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Published on: February 28, 2012
Anesthesia and perioperative pain management during cardiac electronic device implantation
Marina Biocic1, Dijana Vidosevic2, Matija Boric1,3
1Laboratory for Pain Research, University of Split School of Medicine.
Insights
Patients undergoing cardiac electronic device (CED) implantation often experience severe pain during and after the procedure. Current perioperative pain management is insufficient, indicating a need for improved sedation and analgesia strategies.
Area of Science:
- Cardiology
- Anesthesiology
- Pain Management
Background:
- Pain associated with cardiac electronic device (CED) implantation and its management are understudied.
- Existing perioperative pain management practices for CED implantation require further investigation.
Purpose of the Study:
- To analyze perioperative pain management strategies used during CED implantation.
- To assess the intensity and location of pain experienced by patients undergoing CED implantation.
- To compare current practices with established guidelines for acute perioperative pain management.
Main Methods:
- A combined retrospective (321 patients) and prospective (51 patients) study design.
- Data collected from a tertiary hospital, University Hospital Split, Croatia.
- Pain intensity measured using a numerical rating scale (NRS) from 0 to 10.
Main Results:
- Only a quarter of patients received pre-operative analgesia or sedation; all received local lidocaine anesthesia.
- Post-operatively, 31% of patients received pain medication or sedation.
- Severe pain (NRS >5) was reported during and up to 24 hours after implantation, with common locations including the surgical site, shoulder, and chest.
- Adherence to acute perioperative pain management guidelines was insufficient.
Conclusions:
- Patients undergoing CED implantation frequently experience severe pain.
- Current perioperative pain management is suboptimal, necessitating increased sedation and analgesia.
- Development of specific guidelines for anesthesia and pain management during CED implantation is recommended.
Background:
The degree of pain caused by the implantation of cardiac electronic devices (CEDs) and the type of anesthesia or perioperative pain management used with the procedure have been insufficiently studied. The aim of this study was to analyze perioperative pain management, as well as intensity and location of pain among patients undergoing implantation of CED, and to compare the practice with published guidelines.
Patients And Methods:
This was a combined retrospective and prospective study conducted at the tertiary hospital, University Hospital Split, Croatia. The sample included 372 patients who underwent CED implantation. Perioperative pain management was analyzed retrospectively in 321 patients who underwent CED implantation during 2014. In a prospective study, intensity and location of pain before, during, and after the procedure were measured by using a numerical rating scale (NRS) ranging from 0 to 10 in 51 patients at the same institution from November 2014 to August 2015.
Results:
A quarter of patients received analgesia or sedation before surgery. All the patients received local lidocaine anesthesia. After surgery, 31% of patients received pain medication or sedation. The highest pain intensity was observed during CED implantation with the highest NRS pain score being 8. Some patients reported severe pain (NRS >5) also at 1, 3, 6, 8, and 24 hours after surgery. The most common pain locations were surgical site, shoulder, and chest. Adherence to guidelines for acute perioperative pain management was insufficient.
Conclusion:
Patients may experience severe pain during and after CED implantation. Perioperative pain management was suboptimal, and higher doses of sedation and intensive analgesia are required. Guidelines for acute perioperative pain management and anesthesia during CED implantation should be developed.
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