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Kentuckiana Pain Specialists Reviews — What informed consent should clarify

A consent form should follow a conversation about the procedure proposed for you. The useful question is whether you understand what it aims to do and what happens if it does not.

Care planning · Updated October 6, 2026

Name the intended purpose

Ask whether a procedure is diagnostic, intended to relieve symptoms, or both. Confirm the exact area and side, what medication or device is involved and how the result will be interpreted. A temporary response to a diagnostic block should not be described as a guaranteed long-term outcome.

Discuss alternatives and risks

Ask what reasonable alternatives exist, including waiting for more evaluation. Risks differ across injections, ablation and implants. For example, epidural injections have procedure-specific risks, and an implanted stimulator adds surgery and device maintenance. The discussion should relate those risks to your medical history.

Know the aftercare pathway

Before consenting, find out who to contact after hours, which symptoms require urgent evaluation and when follow-up will occur. Ask whether sedation, transportation or activity limits apply to this particular plan. Individual instructions come from the treating team.

After the explanation, try stating the plan back in ordinary language: what the procedure targets, what benefit is uncertain, what the main alternatives are and whom you would call afterward. If any part is unclear, ask again before signing. A written form cannot replace a clear answer about your own condition or the exact procedure site.

Questions to ask

  • What problem is this procedure meant to test or treat?
  • What are the main alternatives for me?
  • Which risks are most relevant to my history?
  • Who should I call if something changes afterward?

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