Anticoagulation for people with cancer and central venous catheters

dc.contributor.authorKahale, Lara A.
dc.contributor.authorTsolakian, Ibrahim George
dc.contributor.authorHakoum, Maram B.
dc.contributor.authorMatar, Charbel F.
dc.contributor.authorBarba, Maddalena
dc.contributor.authorYosuico, Victor E.D.
dc.contributor.authorTerrenato, Irene
dc.contributor.authorSperati, Francesca
dc.contributor.authorSchunëmann, Holger J.
dc.contributor.authorAkl, Elie A.
dc.contributor.departmentFamily Medicine
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:42:22Z
dc.date.available2025-01-24T11:42:22Z
dc.date.issued2018
dc.description.abstractBackground: Central venous catheter (CVC) placement increases the risk of thrombosis in people with cancer. Thrombosis often necessitates the removal of the CVC, resulting in treatment delays and thrombosis-related morbidity and mortality. This is an update of the Cochrane Review published in 2014. Objectives: To evaluate the efficacy and safety of anticoagulation for thromboprophylaxis in people with cancer with a CVC. Search methods: We conducted a comprehensive literature search in May 2018 that included a major electronic search of Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE (Ovid), and Embase (Ovid); handsearching of conference proceedings; checking of references of included studies; searching for ongoing studies; and using the 'related citation' feature in PubMed. This update of the systematic review was based on the findings of a literature search conducted on 14 May 2018. Selection criteria: Randomized controlled trials (RCTs) assessing the benefits and harms of unfractionated heparin (UFH), low-molecular-weight heparin (LMWH), vitamin K antagonists (VKA), or fondaparinux or comparing the effects of two of these anticoagulants in people with cancer and a CVC. Data collection and analysis: Using a standardized form, we extracted data and assessed risk of bias. Outcomes included all-cause mortality, symptomatic catheter-related venous thromboembolism (VTE), pulmonary embolism (PE), major bleeding, minor bleeding, catheter-related infection, thrombocytopenia, and health-related quality of life (HRQoL). We assessed the certainty of evidence for each outcome using the GRADE approach (Balshem 2011). Main results: Thirteen RCTs (23 papers) fulfilled the inclusion criteria. These trials enrolled 3420 participants. Seven RCTs compared LMWH to no LMWH (six in adults and one in children), six RCTs compared VKA to no VKA (five in adults and one in children), and three RCTs compared LMWH to VKA in adults. LMWH versus no LMWHSix RCTs (1537 participants) compared LMWH to no LMWH in adults. The meta-analyses showed that LMWH probably decreased the incidence of symptomatic catheter-related VTE up to three months of follow-up compared to no LMWH (risk ratio (RR) 0.43, 95% confidence interval (CI) 0.22 to 0.81; risk difference (RD) 38 fewer per 1000, 95% CI 13 fewer to 52 fewer; moderate-certainty evidence). However, the analysis did not confirm or exclude a beneficial or detrimental effect of LMWH on mortality at three months of follow-up (RR 0.82, 95% CI 0.53 to 1.26; RD 14 fewer per 1000, 95% CI 36 fewer to 20 more; low-certainty evidence), major bleeding (RR 1.49, 95% CI 0.06 to 36.28; RD 0 more per 1000, 95% CI 1 fewer to 35 more; very low-certainty evidence), minor bleeding (RR 1.35, 95% CI 0.62 to 2.92; RD 14 more per 1000, 95% CI 16 fewer to 79 more; low-certainty evidence), and thrombocytopenia (RR 1.03, 95% CI 0.80 to 1.33; RD 5 more per 1000, 95% CI 35 fewer to 58 more; low-certainty evidence). VKA versus no VKAFive RCTs (1599 participants) compared low-dose VKA to no VKA in adults. The meta-analyses did not confirm or exclude a beneficial or detrimental effect of low-dose VKA compared to no VKA on mortality (RR 0.99, 95% CI 0.64 to 1.55; RD 1 fewer per 1000, 95% CI 34 fewer to 52 more; low-certainty evidence), symptomatic catheter-related VTE (RR 0.61, 95% CI 0.23 to 1.64; RD 31 fewer per 1000, 95% CI 62 fewer to 51 more; low-certainty evidence), major bleeding (RR 7.14, 95% CI 0.88 to 57.78; RD 12 more per 1000, 95% CI 0 fewer to 110 more; low-certainty evidence), minor bleeding (RR 0.69, 95% CI 0.38 to 1.26; RD 15 fewer per 1000, 95% CI 30 fewer to 13 more; low-certainty evidence), premature catheter removal (RR 0.82, 95% CI 0.30 to 2.24; RD 29 fewer per 1000, 95% CI 114 fewer to 202 more; low-certainty evidence), and catheter-related infection (RR 1.17, 95% CI 0.74 to 1.85; RD 71 more per 1000, 95% CI 109 fewer to 356; low-certainty evidence). LMWH versus VKAThree RCTs (641 participants) compared LMWH to VKA in adults. The available evidence did not confirm or exclude a beneficial or detri ental effect of LMWH relative to VKA on mortality (RR 0.94, 95% CI 0.56 to 1.59; RD 6 fewer per 1000, 95% CI 41 fewer to 56 more; low-certainty evidence), symptomatic catheter-related VTE (RR 1.83, 95% CI 0.44 to 7.61; RD 15 more per 1000, 95% CI 10 fewer to 122 more; very low-certainty evidence), PE (RR 1.70, 95% CI 0.74 to 3.92; RD 35 more per 1000, 95% CI 13 fewer to 144 more; low-certainty evidence), major bleeding (RR 3.11, 95% CI 0.13 to 73.11; RD 2 more per 1000, 95% CI 1 fewer to 72 more; very low-certainty evidence), or minor bleeding (RR 0.95, 95% CI 0.20 to 4.61; RD 1 fewer per 1000, 95% CI 21 fewer to 95 more; very low-certainty evidence). The meta-analyses showed that LMWH probably increased the risk of thrombocytopenia compared to VKA at three months of follow-up (RR 1.69, 95% CI 1.20 to 2.39; RD 149 more per 1000, 95% CI 43 fewer to 300 more; moderate-certainty evidence). Authors' conclusions: The evidence was not conclusive for the effect of LMWH on mortality, the effect of VKA on mortality and catheter-related VTE, and the effect of LMWH compared to VKA on mortality and catheter-related VTE. We found moderate-certainty evidence that LMWH reduces catheter-related VTE compared to no LMWH. People with cancer with CVCs considering anticoagulation should balance the possible benefit of reduced thromboembolic complications with the possible harms and burden of anticoagulants. © 2018 The Cochrane Collaboration.
dc.identifier.doihttps://doi.org/10.1002/14651858.CD006468.pub6
dc.identifier.eid2-s2.0-85047930218
dc.identifier.pmid29856471
dc.identifier.urihttp://hdl.handle.net/10938/29980
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.ispartofCochrane Database of Systematic Reviews
dc.sourceScopus
dc.subjectAdult
dc.subjectAnticoagulants
dc.subjectCatheter-related infections
dc.subjectCatheterization, central venous
dc.subjectChild
dc.subjectHeparin
dc.subjectHeparin, low-molecular-weight
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectRandomized controlled trials as topic
dc.subjectSecondary prevention
dc.subjectThrombocytopenia
dc.subjectVenous thrombosis
dc.subjectVitamin k
dc.subjectAnticoagulant agent
dc.subjectAntivitamin k
dc.subjectFondaparinux
dc.subjectLow molecular weight heparin
dc.subjectVitamin k group
dc.subjectAll cause mortality
dc.subjectAnticoagulation
dc.subjectBleeding
dc.subjectCancer staging
dc.subjectCatheter infection
dc.subjectCatheter removal
dc.subjectCatheter thrombosis
dc.subjectClinical effectiveness
dc.subjectClinical evaluation
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectHuman
dc.subjectLung embolism
dc.subjectMalignant neoplasm
dc.subjectMeta analysis
dc.subjectOutcome assessment
dc.subjectPriority journal
dc.subjectQuality of life
dc.subjectRandomized controlled trial (topic)
dc.subjectReview
dc.subjectRisk assessment
dc.subjectSystematic review
dc.subjectThrombosis prevention
dc.subjectTreatment planning
dc.subjectVenous thromboembolism
dc.subjectAntagonists and inhibitors
dc.subjectCentral venous catheterization
dc.subjectChemically induced
dc.subjectMortality
dc.subjectNeoplasm
dc.subjectProcedures
dc.subjectVein thrombosis
dc.titleAnticoagulation for people with cancer and central venous catheters
dc.typeReview

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