Advances in Oral and Maxillofacial Surgery
Effect of Replacing the Pharyngeal Pack After Surgical Preparation with Chlorhexidine- or Normal Saline-Soaked Packs on Postoperative Throat Pain and Burning Following Oral and Maxillofacial Surgery
By Seyed Hesam Aldin Haeri Araghi, Hassan Mesgari, Romina Mahdiroudi and 6 others.
Abstract
Purpose Pharyngeal packs are commonly used during oral and maxillofacial surgery to limit blood ingestion and aspiration of surgical debris. However, packing and residual povidone-iodine from surgical preparation may irritate the pharyngeal mucosa and contribute to postoperative throat discomfort. This study compared chlorhexidine-soaked and saline-soaked replacement pharyngeal packs for reducing postoperative throat pain and irritation. Methods In this prospective, randomized, double-blind clinical trial, 66 patients undergoing oral and maxillofacial surgery at Farhikhtegan Hospital were randomly assigned to receive a replacement pharyngeal pack soaked in either 0.2% chlorhexidine gluconate or 0.9% normal saline after routine preparation with diluted povidone-iodine. Throat pain and irritation were assessed by blinded investigators at 2, 4, 6, and 12 hours postoperatively using a 0–10 visual analog scale (VAS) and a five-point Likert scale. Repeated-measures analysis evaluated group, time, and group-by-time effects. Results The groups were comparable in age and sex distribution. Overall, VAS scores were significantly lower in the chlorhexidine group for throat irritation (P = 0.002) and throat pain (P = 0.001). Both outcomes decreased significantly over time (P < 0.001). Group-by-time interactions were not significant for irritation (P = 0.753) or pain (P = 0.348), indicating similar patterns of improvement. Between-group differences were not significant for Likert irritation (P = 0.260) or pain scores (P = 0.065). Conclusion Chlorhexidine-soaked replacement pharyngeal packs were associated with lower early postoperative VAS throat pain and irritation than saline-soaked packs. However, this benefit was not confirmed by Likert-scale assessments. Further trials should evaluate clinical significance and safety in larger, procedure-specific populations with longer postoperative follow-up.



