primarily an infection of the respiratory tract, but it can have multisystem manifestations. Cardiac complications of COVID-19 can range from acute myocardial injury, cardiac arrhythmias, or heart failure, amongst others. Heart failure (HF) in COVID-19 can be a de novo process or due to worsening of pre-existing cardiovascular ailment. HF in a patient with COVID-19 not only poses challenges in clinical presentation and management of COVID-19 but also affect prognosis of the patient. This article aims to succinctly revisit the implications of this pandemic regarding pre-existing HF or new-onset HF based on prevailing data. It also focuses on the management and special recommendations from prior studies and guidelines.

Key Words: COVID-19; Coronavirus; Cardiomyopathy; Heart failure; Cardiomyopathy

Core Tip: The mini-review is composed of assimilation of guidelines and current literature recommendations for managing heart failure in coronavirus disease 2019 (COVID-19) patients. We discuss many important aspects of heart-failure in COVID-19 from epidemiology to post recovery rehabilitation.

INTRODUCTION

Since its emergence in December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has affected all continents. The case count of coronavirus disease 2019 (COVID-19) continues to soar to-date, as evident by more than 300 million global caseloads[1]. COVID-19 typically presents as a respiratory tract infection, but we have witnessed it herald a multisystem disorder in a lot of patients, including but not limited to the cardiovascular system. Cardiac manifestations of COVID-19 can be broad, and symptoms generally stem from myocardial injury, cardiac arrhythmias, cardiogenic shock, heart failure (HF), or sudden cardiac death[2-5]. This article attempts to provide a brief review of all the major topics related to heart failure and covid-19 from epidemiology, diagnostic tools to the important management options, and post-recovery rehabilitation. It gives insights on breakthrough vaccination and cardiac complications post COVID-19. It attempts to touch on treatment options in various situations encountered while treating heart failure patients.

EPIDEMIOLOGY

An accurate incidence of HF in COVID-19 is difficult to determine as there are not abundant definitive data on it. HF in COVID-19 can be due to worsening of preexisting known or undiagnosed heart disease. Besides, it could also be a new onset HF due to hemodynamic stress, ischemic cardiomyopathy, or nonischemic cardiomyopathy. Available studies have not always clearly discerned a new-onset HF from worsening of chronic HF. As evident in Table 1, HF was present at baseline in up to 23% of cases while up to 7% of patients with COVID-19 had a new-onset HF as a complication of the infection[6-9]. However, we must bear in mind that there seems to be a wider range in these data reported. The other caveat is that not all studies have clearly demarcated the incidence and acuity of pure right heart failure from left heart failure to biventricular loss. Creel-Bulos C et al[10], described five patients with acute right HF in their case series from March 23 to April 4, 2020, in an intensive care unit in Georgia, United States. With the progression of the pandemic, Corica et al[11] conducted a combined pooled analysis of 3813 patients and found to have right HF in as high as 20.4% of patients with COVID-19.

Table 1 It shows data on incidences of acute, chronic heart failure, and acute heart failure.

Ref.	Study type	Country of origin	Incidences
Zhou et al[6], 2020	Retrospective cohort study	China	Total patients 191. deceased 54 patients (28 had chronic hf exacerbation, i.e., 52%) survived 137 patients (16 had chronic hf exacerbation, i.e., 12%) P < 0.0001
Arentz et al[7], 2020	Case series	United states	Total patients 21. nine patients (42.9%) acute on chronic hf
Ruan et al[8], 2020	Multicenter retrospective analysis	China	Total patients 150. death 68 acute on chronic hf 5 (7%)
Shis et al[9], 2020	Single-center cohort jan 2020 - feb 2020	China	Total patients 416. new-onset heart failure 4.1%
Chen et al[12], 2020	Retrospective study	China	Total patients 274. acute on chronic hf 1 (< 1%) new-onset hf 21 (7.7%). 1 recovered and 20 died
Inciardi et al[13], 2020	Retrospective study	Italy	Total patients 99. acute on chronic hf 21 (21%)

ETIOPATHOLOGY

Two types of mechanisms for myocardial injury are described in prior literature. ie direct or specific and indirect effects[24].

SARS-CoV-2 directly attaches to the ACE2 on the myocardium and causes cell damage and death. It also decreases the protective and anti-inflammatory properties of ACE2 on the myocardium through its downregulation.

Sympathetic activity causing Tachycardia from underlying infection, prolonged immobility causing coagulopathy, hypoxemia, hemodynamic changes are indirect effects worsening the cardiac status[24]. Severe inflammatory response causing surge of cytokines like Interleukins, Tumor necrosis factor, interferons' play a major role in the pathogenesis of pulmonary and myocardial damage leading to acute respiratory distress syndrome (ARDS) and various cardiac complications[25]. It can precipitate new cardiac failure and worsen the course in underlying failure patients[25].

Pre-existing HF can exacerbate during COVID-19, as evident in other viral illnesses such as Influenza [15]. Stress cardiomyopathy, vasculitis, thrombosis of coronary arteries, fissuring, and rupture of atheromatous plaque leading to acute myocardial ischemia can be some of the ischemic and nonischemic causes of acute cardiomyopathy and subsequent HF[16,17]. One study evaluated that cardiogenic shock resulting from myocardial injury occurred in up to 10% of patients in shock and can result in worse prognosis compared to hypovolemic or distributive shock in COVID-19 patients[26]. 48% of patients had normal Ejection fraction and low cardiac index shock from low end diastolic volumes which was due to use of Peak end expiratory pressures and mechanical ventilation causing decreased venous return. Cytokine storm detailed above can result in distributive shock[26]. Pulmonary embolism from coagulopathy and pericardial tamponade can cause obstructive shock which are reported in COVID-19. Worsening of chronic kidney disease or onset of acute kidney injury leading to volume overload has been reported in up to 29% of patients with COVID-19 and chronic HF[6,18].

Acute right heart failure (RHF) in COVID-19 has been primarily thought to be due to ARDS and severe hypoxemia. RHF due to acute pulmonary embolism has also been reported in 5%-22% of cases by different authors[19,20]. High clot burden was also found in patients with right heart strain from pulmonary embolism[21]. Patients with COVID-19 are several times at higher risk of pulmonary embolism compared to non-COVID-19 patients and is also associated with higher mortality[20]. Severe Acute Respiratory distress syndrome may lead to pulmonary hypertension and cause right-sided heart failure. Myocardial injury and myocarditis can also weaken the right heart ventricle in COVID-19. Right heart failure in COVID-19 is associated with increased mortality[22,23] Etiopathology of HF in COVID-19 has been summarized in inline diagrams in Figures 1 and 2.

Figure 1 Pathogenesis of heart failure in coronavirus disease 2019.

Figure 2 Causes of acute right heart failure in coronavirus disease 2019.

Clinical evaluation and utility of diagnostic tools

Symptoms of HF, in general, can be due to reduced cardiac output causing fatigue and weakness. It could also be due to excessive fluid accumulation resulting in dyspnea, orthopnea, paroxysmal nocturnal dyspnea, cough, and edema. Patients in cardiogenic shock could have a low cardiac output state. Overall, it can be difficult to accurately distinguish most of the symptoms of HF from COVID-19 itself, so careful examination and use of diagnostic tools are imperative. Signs of fluid overload like weight gain, Jugular venous distension, fine crackles at lung bases, wheezing, third heart sound, abdominal distension, ascites, and pitting pedal edema can be used as important clues at the bedside to determine new-onset or exacerbation of HF in COVID-19 patients.

Plasma B-type natriuretic peptide (BNP) and N-terminal pro-BNP (NT-pro BNP) are useful laboratory markers in suspected HF. High sensitivity troponins (hs-cTn) are often elevated as a marker of myocardial inflammation[16]. BNP less than 100 pg/mL and NT-proBNP less than 450 pg/mL have high negative predictive for HF[27]. Elevated plasma BNP and NT-proBNP also indicate poor prognosis in general, and this relationship holds true for HF in COVID-19 as well[28]. Elevated NT-proBNP level was detected in 12.9% of 3219 patients in a study from Wuhan, China. The adjusted hazard ratio for NT-proBNP was 5.71 (95%CI 3.50-7.47)[29]. In another study conducted on 397 patients with COVID-19 in Milan, Italy, 14.9% had elevated BNP levels, and the mortality rate was higher by 33.9% in these patients[30]. Elevation of BNP, NT-Pro BNP or troponin, hs-cTn should be interpreted with caution. It should not trigger evaluation for heart failure or Myocardial infarction unless patients have accompanying signs and symptoms or EKG changes to suggest diagnosis.

Electrocardiogram (EKG) may not receive ample attention in the diagnosis of HF beyond the milieu of a cardiologist. Perhaps, it is highly unlikely that a patient with a normal EKG will have a dysfunctional left ventricle (LV). Atrial fibrillation, old myocardial infarction, left ventricular hypertrophy, axis deviation, bundle branch block, and ST-T wave abnormalities may hint towards underlying acute or chronic HF in patients with COVID-19[16]. EKG changes commonly observed in COVID-19 patients were atrial fibrillation or flutter, Premature atrial (APCs) and ventricular contractions, Bundle branch block, interventricular conduction delay, and repolarization abnormalities[31]. Abnormal EKGs changes like APCs, Right BBB/Intraventricular block, Ischemic T wave inversions, and non-specific repolarization abnormalities were associated with an increased risk of adverse cardiac events or death in patients with underlying comorbidities like cardiovascular or renal diseases[31,32].

An echocardiogram is one of the most important diagnostic tools for HF. There have been some studies utilizing echocardiograms in patients with COVID-19. Szekely et al[33], performed an echocardiogram in 100 patients within 24 h of hospitalization with COVID-19. 32% of patients had a normal echocardiogram, 39% had right ventricle (RV) dilatation and dysfunction, 16% had LV diastolic dysfunction, and 10% had LV systolic abnormality. Reassessment with echocardiogram due to deterioration during hospital course showed worsening of RV failure in 12 patients and LV systolic failure in 5 patients[33]. In a prospective international study of 1216 patients from 69 countries, 667 patients (55%) were found to have an abnormal echocardiogram. 479 (39%) had LV dysfunction while 397 (33%) had RV dysfunction. Echocardiography findings changed management in 33% of these patients[34]. In an International multicenter study of 305 patients admitted with COVID-19, RV dysfunction was found in 26.3%, LV diastolic dysfunction in 13.2%, and LV global systolic dysfunction in 18.4% of patients. Moreover, multivariate adjustments showed that myocardial injury with abnormal echocardiograms represented higher mortality in comparison to normal echocardiograms[35]. Hence, an echocardiogram is a vital diagnostic tool that should be used by clinicians taking care of COVID-19 patients in a timely and appropriate manner. The Trans-thoracic echocardiogram has also been performed successfully among COVID-19 patients with ARDS who were in prone position by temporarily deflating the lower thoracic portion of the air mattress. This helps in placing the probe between the thorax and the mattress surface[36].

The role of cardiac magnetic resonance imaging (MRI) has been so far more relevant in patients that are on the road to recovery from acute COVID-19 illness. Because of inflammatory cardiomyopathy, some of these patients can develop HF as a sequela. In a German study of 100 patients that were in the recovery phase from acute COVID-19 illness, cardiac MRI was abnormal in 78% of patients at an average of 71 days from initial diagnosis. Compared to the control group, these patients had lower LV and RV ejection fractions. Furthermore, endomyocardial biopsy in three patients with elevated T1/T2 signal, late gadolinium enhancement, and LV ejection fraction less than 50% revealed lymphocytic infiltration with no detection of the viral genome[37]. In another study of 148 patients with severe COVID-19 infection, cardiac MRI was done at a median of 68 days post-discharge from the hospital. The myocarditis-like scar was seen in 26%, and infarction was found in 54%, but 89% of these patients had normal LV function[38]. Thus, cardiac MRI and endomyocardial biopsy in selected COVID-19 patients may be of value in timely diagnosis and initiation of goal-directed medical therapy where HF arises as a late complication in subacute and chronic recovery phases (Table 2).

Table 2 A late complication in subacute and chronic recovery phases.

Diagnostic tools	Likely heart failure	Likely COVID/ARDS
BNP/NT-Pro BNP and clinical findings	BNP > 100 pg/mL or NT-Pro BNP > 450 pg/mL Signs and symptoms of right and left heart failure	< 450 pg/mL Absence of signs and symptoms of volume overload
EKG	Abnormal ekg findings of LVH, LAE, Sinus tachycardia, LAD, RAD, AF, PVCs, BBB	Nonspecific findings or symptoms of pulmonary embolism, Right heart strain or myocardial ischemia
ECHO	Ejection Fraction%, RV dilatation and dysfunction, LV Diastolic dysfunction, LV global systolic dysfunction	Findings of pulmonary arterial hypertension; RV dysfunction, enlargement and abnormal contraction, septal dyskinesia. Acute Cor pulmonale
CMRI	Establishes ischemic vs nonischemic heart failure, quantification of ventricular function and scar burden	Distinguishes pulmonary vs extrapulmonary causes for acute respiratory distress syndrome

LVH: Left ventricular hypertrophy; LAE: Left atrial Enlargement; LAD: Left axis deviation; RAD: Right axis deviation; AF: Atrial fibrillation; PVCs: Premature ventricular complexes; BBB: Bundle branch blocks.

MANAGEMENT

Management of HF exacerbation during COVID-19 should be based on the volume status, the previous history of heart failure, and vital signs. Patients with heart failure and COVID-19 have worse hospitalization and in-hospital mortality outcomes in a systematic review and meta-analysis of 18 studies[39].

Shared decision-making among consultants is necessary to guide clinical management regarding immunosuppression, multiple treatments, multiorgan involvement, and associated complications in COVID-19.

Chronic heart failure patients have a higher risk of in-hospital complications like acute heart failure, acute renal failure, sepsis and length of stay, and in-hospital mortality[40,41].

Medications should be initiated per Guideline-directed medical therapy and continued. Special considerations exist for each class of drugs which are discussed below.

Diuretics

Diuretics in heart failure and COVID-19 help to decongest the lungs. Prior to starting diuretics, they require careful monitoring of the volume status by physical examination, BNP, and bedside ultrasound assessment for the IVC (inferior vena cava) collapsibility[42]. Pulmonary artery catheter, Echocardiography, and cardiac output monitoring are other methods for advanced hemodynamic monitoring in patients with complex hemodynamics. Conservative fluid strategy with judicious initiation or up-titration of diuretics with daily weights is recommended[43]. Aiming for a negative fluid balance is necessary for these patients. Watching for signs of hypotension and over diuresis which can result in kidney injury is necessary. Nephrotoxic medications should be used carefully along with diuretics, i.e., NSAIDs, Remdesivir, or nephrotoxic antibiotics like vancomycin[42,44]. If there is diuretic resistance, then ultrafiltration can be considered to treat heart failure and AKI[42].

It was hypothesized that medications associated with upregulation of ACE2 receptors could worsen the COVID-19 infection, which was not proven in further studies. Outcomes among heart failure patients were similar regardless of ACE inhibitor or ARB use[40].

Heart failure society of America/American College of Cardiology/American Heart Association guidelines recommends against adding or discontinuing these medications beyond the standard of practice in patients with preexisting heart failure, hypertension, or ischemic heart disease. However, careful decision-making and medication discontinuation should be done in acute kidney injury, hypotension, hyperkalemia, and shock on a patient-to-patient basis[45].

Beta-blockers

Carvedilol is the recommended beta-blocker in patients with heart failure and COVID-19 due to its anti-cytokine action[46,47]. However, these medications should not be started for COVID-19 and HF beyond the standard of practice. Assessment of hemodynamic stability is necessary before the initiation of beta-blockers[42]. Patients previously on beta-blockers can have inappropriate bradycardia with COVID-19. Dose changes should be made if patients develop a low output state[45]. Betablockers also help patients with sinus tachycardia and tachyarrhythmias[45]. Antiviral medications like Remdesivir and Tocilizumab can influence the pharmacokinetics of cardiovascular medications, increasing the risk of toxicities and arrhythmias.

Digoxin

Most of the indications for digoxin in HF with reduced ejection fraction are as a rate control agent in those with low blood pressure and atrial fibrillation[48]. Digoxin has antiviral and anti-inflammatory properties per prior literature[46]. Again, there is no recommendation to start patients with new-onset HF and COVID-19 on these medications beyond clinical practice. Digoxin levels should be closely monitored when given anti-viral medications and immunomodulators that may interact with it[42].

Anticoagulation therapy

Consideration should be given for interaction between anticoagulants' current and emerging COVID-19 therapies. Monitoring the liver and kidney function is also necessary. Unfractionated Heparin or Low molecular weight heparin (LMWH) is the preferred anticoagulant in hospitalized patients with prior anticoagulation for other causes. It is particularly preferred in sick patients due to drug interactions with oral anticoagulants[45]. If oral anticoagulants are needed in less sick patients, switching to direct oral anticoagulants is preferred over Vitamin K antagonists. Prophylactic Anticoagulation with LMWH can be considered in all inpatients if there is no hemorrhagic risk[49].

Mineralocorticoid receptor antagonists

Careful use in heart failure patients based on volume status and kidney function. Electrolytes should also be monitored.

Recommendations regarding guideline-directed medical therapy

Stopping GDMT, i.e., Beta-blockers, ACE/ARB, and mineralocorticoid receptor antagonists in patients with chronic heart failure with COVID, are associated with increased in-hospital mortality per prior studies[50]. If GDMT therapy has been discontinued inpatient for AKI or hemodynamic instability, during discharge of patients post heart failure exacerbation, they should be restarted as they have favorable outcomes in heart failure patients[50].They should follow up with the cardiologist or physician for heart failure to review and adjust the dose of GDMT.

Ionotropic/ vasopressor medications and respiratory support

Patients with heart failure have pulmonary edema superimposed on COVID-19 pneumonia. High BNP levels elevation in patients with ARDS indicates cardiogenic shock and pulmonary edema. Use of non-invasive ventilation and prone ventilation help to decrease pulmonary edema. Heart Failure patients are susceptible to hypoxia and ARDS and therefore may require intubation and lung-protective ventilation. These methods also help to manage right heart failure from ARDS[51].

The shock from sepsis and heart failure can develop. Dehydration and hypoperfusion can worsen symptoms. Clinical assessment, bedside echo, and monitoring of hemodynamics help in assessing the pathophysiology of shock. Volume status assessment, careful use of diuretics, and intravenous fluid repletion are needed. The greatest benefit of fluid resuscitation was seen in patients with signs of hypoperfusion who are in hypovolemic shock[26]. In patients with Mixed shock (cardiogenic and septic), vasopressors or inotropes should be started.

Norepinephrine is the preferred vasopressor agent for septic and cardiogenic shock, especially in hypotensive patients[51].If there are signs of low organ perfusion or severe decreased cardiac output, inotropes such as dobutamine and epinephrine can be added[51].Cardiac output monitoring helps in the selection and titration of inotropes and vasopressors.

Bedside, Intra-aortic balloon pump should be considered in severe cardiogenic shock refractory to vasopressors or inotropes[52]. ECMO as mechanical circulatory support is used in the setting of ARDS/hypoxemia with refractory cardiogenic shock in available centers[45,51].

Myocarditis in COVID-19: Patients can present with Heart failure symptoms. Inotropes and vasopressors, mechanical circulatory support, and mechanical ventilation can be used in severe cases.

COVID-19 with HF in heart and lung transplant recipients

Heart Transplant and Heart and lung transplant recipients are on immunosuppression with medications like calcineurin inhibitors, prednisone, and antimetabolites. They are prone to COVID-19 infection from immunosuppression and can have severe symptoms and outcomes[53,54]. For patients with mild symptoms, supportive treatment with the continuation of immunosuppression is recommended.

In patients with moderate to severe illness, anti-metabolites such as azathioprine and mycophenolate mofetil can be held inpatient per the international society of heart and lung transplantation recommendations[55].

These patients should be treated at a heart transplant center. After the infection resolves, careful monitoring is required when restarting immunosuppression in these patients due to effects from the allograft[53].

Breakthrough infection

Breakthrough infections after the COVID-19 vaccination have been frequently observed in older patients and those with comorbidities. One study described close to 12% of breakthrough infections after vaccination[56]. In another study of 700 breakthrough cases close to 49% of the patients were symptomatic[57]. Despite increased breakthrough infection in this patient population, they did not develop disease severe enough to require supplemental oxygen or ICU admission[56,58].

Vaccinated people have a shorter duration of virus transmission, short symptom duration, and restricted tissue dissemination[59].

Chronic heart failure patients with breakthrough infections who are stable can be treated as outpatients with GDMT.

Rehabilitation post-recovery

In the Post-Acute phase, exercise training should be done in these patients, considering oxygen saturation, heart rate, systolic blood pressure, and symptoms[60]. Cardiac rehabilitation includes a variety of programs such as aerobic endurance training, interval training (IT), High intensity IT and resistance training done around 2-5 times per week[60].Thoracic expansion exercises to increase lung ventilation and airway clearance are some of the recommended methods for respiratory rehabilitation in these patients. Home-based cardiac telerehabilitation- is another alternative strategy to follow for these patients. Psychological support and nutritional interventions should also be a part of rehabilitation programs[60].

Complications

Direct viral infection of the myocardium can cause myocardial injury and complications such as myocarditis and myocardial interstitial fibrosis[61,62]. System-wide inflammatory response and release of pro-inflammatory markers like Tumor necrosis factor, interleukin-6, and interleukin-1β are associated with direct myocardial injury and can cause myocardial infarction[24,63]. The prothrombotic state can result in acute coronary events[61,62]. Cardiac Arrhythmias such as atrial arrhythmias, bradyarrhythmia, and non-sustained ventricular tachycardia can occur due to inflammation of the myocardium, fibrosis, edema of interstitial tissues, medication side-effects, and myocarditis[61,62]. Atrial fibrillation can predispose patients to cardiogenic shock[62].

Patients who recover after severe COVID-19 are at high risk of Pulmonary hypertension, Diastolic dysfunction, and right heart failure[9,64]. Stress-induced cardiomyopathy or Takutsubo cardiomyopathy can develop from microvascular dysfunction and inflammatory response[65,66]. The summary of management is illustrated in Table 3.

Table 3 Summary of management.

Management of heart failure

We should know that the development of heart failure in COVID-19 patients can complicate management and worsen the prognosis; Chronic heart failure patients have adverse outcomes compared to new-onset heart failure patients; GDMT guided medical therapy should be used in heart failure with individualized patient decision making based on hemodynamic status and development of complications; Avoiding over diuresis to prevent kidney injury and hypoperfusion is necessary; Watching for signs of deterioration and shock with early initiation of vasopressors in mixed shock should be practiced; Cardiac arrhythmias and acute myocardial infarction are some major complications to look out for.; Advanced hemodynamic monitoring helps to guide management in these patients; Post-recovery cardiac, pulmonary rehabilitation with psychological support and nutritional interventions is necessary

COVID-19: Coronavirus disease 2019.

CONCLUSION

Heart Failure can occur as a complication in patients with COVID-19 infection. It can worsen the course of COVID-19 and is associated with poor outcomes. It requires early diagnosis and appropriate management on a patient-to-patient basis. Continuing Guideline Directed medical therapy is recommended. We need to watch out for complications during its management. Post the acute phase of COVID physical, psychological and nutritional rehabilitation for these individuals is necessary to aid in recovery.