Main Article Content
Abstract
Background: Hydatid disease caused by Echinococcus granulosus is endemic in Iraq and the Middle East. Surgery remains the definitive treatment for liver hydatid cysts, and the choice of scolicidal agent is critical to minimising intraoperative spillage complications and postoperative morbidity. Povidone-iodine and hypertonic saline are the most widely used scolicidal agents, yet their comparative efficacy and safety in clinical practice require further evaluation.
Objectives: To evaluate the effectiveness and safety of 10% povidone-iodine compared with 15–20% hypertonic saline as a scolicidal agent in the surgical management of liver hydatid cysts, with respect to postoperative complications and recurrence rate.
Patients and Methods: A prospective single-centre study including 110 patients with liver hydatidosis managed surgically at Al-Nasiriyah Teaching Hospital and Al-Hussain Teaching Hospital, Nasiriyah, Iraq, from January 2022 to December 2024. Patients were divided into two groups: Group A (povidone-iodine, n=91) and Group B (hypertonic saline, n=19). All patients were followed up for up to 24 months with ultrasonography and CT, liver enzyme assays, and clinical assessment for wound infection, collection, and abscess formation.
Results: The mean age was 33.24±13.96 years and 65.45% were female. Laparoscopic surgery was performed in 63.64% of patients. The overall recurrence rate was 12.73%. Elevated liver enzymes (9.89% vs. 42.11%, p<0.001), wound infection (8.79% vs. 26.32%, p=0.031), fluid collection (10.99% vs. 31.58%, p=0.021), and abscess formation (4.40% vs. 21.05%, p=0.029) were all significantly less frequent in the povidone-iodine group. No significant differences were found between groups in hospital stay (p=0.567) or recurrence rate (p=0.752). Prolonged hospital stay was the only factor significantly associated with recurrence (p=0.001).
Conclusions: Povidone-iodine (10%) is superior to hypertonic saline as a scolicidal agent in reducing liver enzyme elevation, wound infection, fluid collection, and abscess formation following liver hydatid cyst surgery. Both agents have comparable hospital stay and recurrence rates.
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Copyright (c) 2026 Ahmed Ali Ismael, Abdul-Hussein Segeel Ashour Al-Jaberi (Author)

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References
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References
Geller DA, Goss JA, Busuttil RW, et al. Liver. In: Brunicardi FC, Andersen DK, Billiar T, et al., editors. Schwartz's Principles of Surgery. 11th ed. New York: McGraw Hill; 2019. p. 1370.
Meshikhes AN. Current treatment of hydatid liver disease: surgical perspective. Adv Res Gastroentero Hepatol. 2019;13(3):555861. https://doi.org/10.19080/ARGH.2019.13.555861
Shaw JM, Bornman PC, Krige JE. Hydatid disease of the liver. S Afr J Surg. 2006;44(2):70–72.
Gupta P, Debi U, Sinha SK, et al. Role of endoscopic retrograde cholangiography in ruptured hepatic hydatid cyst. Trop Gastroenterol. 2015;36(1):21–24. https://doi.org/10.7869/tg.245
Meshikhes AN. An unusual cause of acute abdominal pain in a young man. BMJ Case Rep. 2013;2013:bcr2013009477. https://doi.org/10.1136/bcr-2013-009477
Jedidi M, Mlayeh S, Masmoudi T, et al. Sudden death due to hydatid cyst: thirty-four medicolegal autopsy cases. Am J Forensic Med Pathol. 2014;35(1):29–33. https://doi.org/10.1097/PAF.0000000000000065
Mihmanli M, Tanal M, Bozkurt E, et al. The surgical management of hydatid cyst of the liver: what is new? IntechOpen; 2019. https://doi.org/10.5772/intechopen.90726
Meshikhes AN. Surgical treatment of hydatid cysts of the liver. Br J Surg. 2004;91(4):510–511. https://doi.org/10.1002/bjs.4470
Nazligul Y, Kucukazman M, Akbulut S. Role of chemotherapeutic agents in the management of cystic echinococcosis. Int Surg. 2015;100(1):112–114. https://doi.org/10.9738/INTSURG-D-13-00201.1
Kapan S, Turhan AN, Kalayci MU, et al. Albendazole is not effective for primary treatment of hepatic hydatid cysts. J Gastrointest Surg. 2008;12(5):867–71. https://doi.org/10.1007/s11605-008-0481-8
Akhan O, Akkaya S, Dagoğlu MG, et al. Percutaneous treatment of splenic cystic echinococcosis: results of 12 cases. Cardiovasc Intervent Radiol. 2016;39(3):441–446. https://doi.org/10.1007/s00270-015-1182-9
Kismet K, Kilicoglu SS, Kilicoglu B, et al. The effects of scolicidal agent propolis on liver and biliary tree. J Gastrointest Surg. 2008;12(8):1406–1411. https://doi.org/10.1007/s11605-008-0526-z
Sokouti M, Sadeghi R, Pashazadeh S, et al. A systematic review and meta-analysis on the treatment of liver hydatid cyst using meta-MUMS tool: comparing PAIR and laparoscopic procedures. Arch Med Sci. 2019;15(2):284–308. https://doi.org/10.5114/aoms.2018.77420
Georgiou GK, Lianos GD, Lazaros A, et al. Surgical management of hydatid liver disease. Int J Surg. 2015;20:118–22. https://doi.org/10.1016/j.ijsu.2015.06.075
Tuxun T, Zhang JH, Zhao JM, et al. World review of laparoscopic treatment of liver cystic echinococcosis – 914 patients. Int J Infect Dis. 2014;24:43–50. https://doi.org/10.1016/j.ijid.2014.01.016
Ertem M, Uras C, Karahasanoglu T, et al. Laparoscopic approach to hepatic hydatid disease. Dig Surg. 1998;15(4):333–336. https://doi.org/10.1159/000018639
Rahimi MT, Ahmadpour E, Rahimi Esboei B, et al. Scolicidal activity of biosynthesized silver nanoparticles against Echinococcus granulosus protoscolices. Int J Surg. 2015;19:128–33. https://doi.org/10.1016/j.ijsu.2015.05.010
Gholami SH, Rahimi Esboei B, Ebrahimzadeh MA, et al. In vitro effect of Sambucus ebulus on scolices of hydatid cysts. Eur Rev Med Pharmacol Sci. 2013;17(17):2360–5.
Adas G, Arikan S, Kemik O, et al. Use of albendazole sulfoxide, albendazole sulfone, and combined solutions as scolicidal agents on hydatid cysts (in vitro study). World J Gastroenterol. 2009;15(9):1126–1130. https://doi.org/10.3748/wjg.15.1126
Pérez-Serrano J, Casado N, Guillermo D, et al. The effects of albendazole and albendazole sulphoxide combination therapy on Echinococcus granulosus in vitro. Int J Parasitol. 1994;24(2):219–224. https://doi.org/10.1016/0020-7519(94)90089-2
Sharafi SM, Sefiddashti RR, Sanei B, et al. Scolicidal agents for protoscolices of Echinococcus granulosus hydatid cyst: review of literature. J Res Med Sci. 2017;22:92. https://doi.org/10.4103/jrms.JRMS_478_17
Caglar R, Yuzbasioglu MF, Bulbuloglu E, et al. In vitro effectiveness of different chemical agents on scolices of hydatid cyst. J Invest Surg. 2008;21(2):71–75. https://doi.org/10.1080/08941930801892347
Lashkarizadeh MR, Asgaripour K, Saedi Dezaki E, et al. Comparison of scolicidal effects of amphotericin B, silver nanoparticles, and Foeniculum vulgare Mill on hydatid cyst protoscoleces. Iran J Parasitol. 2015;10(2):206–12.
Fakhar M, Chabra A, Rahimi Esboei B, et al. In vitro protoscolicidal effects of fungal chitosan isolated from Penicillium waksmanii and Penicillium citrinum. J Parasit Dis. 2015;39(1):162–7. https://doi.org/10.1007/s12639-013-0310-3
Rahimi Esboei B, Fakhar M, Chabra A, et al. In vitro treatments of Echinococcus granulosus with fungal chitosan, as a novel biomolecule. Asian Pac J Trop Biomed. 2013;3(11):811–5. doi: 10.1016/S2221-1691(13)60162-5
Mahmoudvand H, Dezaki ES, Kheirandish F, et al. Scolicidal effects of black cumin seed (Nigella sativa) essential oil on hydatid cysts. Korean J Parasitol. 2014;52(6):653–9. https://doi.org/10.3347/kjp.2014.52.6.653
Verma VC, Gangwar M, Nath G. Osmoregulatory and tegumental ultrastructural damages to protoscoleces of hydatid cysts Echinococcus granulosus induced by fungal endophytes. J Parasit Dis. 2014;38(4):432–9. https://doi.org/10.1007/s12639-012-0196-6
Colebrook AL, Jenkins DJ, Jones MK, et al. Effect of cyclosporin A on the survival and ultrastructure of Echinococcus granulosus protoscoleces in vitro. Parasitology. 2004;129(Pt 4):497–504. https://doi.org/10.1017/S003118200400599X
Pichon M, Burucoa C, Evplanov V, et al. Efficacy of three povidone-iodine formulations against Cutibacterium acnes assessed through in vitro studies: a preliminary study. Antibiotics (Basel). 2022;11(5):665. https://doi.org/10.3390/antibiotics11050665
Trott AT. Wound cleansing and irrigation. In: Trott AT, editor. Wounds and Lacerations. 4th ed. Philadelphia: W.B. Saunders; 2012. p. 73–81.
Le Veen HH, Le Veen RF, Le Veen EG. The mythology of povidone-iodine and the development of self-sterilizing plastics. Surg Gynecol Obstet. 1993;176(2):183–90.
Zhang T, Li B, Liu Y, et al. Risk factors associated with echinococcosis in the general Chinese population: a meta-analysis and systematic review. Front Public Health. 2022;10:821265. https://doi.org/10.3389/fpubh.2022.821265
Nunnari G, Pinzone MR, Gruttadauria S, et al. Hepatic echinococcosis: clinical and therapeutic aspects. World J Gastroenterol. 2012;18(13):1448–1458. https://doi.org/10.3748/wjg.v18.i13.1448
Velasco-Tirado V, Alonso-Sardon M, Lopez-Bernus A, et al. Medical treatment of cystic echinococcosis: systematic review and meta-analysis. BMC Infect Dis. 2018;18:306. d https://doi.org/10.1186/s12879-018-3201-y
Jastaniah S, Malatani TS, Eshy SA, et al. Hydatid cyst disease (Echinococcus granulosus): experience at Asir central hospital. Saudi J Gastroenterol. 1997;3(3):140–143.
Hazra NK, Batajoo H, Ghimire S, et al. Open conservative surgical management of cystic echinococcosis in a tertiary care hospital, Nepal. J Clin Diagn Res. 2015;9(7):PC01–PC03. https://doi.org/10.7860/JCDR/2015/13193.6190
Ahmadi NA, Hamidi M. A retrospective analysis of human cystic echinococcosis in Hamedan province, an endemic region of Iran. Ann Trop Med Parasitol. 2008;102(7):603–609. https://doi.org/10.1179/136485908X337437
Abebe E, Kassa T, Bekele M, et al. Intra-abdominal hydatid cyst: sociodemographics, clinical profiles, and outcomes of patients operated on at a tertiary hospital in Addis Ababa, Ethiopia. J Parasitol Res. 2017;2017:6. https://doi.org/10.1155/2017/6981567
Polat P, Atamanalp SS. Hepatic hydatid disease: radiographic findings. Eurasian J Med. 2009;41(1):49–55.
Safioleas MC, Misiakos EP, Kouvaraki M, et al. Hydatid disease of the liver: a continuing surgical problem. Arch Surg. 2006;141(11):1101–1108. https://doi.org/10.1001/archsurg.141.11.1101
Hazra NK, Batajoo H, Ghimire S, et al. Open conservative surgical management of cystic echinococcosis in a tertiary care hospital, Nepal. J Clin Diagn Res. 2015;9(7):PC01–PC03. https://doi.org/10.7860/JCDR/2015/13193.6190
Bhutani N, Kajal P. Hepatic echinococcosis: a review. Ann Med Surg (Lond). 2018;36:99–105. https://doi.org/10.1016/j.amsu.2018.10.032
Greco S, Cannella R, Giambelluca D, et al. Complications of hepatic echinococcosis: multimodality imaging approach. Insights Imaging. 2019;10(1):113. https://doi.org/10.1186/s13244-019-0801-z
Hamza A, Krasniqi A, Sada F, et al. ERCP treatment of obstructive jaundice caused by hydatid cyst in extrahepatic ducts 13 years after liver hydatid endocystectomy: a case report. Int J Surg Case Rep. 2020;74:38–41. https://doi.org/10.1016/j.ijscr.2020.08.005
Ahire P, Iyer N, Gada PB. Complication of hepatic hydatid cyst surgery presenting as obstructive jaundice. Cureus. 2023;15(2):e35410. https://doi.org/10.7759/cureus.35410
Ghannouchi M, Rodayna H, Ben Khalifa M, et al. Postoperative morbidity risk factors after conservative surgery of hydatid cyst of the liver: a retrospective study of 151 hydatid cysts. BMC Surg. 2022;22:120. https://doi.org/10.1186/s12893-022-01568-x
Hosseini Shabanan S, Dashti SH, Abbasi M, et al. Retrospective review of complications of liver hydatid cyst surgery with emphasis on outcomes of omentoplasty. Iran J Parasitol. 2020;15(4):488–494. https://doi.org/10.18502/ijpa.v15i4.4841
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