Introduction
Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute
respiratory syndrome coronavirus 2 (SARS-CoV-2), a positive-sense single-stranded
RNA virus belonging to the family Coronaviridae. From its first appearance in the
city of Wuhan (China), the infection spread worldwide, leading to its declaration
as a pandemic on March 11, 2020.[1] Clinical manifestations of COVID-19 vary from mild respiratory symptoms to severe
and critical pulmonary disease and patients with underlying pulmonary and cardiovascular
disease are at increased risk for adverse outcomes.[2] COVID-19 may result in pulmonary and cardiovascular complications, including acute
respiratory distress syndrome (ARDS), venous thromboembolism, and acute cardiac injury.[3]
Clinical research on SARS-CoV-2 suggests that the virus may determine changes in the
pulmonary hemodynamics through mechanisms of endothelial dysfunction, vascular leak,
and thrombotic microangiopathy that are similar to those leading to pulmonary vascular
disease.[4] However, a causative role of COVID-19 in inducing pulmonary hypertension (PH) has
to date not been demonstrated and the prognostic role of PH in COVID-19 is still on
study. The present article aims to review pathophysiological mechanisms, clinical
characteristics, and therapeutical aspects relating COVID-19 and PH.
Definition and Pathophysiology of Pulmonary Hypertension
The term PH refers to the presence of high pulmonary vascular pressure, which can
be the result of different underlying disorders. By definition, PH is an increase
in mean pulmonary arterial pressure (mPAP) ≥25 mmHg at rest as assessed by right heart
catheterization. Precapillary PH is characterized by an mPAP ≥25 mmHg, a pulmonary
capillary wedge pressure (PCWP) ≤15 mmHg, and a pulmonary vascular resistance (PVR)
>3 WU. Postcapillary PH is defined by mPAP ≥25 mmHg and PCWP >15 mmHg. In combined
post- and precapillary PH, PCWP is >15 mmHg, diastolic pressure gradient (diastolic
PAP – mean PCWP) ≥7 mmHg and/or PVR >3 WU. Currently clinical classification of PH
categorizes patients with PH in five distinct groups according to pathophysiology
and possible treatment strategies ([Table 1]).[5]
[6] The pathophysiology of PH is multifactorial and characterized by an imbalance in
vasoconstriction and vasodilation, thrombosis, cell proliferation, and remodeling
of the wall of the pulmonary arteries leading to an increase of PVR. Pulmonary vasoconstriction
is an early component of the PH process and is partly related to endothelial dysfunction,
which is characterized by an imbalance between impaired production of vasodilators
such as nitric oxide and prostacyclin (PGI2) and overexpression of vasoconstrictors,
for example endothelin-1 (ET-1). Autoimmunity and inflammation mediated by cytokines
and chemokines also contribute to pulmonary vascular alterations. These alterations
induce an increase of PVR and promote vascular remodeling, and therefore represent
important pharmacological targets.[7]
Table 1
Classification of pulmonary hypertension
|
Precapillary PH
|
Postcapillary PH
|
|
Isolated postcapillary PH
|
Combined postcapillary and precapillary PH
|
|
Etiology
|
• Pulmonary arterial hypertension
• PH due to lung diseases
• Chronic thromboembolic PH
• PH with unclear and/or multifactorial mechanisms
|
• PH due to left heart disease
• PH with unclear and/or multifactorial mechanisms
|
|
Hemodynamic definition
|
mPAP ≥ 25 mmHg
PCWP ≤ 15 mmHg
PVR > 3 WU
|
mPAP ≥ 25 mmHg
PCWP > 15 mmHg
|
|
DPG < 7 mmHg and/or PVR ≤ 3 WU
|
DPG ≥ 7 mmHg and/or PVR > 3 WU
|
Abbreviations: DPG, diastolic pressure gradient (diastolic PAP – mean PCWP); mPAP,
mean pulmonary arterial pressure; PCWP, pulmonary arterial wedge pressure; PH, pulmonary
hypertension; PVR, pulmonary vascular resistance; WU, Wood units.
PH in Patients with COVID-19
Epidemiology
PH is a common condition in patients with COVID-19. Currently available observational
studies report echocardiographic signs of PH in approximately 12 to 13% of hospitalized
patients with COVID-19.[8]
[9] A small study with right heart catheterization found a prevalence of PH of nearly
80% in ventilated patients with severe COVID-19.[10]
The current clinical research does not distinguish between PH of new onset in the
context of acute viral infection and pre-existent and/or worsened PH. Considering
the high prevalence of chronic lung and heart disease among patients with COVID-19,
it can be expected that many patients already had signs of PH before. Data on patients
with pulmonary arterial hypertension (PAH) experiencing COVID-19 are to date very
limited.[11]
[12]
Pathophysiology
SARS-CoV-2 infection may alter pulmonary hemodynamics through different mechanisms,
partially overlapping the general pathophysiology of PH. These include: (1) endotheliitis
and vasculitis; (2) thrombotic microangiopathy; (3) venous thromboembolism; and (4)
hemodynamic alterations consequent to ARDS and mechanical ventilation ([Fig. 1]).[4]
[13]
[14]
[15] A small autopsy study found a recurrent distinctive morphological pattern in lung
samplings infected by SARS-CoV-2, including: (1) severe endothelial injury associated
with intracellular SARS-CoV-2 virus; (2) widespread vascular thrombosis with microangiopathy
and occlusion of alveolar capillaries; and (3) significant new vessel growth through
a mechanism of intussusceptive angiogenesis.[13] Furthermore, intense platelet activation has been reported in several studies.[16]
[17]
[18] In particular, Zaid and colleagues[16] described that platelets express proinflammatory molecules, contain viral RNA, and
are hyperactivated, contributing to the cytokine storm and thrombosis. Thrombotic
sequelae of SARS-CoV-2 infection may affect both macro- and microcirculation and pulmonary
embolism (PE) is a recurrent complication that may result in acute PH and right ventricular
(RV) failure.[19]
[20]
[21]
[22]
[23]
[24] Hemodynamic alterations consequent to ARDS may finally contribute to the development
of PH in severe COVID-19. Classically ARDS is characterized by acute respiratory failure
with noncardiogenic pulmonary edema and consequent impaired gas exchange, decreased
lung compliance, and PH.[25] ARDS may present with an atypical form in COVID-19, characterized by significant
dissociation between the relatively well-preserved lung mechanics and compliance,
and the severity of hypoxemia associated with large intrapulmonary shunts.[26]
[27] Consistently with this observation, patients often display little dyspnea despite
profound hypoxemia (“happy hypoxemia”), as reported by Guan and colleagues.[28] This is supposed to result from the failure of the homeostatic oxygen-sensing systems,
including the mechanism of hypoxic vasoconstriction (HPV) and the carotid body function.[4]
[26]
[27] HPV physiologically diverts blood flow from poorly ventilated alveoli, therefore
optimizing ventilation–perfusion (VQ) matching; on the contrary its loss causes intrapulmonary
shunts with consequent hypoxemia. The hypothesis of the loss of HPV seems to be supported
by data from a small study reporting atypical low values of PVR measured through right
heart catheterization in ventilated patients with COVID-19-associated ARDS.[10]
Fig. 1 Pathogenesis of pulmonary hypertension in COVID-19.
As already underlined, many patients experiencing COVID-19 are affected by chronic
cardiopulmonary disease, including chronic obstructive pulmonary disease (COPD) and
congestive heart failure, which are proven risk factors for SARS-CoV-2 infection in
terms of prevalence and adverse outcome.[5]
[9] In these patients, pre-existent PH may be worsened by the acute viral infection
through the pathophysiological mechanisms cited above.
Diagnostics
Distinct diagnostics of PH would require a comprehensive setting of investigations
including right heart catheterization.[5] However, in the current COVID-19 pandemic, which requires care delivery to an increased
number of patients in emergency setting, transthoracic echocardiographic assessment
is used for diagnosis of PH in most studies. Echocardiography allows Doppler measurement
of peak tricuspid regurgitation velocity (TRV). Together with estimation of right
atrial pressure based on measurement of inferior vena cava diameter and simplified
Bernoulli equation, estimation of systolic pulmonary arterial pressure (sPAP) in mmHg
can be performed. Other echocardiographic signs suggesting PH include: (1) right ventricle/left
ventricle basal diameter ratio >1.0; (2) flattering of the interventricular septum
(left ventricular eccentricity index >1.1 in systole and/or diastole); (3) RV outflow
Doppler acceleration time <105 milliseconds and/or mid-systolic notching; (4) early
diastolic pulmonary regurgitation velocity >2.2 m/s; (5) inferior vena cava diameter
>21 mm with decreased inspiratory collapse (<50% with a sniff or <20% with quiet inspiration);
and (6) right atrial area (end-systole) >18 cm2. A TRV >2.9 milliseconds together with other echocardiographic signs cited above
suggests a high probability of PH.[5] Although not such accurate as right heart catheterization, echocardiography allows
sufficient identification of patients with severe PH. However, this method may be
less sensitive in patients with mild PH. Computed tomography (CT) allows sensitive
diagnostics of pulmonal impairment in COVID-19. Typical findings are ground-glass
opacifications with eventual consolidation. Chest CT is not performed in all hospitalized
patients with COVID-19 and is usually reserved for severe cases. Patients with echocardiographic
signs of PH may be good candidates for further CT scan, as it allows the diagnosis
of concomitant PE and can identify high-risk patients with profound radiographic pulmonary
impairment.
Right heart catheterization may be performed to measure pulmonary pressure directly
and to monitor volume status, vascular resistance, and cardiac output in severe cases
on mechanical ventilation and/or extracorporeal membrane oxygenation (ECMO). Although
pulmonary artery catheter allows precise monitoring, no clinical benefit of routine
use was found in the past for critically ill patients with ARDS.[29] An observational study run on 21 patients with COVID-19-associated ARDS examined
with right heart catheterization reported that PH was mostly postcapillary, underlining
complex pathogenesis of COVID-19 and association with the cardiovascular system.[10]
Clinical and Prognostic Significance
PH is investigated in many studies concerning COVID-19. For this review of current
evidence, we performed a comprehensive systematic search on major electronic databases
including PubMed, Google scholar, Medline, and Scopus to find articles published between
December 1, 2019 and March 1, 2021. In addition, public databases such as the World
Health Organization Centers for Disease Control were used. The following keywords
were adopted: “coronavirus disease 2019,” “COVID-19,” “pulmonary arterial hypertension,”
and “pulmonary hypertension.” In our search we analyzed prospective and retrospective
observational studies, as well as case publications in English in scientific journals
and references cited in those articles ([Table 2]).
Table 2
Pulmonary hypertension in COVID-19 patients
|
Author
|
Study design
|
Number of patients
|
Purpose
|
Results
|
Reference
|
|
Deng et al.
|
Retrospective
|
122
|
To investigate myocardial injury in COVID-19 patients.
PH was assessed in TTE according to the ESC-guidelines criteria.
|
• Signs of PH were present in 13% of all patients, in 21% with severe COVID-19, and
2% with mild to moderate disease.
• Evidence of PH was statistically significant in predicting an adverse outcome (admission
to intensive care unit, requirement of mechanical ventilation or extracorporeal membrane
oxygenation, and mortality).
|
[8]
|
|
Pagnesi et al.
|
Prospective
|
200
|
To investigate presence and prognostic significance of echocardiographic signs of
PH and RVD in COVID-19 patients.
|
• PH and RVD were present in 12 and 14.5% of all patients respectively, 4% had both
PH and RVD.
• Patients with PH and/or RVD had more frequently a history of prior cardiac comorbidities
including congestive heart failure, AF and known cardiomyopathy, and higher biomarkers
of cardiac involvement (high-sensitivity troponin-T and NT-proBNP).
• Patients with PH showed signs of more severe infection in terms of radiological
lung involvement, laboratory findings, oxygenation status, and need of NIV compared
with patients without PH.
• PH was associated with higher rates of in-hospital death or ICU admission.
|
[9]
|
|
Scudiero et al.
|
Retrospective
|
224
|
To assess prevalence, predictors, and clinical outcome of PE in COVID-19 patients.
All patients underwent CT pulmonary angiography and TTE.
|
• PE was observed in 14% patients.
• PE patients had higher D-dimer level and higher prevalence of myocardial injury,
cardiogenic shock, and increased mortality rate.
• PE patients had lower values of TAPSE and higher sPAP.
|
[20]
|
|
Li et al.
|
Prospective
|
120
|
To evaluate the prognostic value of RVLS assessed through speckle-tracking echocardiography
in COVID-19 patients.
|
• RVLS was able to predict higher risk of mortality in patients with COVID-19 independently
of other echocardiographic parameters.
|
[30]
|
|
Feng et al.
|
Case series
|
5
|
To analyze whether iNO was beneficial in patients with severe COVID-19 requiring mechanical
ventilation. Patients with pre-existent heart diseases were excluded.
|
• Three patients received iNO treatment. Normalization or not worsening of sPAP and
increase of PaO2/FiO2 were observed in all cases. Two of them survived.
• Two patients did not receive iNO. Both cases experienced right heart failure, sudden
decrease of sPAP and PaO2/FiO2, and finally died.
|
[40]
|
|
Sonti et al.
|
Retrospective study
|
80
|
To analyze potential effect of iEpo in the management of hypoxemia in patients mechanically
ventilated for COVID-19.
|
• Clinically significant improvement in PaO2/FiO2 (+10% from the baseline value) was observed in 50% of patients.
|
[47]
|
|
Moezinia et al.
|
Case series
|
8
|
To explore potential benefit of iloprost in patients with severe COVID-19 and digital
ischemia.
|
• After a continuous 5-day infusion, a sustained clinical improvement in the digital
ischemia and in cardiovascular and respiratory parameters (decreasing oxygen requirements,
increasing PaO2/FiO2, and normalization of HR) were observed.
• The treatment was well tolerated.
|
[48]
|
Abbreviations: AF, atrial fibrillation; CT, computed tomography; HR, heart rate; ICU,
intensive care unit; iEpo, inhaled epoprostenol; iNO, inhaled nitric oxide; NIV, noninvasive
ventilation; PAH, pulmonary arterial hypertension; PE, pulmonary embolism; PH, pulmonary
hypertension; RVD, right ventricular dysfunction; RVLS, right ventricular longitudinal
strain; sPAP, systolic pulmonary artery pressure; TAPSE, tricuspid annular plane systolic
excursion; TTE, transthoracic echocardiography.
The presence of PH seems to be associated with increased disease severity and poor
outcome in COVID-19, in terms of requirement of mechanical ventilation, admission
to intensive care unit, and mortality.[8]
[9]
[30] In particular, Deng and colleagues[8] reported that PH was more frequent in patients with severe COVID-19 compared with
those experiencing mild to moderate course. Moreover, evidence of PH was statistically
significant in predicting an adverse outcome (primary composite endpoint including
admission to intensive care unit, requirement of mechanical ventilation or ECMO, and
mortality). Similarly, it was found that an increase of sPAP detected by echocardiography
was associated with disease severity in terms of radiological lung involvement, laboratory
findings, oxygenation status, and need of noninvasive ventilation.[9]
PH can result in RV overload and thus acute RV failure, which may further complicate
the clinical course of the viral infection. RV longitudinal strain (RVLS) assessed
with speckle-tracking echocardiography was able to predict higher mortality risk in
patients with COVID-19 in a retrospective study by Li and colleagues.[30] Patients with lower RVLS had also enlarged RV chamber, reduced tricuspid annular
plane systolic excursion (TAPSE), and increased sPAP compared with those with higher
RVLS. These findings were also supported by Rath et al,[31] who reported that impaired RV function and tricuspid regurgitation > grade 1 were
significantly associated with higher mortality.
Echocardiographic signs of PH and RV failure may also be related with acute PE, as
observed by Scudiero and colleagues.[20] Consistent with previous data reporting a prevalence of PE of 7 to 30%,[19]
[21]
[22] they described PE in 14% of hospitalized patients with COVID-19. Patients with PE
showed lower values of TAPSE and higher sPAP compared with those without PE. Moreover,
the presence of PE was associated with higher prevalence of myocardial injury, cardiogenic
shock, and increased mortality rate.[20] Due to the prognostic significance of PH, current studies underline the importance
of transthoracic echocardiography in the diagnostic evaluation of patients with COVID-19.
Signs of PH may identify low-symptomatic patients who are at increased risk of adverse
outcome and thus candidates for close monitoring and aggressive treatment.
Therapeutic Perspectives
Based on the discussed importance of pulmonary hemodynamics in the pathophysiology
of COVID-19, indirect evidence suggests that current therapies of PAH targeting nitric
oxide (NO), prostaglandin, and endothelin pathways may partially influence the outcome
of COVID-19 patients, especially in the context of ARDS.
NO is a vasodilative molecule produced from l-arginine in vascular endothelial cells. It diffuses into adjacent vascular smooth
muscle and, through activation of the cyclic guanosine monophosphate (cGMP) pathway,
induces smooth muscle relaxation, which results in decreased vascular tone in systemic
and pulmonary circulation. Additional effects of NO include anti-inflammatory functions
as well as suppression of smooth muscle proliferation and platelet aggregation.[32] Phosphodiesterase 5 (PDE-5) inhibitors are potent unselective vasodilative drugs
targeting the NO pathway. Their mechanism derives from inhibition of PDE-5, which
prolongs the action of cGMP avoiding its enzymatic degradation. PDE-5 inhibitors have
been traditionally successfully used in the treatment of PAH, while clinical research
failed to demonstrate their efficacy in the management of ARDS.[33]
[34] The use of PDE-5 inhibitors has been supposed to be beneficial in COVID-19 to counteract
the changes in pulmonary hemodynamics and the intense inflammatory response.[34] However, clinical data reporting the use of this class of drugs in COVID-19 are
still lacking.
Unlike PDE5 inhibitors, inhaled nitric oxide (iNO) induces selective pulmonary vasodilation
in ventilated areas of the lung, resulting in improvement of oxygenation due to better
VQ-matching and amelioration of PH.[35] Clinical trials and meta-analysis in ARDS showed that treatment with iNO induces
a transitory improvement of oxygenation but has no impact on patients' outcome and
therefore is not routinely recommended.[36]
[37]
[38]
[39] Small studies suggest that treatment with iNO may be beneficial in patients with
COVID-19 through improvement of systemic oxygenation and reduction of PAP and thus
RV afterload.[12]
[40]
PGI2 is produced by endothelial cells and induces vascular smooth muscle relaxation
and inhibition of platelet aggregation. Furthermore, it seems to have cytoprotective
and antiproliferative properties.[41]
[42] Inhaled PGI2 analogs represent a cornerstone of therapy of PAH, while they are not
beneficial in the context of ARDS.[43]
[44]
[45]
[46] Their use in patients with severe COVID-19 showed positive results in two clinical
studies, reporting modest but statistically significant improvement of cardiovascular
and respiratory parameters, including systemic oxygenation.[47]
[48] Despite some promising results, potential benefits of therapies with iNO and PGI2
analogs must be supported by stronger evidence from randomized trials.
The use of endothelin receptor antagonists (ERAs) may also be of interest in the management
of PH in COVID-19. ET-1 is a potent vasoconstrictor, proinflammatory, proliferative,
and pro-oxidative glycopeptide, which is overexpressed in PAH.[49] It has been postulated that in inflammatory stress conditions, such as SARS-CoV-2
infection, high levels of ET-1 may aggravate the lung injury through activation of
necroptotic pathways and promoting fibroblast differentiation.[42]
[50]
[51] On this basis, the use of ERAs may be beneficial in the management of PH in COVID-19.
Clinical data are still lacking.
Summary
PH is a common condition associated with COVID-19. Its pathogenesis is complex and
includes the following mechanisms: endotheliitis and vasculitis, thrombotic microangiopathy,
venous thromboembolism, and ARDS. Many patients with signs of PH suffer from chronic
cardiopulmonary diseases such as COPD and congestive heart failure. Current clinical
evidence suggests that evidence of PH in patients with COVID-19 may be associated
with increased disease severity and poor outcome. This underlines the importance of
transthoracic echocardiography in the diagnostic evaluation of patients with COVID-19,
to identify those at increased risk of adverse outcome. Because of the importance
of the pulmonary hemodynamics in the pathophysiology of COVID-19, indirect evidence
suggests that current therapies of PAH targeting the NO, the prostaglandin, and the
endothelin pathways may partially influence the outcome of COVID-19 patients, especially
in the context of ARDS. Treatments with iNO and inhaled PGI2 have shown encouraging
results in small trials through improvement of systemic oxygenation, reduction of
sPAP, and prevention of RV failure. However, further investigation in large randomized
clinical trials is required.
Zusammenfassung
Die pulmonale Hypertonie (PH) stellt eine relativ häufige Komplikation von COVID-19
dar. Es entsteht aus einer Kombination von verschiedenen pathophysiologischen Mechanismen,
welche mit SARS-CoV-2-Infektion assoziiert sind: 1) Endotheliitis und Vaskulitis;
2) thrombotische Mikroangiopathie; 3) venöse Thromboembolie; 4) ARDS. Anhand von aktuellen
Daten, erscheinen vorbestehende chronische Herz- und Lungenerkrankungen relevante
Risikofaktoren für die Entwicklung einer PH im Rahmen der viralen Infektion zu sein.
Anderseits korreliert das Vorhandseien einer PH mit einem schwereren Krankheitsbild
und einer schlechteren Prognose von COVID-19. Das stellt die Bedeutung der transthorakalen
Echokardiographie in diesem Kontext heraus, welche eine Risikostratifizierung von
COVID-19 Patienten ermöglicht. In Hinblick auf die Beteiligung des pulmonalen Kreislaufs
in Rahmen der viralen Infektion, besteht ein wachsendes Interesse an der konventionellen
medikamentösen Therapie der PAH mit iNO und inhalativem Prostacyclin, insbesondere
in Rahmen von COVID-19-assoziierten ARDS. Obwohl vorläufige Studien ermutigenden Ergebnisse
gezeigt haben, ist eine stärkere Evidenzen hinsichtlich Nutzens und Risikos einer
solchen Therapie zwingend erforderlich.
What Is Known about This Topic?
-
Coronavirus disease 2019 can result in pulmonary and cardiovascular complications.
-
Radiological and histological findings suggest that the virus may determine changes
in the pulmonary circulation similar to those leading to pulmonary hypertension.
What Does This Paper Add?
-
This review collects and discusses current available data about the relationship between
COVID-19 and pulmonary hypertension.
-
Diagnostic and therapeutical options are presented, with particular attention to bed-side
echocardiography.
-
The detection of pulmonary hypertension may be helpful to identify patients at increased
risk of adverse outcome.
