TY - JOUR
T1 - Anticoagulation in chronic thromboembolic pulmonary hypertension
T2 - A systematic review and meta-analysis
AU - Ishisaka, Yoshiko
AU - Watanabe, Atsuyuki
AU - Takagi, Hisato
AU - Steiger, David
AU - Kuno, Toshiki
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/11
Y1 - 2023/11
N2 - Introduction: Life-long anticoagulation is the recommended management for chronic thromboembolic pulmonary hypertension (CTEPH). Evidence regarding the use of direct oral anticoagulants (DOAC) for CTEPH is yet to be established. We performed a systematic review and meta-analysis to clarify the outcomes of CTEPH in patients who used DOAC or vitamin K antagonists (VKA). Methods: We reviewed literature in PubMed and EMBASE through March 2023. We included studies involving patients with CTEPH where DOAC and VKA were compared. We collected data including intervention history for CTEPH, bleeding events, recurrence of VTE (venous thromboembolism), and mortality. We performed a meta-analysis using the Mantel-Haenszel method with a fixed-effects model. Results: We included one randomized clinical trial and six observational studies, with a total of 2969 patients. Six studies investigated major bleeding outcomes, and seven investigated all bleeding outcomes. There were no differences in major bleeding (RR 0.59, 95 % CI [0.34–1.02], I2 = 0 %) and all–bleeding (RR 0.87, 95 % CI [0.67–1.13], I2 = 0 %). Based on the five studies we included, DOAC was associated with a lower risk of mortality (RR 0.54, 95 % CI: 0.37–0.79, I2 = 5 %). However, a higher risk of recurrent pulmonary embolism (PE) was seen in three studies (RR 3.80, 95 % CI: [1.93–7.50], I2 = 11 %). No significant differences were noted in terms of VTE. Conclusion: DOAC compared to VKA was associated with a significantly lower mortality and higher risk of recurrent PE. Since most of the included studies are observational, we must consider the existence of multiple biases and confounding factors.
AB - Introduction: Life-long anticoagulation is the recommended management for chronic thromboembolic pulmonary hypertension (CTEPH). Evidence regarding the use of direct oral anticoagulants (DOAC) for CTEPH is yet to be established. We performed a systematic review and meta-analysis to clarify the outcomes of CTEPH in patients who used DOAC or vitamin K antagonists (VKA). Methods: We reviewed literature in PubMed and EMBASE through March 2023. We included studies involving patients with CTEPH where DOAC and VKA were compared. We collected data including intervention history for CTEPH, bleeding events, recurrence of VTE (venous thromboembolism), and mortality. We performed a meta-analysis using the Mantel-Haenszel method with a fixed-effects model. Results: We included one randomized clinical trial and six observational studies, with a total of 2969 patients. Six studies investigated major bleeding outcomes, and seven investigated all bleeding outcomes. There were no differences in major bleeding (RR 0.59, 95 % CI [0.34–1.02], I2 = 0 %) and all–bleeding (RR 0.87, 95 % CI [0.67–1.13], I2 = 0 %). Based on the five studies we included, DOAC was associated with a lower risk of mortality (RR 0.54, 95 % CI: 0.37–0.79, I2 = 5 %). However, a higher risk of recurrent pulmonary embolism (PE) was seen in three studies (RR 3.80, 95 % CI: [1.93–7.50], I2 = 11 %). No significant differences were noted in terms of VTE. Conclusion: DOAC compared to VKA was associated with a significantly lower mortality and higher risk of recurrent PE. Since most of the included studies are observational, we must consider the existence of multiple biases and confounding factors.
KW - Chronic thromboembolic pulmonary hypertension
KW - Direct oral anticoagulants
KW - Pulmonary embolism
KW - Venous thromboembolism
KW - Vitamin K antagonists
UR - http://www.scopus.com/inward/record.url?scp=85173975371&partnerID=8YFLogxK
U2 - 10.1016/j.thromres.2023.10.003
DO - 10.1016/j.thromres.2023.10.003
M3 - Article
C2 - 37839150
AN - SCOPUS:85173975371
SN - 0049-3848
VL - 231
SP - 91
EP - 98
JO - Thrombosis Research
JF - Thrombosis Research
ER -