Cochrane · systematic review · CD000985

Infusion techniques for peripheral arterial thrombolysis

Broderick, C, Patel, JV · Cochrane Database of Systematic Reviews · 2021 · Cochrane Library

VascularAMSTAR 2: not assessed
SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
28
current version
GRADE rated
25
No studies
0
Included studies
NR
No studies 0 · 0%Ungraded 3 · 10.7%Very low 20 · 71.4%Low 5 · 17.9%Moderate 0 · 0%High 0 · 0%

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.

Questions and results

Intra‐arterial delivery compared to intravenous delivery for peripheral arterial thrombolysis

Population: patients with < 30 days' limb ischaemiaa
7 questions
OutcomeEffectEvidenceStatus / GRADE
30‐Day amputation‐free survival
Intra‐arterial delivery vs intravenous delivery
OR 1.71 [0.4, 7.34]1 study · 40 participantsVery low
Downgraded: risk of bias, imprecision, inconsistency
Amputation (up to 6 months)
Intra‐arterial delivery vs intravenous delivery
no estimate extracted2 studies · 78 participantsLow
Downgraded: risk of bias, imprecision, inconsistency
30‐Day mortality
Intra‐arterial delivery vs intravenous delivery
no estimate extracted2 studies · 78 participantsLow
Downgraded: risk of bias, imprecision, inconsistency
Vessel patency ‐ radiological success ‐ complete (to end of treatment)
Intra‐arterial delivery vs intravenous delivery
OR 13.22 [2.79, 62.67]1 study · 40 participantsLow
Downgraded: risk of bias, imprecision, inconsistency
Duration of thrombolysis (to end of treatment)
Intra‐arterial delivery vs intravenous delivery
no estimate extracted2 studies · 78 participantsVery low
Downgraded: risk of bias, imprecision, inconsistency
CVA (up to 6 months)
Intra‐arterial delivery vs intravenous delivery
no estimate extracted2 studies · 78 participantsVery low
Downgraded: risk of bias, imprecision, inconsistency
Major bleeding (up to 6 months)
Intra‐arterial delivery vs intravenous delivery
OR 0.12 [0.01, 2.53]1 study · 40 participantsVery low
Downgraded: risk of bias, imprecision, inconsistency

High‐dose compared to low‐dose regimens of thrombolytic agents

Population: patients with < 42 days' limb ischaemiaa
7 questions
OutcomeEffectEvidenceStatus / GRADE
30‐Day amputation‐free survival
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Amputation (
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
30‐Day mortality
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Vessel patency (at end of treatment)
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Duration of thrombolysis (to end of treatment)
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
CVA (
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Major bleeding (
High‐dose vs low‐dose regimens of thrombolytic agents
no estimate extracted4 studies · 302 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness

Continuous infusion compared to forced (or pulse) infusion of thrombolytic agents

Population: patients with less than 42 days' lower limb ischaemiaa
7 questions
OutcomeEffectEvidenceStatus / GRADE
30‐Day amputation‐free survival
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted4 studies · 304 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Amputation (
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted3 studies · 164 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
30‐Day mortality
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted4 studies · 304 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Vessel patency (up to 30 days)
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted4 studies · 304 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Duration of thrombolysis (to end of treatment)
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted4 studies · 304 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
CVA (
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted4 studies · 304 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness
Major bleeding (
Continuous infusion vs forced (or pulse) infusion of thrombolytic agents
no estimate extracted4 studies · 304 participantsVery low
Downgraded: risk of bias, inconsistency, indirectness

Thrombolysis with or without adjunctive antiplatelet agents

Population: patients with less than 42 days' lower limb ischaemia
7 questions
OutcomeEffectEvidenceStatus / GRADE
30‐Day amputation‐free survival
no estimate extracted1 study · 70 participantsUngraded
Amputation (
no estimate extracted1 study · 70 participantsUngraded
30‐Day mortality
no estimate extracted1 study · 70 participantsUngraded
Vessel patency (
OR 1.2 [0.39, 3.69]1 study · 70 participantsVery low
Downgraded: risk of bias, imprecision, indirectness
Duration of thrombolysis (
no estimate extracted1 study · 70 participantsLow
Downgraded: risk of bias, imprecision
CVA (
no estimate extracted1 study · 70 participantsLow
Downgraded: risk of bias, imprecision
Major bleeding (
OR 0.25 [0.01, 4.9]1 study · 70 participantsVery low
Downgraded: risk of bias, imprecision, inconsistency