World Journal of Pharmaceutical
and Medical Research

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An International Peer Reviewed Journal for Pharmaceutical and Medical Research and Technology
An Official Publication of Society for Advance Healthcare Research (Reg. No. : 01/01/01/31674/16)
ISSN (O) : 2455-3301
ISSN (P) : 3051-2557
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ICV : 78.6

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Abstract

A SINGLE CASE STUDY OF PILONIDAL SINUS MANAGED BY CHEDANA KARMA (WIDE EXCISION) WITH AYURVEDIC POSTOPERATIVE CARE

Dr. Rahul Kumar*, Dr. Vishnu Dutt Sharma, Dr. Prem Kumar, Prof. (Dr) Rajesh Kumar Gupta, Dr. Aanchal Meena5, Dr. Piyush Sharma

ABSTRACT

Background: Pilonidal sinus is a chronic inflammatory condition of the sacrococcygeal region, characterised by a sinus tract containing hair tufts. In modern surgery, wide excision (open technique) remains the gold standard, yet postoperative wound healing is frequently prolonged, painful and complicated by secondary infection.[1] Ayurveda describes a comparable entity under Nadi Vrana (sinus wound) and offers a rich pharmacopoeia of wound-healing agents that may complement conventional surgical management. Case Presentation: A 34-year-old male presented with a recurrent midline pit and purulent discharge in the natal cleft of 14 months' duration. He was diagnosed with sacrococcygeal pilonidal sinus (Nadi Vrana / Nadi Shotha) and underwent Chedana Karma (wide excision under local anaesthesia). Postoperatively, wound care was carried out with Ayurvedic formulations including Jatyadi Taila.[2] dressing, Panchavalkala Kashaya irrigation, oral Triphala Guggulu, and dietary regulation (Pathya-Apathya). Outcome: Complete wound healing was achieved by the 42nd postoperative day without secondary infection, wound dehiscence, or recurrence at 6-month follow-up. Pain scores (VAS) reduced significantly by Day 7, and the patient resumed normal activities by Day 21. Conclusion: Chedana Karma combined with Ayurvedic postoperative wound care may provide an effective and cost-efficient integrative management strategy for pilonidal sinus, reducing healing time, pain, and recurrence. Further prospective clinical trials with larger sample sizes are warranted.[3]

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