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암환자의 수술중 혈전증강하제 항응고

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배경

암에 걸린 사람들에게 적절한 수술 주기의 혈전증(trombopropylaxis)의 선택은 다른 항응고제의 상대적 이점과 해악에 달려 있다.

목적

암에 걸린 사람의 수술 주기에 대한 항응고제의 상대적 효능과 안전성에 대한 증거를 체계적으로 검토한다.

검색 전략

이번 체계적 검토의 업데이트는 2018년 6월 14일 코크란 중앙 통제 재판 등록부(Central, 2018, Essue 6), MEDLINE(Ovid), 엠바세(Ovid)의 주요 전자 검색, 회의 절차의 손 검색, 관련 참고문헌의 확인 등을 포함한 종합적인 문헌 검색 결과에 근거한 것이다.ed studies, 진행 중인 연구 검색, PubMed의 '관련 인용' 기능 사용.

선정 기준

수술적 개입을 받고 있는 암환자를 등록하고 저분자량 헤파린(LMWH)이 불연속 헤파린(UFH) 또는 폰다파린룩스에 미치는 영향, 사망률, 깊은 정맥혈전증(DVT), 폐색전증(PE), 출혈 결과, 혈소판감소증에 대한 영향을 평가한 RCT.

자료 수집 및 분석

표준화된 양식을 사용하여 연구 설계, 참가자, 관심의 결과, 편향 위험 등에 대한 데이터를 중복 추출했다. 관심의 결과는 모든 원인 사망률, PE, 증상 정맥 혈전증(VTE), 무증상 DVT, 주요 출혈, 경미한 출혈, 후두혈증후군, 건강 관련 삶의 질, 혈소판감소증 등을 포함했다. GRADE 접근법 ( GRADE Handbook )을 사용하여 각 결과에 대한 증거의 확실성을 평가했습니다.

주요 결과

확인된 7670개의 고유 인용문 중, 수술 전 예방적 항응고 작용을 받는 암이 있는 무작위적인 9771명의 RCT 20개를 포함했다. 우리는 이 업데이트에 대한 7개의 새로운 RCT에 대한 7개의 보고서를 확인했다.

메타분석에서는 사망률(RR) 0.82, 95% 신뢰구간(CI) 0.63~1.07, 1000명당 위험차(RD) 9개 감소, 95% CI 19~4개 이상, 중간정확성 근거 PE(0R)와 비교하여 LMWH의 유익하거나 유해한 영향을 결정적으로 배제하지 않았다. 1000당 감소, 95% CI 5 ~ 3 이상, 중간‐확률 근거), 증상 DVT(RR 0.67, 95% CI 0.27 ~ 1.69, 1000당 RD 3 감소, 95% CI 7 ~ 7 이상, 중간‐확률 근거), 무증상 DVT(RR 0.86, 95% CI 0.71 ~ 1.05; RD) 0.69 ~ 1.48, RD 0 1000 당 감소, 95% CI 10 ~ 15 더 적음, 중간‐확률 증거, 경미한 출혈(RR 1.01, 95% CI 0.76 ~ 1.33), RD 1 1000 당 증가, 95% CI 34 ~ 47 더 적음, 중간‐확률 증거), 출혈 재수술(RRR 0.93, 95% CI 0.57 ~ 150)), 수술 후 수혈(평균 차이(MD) ‐35.36 mL, 95% CI ‐253.19 ~ 182.47, 저확률 증거), 수술 후 수혈(MD 190.03 mL, 95% CI ‐23.65 ~ 403.72, 저확률 증거), 혈전소판증(RRR 3.07, 95% CI 032). LMWH는 상처 혈종 발생률이 낮은 것과 관련이 있었다(RR 0.70, 95% CI 0.54~0.92, RD 26 1000명당 감소, 95% CI 39~7명 감소, 중간확률 증거). 메타 분석 결과, 수술 중 출혈 결과(MD ‐6.75 mL, 95% CI ‐85.49 ~ 71.99, 중간‐확률 근거) 및 수술 후 배수량(MD 30.18 mL, 95% CI ‐36.26 ~ 96.62; 중간‐확률 근거)이 추가적으로 나타났다.

또한 메타 분석은 VTE(DVT 또는 PE, 또는 둘 다), RR 2.51, 95% CI 0.89~7.03, RD 57, 1000당 95% CI 4~228개, 낮은 확률에 대한 폰다파린룩스와 비교하여 LMWH의 유익하거나 유해한 영향을 결정적으로 배제하지 않았다.r 1000당, 95% CI 16 ~ 7개 더 적음, 저확률 증거, 경미한 출혈(RR 0.83, 95% CI 0.34 ~ 2.05, RD 8fewer per 1000, 95% CI 33 ~ 52개 더 적음, 저확률 증거), 혈소판감소증(RRR 0.35, 95% CI 0.04 ~ 3.30, RD 14 1000명 더 적음) 1000명당 더 많은, 95% CI 1에서 78명 더 적음, 저확률 증거) 및 수술 후 배수량(MD ‐20.00 mL, 95% CI ‐114.34 ~ 74.34, 저확률 증거)

연구진 결론

우리는 사망률, 혈전증 결과, 주요 출혈 또는 암에 걸린 사람들의 경미한 출혈에 대한 효과에서 폰다파린룩스와 비교했을 때 LMWH에 대한 수술중 혈전증 대 UFH 및 LMWH의 혈전증 간 차이를 발견하지 못했다. UFH에 비해 LMWH로 상처입은 혈종 발생률이 낮았다.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

수술을 받는 암 환자의 혈액 응고 예방을 위한 혈액 희석제

배경
암 수술을 받고 있는 사람들은 혈전의 위험이 높아진다. 이러한 응고를 예방하기 위해 투여되는 혈액 희석제(항응고제)는 정맥에 정맥에 주입되지 않은 헤파린(UFH), 피하피부(피부 아래)를 하루에 한두 번 주입한 저분자 헤파린(LMWH), 폰다파린룩스 등이다. 이러한 혈액 희석제는 서로 다른 효과와 안전 프로파일을 가질 수 있다.

연구 특징
혈액 희석제가 죽음에 미치는 영향, 폐색전증(폐색전증), 심맥혈전증(다리의 정맥 혈전), 타박상, 출혈, 암 수술을 받은 사람의 수혈 필요성 등을 살펴보는 임상실험을 위해 과학 데이터베이스를 조사했다. 우리는 암 치료의 종류와 상관없이 고형종양이나 혈액암을 가진 모든 연령의 성인들과 어린이들의 실험을 포함했다. 증거는 2018년 6월 14일까지이다.

주요 결과
우리는 9771명의 암환자를 포함한 20개의 연구를 발견했다. 그 증거는 LMWH와 UFH가 사망, 혈전, 출혈에 미치는 영향의 차이를 확인하지 않았다. LMWH로 작업한 후 상처 주변은 UFH에 비해 타박상이 적었다. 폰다파리눅스는 혈전을 맞을 위험을 줄였을지도 모른다.

근거의 신뢰성
증거의 신뢰성은 관심 결과에 따라 낮은 수준에서 중간 수준으로 다양했다.

Authors' conclusions

Implications for practice

Given the lack of clear evidence of superiority of one medicine over the other as a result of this imprecision, clinicians should base their choice on cost and patient preferences using an individualized decision‐making process. The American College of Chest Physicians (ACCP) 9th iteration of the antithrombotic guidelines does not recommend using either of the two anticoagulants of interest over the other in people with cancer undergoing surgical interventions (Gould 2012).

Implications for research

Despite the large number of participants enrolled in these trials, there is still some lack of precision for several critical outcomes. This is partly because several trials assessed surrogate outcome (asymptomatic deep venous thrombosis (DVT)) instead of patient‐important outcomes such as DVT and pulmonary embolism. Researchers can use these results to plan additional randomized controlled trials to either exclude or confirm a superiority of one of the two drugs over the other on patient‐important outcomes.

Summary of findings

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Summary of findings for the main comparison. LMWH prophylaxis compared to UFH prophylaxis in people with cancer without VTE undergoing a surgery

LMWH prophylaxis compared to UFH prophylaxis in people with cancer without VTE undergoing a surgery

Patient or population: People with cancer with perioperative thromboprophylaxis
Settings: Inpatient
Intervention: LMWH
Comparison: UFH

Outcomes

№ of participants
(studies)
Follow up

Certainty of the evidence
(GRADE)

Relative effect
(95% CI)

Anticipated absolute effects* (95% CI)

Risk with UFH prophylaxis

Risk difference with LMWH prophylaxis

Mortality
follow up: range 1 weeks to 3 months

4260
(8 RCTs)

⊕⊕⊕⊝
MODERATE 1

RR 0.82
(0.63 to 1.07)

Study population

51 per 1000

9 fewer per 1000
(19 fewer to 4 more)

Any PE
follow up: range 1 weeks to 3 months

5588
(14 RCTs)

⊕⊕⊕⊝
MODERATE 2

RR 0.49
(0.17 to 1.47)

Study population

6 per 1000

3 fewer per 1000
(5 fewer to 3 more)

Symptomatic DVT
follow up: range 1 weeks to 3 months

2250
(8 RCTs)

⊕⊕⊕⊝
MODERATE 3

RR 0.67
(0.27 to 1.69)

Study population

10 per 1000

3 fewer per 1000
(7 fewer to 7 more)

Symptomatic DVT measured as asymptomatic DVT
follow up: range 1 weeks to 3 months

4938
(12 RCTs)

⊕⊕⊝⊝
LOW 4 5

RR 0.86
(0.71 to 1.05)

Study population

79 per 1000

11 fewer per 1000
(23 fewer to 4 more)

Major bleeding
follow up: range 1 weeks to 3 months

3473
(9 RCTs)

⊕⊕⊕⊝
MODERATE 6

RR 1.01
(0.69 to 1.48)

Study population

31 per 1000

0 fewer per 1000
(10 fewer to 15 more)

Minor bleeding
follow up: range 1 weeks to 3 months

1194
(2 RCTs)

⊕⊕⊕⊝
MODERATE 7

RR 1.01
(0.76 to 1.33)

Study population

142 per 1000

1 more per 1000
(34 fewer to 47 more)

Wound hematoma
follow up: range 1 weeks to 3 months

2827
(6 RCTs)

⊕⊕⊕⊝
MODERATE 8 9

RR 0.70
(0.54 to 0.92)

Study population

86 per 1000

26 fewer per 1000
(39 fewer to 7 fewer)

Reoperation for bleeding
follow up: range 1 weeks to 3 months

1246
(4 RCTs)

⊕⊕⊕⊝
MODERATE 10

RR 0.93
(0.57 to 1.50)

Study population

51 per 1000

4 fewer per 1000
(22 fewer to 26 more)

Intraoperative transfusion
follow up: range 1 weeks to 3 months

737
(2 RCTs)

⊕⊕⊝⊝
LOW 11 12

MD 35.36 lower
(253.19 lower to 182.47 higher)

Postoperative transfusion
follow up: range 1 weeks to 3 months

734
(2 RCTs)

⊕⊕⊝⊝
LOW 13 14

MD 190.03 higher
(23.65 lower to 403.72 higher)

Intraoperative blood loss
follow up: range 1 weeks to 3 months

761
(4 RCTs)

⊕⊕⊕⊝
MODERATE 15

MD 6.75 lower
(85.49 lower to 71.99 higher)

Postoperative drain volume
follow up: range 1 weeks to 3 months

1459
(3 RCTs)

⊕⊕⊕⊝
MODERATE 16

MD 30.18 higher
(36.26 lower to 96.62 higher)

Thrombocytopenia
follow up: range 1 weeks to 3 months

683
(2 RCTs)

⊕⊕⊕⊝
MODERATE 17

RR 3.07
(0.32 to 29.33)

Study population

3 per 1000

6 more per 1000
(2 fewer to 82 more)

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio; OR: Odds ratio;

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (19 fewer per 1000 absolute reduction) and possibility of no effect (4 more per 1000 absolute increase), including 197 events in total.

2 Downgraded due to serious imprecision. Low event rate, 26 events in total

3 Downgraded due to serious imprecision. Low event rate, 18 events in total

4 Downgraded by one level due to serious inconsistency, outcome measured as surrogate outcome

5 Downgraded due to serious imprecision. 95% CI is consistent with the possibility of important benefit (23 fewer more per 1000 absolute reduction) and possibility of harm (4 more per 1000 increase), including 367 events in total.

6 Downgraded due to serious imprecision. 95% CI is consistent with the possibility of important benefit (10 fewer more per 1000 absolute reduction) and possibility of harm (15 more per 1000 increase), including 107 events in total.

7 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (34 fewer per 1000 absolute reduction) and possibility of no effect (47 more per 1000 absolute increase), including 170 events in total.

8 Downgraded due to serious risk of bias; allocation concealment was not clear in 5 out of 6 studies.

9 Downgraded due to serious imprecision. Low event rate, 206 events in total

10 Downgraded due to serious imprecision. 95% CI is consistent with the possibility of benefit (22 fewer per 1000 absolute reduction) and possibility of important harm (26 more per 1000 absolute increase), including 61 events in total.

11 Downgraded due to serious inconsistency. I2= 98%; Dahan 1990 included patients undergoing thoracic surgery for cancer whereas Koppenhagen 1992 included patients undergoing major elective abdominal surgery

12 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (253.19 mL less) and possibility of harm (182.47 mL more)

13 Downgraded due to serious inconsistency. I2 = 83%; Dahan 1990 included patients undergoing thoracic surgery for cancer whereas Koppenhagen 1992 included patients undergoing major elective abdominal surgery

14 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (23.65mL less) and possibility of harm (40.3.72mL more)

15 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (85.49 mL less) and possibility of harm (71.99 mL more)

16 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (36.26 mL less) and possibility of harm (96.62 mL more)

17 Downgraded due to serious imprecision. Low event rate, 4 events in total

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Summary of findings 2. LMWH prophylaxis compared to fondaparinux prophylaxis in people with cancer without VTE undergoing a surgical procedure

LMWH prophylaxis compared to fondaparinux prophylaxis in people with cancer without VTE undergoing a surgical procedure

Patient or population: People with perioperative thromboprophylaxis in people with cancer
Settings: Inpatient
Intervention: LMWH
Comparison: Fondaparinux

Outcomes

№ of participants
(studies)
Follow up

Certainty of the evidence
(GRADE)

Relative effect
(95% CI)

Anticipated absolute effects* (95% CI)

Risk with Fondaparinux prophylaxis

Risk difference with LMWH prophylaxis

Mortality ‐ not reported

Any VTE
follow up: 3 months

1806
(3 RCTs)

⊕⊕⊝⊝
LOW 1 2

RR 2.51
(0.89 to 7.03)

Study population

38 per 1000

57 more per 1000
(4 fewer to 228 more)

Major Bleeding
follow up: 3 months

2339
(3 RCTs)

⊕⊕⊝⊝
LOW 2 4

RR 0.74
(0.45 to 1.23)

Study population

29 per 1000

8 fewer per 1000
(16 fewer to 7 more)

Minor Bleeding

398
(2 RCTs)

⊕⊕⊝⊝
LOW 5 6

RR 0.83
(0.34 to 2.05)

Study population

49 per 1000

8 fewer per 1000
(33 fewer to 52 more)

Thrombocytopenia

282
(1 RCT)

⊕⊕⊝⊝
LOW 7 8

RR 0.35
(0.04 to 3.30)

Study population

21 per 1000

14 fewer per 1000
(20 fewer to 48 more)

Any Pulmonary embolism

116
(1 RCT)

⊕⊕⊝⊝
LOW 9

RR 3.10
(0.13 to 74.64)

Study population

0 per 1000

0 fewer per 1000
(0 fewer to 0 fewer)

Low

1 per 1000

2 more per 1000
(1 fewer to 74 more)

Postoperative drain volume

116
(1 RCT)

⊕⊕⊝⊝
LOW 10

The mean postoperative drain volume was 0 ml

MD 20 ml lower
(114.34 lower to 74.34 higher)

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio; OR: Odds ratio;

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded by one level for concerns about both imprecision and indirectness. 95% CI is consistent with the possibility for benefit (4 per 1000 absolute reduction) and possibility of important harm (22 per 1000 absolute increase), including 99 events in total. VTE events included both symptomatic and asymptomatic events for patients with cancer which introduces some level of indirectness.

2 Downgraded by one level due to high risk of bias (lack of allocation concealment and incomplete outcome data in Agnelli 2005; lack of blinding of patients and personnel and incomplete outcome data in Hata 2016 unclear allocation concealment in song 2018)

3 Although the event rate used from the fondaprinux arm includes asymptomatic events, it is very close to rate of symptomatic VTE (3.1%) found in a retrospective cohort Changolkar 2014

4 Downgraded for serious imprecision. 95% CI is consistent with the possibility for important benefit (16 per 1000 absolute reduction) and possibility of important harm (7 per 1000 absolute increase), including 60 events in total.

5 Downgraded for high risk of bias (lack of blinding of patients and personnel and incomplete outcome data in Hata 2016 and unclear allocation concealment in Song 2018)

6 Downgraded for serious imprecision. 95% CI is consistent with the possibility for important benefit (33 per 1000 absolute reduction) and possibility of important harm (52 per 1000 absolute increase), including 18 events in total.

7 Downgraded for high risk of bias (lack of blinding of patients and personnel and incomplete outcome data in Hata 2016)

8 Downgraded for serious imprecision. 95% CI is consistent with the possibility for important benefit (20 per 1000 absolute reduction) and possibility of important harm (48 per 1000 absolute increase), including 4 events in total.

9 Downgraded by two levels for very serious imprecision. 95% CI is consistent with the possibility for important benefit (1 per 1000 absolute reduction) and possibility of important harm (78 per 1000 absolute increase), including 1 event in total.

10 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (114.34 mL less) and possibility of harm (74.34 mL more)

Background

Description of the condition

People with cancer undergoing surgical procedures have a higher risk of venous thromboembolism (VTE) (deep venous thrombosis (DVT) or pulmonary embolism (PE), or both) than people without cancer (Gallus 1997; Kakkar 1970; Rahr 1992). It is estimated that cancer triples the risk of postoperative DVT (Edmonds 2004). Moreover, people with cancer and VTE have an increased risk of dying than people with VTE alone or with cancer alone (Levitan 1999; Sorensen 2000). It has been suggested that thromboprophylaxis might be less effective in people with cancer due to the prothrombotic state associated with malignancy (Flordal 1996; Gallus 1997).

Description of the intervention

Unfractionated heparin (UFH), and low‐molecular weight heparins (LMWH) do not have intrinsic anticoagulant activity but potentiate the activity of antithrombin III in inhibiting activated coagulation factors. These agents constitute indirect anticoagulants as their activity is mediated by plasma cofactors. Heparin and its low molecular weight derivatives are not absorbed orally and must be administered parenterally (Hirsh 1993). Both UFH and LMWH, in addition to fondaparinux, have been used for perioperative thromboprophylaxis in people with cancer undergoing surgery.

How the intervention might work

Through their anticoagulant effect, UFH and LMWH reduce the incidence of both DVT and PE and subsequently reduce the incidence of VTE‐associated mortality (Barritt 1960). At the same time, they increase the risk of bleeding that might be potentiated by the presence of surgical wounds.

Why it is important to do this review

Two systematic reviews found that heparins were superior to no anticoagulation in the prevention of DVT and PE in people undergoing colorectal (Borly 2005) or general surgery (Mismetti 2001). Mismetti 2001 found that among general surgery people, LMWH and UFH had similar efficacy and safety irrespective of cancer status. However, the authors did not provide the estimates of the relative effects of the two medications in people with cancer. The last update of this Cochrane systematic review (16 trials enrolling 12,890 participants) found no any significant differences in the relative benefits and harms of the two medications (Akl 2014).

Objectives

To systematically review the evidence for the relative efficacy and safety of anticoagulants for perioperative thromboprophylaxis in people with cancer.

Methods

Criteria for considering studies for this review

Types of studies

Randomized controlled trials (RCTs).

Types of participants

People with cancer planned to undergo a surgical intervention. People could have been of any age with either solid or hematologic cancer and at any stage of their cancer irrespective of the type of cancer therapy.

We included studies with subgroups of people with cancer that did not report subgroup specific data when people with cancer constituted 50% or more of the total population. Otherwise, we excluded them from the systematic review.

Types of interventions

Experimental arms: any anticoagulant.

  • Low‐molecular weight heparin (LMWH)

  • Unfractionated heparin (UFH)

  • Fondaparinux

We were interested in comparisons of any combination of the three management options listed above. We excluded studies that compared different types of LMWH or any anticoagulant to placebo. The protocol should have planned to provide all other co interventions (e.g. chemotherapy) similarly in the intervention and comparison group.

Types of outcome measures

Primary outcomes

  • All‐cause mortality.

Secondary outcomes

  • Pulmonary embolism (PE). PE events had to be suspected clinically, and diagnosed using an objective diagnostic test such as: pulmonary perfusion/ventilation scans, computed tomography, pulmonary angiography, or autopsy.

  • Symptomatic deep venous thrombosis (DVT). DVT events had to be suspected clinically, and diagnosed using an objective diagnostic test such as: venography, 125I‐fibrinogen‐uptake test, impedance plethysmography, or compression ultrasound.

  • Asymptomatic DVT. DVT detected by screening and diagnosed using an objective diagnostic test such as: venography, 125I‐fibrinogen‐uptake test, impedance plethysmography, or compression ultrasound.

  • Bleeding outcomes:

    • major bleeding: we accepted the authors' definitions of major bleeding

    • minor bleeding: we accepted the authors' definitions of minor bleeding

    • wound hematoma

    • reoperation for bleeding

    • transfusion (intraoperative, postoperative)

    • intraoperative blood loss

    • postoperative drain volume

  • Thrombocytopenia.

  • Health related quality of life.

Search methods for identification of studies

Electronic searches

The search was part of a comprehensive search for studies of anticoagulation in participants with cancer. We conducted comprehensive searches on 14 June 2018, following the original electronic searched in January 2007, February 2010, February 2013, and February 2016. We electronically searched the following databases: the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 6), MEDLINE Ovid (starting 1946), and Embase Ovid (starting 1980). For each database, the search strategies combined terms for anticoagulants, terms for cancer, and a search filter for RCTs. We used no language restrictions. We listed the full search strategies for each of the electronic databases in Appendix 1; Appendix 2; and Appendix 3.

Searching other resources

We handsearched the conference proceedings of the American Society of Clinical Oncology (ASCO, starting with its first volume, 1982 up to June 2018) and of the American Society of Hematology (ASH, starting with its 2003 issue up to June 2018). We also searched ClinicalTrials.gov and World Health Organization International Clinical Trials Registry Platform for ongoing studies. We reviewed the reference lists of papers included in this review and of other relevant systematic reviews. We used the 'related citation' feature in PubMed to identify additional articles and 'citation tracking' of included studies in Web of Science Core Collection. In addition, we contacted experts in the field to check for unpublished and ongoing trials.

Data collection and analysis

Selection of studies

Two review authors (CFM and LAK) independently screened the title and abstract of identified citations for potential eligibility. We retrieved the full text of articles judged potentially eligible by at least one review author. Two review authors then independently screened the full‐text articles for eligibility using a standardized form with explicit inclusion and exclusion criteria (as detailed in the Criteria for considering studies for this review section). The two review authors resolved any disagreements about which articles were eligible by discussion or by consulting a third review author (EAA).

Data extraction and management

Two review authors (CFM and IGT) independently extracted data from each included study and resolved their disagreements by discussion. We aimed to collect data related to participants, interventions, outcomes, and others.

Participants

  • Number of people in each treatment arm

  • Number of people randomized to each treatment arm

  • Number of people followed up in each treatment arm

  • Number of withdrawals from treatment in each treatment arm

  • Demographic characteristics (e.g. age, sex)

  • Cancer characteristics (e.g. type, location, site of origin, stage, time since diagnosis, estimated life expectancy, current cancer treatments, performance status)

  • Description of the surgical procedure

  • History of VTE

  • Use of indwelling central venous catheters (CVC)

Interventions

  • Type of anticoagulant: LMWH, UFH, or fondaparinux

  • Dose: prophylactic versus therapeutic

  • Duration of treatment

  • Cointerventions including radiation therapy, chemotherapy, and hormonal therapy (type and duration)

Outcomes

We attempted to extract both time‐to‐event data (for all‐cause mortality) and categorical data (for all outcomes). However, none of the studies reported time‐to‐event data for people with cancer. For dichotomous data, we extracted data necessary to conduct a complete‐case analysis as the primary analysis. For continuous data, we extracted mean and standard deviation (SD) separately for each arm.

We attempted to contact study authors for incompletely reported data. We determined a priori to consider abstracts in the main analysis only if study authors supplied us with full reports of their methods and results.

Other

We extracted from each included trial any information on the following points:

  • source of funding

  • ethical approval

  • conflict of interest

  • intention‐to‐treat (ITT) analysis

Assessment of risk of bias in included studies

We assessed risk of bias at the trial level using Cochrane's 'Risk of bias' tool (Higgins 2011). Two review authors (CFM and LAK) independently assessed the risk of bias for each included trial and resolved any disagreements by discussion. 'Risk of bias' criteria included:

  • random sequence generation

  • allocation concealment

  • blinding of participants and personnel

  • blinding of outcome assessment

  • incomplete outcome data (percentage of follow‐up and whether this was addressed)

  • selective reporting

  • other bias (whether the trial was stopped early for benefit)

See Dealing with missing data section about assessing risk of bias associated with participants with missing data.

Measures of treatment effect

We collected and analyzed risk ratios (RRs) for categorical data, and mean differences (MD) for continuous data, with 95% confidence intervals (CI).

Unit of analysis issues

The unit of analysis was the individual participant.

Dealing with missing data

Determining participants with missing data

It was not clear whether certain participant categories (e.g. those described as "withdrew consent" or "experienced adverse events") were actually followed up by the trial authors (versus had missing participant data) (Akl 2016). To deal with this issue, we made the following considerations:

  • "ineligible participants," "did not receive the first dose" participant categories, which were defined prior to the initiation of the study intervention, most likely had missing participant data;

  • "withdrew consent," "lost to follow‐up" (LTFU), and "outcome not assessable" participant categories and other category explicitly reported as not being followed up, which were defined after the initiation of the study intervention, most likely had missing participant data;

  • "dead," "experienced adverse events," "noncompliant," and "discontinued prematurely" (and similarly described) participant categories, less likely have had missing participant data

Dealing with participants with missing data in the primary meta‐analysis

In the primary meta‐analysis, we used a complete‐case analysis approach, that is, we excluded participants considered to have missing data (Guyatt 2017).

For categorical data, we used the following calculations for each study arm:

  • denominator: (number of participants randomized) – (number of participants most likely with missing data, both pre‐ and postintervention initiation);

  • numerator: number of participants with observed events (i.e. participants who had at least one event for the outcome of interest during their available follow‐up time).

For continuous data, we planned to use the reported mean and SD for each study arm for participants actually followed up by the trial authors.

Assessing the risk of bias associated with participants with missing data

When the primary meta‐analysis of a specific outcome found a statistically significant effect, we conducted sensitivity meta‐analyses to assess the risk of bias associated with missing participant data. Those sensitivity meta‐analyses used a priori plausible assumptions about the outcomes of participants considered to have missing data. The assumptions we used in the sensitivity meta‐analyses were increasingly stringent in order to challenge the statistical significance of the results of the primary analysis progressively (Akl 2013; Ebrahim 2013).

For categorical data, and for RR showing a reduction in effect (RR less than 1), we used the following increasingly stringent but plausible assumptions (Akl 2013):

  • for the control arm, relative incidence (RI) among participants with missing data (LTFU) compared with participants with available data (FU) in the same arm (RILTFU/FU) = 1; for the intervention arm, RILTFU/FU = 1.5;

  • for the control arm, RILTFU/FU = 1; for the intervention arm, RILTFU/FU = 2;

  • for the control arm, RILTFU/FU = 1; for the intervention arm, RILTFU/FU = 3;

  • for the control arm, RILTFU/FU = 1; for the intervention arm, RILTFU/FU = 5.

For RR showing an increase in effect (RR greater than 1), we switched the above assumptions between the control and interventions arms (i.e. used RILTFU/FU = 1 for the intervention arm).

Specifically, we used the following calculations for each study arm:

  • denominator: (number of participants randomized) – (number of participants most likely with missing data, preintervention initiation);

  • numerator: (number of participants with observed events) + (number of participants most likely with missing data postintervention initiation, with assumed events).

Assumed events were calculated by applying the a priori plausible assumptions to the participants considered most likely with missing data postintervention initiation.

For continuous data, we planned to use the four strategies suggested by Ebrahim and colleagues (Ebrahim 2013). The strategies imputed the means for participants with missing data based on the means of participants actually followed up in individual trials included in the systematic review. To impute SD, we used the median SD from the control arms of all included trials (Ebrahim 2013).

Assessment of heterogeneity

We assessed heterogeneity among trials by visual inspection of forest plots, estimation of the percentage heterogeneity among trials that could not be ascribed to sampling variation (I2 test) (Higgins 2003), and by a formal statistical test of the significance of the heterogeneity (Deeks 2001). If there was evidence of substantial heterogeneity, we investigated and reported the possible reasons for this (see Subgroup analysis and investigation of heterogeneity section).

Assessment of reporting biases

We assessed for selective outcome reporting by trying to identify whether the study was included in a trial registry, whether a protocol was available, and whether the methods section provided a list of outcomes. We compared the list of outcomes from those sources to the outcomes reported in the published paper. Also, we created funnel plots to assess publication.

Data synthesis

For dichotomous data, we calculated the RR separately for each study (DerSimonian 1986; RevMan 2014), and for continuous data, we calculated the MD separately for each trial. When analyzing data related to participants who were reported as not compliant, we attempted to adhere to the principles of ITT analysis. We approached the issue of non‐compliance independently from that of missing data (Alshurafa 2012). We then pooled the results of the different studies using a random‐effects model.

'Summary of findings' tables

We created 'Summary of findings' tables and assessed the certainty of evidence for all outcomes using the GRADE approach (GRADE Handbook).

Subgroup analysis and investigation of heterogeneity

We planned to explore substantial heterogeneity by conducting subgroup analyses based on the characteristics of participants (type, severity, and stage of cancer, and whether people were on cancer treatment or not). We did not conduct any subgroup analyses because of the relatively small number of trials and the inclusion of different types of cancer in the same trial.

Sensitivity analysis

Unlike the 2014 update of this review, we included studies published as abstracts only in the sensitivity analysis. When the primary meta‐analysis of a specific outcome found a statistically significant effect, we conducted sensitivity meta‐analyses to assess the risk of bias associated with missing participant data.

Results

Description of studies

Results of the search

Figure 1 shows the study flow diagram. As of June 2018, the search strategy identified 7670 unique citations after removal of duplicates. In total, the title and abstract screening identified 167 citations as potentially eligible for this review. The full‐text screening of the 167 citations identified 32 full reports for 20 eligible RCTs (Agnelli 2005; Baykal 2001; Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Dahan 1990; Encke 1988 (EFS); Fricker 1988; Gallus 1993; Goldhaber 2002; Hata 2016; Kakkar 1997; Kakkar 2005; Koppenhagen 1992; Onarheim 1986; Song 2018; Von Tempelhoff 1997; Von Tempelhoff 2000; Ward 1998), and one RCT published as an abstract (Godwin 1993). We excluded the remaining 135 full texts. One eligible study did not provide outcome data that could be included in the meta‐analysis so we summarized its results narratively (Kakkar 2005). We identified seven reports for six RCTs not included in previous version of this review. We identified one ongoing study (Safi 2011).


Study flow diagram. CVC: central venous catheter; LMWH: low‐molecular weight heparin; RCT: randomized controlled trial; UFH: unfractionated heparin; VTE: venous thromboembolism.

Study flow diagram. CVC: central venous catheter; LMWH: low‐molecular weight heparin; RCT: randomized controlled trial; UFH: unfractionated heparin; VTE: venous thromboembolism.

Included studies

We included 20 RCTs in this review (Agnelli 2005; Baykal 2001; Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Dahan 1990; Encke 1988 (EFS); Fricker 1988; Gallus 1993; Godwin 1993; Goldhaber 2002; Hata 2016; Kakkar 1997; Kakkar 2005; Koppenhagen 1992; Onarheim 1986; Song 2018; Von Tempelhoff 1997; Von Tempelhoff 2000; Ward 1998). One of these trials was published as an abstract (Godwin 1993). See Characteristics of included studies table.

Participant characteristics

Trials were conducted in people with cancer undergoing the following types of surgery: gynecologic (four trials; Baykal 2001; Von Tempelhoff 1997; Von Tempelhoff 2000; Ward 1998), abdominal or pelvic (eight trials; Agnelli 2005; Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Encke 1988 (EFS); Fricker 1988; Godwin 1993; Koppenhagen 1992; Onarheim 1986), thoracic (one trial; Dahan 1990), abdominal or thoracic (two trials; Gallus 1993; Song 2018), prostate (one trial; Boncinelli 2001), neurosurgery (one trial; Goldhaber 2002), urologic (one trial: Hata 2016), and unspecified (two trials; Kakkar 1997; Kakkar 2005). Mean age of participants varied from 46 to 71 years across included trials.

Interventions

Types of LMWH studied were: enoxaparin (four trials; Baykal 2001; Bergqvist 1997 (ENOXACAN); Goldhaber 2002; Hata 2016); dalteparin (five trials; Agnelli 2005; Bergqvist 1990; Fricker 1988; Onarheim 1986; Ward 1998); nadroparin (four trials; Boncinelli 2001; Dahan 1990; Encke 1988 (EFS); Song 2018); orgaran (one trial; Gallus 1993); normiflo (one trial; Godwin 1993); certoparin (two trials; Kakkar 2005; Von Tempelhoff 2000); clivarine (one trial; Kakkar 1997); and not specified (two trials; Koppenhagen 1992; Von Tempelhoff 1997). All trials started thromboprophylaxis preoperatively.

Outcomes
Comparison 1: low‐molecular weight heparin versus unfractionated heparin

Comparison 2: low‐molecular weight heparin versus fondaparinux

Excluded studies

We excluded 135 reports of 80 trials from this review for the following reasons: not population of interest, hospitalized people (11 studies); not population of interest, ambulatory people (27 studies); not population of interest, people with CVC (seven studies); not population of interest, people with VTE (19 studies): not comparison of interest, preoperative versus postoperative anticoagulation (two studies); not comparison of interest, mechanical versus pharmacologic (12 studies); not comparison of interest, different dosages of LMWH (one study); not comparison of interest, different dosages of UFH (two studies); not comparison of interest, UFH versus placebo (four studies); not comparison of interest, LMWH versus placebo (six studies); not comparison of interest, different types of LMWH (two studies); not comparison of interest, defibrotide versus UFH (one study); not comparison of interest, defibrotide versus placebo (one study); not comparison of interest, extended versus limited duration of anticoagulation (25 studies); not design of interest, a systematic review (one study); no outcomes of interest (two studies), and no outcome data available for cancer people (12 studies). See Characteristics of excluded studies table.

Risk of bias in included studies

Figure 2 presents the 'Risk of bias' graph while Figure 3 presents the 'Risk of bias' summary associated with the outcomes: mortality, PE, DVT, and major bleeding.


Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.

Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.


Risk of bias summary: review authors' judgments about each risk of bias item for each included study.

Risk of bias summary: review authors' judgments about each risk of bias item for each included study.

Allocation

The method of sequence generation was unclear in five studies (Dahan 1990; Fricker 1988; Godwin 1993; Kakkar 1997; Von Tempelhoff 1997), but adequate in the remaining one.

Allocation was adequately concealed in five trials (Baykal 2001; Gallus 1993; Hata 2016; Von Tempelhoff 2000; Ward 1998). It was unclear whether it was adequately concealed in the remaining 14 trials.

Blinding

Blinding of participants and personnel (performance bias)

We judged participants and personnel to be definitely blinded in 12 studies (Agnelli 2005; Baykal 2001; Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Goldhaber 2002; Kakkar 1997; Kakkar 2005; Koppenhagen 1992; Onarheim 1986; Song 2018; Von Tempelhoff 1997; Von Tempelhoff 2000), and definitely not blinded in the remaining eight studies.

Blinding of outcome assessment (detection bias)

We judged outcome assessors to be definitely blinded in all 20 studies.

Incomplete outcome data

Follow‐up was satisfactory in all the trials with the following percentages: 72% in Agnelli 2005; 100% in Baykal 2001; 100% in Bergqvist 1990; 56% in Bergqvist 1997 (ENOXACAN); 100% in Boncinelli 2001; 100% in Dahan 1990; 100% in Encke 1988 (EFS); 100% in Fricker 1988; 95% in Gallus 1993; 100% in Godwin 1993; 96% in Goldhaber 2002; 94% in Hata 2016; 99% in Kakkar 1997; 100% in Kakkar 2005; 97% in Koppenhagen 1992; 100% in Onarheim 1986; 100% in Song 2018; 100% in Von Tempelhoff 1997; 100% in Von Tempelhoff 2000; and 97% in Ward 1998.

We judged incomplete outcome data to be with low risk of bias in 10 studies (Baykal 2001; Bergqvist 1990; Boncinelli 2001; Dahan 1990; Fricker 1988; Godwin 1993; Onarheim 1986; Song 2018; Von Tempelhoff 1997; Von Tempelhoff 2000); high risk in seven studies (Agnelli 2005; Bergqvist 1997 (ENOXACAN); Goldhaber 2002; Hata 2016; Kakkar 1997; Koppenhagen 1992; Ward 1998); and unclear risk of bias in the remaining studies.

Selective reporting

The outcomes listed in the methods section were reported in the results section for all trials. Von Tempelhoff 2000 appeared to have collected data on VTE outcomes but did not report them, so was at high risk of bias. It was unclear whether Dahan 1990 had any reporting bias.

Other potential sources of bias

The only trial that was stopped early was Kakkar 2005. We judged the associated risk of bias to be high because the reason to stop was that the study would not be sufficiently powered to show superiority of certoparin over UFH.

Effects of interventions

See: Summary of findings for the main comparison LMWH prophylaxis compared to UFH prophylaxis in people with cancer without VTE undergoing a surgery; Summary of findings 2 LMWH prophylaxis compared to fondaparinux prophylaxis in people with cancer without VTE undergoing a surgical procedure

Comparison 1: low‐molecular weight heparin versus unfractionated heparin

Fourteen trials reported LMWH versus UFH (Baykal 2001; Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Dahan 1990; Encke 1988 (EFS); Fricker 1988; Gallus 1993; Goldhaber 2002; Kakkar 1997; Koppenhagen 1992; Onarheim 1986; Von Tempelhoff 1997; Ward 1998).

All‐cause mortality

Meta‐analysis of eight trials reporting data on 4260 participants did not conclusively rule out a mortality reduction with LMWH compared with UFH (RR 0.82, 95% CI 0.63 to 1.07; RD 9 fewer per 1000, 95% CI 19 fewer to 4 more; Analysis 1.1); the percentage of the variability in effect estimates that was due to heterogeneity between studies rather than sampling error (chance) was not important (I2 = 0%; ) (Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Gallus 1993; Goldhaber 2002; Kakkar 1997; Koppenhagen 1992; Onarheim 1986; Von Tempelhoff 2000). Kakkar 2005 found no difference in outcomes between the two treatment regimens. The inverted funnel plot for the primary outcome of mortality did not suggest publication bias, but there were relatively few trials to permit an accurate assessment ().

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Pulmonary embolism

Meta‐analysis of 14 trials reporting data on 5588 participants did not conclusively rule out a reduction or increase in PE with LMWH compared with UFH (RR 0.49, 95% CI 0.17 to 1.47; RD 3 fewer per 1000, 95% CI 5 fewer to 3 more; I2 = 0%; Analysis 1.2) (Baykal 2001; Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Dahan 1990; Encke 1988 (EFS); Fricker 1988; Gallus 1993; Goldhaber 2002; Kakkar 1997; Koppenhagen 1992; Onarheim 1986; Von Tempelhoff 1997; Ward 1998). These results did not change in a meta‐analysis including the study published as an abstract (RR 0.52, 95% CI 0.20 to 1.34; ) (Godwin 1993). The inverted funnel plot for PE did not suggest publication bias, but there were relatively few trials to permit an accurate assessment.

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Symptomatic deep venous thrombosis

Meta‐analysis of eight trials reporting data on 2250 participants did not conclusively rule out a symptomatic DVT reduction or increase with LMWH compared with UFH (RR 0.67, 95% CI 0.27 to 1.69; RD 3 fewer per 1000, 95% CI 7 fewer to 7 more; I2 = 0%; Analysis 1.3) (Baykal 2001; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Fricker 1988; Goldhaber 2002; Koppenhagen 1992; Onarheim 1986; Ward 1998).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Asymptomatic deep venous thrombosis

Meta‐analysis of 12 trials reporting data on 4938 participants did not conclusively rule out a reduction in asymptomatic DVT with LMWH compared with UFH (RR 0.86, 95% CI 0.71 to 1.05; RD 11 fewer per 1000, 95% CI 23 fewer to 4 more; I2 = 0%;Analysis 1.4) (Bergqvist 1990; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Dahan 1990; Encke 1988 (EFS); Fricker 1988; Gallus 1993; Goldhaber 2002; Kakkar 1997; Koppenhagen 1992; Onarheim 1986; Von Tempelhoff 1997). These results did not substantively change in a meta‐analysis including the study published as an abstract (RR 0.87, 95% CI 0.70 to 1.07) (Godwin 1993). The inverted funnel plot for asymptomatic DVT did not suggest publication bias, but there were relatively few trials to permit an accurate assessment (Figure 10).

The certainty of evidence was low (summary of findings Table for the main comparison).

Bleeding outcomes
Major bleeding

Meta‐analysis of nine trials reporting data on 3473 participants did not conclusively rule out a reduction or increase in major bleeding with LMWH compared with UFH (RR 1.01, 95% CI 0.69 to 1.48; RD 0 fewer per 1000, 95% CI 10 fewer to 15 more; I2 = 0%; Analysis 1.5) (Baykal 2001; Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Dahan 1990; Fricker 1988; Gallus 1993; Goldhaber 2002; Kakkar 1997; Onarheim 1986). The inverted funnel plot for major bleeding did not suggest publication bias, but there were relatively few trials to permit an accurate assessment.

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Minor bleeding

Meta‐analysis of two trials reporting data on 1194 participants did not conclusively rule out a reduction or increase in minor bleeding with LMWH compared with UFH (RR 1.01, 95% CI 0.76 to 1.33; RD 1 more per 1000, 95% CI 34 fewer to 47 more; I2 = 0%; Analysis 1.6) (Bergqvist 1997 (ENOXACAN); Fricker 1988).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Wound hematoma

Meta‐analysis of six trials assessing 2827 participants found a reduction in wound hematomas with LMWH compared with UFH (RR 0.70, 95% CI 0.54 to 0.92; RD 26 fewer per 1000, 95% CI 39 fewer to 7 fewer; I2 = 0%; Analysis 1.7) (Baykal 2001; Bergqvist 1990; Boncinelli 2001; Kakkar 1997; Koppenhagen 1992; Onarheim 1986).

Since the primary meta‐analysis found a statistically significant effect, and to assess the risk of bias associated with missing participant data, we conducted sensitivity meta‐analyses used the priori plausible assumptions detailed in the Methods section. The effect estimate remained statistically significant even when using the most stringent plausible assumption (RR 0.73, 95% CI 0.56 to 0.95).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Reoperation for bleeding

Meta‐analysis of four trials reporting data on 1246 participants did not conclusively rule out a reduction or increase in re operations for bleeding with LMWH compared with UFH (RR 0.93, 95% CI 0.57 to 1.50; RD 4 fewer per 1000, 95% CI 22 fewer to 26 more; I2 = 0%; Analysis 1.8) (Bergqvist 1997 (ENOXACAN); Boncinelli 2001; Gallus 1993; Onarheim 1986).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Transfusion: intraoperative

Two trials reporting data on 737 participants found no difference in intraoperative transfusion volume with LMWH compared with UFH (MD ‐35.36 mL, 95% CI ‐253.19 to 182.47; Analysis 1.9) (Dahan 1990; Koppenhagen 1992).

The certainty of evidence was low (summary of findings Table for the main comparison).

Transfusion: postoperative

Two trials assessing 734 participants found no difference in postoperative transfusions with LMWH compared with UFH (MD 190.03 mL, 95% CI ‐23.65 to 403.72; Analysis 1.10) (Dahan 1990; Koppenhagen 1992).

The certainty of evidence was low (summary of findings Table for the main comparison).

Intraoperative blood loss

Meta‐analysis of four trials reporting data on 761 participants found no difference in intraoperative blood loss with LMWH compared with UFH (MD ‐6.75 mL, 95% CI to ‐85.49 to 71.99; Analysis 1.11) (Baykal 2001; Dahan 1990; Gallus 1993; Onarheim 1986).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Postoperative drain volume

Meta‐analysis of three trials reporting data on 1459 participants found no difference in postoperative drain volume with LMWH compared with UFH (MD 30.18 mL, 95% CI ‐36.26 to 96.62; Analysis 1.12) (Baykal 2001; Encke 1988 (EFS); Koppenhagen 1992).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Thrombocytopenia

Meta‐analysis of two trials reporting data on 683 participants did not conclusively rule out a thrombocytopenia reduction or increase with LMWH compared to UFH (RR 3.07, 95% CI 0.32 to 29.33; RD 6 more per 1000, 95% CI 2 fewer to 82 more; Analysis 1.13) (Bergqvist 1997 (ENOXACAN); Onarheim 1986). The RR was reduced substantively in a meta‐analysis including the study published as an abstract (Godwin 1993) (RR 1.20, 95% CI 0.41 to 3.50).

The certainty of evidence was moderate (summary of findings Table for the main comparison).

Heparin‐induced thrombocytopenia

We found no trials reporting the relative effects of LMWH and UFH on heparin‐induced thrombocytopenia (HIT).

Health related quality of life

We found no trials reporting the relative effects of LMWH and UFH on health related quality of life.

Comparison 2: low‐molecular weight heparin versus fondaparinux

Three trials compared LMWH versus fondaparinux (Agnelli 2005; Hata 2016; Song 2018).

All‐cause mortality

Neither trial reported all‐cause mortality.

Any pulmonary embolism

The one study reporting data on 116 participants did not rule out an increase or decrease risk of any PE with LMWH compared with fondaparinux (RR 3.13, 95% CI 0.13 to 74.64; RD 2 more per 1000, 95% CI 1 fewer to 78 more; Analysis 2.1) (Song 2018).

The certainty of evidence was low (summary of findings Table 2).

Symptomatic and asymptomatic deep venous thrombosis
Venous thromboembolism

Meta‐analysis of three trials reporting data on 1806 participants did not rule out an increase or decrease risk in VTE with LMWH compared with fondaparinux (RR 2.51, 95% CI 0.89 to 7.03; RD 57 more per 1000, 95% CI 4 fewer to 228 more; Analysis 2.2); I2 = 31%) (Agnelli 2005; Hata 2016; Song 2018).

The certainty of evidence was low (summary of findings Table 2).

Bleeding outcomes
Major bleeding

Meta‐analysis of three trials reporting data on 2339 participants did not rule out an increase or decrease in major bleeding with LMWH compared with fondaparinux (RR 0.74, 95% CI 0.45 to 1.23; RD 8 fewer per 1000, 95% CI 16 fewer to 7 more; I2 = 0%; Analysis 2.3) (Agnelli 2005; Hata 2016; Song 2018).

The certainty of evidence was low (summary of findings Table 2).

Minor bleeding

Meta‐analysis of two trials reporting data on 398 participants did not rule out an increase or decrease in minor bleeding with LMWH compared with fondaparinux (RR 0.83, 95% CI 0.34 to 2.05; RD 8 fewer per 1000, 95% CI 33 fewer to 52 more;;Analysis 2.4; ) (Hata 2016; Song 2018).

The certainty of evidence was low (summary of findings Table 2).

Wound hematoma

Neither trial reported wound hematoma.

Reoperation for bleeding

Neither trial reported reoperation for bleeding.

Transfusion: intraoperative

Neither trial reported intraoperative transfusion.

Transfusion: postoperative

Neither trial reported postoperative transfusion.

Intraoperative blood loss

Neither trial reported intraoperative blood loss.

Postoperative drain volume

The one study reporting data on 116 participants found no difference in postoperative drain volume with LMWH compared with fondaparinux (MD ‐20 mL, 95% CI ‐114.34 to 74.34; Analysis 2.5) (Song 2018).

The certainty of evidence was low (summary of findings Table 2).

Thrombocytopenia

The one study reporting data on 282 participants did not rule out an increase or decrease in thrombocytopenia with LMWH compared with fondaparinux (RR 0.35, 95% CI 0.04 to 3.30; RD 14 fewer per 1000, 95% CI 20 fewer to 48 more; Analysis 2.6) (Hata 2016).

The certainty of evidence was low (summary of findings Table 2).

Health related quality of life

We found no trials reporting the relative effects of LMWH an fondaparinux on health related quality of life.

Discussion

Summary of main results

We did not conclusively rule out either beneficial or harmful effects of LMWH compared with UFH; and LMWH compared with fondaparinux for the outcomes of mortality, symptomatic DVT, PE, minor bleeding, and major bleeding. There was a lower incidence of wound hematoma with LMWH compared to UFH; None of the trials reported on HIT. The certainty of evidence per outcome ranged from low to moderate.

Overall completeness and applicability of evidence

While the absence of a statistically significant difference might reflect a true absence of effect of LMWH on some VTE outcomes, this could also be related to insufficient power to detect important differences between drugs. Another potential explanation is the relatively low baseline risks for the different outcomes (e.g. the baseline risk for PE was 0.6%).

These trials recruited people with variety of cancer types and stages, which should increase the applicability of the results.

All included trials started anticoagulant treatment preoperatively. Consequently, it is not certain how the results apply to anticoagulant treatment started postoperatively. However, one systematic review found no statistically significant differences in blood loss when the first dose of enoxaparin was administered 12 hours before surgery versus postoperatively (Einstein 2007).

Quality of the evidence

For the comparison of LMWH versus UFH, we judged the certainty of evidence as moderate for mortality, PE, symptomatic DVT, asymptomatic DVT, minor bleeding, major bleeding, wound hematoma, reoperation for bleeding, intraoperative blood loss, postoperative drain volume, and thrombocytopenia, and as low for intraoperative transfusion and postoperative transfusion. The certainty of evidence per outcome ranged from low to moderate.

For the comparison of LMWH versus fondaparinux, we judged the certainty of evidence as low for all outcomes.

Screening participants for DVT may have biased the results of 13 included trials (Agnelli 2005; Bergqvist 1990; Bergqvist 1997 (ENOXACAN);Dahan 1990; Encke 1988 (EFS); Fricker 1988; Gallus 1993; Godwin 1993; Goldhaber 2002; Kakkar 1997; Koppenhagen 1992; Onarheim 1986; Song 2018). If screening detects thromboses, participants are typically therapeutically anticoagulated. Some of the participants with asymptomatic events may have developed symptomatic VTE, had screening testing not been undertaken and anticoagulant therapy not been administered. As a result, the number of symptomatic VTE events in this review, and the differential effect of LMWH versus UFH on symptomatic events, may have been underestimated.

Potential biases in the review process

Our systematic approach to searching, study selection, and data extraction should have minimized the likelihood of missing relevant trials. We excluded 12 trials that included participants with cancer as subgroups but did not report on their outcome data. The cancer subgroups in these trials included 3185 participants compared with 9771 randomized participants included in the current analysis. This may have introduced bias.

The relatively small number of trials and the inclusion of different types of malignancies, different types of surgical procedures, different dosing of anticoagulant medications, and different follow‐up periods in the same trials precluded us from conducting the subgroup analyses to explore effect modifiers.

Agreements and disagreements with other studies or reviews

One systematic review of thromboprophylaxis in colorectal surgery reported no differences between LMWH and UFH in their effects on preventing DVT or PE, or both (odds ratio (OR) 1.01, 95% CI 0.67 to 1.52) (Borly 2005). One systematic review compared the effects of UFH and LMWH thromboprophylaxis on thrombocytopenia and HIT (Martel 2005). Most of the included trials were in orthopedic surgery and only two trials prospectively examined HIT and reported 10 events (all in the UFH group). The meta‐analysis found an OR of 0.10 (95% CI 0.01 to 0.82) for HIT and 0.47 (95% CI 0.22 to 1.02) for thrombocytopenia, favoring LMWH. Another meta‐analysis comparing therapeutic doses of UFH and LMWH reported no differential effect on HIT (RR 1.33, 95% CI 0.77 to 2.30) (Morris 2007). One other systematic review comparing the effects of UFH and LMWH thromboprophylaxis reported no difference in minor complications, major complications, or the discontinuation of prophylaxis (Leonardi 2007).

Study flow diagram. CVC: central venous catheter; LMWH: low‐molecular weight heparin; RCT: randomized controlled trial; UFH: unfractionated heparin; VTE: venous thromboembolism.
Figures and Tables -
Figure 1

Study flow diagram. CVC: central venous catheter; LMWH: low‐molecular weight heparin; RCT: randomized controlled trial; UFH: unfractionated heparin; VTE: venous thromboembolism.

Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.
Figures and Tables -
Figure 2

Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgments about each risk of bias item for each included study.
Figures and Tables -
Figure 3

Risk of bias summary: review authors' judgments about each risk of bias item for each included study.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 1 All‐cause mortality.
Figures and Tables -
Analysis 1.1

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 1 All‐cause mortality.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 2 Pulmonary embolism (PE).
Figures and Tables -
Analysis 1.2

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 2 Pulmonary embolism (PE).

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 3 Symptomatic deep venous thrombosis (DVT).
Figures and Tables -
Analysis 1.3

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 3 Symptomatic deep venous thrombosis (DVT).

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 4 Asymptomatic DVT.
Figures and Tables -
Analysis 1.4

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 4 Asymptomatic DVT.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 5 Major bleeding.
Figures and Tables -
Analysis 1.5

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 5 Major bleeding.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 6 Minor bleeding.
Figures and Tables -
Analysis 1.6

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 6 Minor bleeding.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 7 Wound hematoma.
Figures and Tables -
Analysis 1.7

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 7 Wound hematoma.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 8 Reoperation for bleeding.
Figures and Tables -
Analysis 1.8

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 8 Reoperation for bleeding.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 9 Intraoperative transfusion.
Figures and Tables -
Analysis 1.9

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 9 Intraoperative transfusion.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 10 Postoperative transfusion.
Figures and Tables -
Analysis 1.10

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 10 Postoperative transfusion.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 11 Intraoperative blood loss.
Figures and Tables -
Analysis 1.11

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 11 Intraoperative blood loss.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 12 Postoperative drain volume.
Figures and Tables -
Analysis 1.12

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 12 Postoperative drain volume.

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 13 Thrombocytopenia.
Figures and Tables -
Analysis 1.13

Comparison 1 Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH), Outcome 13 Thrombocytopenia.

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 1 Any pulmonary embolism.
Figures and Tables -
Analysis 2.1

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 1 Any pulmonary embolism.

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 2 Any venous thromboembolism (VTE).
Figures and Tables -
Analysis 2.2

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 2 Any venous thromboembolism (VTE).

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 3 Major Bleeding.
Figures and Tables -
Analysis 2.3

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 3 Major Bleeding.

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 4 Minor Bleeding.
Figures and Tables -
Analysis 2.4

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 4 Minor Bleeding.

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 5 Postoperative drain volume.
Figures and Tables -
Analysis 2.5

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 5 Postoperative drain volume.

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 6 Thrombocytopenia.
Figures and Tables -
Analysis 2.6

Comparison 2 Low molecular weight heparin (LMWH) versus Fondaparinux, Outcome 6 Thrombocytopenia.

Summary of findings for the main comparison. LMWH prophylaxis compared to UFH prophylaxis in people with cancer without VTE undergoing a surgery

LMWH prophylaxis compared to UFH prophylaxis in people with cancer without VTE undergoing a surgery

Patient or population: People with cancer with perioperative thromboprophylaxis
Settings: Inpatient
Intervention: LMWH
Comparison: UFH

Outcomes

№ of participants
(studies)
Follow up

Certainty of the evidence
(GRADE)

Relative effect
(95% CI)

Anticipated absolute effects* (95% CI)

Risk with UFH prophylaxis

Risk difference with LMWH prophylaxis

Mortality
follow up: range 1 weeks to 3 months

4260
(8 RCTs)

⊕⊕⊕⊝
MODERATE 1

RR 0.82
(0.63 to 1.07)

Study population

51 per 1000

9 fewer per 1000
(19 fewer to 4 more)

Any PE
follow up: range 1 weeks to 3 months

5588
(14 RCTs)

⊕⊕⊕⊝
MODERATE 2

RR 0.49
(0.17 to 1.47)

Study population

6 per 1000

3 fewer per 1000
(5 fewer to 3 more)

Symptomatic DVT
follow up: range 1 weeks to 3 months

2250
(8 RCTs)

⊕⊕⊕⊝
MODERATE 3

RR 0.67
(0.27 to 1.69)

Study population

10 per 1000

3 fewer per 1000
(7 fewer to 7 more)

Symptomatic DVT measured as asymptomatic DVT
follow up: range 1 weeks to 3 months

4938
(12 RCTs)

⊕⊕⊝⊝
LOW 4 5

RR 0.86
(0.71 to 1.05)

Study population

79 per 1000

11 fewer per 1000
(23 fewer to 4 more)

Major bleeding
follow up: range 1 weeks to 3 months

3473
(9 RCTs)

⊕⊕⊕⊝
MODERATE 6

RR 1.01
(0.69 to 1.48)

Study population

31 per 1000

0 fewer per 1000
(10 fewer to 15 more)

Minor bleeding
follow up: range 1 weeks to 3 months

1194
(2 RCTs)

⊕⊕⊕⊝
MODERATE 7

RR 1.01
(0.76 to 1.33)

Study population

142 per 1000

1 more per 1000
(34 fewer to 47 more)

Wound hematoma
follow up: range 1 weeks to 3 months

2827
(6 RCTs)

⊕⊕⊕⊝
MODERATE 8 9

RR 0.70
(0.54 to 0.92)

Study population

86 per 1000

26 fewer per 1000
(39 fewer to 7 fewer)

Reoperation for bleeding
follow up: range 1 weeks to 3 months

1246
(4 RCTs)

⊕⊕⊕⊝
MODERATE 10

RR 0.93
(0.57 to 1.50)

Study population

51 per 1000

4 fewer per 1000
(22 fewer to 26 more)

Intraoperative transfusion
follow up: range 1 weeks to 3 months

737
(2 RCTs)

⊕⊕⊝⊝
LOW 11 12

MD 35.36 lower
(253.19 lower to 182.47 higher)

Postoperative transfusion
follow up: range 1 weeks to 3 months

734
(2 RCTs)

⊕⊕⊝⊝
LOW 13 14

MD 190.03 higher
(23.65 lower to 403.72 higher)

Intraoperative blood loss
follow up: range 1 weeks to 3 months

761
(4 RCTs)

⊕⊕⊕⊝
MODERATE 15

MD 6.75 lower
(85.49 lower to 71.99 higher)

Postoperative drain volume
follow up: range 1 weeks to 3 months

1459
(3 RCTs)

⊕⊕⊕⊝
MODERATE 16

MD 30.18 higher
(36.26 lower to 96.62 higher)

Thrombocytopenia
follow up: range 1 weeks to 3 months

683
(2 RCTs)

⊕⊕⊕⊝
MODERATE 17

RR 3.07
(0.32 to 29.33)

Study population

3 per 1000

6 more per 1000
(2 fewer to 82 more)

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio; OR: Odds ratio;

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (19 fewer per 1000 absolute reduction) and possibility of no effect (4 more per 1000 absolute increase), including 197 events in total.

2 Downgraded due to serious imprecision. Low event rate, 26 events in total

3 Downgraded due to serious imprecision. Low event rate, 18 events in total

4 Downgraded by one level due to serious inconsistency, outcome measured as surrogate outcome

5 Downgraded due to serious imprecision. 95% CI is consistent with the possibility of important benefit (23 fewer more per 1000 absolute reduction) and possibility of harm (4 more per 1000 increase), including 367 events in total.

6 Downgraded due to serious imprecision. 95% CI is consistent with the possibility of important benefit (10 fewer more per 1000 absolute reduction) and possibility of harm (15 more per 1000 increase), including 107 events in total.

7 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (34 fewer per 1000 absolute reduction) and possibility of no effect (47 more per 1000 absolute increase), including 170 events in total.

8 Downgraded due to serious risk of bias; allocation concealment was not clear in 5 out of 6 studies.

9 Downgraded due to serious imprecision. Low event rate, 206 events in total

10 Downgraded due to serious imprecision. 95% CI is consistent with the possibility of benefit (22 fewer per 1000 absolute reduction) and possibility of important harm (26 more per 1000 absolute increase), including 61 events in total.

11 Downgraded due to serious inconsistency. I2= 98%; Dahan 1990 included patients undergoing thoracic surgery for cancer whereas Koppenhagen 1992 included patients undergoing major elective abdominal surgery

12 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (253.19 mL less) and possibility of harm (182.47 mL more)

13 Downgraded due to serious inconsistency. I2 = 83%; Dahan 1990 included patients undergoing thoracic surgery for cancer whereas Koppenhagen 1992 included patients undergoing major elective abdominal surgery

14 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (23.65mL less) and possibility of harm (40.3.72mL more)

15 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (85.49 mL less) and possibility of harm (71.99 mL more)

16 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (36.26 mL less) and possibility of harm (96.62 mL more)

17 Downgraded due to serious imprecision. Low event rate, 4 events in total

Figures and Tables -
Summary of findings for the main comparison. LMWH prophylaxis compared to UFH prophylaxis in people with cancer without VTE undergoing a surgery
Summary of findings 2. LMWH prophylaxis compared to fondaparinux prophylaxis in people with cancer without VTE undergoing a surgical procedure

LMWH prophylaxis compared to fondaparinux prophylaxis in people with cancer without VTE undergoing a surgical procedure

Patient or population: People with perioperative thromboprophylaxis in people with cancer
Settings: Inpatient
Intervention: LMWH
Comparison: Fondaparinux

Outcomes

№ of participants
(studies)
Follow up

Certainty of the evidence
(GRADE)

Relative effect
(95% CI)

Anticipated absolute effects* (95% CI)

Risk with Fondaparinux prophylaxis

Risk difference with LMWH prophylaxis

Mortality ‐ not reported

Any VTE
follow up: 3 months

1806
(3 RCTs)

⊕⊕⊝⊝
LOW 1 2

RR 2.51
(0.89 to 7.03)

Study population

38 per 1000

57 more per 1000
(4 fewer to 228 more)

Major Bleeding
follow up: 3 months

2339
(3 RCTs)

⊕⊕⊝⊝
LOW 2 4

RR 0.74
(0.45 to 1.23)

Study population

29 per 1000

8 fewer per 1000
(16 fewer to 7 more)

Minor Bleeding

398
(2 RCTs)

⊕⊕⊝⊝
LOW 5 6

RR 0.83
(0.34 to 2.05)

Study population

49 per 1000

8 fewer per 1000
(33 fewer to 52 more)

Thrombocytopenia

282
(1 RCT)

⊕⊕⊝⊝
LOW 7 8

RR 0.35
(0.04 to 3.30)

Study population

21 per 1000

14 fewer per 1000
(20 fewer to 48 more)

Any Pulmonary embolism

116
(1 RCT)

⊕⊕⊝⊝
LOW 9

RR 3.10
(0.13 to 74.64)

Study population

0 per 1000

0 fewer per 1000
(0 fewer to 0 fewer)

Low

1 per 1000

2 more per 1000
(1 fewer to 74 more)

Postoperative drain volume

116
(1 RCT)

⊕⊕⊝⊝
LOW 10

The mean postoperative drain volume was 0 ml

MD 20 ml lower
(114.34 lower to 74.34 higher)

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio; OR: Odds ratio;

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded by one level for concerns about both imprecision and indirectness. 95% CI is consistent with the possibility for benefit (4 per 1000 absolute reduction) and possibility of important harm (22 per 1000 absolute increase), including 99 events in total. VTE events included both symptomatic and asymptomatic events for patients with cancer which introduces some level of indirectness.

2 Downgraded by one level due to high risk of bias (lack of allocation concealment and incomplete outcome data in Agnelli 2005; lack of blinding of patients and personnel and incomplete outcome data in Hata 2016 unclear allocation concealment in song 2018)

3 Although the event rate used from the fondaprinux arm includes asymptomatic events, it is very close to rate of symptomatic VTE (3.1%) found in a retrospective cohort Changolkar 2014

4 Downgraded for serious imprecision. 95% CI is consistent with the possibility for important benefit (16 per 1000 absolute reduction) and possibility of important harm (7 per 1000 absolute increase), including 60 events in total.

5 Downgraded for high risk of bias (lack of blinding of patients and personnel and incomplete outcome data in Hata 2016 and unclear allocation concealment in Song 2018)

6 Downgraded for serious imprecision. 95% CI is consistent with the possibility for important benefit (33 per 1000 absolute reduction) and possibility of important harm (52 per 1000 absolute increase), including 18 events in total.

7 Downgraded for high risk of bias (lack of blinding of patients and personnel and incomplete outcome data in Hata 2016)

8 Downgraded for serious imprecision. 95% CI is consistent with the possibility for important benefit (20 per 1000 absolute reduction) and possibility of important harm (48 per 1000 absolute increase), including 4 events in total.

9 Downgraded by two levels for very serious imprecision. 95% CI is consistent with the possibility for important benefit (1 per 1000 absolute reduction) and possibility of important harm (78 per 1000 absolute increase), including 1 event in total.

10 Downgraded due to serious imprecision. 95% CI is consistent with the possibility for important benefit (114.34 mL less) and possibility of harm (74.34 mL more)

Figures and Tables -
Summary of findings 2. LMWH prophylaxis compared to fondaparinux prophylaxis in people with cancer without VTE undergoing a surgical procedure
Comparison 1. Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 All‐cause mortality Show forest plot

8

4260

Risk Ratio (M‐H, Random, 95% CI)

0.82 [0.63, 1.07]

2 Pulmonary embolism (PE) Show forest plot

14

5588

Risk Ratio (M‐H, Random, 95% CI)

0.49 [0.17, 1.47]

3 Symptomatic deep venous thrombosis (DVT) Show forest plot

8

2250

Risk Ratio (M‐H, Random, 95% CI)

0.67 [0.27, 1.69]

4 Asymptomatic DVT Show forest plot

12

4938

Risk Ratio (M‐H, Random, 95% CI)

0.86 [0.71, 1.05]

5 Major bleeding Show forest plot

9

3473

Risk Ratio (M‐H, Random, 95% CI)

1.01 [0.69, 1.48]

6 Minor bleeding Show forest plot

2

1194

Risk Ratio (M‐H, Random, 95% CI)

1.01 [0.76, 1.33]

7 Wound hematoma Show forest plot

6

2827

Risk Ratio (M‐H, Random, 95% CI)

0.70 [0.54, 0.92]

8 Reoperation for bleeding Show forest plot

4

1246

Risk Ratio (M‐H, Random, 95% CI)

0.93 [0.57, 1.50]

9 Intraoperative transfusion Show forest plot

2

737

Mean Difference (IV, Random, 95% CI)

‐35.36 [‐253.19, 182.47]

10 Postoperative transfusion Show forest plot

2

734

Mean Difference (IV, Random, 95% CI)

190.03 [‐23.65, 403.72]

11 Intraoperative blood loss Show forest plot

4

761

Mean Difference (IV, Random, 95% CI)

‐6.75 [‐85.49, 71.99]

12 Postoperative drain volume Show forest plot

3

1459

Mean Difference (IV, Random, 95% CI)

30.18 [‐36.26, 96.62]

13 Thrombocytopenia Show forest plot

2

683

Risk Ratio (M‐H, Random, 95% CI)

3.07 [0.32, 29.33]

Figures and Tables -
Comparison 1. Low‐molecular weight heparin (LMWH) versus unfractionated heparin (UFH)
Comparison 2. Low molecular weight heparin (LMWH) versus Fondaparinux

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Any pulmonary embolism Show forest plot

1

116

Risk Ratio (M‐H, Random, 95% CI)

3.10 [0.13, 74.64]

2 Any venous thromboembolism (VTE) Show forest plot

3

1806

Risk Ratio (M‐H, Random, 95% CI)

2.51 [0.89, 7.03]

3 Major Bleeding Show forest plot

3

2339

Risk Ratio (M‐H, Random, 95% CI)

0.74 [0.45, 1.23]

4 Minor Bleeding Show forest plot

2

398

Risk Ratio (M‐H, Random, 95% CI)

0.83 [0.34, 2.05]

5 Postoperative drain volume Show forest plot

1

116

Mean Difference (IV, Random, 95% CI)

‐20.0 [‐114.34, 74.34]

6 Thrombocytopenia Show forest plot

1

282

Risk Ratio (M‐H, Random, 95% CI)

0.35 [0.04, 3.30]

Figures and Tables -
Comparison 2. Low molecular weight heparin (LMWH) versus Fondaparinux