TY - JOUR
T1 - Clinical Presentation and Short- and Long-term Outcomes in Patients with Isolated Distal Deep Vein Thrombosis vs Proximal Deep Vein Thrombosis in the RIETE Registry
AU - Bikdeli, Behnood
AU - Caraballo, César
AU - Trujillo-Santos, Javier
AU - Galanaud, Jean Philippe
AU - Di Micco, Pierpaolo
AU - Rosa, Vladimir
AU - Cusidó, Gemma Vidal
AU - Schellong, Sebastian
AU - Mellado, Meritxell
AU - Del Valle Morales, María
AU - Gavín-Sebastián, Olga
AU - Mazzolai, Lucia
AU - Krumholz, Harlan M.
AU - Monreal, Manuel
AU - The RIETE Investigators
A2 - Kigitovica, Dana
A2 - Skride, Andris
A2 - Rusa, Elina
N1 - Full list of the RIETE Investigators is given in Pubmed publication. Article can be found in A.Skride's and D.Kigitoviča's profiles in Web of Science but not in Scopus.
Funding Information:
Funding/Support: This work was supported by an unrestricted educational grant from Sanofi Spain, Leo Pharma, and Rovi; the Scott Schoen and Nancy Adams IGNITE Award from the Mary Horrigan Connors Center for Women’s Health and Gender Biology at Brigham and Women’s Hospital (Dr Bikdeli); and a Career Development Award (938814) from the American Heart Association (Dr Bikdeli).
Funding Information:
registry has been supported by Sanofi Spain, Leo Pharma, and Rovi with an unrestricted educational grant. Dr Bikdeli reported receiving consulting fees serving as an expert on behalf of the plaintiff for litigation related to 2 specific brand models of inferior vena cava filters. Dr Krumholz reported receiving personal fees from UnitedHealth, Element Science, Aetna, Reality Labs, F-Prime, Tesseract/4Catalyst, Martin/Baughman Law Firm, Arnold and Porter Law Firm, and Siegfried and Jensen Law Firm; being a cofounder of HugoHealth, a personal health information platform; being a cofounder of Refactor Health, an Enterprise Health Care artificial intelligence–augmented data management company; having contracts with the Centers for Medicare & Medicaid Services Association through Yale New Haven Hospital, to develop and maintain performance measures that are publicly reported; and receiving grants from Johnson & Johnson outside the submitted work. Dr Monreal reported receiving grants from Sanofi and Rovi sponsorship of the RIETE registry outside the submitted work. No other disclosures were reported.
Publisher Copyright:
© 2022 American Medical Association. All rights reserved.
PY - 2022/8
Y1 - 2022/8
N2 - Importance: Insufficient data exist about the clinical presentation, short-term, and long-term outcomes of patients with isolated distal deep vein thrombosis (IDDVT), that is, thrombosis in infrapopliteal veins without proximal extension or pulmonary embolism (PE). Objective: To determine the clinical characteristics, short-term, and 1-year outcomes in patients with IDDVT and to compare the outcomes in unadjusted and multivariable adjusted analyses with patients who had proximal DVT. Design, Setting, and Participants: This was a multicenter, international cohort study in participating sites of the Registro Informatizado Enfermedad Tromboembólica (RIETE) registry conducted from March 1, 2001, through February 28, 2021. Patients included in this study had IDDVT. Patients with proximal DVT were identified for comparison. Patients were excluded if they had a history of asymptomatic DVT, upper-extremity DVT, coexisting PE, or COVID-19 infection. Main Outcomes and Measures: Primary outcomes were 90-day and 1-year mortality, 1-year major bleeding, and 1-year venous thromboembolism (VTE) deterioration, which was defined as subsequent development of proximal DVT or PE. Results: A total of 33897 patients were identified with isolated DVT (without concomitant PE); 5938 (17.5%) had IDDVT (mean [SD] age, 61 [17] years; 2975 male patients [50.1%]), and 27959 (82.5%) had proximal DVT (mean [SD] age, 65 [18] years; 14315 male patients [51.2%]). Compared with individuals with proximal DVT, those with IDDVT had a lower comorbidity burden but were more likely to have had recent surgery or to have received hormonal therapy. Patients with IDDVT had lower risk of 90-day mortality compared with those with proximal DVT (odds ratio [OR], 0.47; 95% CI, 0.40-0.55). Findings were similar in 1-year unadjusted analyses (hazard ratio [HR], 0.52; 95% CI, 0.46-0.59) and adjusted analyses (HR, 0.72; 95% CI, 0.64-0.82). Patients with IDDVT had a lower 1-year hazard of VTE deterioration (HR, 0.83; 95% CI, 0.69-0.99). In 1-year adjusted analyses of patients without an adverse event within the first 3 months, IDDVT was associated with lower risk of VTE deterioration (adjusted HR, 0.48; 95% CI, 0.24-0.97). By 1-year follow-up, symptoms or signs of postthrombotic syndrome were less common in patients with IDDVT (47.6% vs 60.5%). Conclusions and Relevance: Results of this cohort study suggest that patients with IDDVT had a less ominous prognosis compared with patients with proximal DVT. Such differences were likely multifactorial, including the differences in demographics, risk factors, comorbidities, particularly for all-cause mortality, and a potential association of thrombus location with VTE deterioration and postthrombotic syndrome. Randomized clinical trials are needed to assess the optimal long-term management of IDDVT.
AB - Importance: Insufficient data exist about the clinical presentation, short-term, and long-term outcomes of patients with isolated distal deep vein thrombosis (IDDVT), that is, thrombosis in infrapopliteal veins without proximal extension or pulmonary embolism (PE). Objective: To determine the clinical characteristics, short-term, and 1-year outcomes in patients with IDDVT and to compare the outcomes in unadjusted and multivariable adjusted analyses with patients who had proximal DVT. Design, Setting, and Participants: This was a multicenter, international cohort study in participating sites of the Registro Informatizado Enfermedad Tromboembólica (RIETE) registry conducted from March 1, 2001, through February 28, 2021. Patients included in this study had IDDVT. Patients with proximal DVT were identified for comparison. Patients were excluded if they had a history of asymptomatic DVT, upper-extremity DVT, coexisting PE, or COVID-19 infection. Main Outcomes and Measures: Primary outcomes were 90-day and 1-year mortality, 1-year major bleeding, and 1-year venous thromboembolism (VTE) deterioration, which was defined as subsequent development of proximal DVT or PE. Results: A total of 33897 patients were identified with isolated DVT (without concomitant PE); 5938 (17.5%) had IDDVT (mean [SD] age, 61 [17] years; 2975 male patients [50.1%]), and 27959 (82.5%) had proximal DVT (mean [SD] age, 65 [18] years; 14315 male patients [51.2%]). Compared with individuals with proximal DVT, those with IDDVT had a lower comorbidity burden but were more likely to have had recent surgery or to have received hormonal therapy. Patients with IDDVT had lower risk of 90-day mortality compared with those with proximal DVT (odds ratio [OR], 0.47; 95% CI, 0.40-0.55). Findings were similar in 1-year unadjusted analyses (hazard ratio [HR], 0.52; 95% CI, 0.46-0.59) and adjusted analyses (HR, 0.72; 95% CI, 0.64-0.82). Patients with IDDVT had a lower 1-year hazard of VTE deterioration (HR, 0.83; 95% CI, 0.69-0.99). In 1-year adjusted analyses of patients without an adverse event within the first 3 months, IDDVT was associated with lower risk of VTE deterioration (adjusted HR, 0.48; 95% CI, 0.24-0.97). By 1-year follow-up, symptoms or signs of postthrombotic syndrome were less common in patients with IDDVT (47.6% vs 60.5%). Conclusions and Relevance: Results of this cohort study suggest that patients with IDDVT had a less ominous prognosis compared with patients with proximal DVT. Such differences were likely multifactorial, including the differences in demographics, risk factors, comorbidities, particularly for all-cause mortality, and a potential association of thrombus location with VTE deterioration and postthrombotic syndrome. Randomized clinical trials are needed to assess the optimal long-term management of IDDVT.
UR - http://www.scopus.com/inward/record.url?scp=85134696905&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/35830171/
UR - https://www.riete.org/info/centros_participantes/index.php
U2 - 10.1001/jamacardio.2022.1988
DO - 10.1001/jamacardio.2022.1988
M3 - Article
C2 - 35830171
AN - SCOPUS:85134696905
SN - 2380-6583
VL - 7
SP - 857
EP - 865
JO - JAMA Cardiology
JF - JAMA Cardiology
IS - 8
ER -