** Abnormality of [[cardiac]] chambers ([[Hypertrophy (medical)|hypertrophy]], dilation)
** Delayed enhancement [[MRI]] may help characterize the [[myocardial]] [[Tissue (biology)|tissue]] ([[fibrosis]])
** Late enhancement of contrast in conditions such as [[myocarditis]], [[sarcoidosis]], [[amyloidosis]], [[Anderson-Fabry disease|Anderson-Fabry]]'s disease, [[Chagas disease]])
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*Goldberg's criteria may aid in diagnosis of left ventricular dysfunction: (High specificity)
**[[S wave|S]]V1 or [[S wave|S]]V2 + [[R wave|R]]V5 or [[R wave|R]]V6 ≥3.5 mV
**Total [[QRS complex|QRS]] amplitude in each of the limb leads ≤0.8 mV
** [[R wave|R]]/[[S wave|S]] ratio <1 in lead V4
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*[[Cardiomegaly]]
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*Previous [[myocardial infarction]]
*[[Hypertension]] ([[Systemic hypertension|systemic]] and [[Pulmonary hypertension|pulmonary]])
*Non-specific [[ST interval|ST segment]] and [[T wave]] changes
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*[[Nodule (medicine)|Nodules]]
*[[Cavitation]]
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*[[Takayasu's arteritis|Takayasu arteritis]] usually found in persons aged 4-60 years with a mean of 30
*[[Giant-cell arteritis]] usually occurrs in persons aged > 60 years
*[[Churg-Strauss syndrome]] may present with [[asthma]], [[sinusitis]], transient [[pulmonary]] infiltrates and neuropathy alongwith [[cardiac]] involvement
*Granulomatous vasculitides may present with [[nephritis]] and [[upper airway]] ([[nasopharyngeal]]) destruction
Proposed mechanism of multiple organ dysfunction that occurs in COVID-19 patients are multifactorial but they include a hypercoagulable state with micro and macro-circulatory thrombosis.
Based on these case reports and case series, various guidelines have been proposed now to initiate anticoagulants in critically ill patients and those who are admitted to the hospital.
Classification
Acute Pulmonary Embolism
Pathologically an embolus is said to be acute when it is situated centrally within in the vascular lumen, or in other case it causes the occlusion of vessel. It can cause immediate occurence of symptoms.
Chronic Pulmonary Embolism
An embolus is said to be chronic , if it is eccentric and lies in lies with the vessel wall.
It occouleds the lumen of vessel wall by more than 50 %.
There is also evidence of recanalization within the thrombus.
Chronic thromboembolism can cause pulmonary hypertension especially when there is >3 months of effective anticoagulation therapy and one of the following criteria. a) Mean pulmonary arterial pressure greater than or equal to 25 mmHg b) Pulmonary arterial wedge pressure less than or equal to 15 mmgHg c) Abnormal lung V/Q scan or imaging findings suggestive of chronic pulmonary embolism on CTPA, CMR, CPA.
Pathophysiology
As data on COVID-19 has been incomplete and evolving, the pathogenesis of pulmonary embolism has not yet been completely understood. Various contributors to the pathogenesis of pulmonary embolism in these patients are listed in the table below:
It has been proposed that endothelial cells contribute towards the initiation and propagation of ARDS by changing the vascular barrier permeability, increasing the chance of procoagulative state that leads to endotheliitis and infiltration of inflammatory cells in the pulmonary vasculature.
It has been proposed that COVID-19 can directly affect endothelial cells leading to widespread endotheliitis. SARS-CoV-2 also binds to the ACE2 receptors which alter the activity of ACE2.
Reduced ACE2 activity leads to activation of the kallikrein-bradykinin pathway, which increases vascular permeability.
The activated neutrophils migrate towards the pulmonary endothelial cells and produce cytotoxic mediators including reactive oxygen species.
Most hospitalized critically ill immobile COVID-19 patients are prone to stasis of blood flow leading to another contributor towards the pathogenesis of pulmonary embolism.
Various clinical studies have reported different prothrombotic factors in patients who are critically ill and are hospitalized due to COVID-19. These studies report various key lab factors that play an important role in the pathogenesis of pulmonary embolism.
Recently, SARS-CoV-2 has been associated with pulmonary embolism and other coagulopathic disorders. Other than SARS-CoV-2, pulmonary embolism can be caused by a number of different factors
Etiologies of Pulmonary Embolism
Hereditary Causes
Comorbidities
Miscellaneous
Factor V Leiden Mutation
Heart failure
Surgery
Factor C & S deficiency
Congenital heart disease
Pregnancy
Antithrombin deficiency
Antiphospholipid syndrome
OCPs
Obesity
Immobilization
Myeloproliferative Disorders
Trauma
Paroxysmal nocturnal hemoglobinuria
Malignancy
Differentiating Pulmonary Embolism from other Diseases
Pulmonary embolism in COVID-19 patients can be sudden and can mimic symptoms of other disorders like pneumonia and ARDS. Therefore it has been suggested there should be lower threshold of imaging like DVT or CTPA reserved for pulmonary embolism in COVID-19 patients admitted to the ICU setting.
Epidemiology and demographics
Various case reports and case series report relatively high incidence of pulmonary embolism in ICU patients.
The incidence of thrombotic complications is reported to be 31 % in one study. In this study pulmonary embolism was the most common thrombotic complication.
Another study reported an overall 24% cumulative incidence of pulmonary embolism in patients with COVID-19 pneumonia, 50% (30–70%) in ICU and 18% (12–27%) in other patients.
In Non-ICU settings (In-patient), pulmonary embolism is reported to occur in 3% percent of patients in one study.
Risk Factors
Multivariate analysis showed following risk factors that predispose a patient of COVID-19 to pulmonary embolism
Pulmonary embolism in critically ill patients of COVID-19 is a frequent finding. It can lead to the development of cardiogenic shock, sudden cardiac arrest and pulmonary hypertension if developed chronically. There has been various investigational and treatment approach to treat the hypercoagulability leading to these complications in COVID-19 patients. Patients that are at risk of pulmonary embolism such as those with deep venous thrombosis are advised to take oral anticoagulants. Studies show that there is high cumulative incidence of PE in COVID-19 patients which suggests more frequent use of contrast medium on CT for the evaluation of COVID-19 patients.
COVID-19 patients presenting with pulmonary embolism have a poor prognosis. It has been reported that despite adequate anticoagulation being advised to patients in ICU, there is still relatively high incidence of PE in these patients. Few studies showed VTE to be the main cause of death in COVID-19 patients which suggests setting a lower threshold for diagnostic imaging for DVT or PE.
Diagnosis
History and Symptoms
COVID-19 patients are usually at high risk of hypercoagulability and as there is an increased incidence of pulmonary embolism in ICU patients, they mostly have overlapping symptoms with pneumonia, ARDS, and sometimes present only with fever progressing to pulmonary embolism and sudden cardiac arrest.
Prompt diagnosis of PE in COVID-19 patient is difficult in this regard that various symptoms of COVID-19 overlap with that of pulmonary embolism. American Society of Hematology provides the following guidelines regarding the diagnosis of pulmonary embolism:
Normal d-dimers level in a patient with low to moderate pretest probability is sufficient to rule out the diagnosis of PE. D-dimers level is usually elevated in COVID-19 patients. This is not applicable to a patient with a high pretest probability.
All hospitalized patients with COVID 19 should get proper venous thromboembolism prophylaxis in the absence of any contraindication of anticoagulation.
In ICU setting, empiric use of intermediate or therapeutic dose anticoagulation should be instituted.
In a non-ICU setting, all hospitalized patients should be treated with prophylactic low dose molecular weight heparin.
Acute Pulmonary embolism
Full dose anti-coagulation is appropriate for diagnosed pulmonary embolism.
Critically ill patients that have recovered from COVID-19 and had a documented VTE are usually given a minimum of 3 months of anticoagulation.
Patients not admitted to hospitals but at risk of VTE, such as prior VTE episode, recent surgery, prolonged immobilization are usually given a prophylactic dose of Rivaroxaban 10 mg daily for 31 days or 39 days.
References
↑Invalid <ref> tag; no text was provided for refs named Hematology.org 2020