Device selection: DCB/DES evidence and paclitaxel safety context
Applied
Type
ReinforcementConfidence
90%
Created
Mar 19, 2026
Evidence
1 source
Rationale
The integration of Zhou 2025 provides high-level evidence (network meta-analysis) that reinforces the existing claims regarding DCB and DES efficacy. It adds value by noting that this efficacy is consistent across various lesion locations and severities, which is a more granular finding than the original text. Abbreviations were standardized according to the provided instructions.
Evidence
Content Changes
removedadded
Paclitaxel-based drug-coated balloons (DCBs)(DCB) and drug-eluting stents (DES) improve patency in femoropopliteal disease compared to uncoated devices. Recent network meta-analysis data reinforces the efficacy of these endovascular treatments across various lesion locations and severities [@zhou2025]. Regulatory review following an initial safety signal (Katsanos 2018) has been ongoing; subsequent large real-world analyses have not confirmed excess mortality. For detailed device evidence, current regulatory guidance, and shared decision-making requirements, see [[Peripheral Artery Disease|Ch. 10]].