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Search review questions
Each row is one question a systematic review asked: who, what, compared with what, and which outcome, with the effect it found and how certain that is. Words match anywhere in the field.
1,558 questions in 115 reviews · Vascular
current versionsNo studies 346 · 22.2%Ungraded 90 · 5.8%Very low 281 · 18%Low 477 · 30.6%Moderate 313 · 20.1%High 51 · 3.3%
Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.
| Question | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Low‐molecular‐weight heparin vs active control (3) Clinically relevant bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Ultra‐low‐molecular‐weight heparin vs placebo Symptomatic VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.36 [0.22, 0.6] | 1 study · 3212 participants | High |
Ultra‐low‐molecular‐weight heparin vs placebo Major bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.05 [0.55, 2] | 1 study · 3172 participants | Moderate |
Ultra‐low‐molecular‐weight heparin vs placebo Symptomatic PE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.48 [0.22, 1.01] | 1 study · 3212 participants | Moderate |
Ultra‐low‐molecular‐weight heparin vs placebo Symptomatic DVT · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.32 [0.16, 0.63] | 1 study · 3212 participants | High |
DOAC vs placebo Symptomatic DVT · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.51 [0.21, 1.22] | 3 studies · 1526 participants | Low |
Ultra‐low‐molecular‐weight heparin vs placebo Any VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.36 [0.22, 0.6] | 1 study · 3212 participants | High |
Ultra‐low‐molecular‐weight heparin vs placebo 1‐year overall mortality · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.02 [0.96, 1.08] | 1 study · 3212 participants | Moderate |
Ultra‐low‐molecular‐weight heparin vs placebo Clinically relevant bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.4 [0.9, 2.19] | 1 study · 3172 participants | Moderate |
Unfractionated heparin vs no thromboprophylaxis Symptomatic VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Unfractionated heparin vs no thromboprophylaxis Major bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Unfractionated heparin vs no thromboprophylaxis Symptomatic PE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Unfractionated heparin vs no thromboprophylaxis Symptomatic DVT · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Unfractionated heparin vs no thromboprophylaxis Any VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Unfractionated heparin vs no thromboprophylaxis 1‐year overall mortality · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.86 [0.72, 1.03] | 1 study · 277 participants | Moderate |
Unfractionated heparin vs no thromboprophylaxis Clinically relevant bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 2.01 [0.18, 21.96] | 1 study · 277 participants | Low |
DOAC vs placebo Any VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.55 [0.34, 0.9] | 2 studies · 1404 participants | Moderate |
Vitamin K antagonists vs placebo or no thromboprophylaxis Symptomatic VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.15 [0.02, 1.2] | 1 study · 311 participants | Low |
Vitamin K antagonists vs placebo or no thromboprophylaxis Major bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 3.82 [0.97, 15.04] | 4 studies · 994 participants | Low |
Vitamin K antagonists vs placebo or no thromboprophylaxis Symptomatic PE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.05 [0.07, 16.58] | 1 study · 311 participants | Very low |
Vitamin K antagonists vs placebo or no thromboprophylaxis Symptomatic DVT · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.08 [0, 1.42] | 1 study · 311 participants | Low |
Vitamin K antagonists vs placebo or no thromboprophylaxis Any VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Vitamin K antagonists vs placebo or no thromboprophylaxis 1‐year overall mortality · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Vitamin K antagonists vs placebo or no thromboprophylaxis Clinically relevant bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Vitamin K antagonists vs active control Symptomatic VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.5 [0.74, 3.04] | 1 study · 440 participants | Moderate |
Vitamin K antagonists vs active control Major bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.14 [0.01, 2.75] | 1 study · 440 participants | Low |
Vitamin K antagonists vs active control Symptomatic PE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1 [0.25, 3.95] | 1 study · 440 participants | Moderate |
DOAC vs placebo 1‐year overall mortality · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | 0 studies · 0 participants | Ungraded |
Vitamin K antagonists vs active control Symptomatic DVT · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.75 [0.75, 4.09] | 1 study · 440 participants | Moderate |
Vitamin K antagonists vs active control Any VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Vitamin K antagonists vs active control 1‐year overall mortality · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Vitamin K antagonists vs active control Clinically relevant bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Antithrombin vs no thromboprophylaxis Symptomatic VTE · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Antithrombin vs no thromboprophylaxis Major bleeding · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.78 [0.03, 18.57] | 1 study · 85 participants | Very low |
Antithrombin vs no thromboprophylaxis Symptomatic PE · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Antithrombin vs no thromboprophylaxis Symptomatic DVT · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Antithrombin vs no thromboprophylaxis Any VTE · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.84 [0.41, 1.73] | 1 study · 85 participants | Very low |
Antithrombin vs no thromboprophylaxis 1‐year overall mortality · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
DOAC vs placebo Clinically relevant bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.61 [0.82, 3.15] | 2 studies · 931 participants | Moderate |
Antithrombin vs no thromboprophylaxis Clinically relevant bleeding · ambulatory paediatric cancer patients newly diagnosed with acute lymphoblastic leukaemia who received chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | no estimate extracted | NR | No studies |
Low‐molecular‐weight heparin vs no thromboprophylaxis Symptomatic VTE · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 0.62 [0.46, 0.83] | 11 studies · 3931 participants | High |
Low‐molecular‐weight heparin vs no thromboprophylaxis Major bleeding · ambulatory cancer patients receiving chemotherapy Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy (2020) · Cochrane | RR 1.63 [1.12, 2.35] | 15 studies · 7282 participants | Moderate |
Alternative modes of exercise vs walking exercise Maximum walking distance (12 weeks) · patients with IC Modes of exercise training for intermittent claudication (2020) · Cochrane | no estimate extracted | 6 studies · 274 participants | Low |
Alternative modes of exercise vs walking exercise Maximum walking distance (at end of training, ranging from 6 to 24 weeks) · patients with IC Modes of exercise training for intermittent claudication (2020) · Cochrane | no estimate extracted | 9 studies · 412 participants | Low |
Alternative modes of exercise vs walking exercise Pain‐free walking distance (12 weeks) · patients with IC Modes of exercise training for intermittent claudication (2020) · Cochrane | no estimate extracted | 5 studies · 249 participants | Low |
Alternative modes of exercise vs walking exercise Pain‐free walking distance (at end of training, ranging from 6 to 24 weeks) · patients with IC Modes of exercise training for intermittent claudication (2020) · Cochrane | no estimate extracted | 8 studies · 382 participants | Low |
Alternative modes of exercise vs walking exercise Health‐related QoL (at end of training, ranging from 12 to 24 weeks) · patients with IC Modes of exercise training for intermittent claudication (2020) · Cochrane | no estimate extracted | NR | No studies |
Alternative modes of exercise vs walking exercise Self‐reported functional impairment (WIQ) (at end of training, ranging from 12 to 24 weeks) · patients with IC Modes of exercise training for intermittent claudication (2020) · Cochrane | no estimate extracted | 2 studies · 96 participants | Low |
Low molecular weight heparin vs unfractionated heparin Success rate of replantation1 (analysed by participant, · patients undergoing digital replantation after traumatic amputation Low molecular weight heparin for prevention of microvascular occlusion in digital replantation (2020) · Cochrane | RR 0.98 [0.87, 1.1] | 2 studies · 130 participants | Very low |
Low molecular weight heparin (LMWH) vs no LMWH Incidence of compromised microcirculation requiring invasive intervention (re‐exploration) (analysed by digit, · patients undergoing digital replantation after traumatic amputation Low molecular weight heparin for prevention of microvascular occlusion in digital replantation (2020) · Cochrane | RR 0.86 [0.21, 3.58] | 1 study · 73 participants | Very low |