Vroegindeweij 1995.
Study characteristics | ||
Methods | Randomisation method: numbered envelopes opened sequentially Allocation: sealed envelopes, not stated if opaque Intervention model: parallel assignment Blinding: not stated, probably not done | |
Participants | Country: Netherlands No. of participants: 73 Simpson atherectomy: 38 BA: 35 Age (mean (years) range): Atherectomy: 64 (range 49 ‐ 77) BA: 64 (range 46 ‐ 80) Inclusion criteria: intermittent claudication of at least 3 months duration and obstructive lesions of the femoropopliteal arteries with a maximum length of 5 cm or complete occlusions shorter than 2 cm. Exclusion criteria: any previous ipsilateral femoropopliteal endovascular or operative intervention; participant unable to comply with the frequent follow‐up visits required by the protocol. |
|
Interventions | BA versus Simpson atherectomy | |
Outcomes | Primary patency during follow‐up Restenosis as determined by duplex ultrasound |
|
Notes | Four participants crossed over to the other treatment group: three participants had angioplasty following atherectomy, one participant had atherectomy in addition to angioplasty. Results were presented in an intention‐to‐treat format | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Numbered envelopes opened sequentially. Randomisation not performed until after inclusion and exclusion criteria evaluated. |
Allocation concealment (selection bias) | Low risk | Sealed envelopes, not stated if opaque. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Not stated, but impractical in trials of this type. |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Not stated, probably not done. |
Incomplete outcome data (attrition bias) All outcomes | High risk | Three participants in the BA group were not followed up to 6 months. One participant in the atherectomy group and 10 in the BA group were not followed up to one year. |
Selective reporting (reporting bias) | Low risk | Primary patency reported fully in life‐table format; restenosis presented graphically. |
Other bias | Low risk | Clear antiplatelet protocol. |