Evidence map›Paper›PMID 39873294›Full record

SynthesisThe Cochrane database of systematic reviews2025

Interrupted versus uninterrupted anticoagulation for cardiac rhythm management device insertion.

Brett Chen, Mi Phan, Vinay Pasupuleti, Yuani M Roman, Adrian V Hernandez

Abstract readComparative StudyMeta-AnalysisSystematic Review
In one paragraph

Synthesis in The Cochrane database of systematic reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Brett ChenDepartment of Medicine, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, USA.
Mi PhanDepartment of Pharmacy Services, Yale New Haven Hospital, CT, USA.
Vinay PasupuletiScientific Services, Oxford PharmaGenesis, Inc., Newtown, PA 18940, USA.
Yuani M RomanDepartment of Pharmacy Practice, University of Connecticut, Storrs, CT 06269, USA.
Adrian V HernandezDepartment of Pharmacy Practice, University of Connecticut, Storrs, CT 06269, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuideline-recommended strategies to interrupt chronic anticoagulation with warfarin or direct oral anticoagulants (DOAC) during the perioperative period of cardiac implantable electronic device (CIED) surgery differ worldwide. There is uncertainty concerning the benefits and harms of interrupted and uninterrupted anticoagulation in patients undergoing CIED surgery.

objectivesTo assess the benefits and harms of interrupted anticoagulation (IAC) with either warfarin or DOAC in the perioperative period of CIED surgery versus uninterrupted anticoagulation (UAC), with or without heparin bridging, during an equivalent time frame, for CIED surgery. SEARCH

methodsCENTRAL, MEDLINE, Embase, Web of Science, and two trials registers were searched on 26 November 2021 together with reference checking, citation searching and contact with study authors to identify additional studies. We plan to update this review imminently. SELECTION CRITERIA: We included randomized controlled trials (RCTs) evaluating IAC vs. UAC in adults with a diagnosed cardiac rhythm disorder, who underwent elective CIED surgery and received at least one month of warfarin or DOAC anticoagulation. Comparisons of interest were: (1) continued warfarin vs. interrupted warfarin anticoagulation, with or without heparin bridging; and (2) continued DOAC (apixaban, betrixaban, dabigatran, edoxaban, or rivaroxaban) vs. interrupted DOAC, with or without heparin bridging. DATA COLLECTION AND ANALYSIS: Primary outcomes were composite thromboembolic events (transient ischemic attack, ischemic stroke, deep vein thrombosis, pulmonary embolism, peripheral embolism, or valve thrombosis) and device-pocket hematoma. Secondary outcomes included individual components of composite thromboembolic events, composite bleeding events, all-cause mortality, adverse events, quality of life and days of hospitalization. Two authors independently selected studies, extracted data, and assessed the risk of bias. We assessed the certainty of evidence using GRADE. The inverse variance random-effects model was used for meta-analyses, and the DerSimonian and Laird method was used for calculating the between-study variance Tau MAIN

resultsWe identified 10 eligible studies (2221 participants), of which one is ongoing. Of these 10 studies, six compared IAC vs. UAC with warfarin (1267 participants) and four compared IAC vs. UAC with DOAC (954 participants). Follow-up duration ranged between 0.5 to three months. The mean age of participants ranged from 68 to 76 years. Definitions of thromboembolic events, device-pocket hematoma, and bleeding events varied across studies. IAC vs. UAC with warfarin IAC with warfarin may result in little to no difference in composite thromboembolic events (RR 0.85, 95% CI 0.18 to 4.11; 5 RCTs, n = 1266; low-certainty evidence). The evidence is very uncertain about the effect of IAC on device-pocket hematoma (RR 1.87, 95% CI 0.83 to 4.22; 5 RCTs, n = 1266; very low-certainty evidence), ischemic stroke (RR 0.70, 95% CI 0.11 to 4.40; 5 RCTs, n = 1266; very low-certainty evidence) and composite bleeding events (RR 1.92, 95% CI 0.84 to 4.43; 5 RCTs, very low-certainty evidence). IAC with warfarin likely results in little to no difference in deep vein thrombosis or pulmonary embolism (0 events in both groups; 2 RCTs, n = 782; moderate-certainty evidence). IAC may result in a slight reduction of all-cause mortality (RR 0.35, 95% CI 0.04 to 2.93; 3 RCTs, n = 953; low-certainty evidence). IAC vs. UAC with DOAC IAC with DOAC may result in little to no difference in composite thromboembolic events (RR 0.98, 95% CI 0.06 to 15.63; 3 RCTs, n = 843; low-certainty evidence) and ischemic stroke (RR 0.98, 95% CI 0.06 to 15.63, 2 RCTs, n = 763; low-certainty evidence). The evidence is very uncertain about the effect of IAC with DOAC on device-pocket hematoma (RR 1.07, 95% CI 0.55 to 2.11; 4 RCTs, n = 954; very low-certainty evidence) and composite bleeding events (RR 1.07, 95% CI 0.55 to 2.06; 4 RCTs, n = 954; very low-certainty evidence). IAC may result in little to no difference in ischemic stroke (RR 0.98, 95% CI 0.06 to 15.63, 2 RCTs, low-certainty evidence). IAC likely results in little to no difference in deep vein thrombosis or pulmonary embolism (0 events in both groups; 2 RCTs, n = 763; moderate-certainty evidence). IAC may result in a slight reduction of all-cause mortality (RR 0.49, 95% CI 0.04 to 5.39; 2 RCTs, n = 763; low-certainty evidence). AUTHORS'

conclusionsInterrupted anticoagulation in people undergoing elective CIED surgery had similar outcomes to uninterrupted anticoagulation with either warfarin or DOAC medications. Certainty of evidence was judged to be low to very low for most of the assessed outcomes. Further RCTs are particularly needed to help identify whether IAC significantly impacts the risks of thromboembolic events and device-pocket hematoma.

Indexed as

AnticoagulantsDefibrillators, ImplantablePacemaker, ArtificialWarfarinArrhythmias, CardiacBiasHematomaHemorrhageHeparinHumansPostoperative ComplicationsPulmonary EmbolismQuality of LifeRandomized Controlled Trials as TopicStrokeThromboembolismAnticoagulantsHeparinWarfarin

Identifiers

PMID39873294
PMCPMC11773630

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.