Safety and Outcomes with Direct Oral Anticoagulants Versus Vitamin-K Antagonists in Chronic Thromboembolic Pulmonary Hypertension: A Systematic Review, Meta-Analysis, and Meta-Regression

Author:

Jain Hritvik1,Odat Ramez M.2,Ahmed Mushood3,Jain Jyoti1,Goyal Aman4,Idrees Muhammad5,Passey Siddhant6,Jha Jagriti7,Shah Janhvi8,Gole Shrey9

Affiliation:

1. Department of Internal Medicine, All India Institute of Medical Sciences (AIIMS), Jodhpur, India

2. Department of Internal Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan

3. Department of Internal Medicine, Rawalpindi Medical University, Rawalpindi, Pakistan

4. Department of Internal Medicine, Seth GS Medical College and KEM Hospital, Mumbai, India

5. Department of Internal Medicine, Lahore General Hospital, Lahore, Pakistan

6. Department of Internal Medicine, University of Connecticut Health Center, CT

7. Department of Pediatrics, University of Connecticut Health Center, CT

8. Department of Internal Medicine, St Luke’s Hospital, Chesterfield, MO

9. Department of Immunology and Rheumatology, Stanford University, CA.

Abstract

Chronic thromboembolic pulmonary hypertension (CTEPH) is a subtype of pulmonary hypertension characterized by organized thrombi inside the pulmonary vasculature, leading to an increase in pulmonary artery pressure. CTEPH is seen in about 3–4% of patients with acute pulmonary embolism and is associated with poor outcomes. Apart from surgical intervention, lifelong anticoagulation is the mainstay of CTEPH management. Traditionally, CTEPH is managed with vitamin-K antagonists (VKA); however, direct oral anticoagulants (DOACs) are recently gaining popularity. However, the current literature comparing DOACs versus VKAs in CTEPH has inconsistent results. An electronic search of the major bibliographic databases was performed to retrieve studies comparing DOACs versus VKAs in CTEPH patients. For dichotomous outcomes, the odds ratio (ORs) with 95% confidence intervals (CI) were pooled using the DerSimonian and Laird random-effects model to generate forest plots. Statistical significance was considered at P < 0.05. Ten studies were included with 3936 patients (1269 in the DOAC group and 2667 in the VKA group). Treatment with DOAC was associated with no statistically significant difference in the risk of all-cause mortality (OR, 0.78; 95% CI, 0.35–1.71; P < 0.53), venous thromboembolism (OR, 1.19; 95% CI, 0.59–2.40; P = 0.63), major bleeding (OR, 0.68; 95% CI, 0.38–1.22; P = 0.20), and clinically relevant nonmajor bleeding (OR, 1.22; 95% CI, 0.80–1.86; P = 0.37). Our analysis demonstrates that DOACs are noninferior to VKAs in terms of their safety and outcomes profile in CTEPH. Further trials are needed to evaluate more robust evidence and to compare additional outcomes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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