Same Day Subcutaneous ICD And Send Home (DASH) — DASH  

Cardiomyopathies Clinical Trial

Official title: Same Day Subcutaneous ICD And Send Home

Status Completed

Clinical Trial Summary

Design: Prospective, non-randomized single center study at The Ohio State University Wexner Medical Center. Purpose: The purpose of this study is to prospectively evaluate a specific analgesia protocol designed to allow for same day discharge following implantation of the subcutaneous implantable cardiac defibrillator (S-ICD) Enrollment: Up to 40 subjects will be enrolled. Subject Population: Consecutive patients undergoing S-ICD implantation under general anesthesia or monitored anesthesia care. Endpoints: Rate of successful completion of the protocol; Procedural complications; Serial assessment of patient perception of pain.

Clinical Trial Description

This is a prospective, nonrandomized, descriptive, single center study designed to assess the rate of successful completion of the study protocol in consecutive patients undergoing S-ICD implantation. Objectives To prospectively evaluate the same day discharge protocol for patients undergoing S-ICD implantation. Primary Endpoint 1. Rate of successful completion of S-ICD implantation and discharge of the patient on the same day the device is implanted using the analgesia protocol. Secondary Endpoints 1. Procedure complication (failed implantation, infection, hematoma/bleeding, etc…) within 30 days of procedure. 2. Serial assessment of patient perception of pain using the graded integer pain scale of 1-10 3. Side effects related to medical therapy of protocol. 4. Time from beginning of recovery (defined as when the patient enters the recovery IPR room) to the time of discharge from the recovery unit. 5. 30 day readmission rate after discharge following S-ICD implant 6. Number of days that oral analgesics are used post discharge. Patients will be approached for participation in the study once they have been consented for implantation of the clinically indicated S-ICD . Pre-procedure analgesia will be given to each patient as follows: Acetaminophen 975 mg PO x 1 will be administered 1-2 hours prior to the procedure. and Oxycodone 10 mg PO x 1 will be administered 1-2 hours prior to the procedure. Anesthesia will be provided by anesthesiology team as MAC or general anesthesia. Local subcutaneous anesthetic will be a 50:50 mixture of 2% lidocaine and 0.5% bupivacaine; which will result in a concentration of 1% lidocaine and 0.25% bupivacaine. Starting at ≈2 hours post procedure, the patient will then enter the "Preparation for Discharge" phase. The modified Aldrete scoring system will be used to determine eligibility for discharge home.Patients with an Aldrete score ≥ 9 will be deemed eligible for discharge home. Additional standard ambulatory discharge criteria per the OSUWMC postanesthesia care policy statement will be applied by the nursing team, akin to all ambulatory surgery patients at OSUWMC. If the above discharge parameters (DP) are not meet, the patient will be reassessed every 30 minutes until parameters are satisfied. Once the patient satisfies the DP, the patient will complete the Pain Perception Questionnaire and be assessed for ambulation, eating/drinking and for understanding of post discharge instructions. The electrophysiology device nursing staff will review management of the S-ICD incision, device and post discharge care instructions with the patient and with the accompanying family member(s)/friend. The patient will be given instructions regarding management of pain and will be provided the following prescription for outpatient pain control Percocet 5mg/325 mg (1 tablet every 6 hours). A 2-day supply will be given. Also, the patient will be provided a phone number to contact during business hours as well as for after hours to address questions/concerns. The electrophysiology nursing staff will contact the patient the following day and again at about 3 days post discharge to administer the Pain Perception Questionnaire as well as to address any patient questions. The patient will then be evaluated in the Device Clinic about 10 days post implantation. The Pain Perception questionnaire will be administered and assessment of the incision and S-ICD will be completed. The last Pain Perception questionnaire will be obtained by telephone at about 30 days post implantation. ;

Related Conditions & MeSH terms

• Cardiac Death, Sudden
• Cardiomyopathies
• Death
• Death, Sudden
• Death, Sudden, Cardiac

• NCT number: NCT03504839
• Study type: Interventional
• Source: Ohio State University
• Status: Completed
• Phase: N/A
• Start date: January 15, 2018
• Completion date: April 12, 2019