section name header

Evidence summaries

Cryoplasty for Peripheral Vascular Disease

Cryoplasty might possibly not be more effective than conventional angioplasty in the treatment of peripheral vascular disease, but the evidence is insufficient. Level of evidence: "D"

A Cochrane review [Abstract] 1 included 7 studies (6 primary cryoplasty and one adjunctive cryoplasty study) with total of 478 subjects. Follow-up ranged from 30 days to 3 years. Target lesion patency measured at various time points in 2 primary cryoplasty studies showed no statistically significant difference between the treatment groups. The adjunctive cryoplasty study showed that cryoplasty was associated with improved patency only at 6 months (OR 5.37, 95% CI 1.09 to 26.49, 1 study, n = 90), not at other time points. Restenosis measured per patient (2 primary cryoplasty studies) showed no statistically significant difference between the treatments. Restenosis measured by lesion (2 primary cryoplasty trials) showed a statistically significant difference only within 24 hours of the procedure (OR 0.08, 95% CI 0.04 to 0.18, 1 study, n = 192) favouring cryoplasty.

Need for re-intervention was not significantly different in primary cryoplasty trial participants (per participant: OR 0.27, 95% CI 0.05 to 1.52; 2 studies, n = 241, I2 = 89%; per lesion: OR 0.59, 95% CI 0.06 to 5.69; 3 studies, n = 307, I2 = 94%). The adjunctive cryoplasty trial did not report on need for intervention. Immediate success of procedure (within 24 hours) was not significantly different in primary cryoplasty trial participants (per participant: OR 1.63, 95% CI 0.14 to 19.55; 3 studies, n=266, I2 = 95%; per lesion: OR 1.81, 95% CI 0.19 to 17.36, n = 307, I2 = 90%). The adjunctive cryoplasty trial reported 100% success. Limb loss, deaths from all causes and the risk of complications immediately after treatment showed no statistically significant differences between the treatments.

Comment: The quality of evidence is downgraded by study limitations (lack of allocation concealment and blinding), by inconsistency (variability in results), and by imprecise results (few patients and outcome events).

References

Primary/Secondary Keywords