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. Author manuscript; available in PMC: 2019 Feb 5.
Published in final edited form as: Reg Anesth Pain Med. 2019 Jan;44(1):100–106. doi: 10.1136/rapm-2018-000007

Figure 3.

Figure 3

Subcategorization of device-related, procedural, patient complaint, and serious adverse event complication categories. *If multiple complications occurred for the same episode, each was recorded each as a separate complication. If a particular complication was considered serious and managed via a separately recorded category, it was reported in both categories. IPG, implantable pulse generator.