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Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma

Year 2022, Volume: 3 Issue: 2, 157 - 166, 01.08.2022

Abstract

Giriş: SARS-CoV-2 enfeksiyonuyla gelişen pandemi son 3 yıldır dünya çapında önemli bir sağlık sorunudur. COVID-19 hastalığında gelişen karaciğer hasarının patogenezi ve sonuçları hala belirsizdir. Biz de bu çalışmamızda, COVID-19 hastalarında karaciğer fonksiyon testi (KCFT) anormalliklerinin prevalansını, ilaçlarla ilişkisini, şiddetli ve şiddetli olmayan COVID-19 hastaları arasındaki farkı, yoğun bakımda ve serviste yatan hastalarda KCFT seyrinin sonuçlarını araştırdık. Yöntemler: Çalışmaya Eskişehir Şehir Hastanesine Mart 2020 ve Ekim 2020 tarihleri arasında başvuran 389 hasta çalışmaya dahil edildi. RT-PCR (+) hasta ve RT-PCR(-) kontrol grubunun demografik verileri (yaş, cinsiyet, komorbiditeler, semptomları), laboratuvar parametreleri, radyolojik tetkikleri, servis ve yoğun bakım takipleri ve kullanılan ilaçlar retrospektif olarak kaydedildi. COVID-19’lu tüm hastalar şiddetli veya hafif ve orta şiddetli vakalar olarak sınıflandırıldı. Bulgular: RT-PCR (+) 321 hastanın 115’inde (%35,2), PCR (-) kontrol grubunda 68 hastanın 10’unda (%14,7) anormal KCFT saptandı. Hastaneye yatış anında karaciğer testleri (Alanin aminotransferaz, Aspartat aminotransferaz, total bilirubin, Gama-glutamil transferaz, Alkalen fosfataz) hasta grubunda sırasıyla %10,3, %22,7, %4,9, %11,4 ve %1,2; kontrol grubunda ise %1,9, %2,9, %2, %3,3, %0,8 oranında yüksekti (p=0,610, p=0,00, p=0,269, p=0,198, P=0,158). Antibiyotik (Levofloksasin, Seftriakson, Klaritromisin, Tazobaktam, Karbapenem), düşük molekül ağırlıklı heparin (DMAH) ve antiviral (favipravir) tedavi alan hastalarda KCFT’de anlamlı yükseklik saptandı (p=0,001, p=0,001, p=0,001). KCFT’de yükselme hafif şiddetli vaka grubunda (%40,2; %8,2) ve şiddetli vaka grubunda (%41,2; %5,2) belirgin iken, kontrol grubunda ise düşüktü (%0,5). Sonuç: SARS-CoV-2 enfeksiyonda, karaciğer hasarı sık görülür ancak oldukça hafiftir. Şiddetli COVID-19 hastalarında anormal karaciğer testlerinin sıklığı, hafif hastalığı olanlara göre daha yüksektir. Hastalık şiddeti, önceden var olan karaciğer hastalığı ve ileri yaş, karaciğer hasarı için risktir. İlaç kaynaklı karaciğer hasarı, sistemik inflamatuvar yanıt sendromu ve hipoksi tarafından tetiklenen karaciğer hasarı, COVID-19'da karaciğer hasarı için esas etiyolojik faktörler olabilir.

Supporting Institution

Çalışmamızda, ticari firma ya da firmaların katkısı bulunmamaktadır.

Thanks

Eskişehir Şehir Hastanesinde COVID-19 hastalarının tanı ve tedavisinde yer alan tüm hekim ve sağlık çalışanlarına teşekkür ediyoruz

References

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  • Referans2. Su Eun Park. Epidemiology, virology, and clinical features of severe acute respiratory syndrome -coronavirus-2 (SARS-CoV-2; Coronavirus Disease-19). Clin Exp Pediatr. 2020 Apr; 63(4): 119–124.
  • Referans3. Jinyang Gu, Bing Han, and Jian Wang et al.COVID-19: Gastrointestinal Manifestations and Potential Fecal–Oral Transmission. Gastroenterology. 2020 Mar 3.
  • Referans4. Li Q., Guan X., Wu P et al. Early Transmission Dynamics in Wuhan, China, of Novel Coronavirus-Infected Pneumonia. N. Engl. J. Med. 2020 Mar 26;382(13):1199-1207
  • Referans5. Toshio Hirano, Masaaki Murakami. COVID-19: A New Virus, but a Familiar Receptor and Cytokine Release Syndrome. Immunity. 2020 May 19;52(5):731-733.
  • Referans6. Hui Li, Liang Liu, Dingyu Zhang et al. SARS-CoV-2 and Viral Sepsis: Observations and Hypotheses. Lancet. 2020 May 9;395(10235):1517-1520.
  • Referans7. Hussin A. Rothana and Siddappa N. Byrareddyb. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak. J Autoimmun. 2020 May; 109: 102433
  • Referans8. Herta T, Berg T. COVID-19 and the liver - Lessons learned. Liver Int. 2021 Jun;41 Suppl 1(Suppl 1):1-8.
  • Referans9. Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395:507‐513
  • Referans10. IBM Corp. Released 2011. IBM SPSS Statistics for Windows, Version 20,0. Armonk, NY: İBM Corp.
  • Referans11. Zhang C, Shi L, Wang FS. Liver injury in COVID-19: management and challenges. Lancet Gastroenterol Hepatol. 2020;5:428-430.
  • Referans12. Jonathan Kopel, Abhilash Perisetti, Mahesh Gajendra. Clinical Insights Into the Gastrointestinal Manifestations of COVID-19. Dig Dis Sci. 2020 May 23;1-8
  • Referans13. Xu L, Liu, J, Lu ML et al. Liver injury during highly pathogenic human coronavirus infections. Liver International. 2020;40:998–1004
  • Referans14. Kulkarni A.V., Kumar P., Tevethia H.V. Systematic review with meta-analysis: liver manifestations and outcomes in COVID-19. Aliment Pharmacol Ther. 2020;52:584–599.
  • Referans15. Cai Q, Huang D, Yu H, et al. COVID-19: Abnormal liver function tests. J Hepatol. 2020 Sep;73(3):566-574.
  • Referans16. Metawea MI, Yousif WI, Moheb I.. COVID 19 and liver: An A-Z literature review. Dig Liver Dis. 2021 Feb;53(2):146-152.
  • Referans17. Marjot T, Webb GJ, Barritt AS 4th et al. COVID-19 and liver disease: mechanistic and clinical perspectives. Nat Rev Gastroenterol Hepatol. 2021 May;18(5):348-364.
  • Referans18. Asselah T, Durantel D, Pasmant E et al. COVID-19: Discovery, diagnostics and drug development. J Hepatol. 2021 Jan;74(1):168-184.
  • Referans19. Saviano A, Wrensch F, Ghany MG et al. Liver Disease and Coronavirus Disease 2019: From Pathogenesis to Clinical Care. Hepatology. 2021 Aug;74(2):1088-1100.
  • ReferansReferans20. Amin M. COVID-19 and the liver: overview. Eur J Gastroenterol Hepatol. 2021 Mar 1;33(3):309-311.
  • Referans21. Alqahtani SA, Schattenberg JM. Liver injury in COVID-19: The current evidence. United European Gastroenterol J. 2020 Jun;8(5):509-519.
  • Referans22. Alexandre Olry, Lucy Meunier, Bénédicte Délire. Drug-Induced Liver Injury and COVID-19 Infection: The Rules Remain the Same. Editorial Drug Saf. 2020 Jul;43(7):615-617.
  • Referans23. Tian D, Ye Q. Hepatic complications of COVID-19 and its treatment. J Med Virol. 2020 May 21:10.1002
  • Referans24. Kumar-M P, Mishra S, Jha DK et al. Coronavirus disease (COVID-19) and the liver: a comprehensive systematic review and meta-analysis. Coronavirus disease (COVID-19) and the liver: a comprehensive systematic review and meta-analysis.
  • Referans25. Tai-Nin Chau, Kam-Cheong Lee, Hung Yao et al. SARS-associated viral hepatitis caused by a novel coronavirus: report of three cases. Hepatology. 2004 Feb;39(2):302-10.
  • Referans26. Chai X, Hu L, Zhang Y, et al. Specific ACE2 expression in cholangiocytes may cause liver damage after 2019-nCoV infection. bioRxiv;2020
  • Referans27. Yafei Zhang, Liang Zheng, Lan Liu et al. Liver impairment in COVID-19 patients: A retrospective analysis of 115 cases from a single centre in Wuhan city, China. Liver Int 2020 Sep;40(9):2095-2103.
  • Referans28. Parohan M, Yaghoubi S, Seraj A. Liver injury is associated with severe Coronavirus disease 2019 (COVID‐19) infection: a systematic review and meta‐analysis of retrospective studies. Hepatol Res. 2020 May 9:10.1111
  • Referans29. Lei F, Liu YM, Zhou F, et al. Longitudinal association between markers of liver injury and mortality in COVID-19 in China. Hepatology. 2020 May 2:10.1002
  • Referans29. Qin S., Li W., Shi X., et al. 3044 Cases reveal important prognosis signatures of COVID-19 patients. Comput. Struct. Biotechnol. J. 2021;19:1163–1175.
  • Referans30. Alqahtani SA, Schattenberg JM. Liver injury in COVID-19: The current evidence. United European Gastroenterol J. 2020 Jun;8(5):509-519
  • Referans31. Zhonghua Liu Xing Bing Xue Za Zhi. Novel Coronavirus Pneumonia Emergency Response Epidemiology T The epidemiological characteristics of an outbreak of 2019 novel coronavirus diseases (COVID-19) in China. 2020;41:145–151.
  • Referans32. Peckham H, de Gruijter NM, Raine C et al. Male sex identified by global COVID-19 meta-analysis as a risk factor for death and ITU admission. Nat Commun. 2020;11:6317.
  • Referans33. Fan Z., Chen L., Li J. et al. Clinical features of COVID-19 related liver damage. MedRxiv. 20
  • Referans34. Wang Q., Wang Q., Zhao H. Pattern of liver injury in adult patients with COVID-19: a retrospective analysis of 105 patients. Mil Med Res. 2020;7:28.
  • Referans35. Li W., Moore M.J., Vasilieva N. et al Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426:450–454
  • Referans36. Hisashi Kai, Mamiko Kai. Interactions of Coronaviruses With ACE2, Angiotensin II, and RAS Inhibitors-Lessons From Available Evidence and Insights Into COVID-19. Hypertens Res . 2020 Apr 27;1-7.
  • Referans37. Markus Hoffmann, Hannah Kleine-Weber, Simon Schroeder et al. SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor. Cell. 2020 Apr 16; 181(2): 271–280.
  • Referans38. Glowacka I., Bertram S., Müller M.A et al. Evidence that TMPRSS2 activates the severe acute respiratory syndrome coronavirus spike protein for membrane fusion and reduces viral control by the humoral immune response. J. Virol. 2011;85:4122–4134
  • Referans39. Qing Ye, Bili Wang, and Jianhua Mao. The pathogenesis and treatment of the `Cytokine Storm' in COVID-19. J Infect. 2020 Jun; 80(6): 607–613.
  • Referans40. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012.
  • Referans41. Ortiz GX, Lenhart G, Becker MW et al. Drug-induced liver injury and COVID-19: A review for clinical practice. 2021 Sep 27; 13(9): 1143–1153.
  • Referans42.Cavalcanti AB, Zampieri FG, Rosa RG et al. Hydroxychloroquine with or without Azithromycin in Mild-to-Moderate Covid-19. N Engl J Med. 2020; 383:2041–2052
  • Referans43.Sodeifian F, Seyedalhosseini ZS, Kian N et al. Suspected cholestatic liver injury induced by favipiravir in a patient with COVID-19. Infect Chemother . Feb;27(2):390-392.
  • Referans44.Yamazaki S, Suzuki T, Sayama M et al. Suspected cholestatic liver injury induced by favipiravir in a patient with COVID-19. J Infect Chemother. 2021 Feb;27(2):390-392.
  • Referans45. Avigan (favipiravir) Review Report. Pharmaceuticals and Medical Devices Agency, 2014
  • Referans46. Pilkington V., Pepperrell T., Hill A. A review of the safety of favipiravir — a potential treatment in the COVID-19 pandemic? J Virus Erad. 2020;6:45–51
  • Referans47. Lin Fu, Jun Fei, Shen Xu et al. Liver Dysfunction and Its Association with the Risk of Death in COVID-19 Patients: A Prospective Cohort StudyJ Clin Transl Hepatol. 2020 Sep 28; 8(3): 246–254.

Hepatobiliary System Effects And Clinical Features of Sars-Cov-2 Infection; Case-Control Study

Year 2022, Volume: 3 Issue: 2, 157 - 166, 01.08.2022

Abstract

Introduction: Pandemic caused by SARS-CoV-2 infection has been an important health problem worldwide for the last 3 years. The pathogenesis and consequences of liver injury developed in COVID-19 disease are still unclear. We investigated the prevalence of liver function tests (LFTs) abnormalities in COVID-19 patients, their relationship with drugs, the difference between severe and non-severe COVID-19 patients, and the results of the course of LFTs among patients hospitalized in intensive care units and clinics. Methods: 389 patients who applied to Eskişehir City Hospital between March 2020 and October 2020 were included in the study. Demographic data of RT-PCR (+) patients and RT-PCR (-) control groups (age, gender, comorbidities, symptoms), laboratory parameters, radiological examinations, follow-ups in the clinics and intensive care units, drugs used for the infection were collected retrospectively. All patients with COVID-19 were classified as severe cases or mild to moderate cases groups. Results: Abnormal LFTs were found in 115 (35.2%) of 321 patients with RT-PCR(+), and in 10 (14.7%) of 68 patients in the PCR(-) control group. LFTs at the time of hospitalization were 10.3%, 22.7%, 4.9%, 11.4% and 1.2% in the patient group, respectively; in the control group, it was 1.9%, 2.9%, 2%, 3.3%, 0.8% (p=0.610, p=0.00, p=0.269, p=0.198, p=0.158). There was a significant increase in LFTs in patients who received antibiotics (Levofloxacin, Ceftriaxone, Clarithromycin, Tazobactam, Carbapenem), low molecular weight heparins and antiviral (favipravir) treatments (p=0.001, p=0.001, p=0.001). While the increase in LFTs were significant in the mild (40.2%; 8.2%) and severe groups (41.2%; 5.2%), the number of patients with elevated LFTs in the control group was low (0.5%). Conclusion: Liver damage is common in SARS-CoV-2 infection, but it is quite mild. Patients with severe COVID-19 have a higher frequency of abnormal LFTs than those with mild disease. Disease severity, pre-existing liver disease, and advanced age are risk factors for liver damage. Drug-induced liver injury, systemic inflammatory response syndrome, and hypoxia-induced liver injury may be the main etiological factors for liver injury in COVID-19.

References

  • Referans1. Catrin Sohrabi, Zaid Alsafi, Niamh O'Neill et al. World Health Organization Declares Global Emergency: A Review of the 2019 Novel Coronavirus (COVID-19). Int J Surg. 2020 Apr;76:71-76
  • Referans2. Su Eun Park. Epidemiology, virology, and clinical features of severe acute respiratory syndrome -coronavirus-2 (SARS-CoV-2; Coronavirus Disease-19). Clin Exp Pediatr. 2020 Apr; 63(4): 119–124.
  • Referans3. Jinyang Gu, Bing Han, and Jian Wang et al.COVID-19: Gastrointestinal Manifestations and Potential Fecal–Oral Transmission. Gastroenterology. 2020 Mar 3.
  • Referans4. Li Q., Guan X., Wu P et al. Early Transmission Dynamics in Wuhan, China, of Novel Coronavirus-Infected Pneumonia. N. Engl. J. Med. 2020 Mar 26;382(13):1199-1207
  • Referans5. Toshio Hirano, Masaaki Murakami. COVID-19: A New Virus, but a Familiar Receptor and Cytokine Release Syndrome. Immunity. 2020 May 19;52(5):731-733.
  • Referans6. Hui Li, Liang Liu, Dingyu Zhang et al. SARS-CoV-2 and Viral Sepsis: Observations and Hypotheses. Lancet. 2020 May 9;395(10235):1517-1520.
  • Referans7. Hussin A. Rothana and Siddappa N. Byrareddyb. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak. J Autoimmun. 2020 May; 109: 102433
  • Referans8. Herta T, Berg T. COVID-19 and the liver - Lessons learned. Liver Int. 2021 Jun;41 Suppl 1(Suppl 1):1-8.
  • Referans9. Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395:507‐513
  • Referans10. IBM Corp. Released 2011. IBM SPSS Statistics for Windows, Version 20,0. Armonk, NY: İBM Corp.
  • Referans11. Zhang C, Shi L, Wang FS. Liver injury in COVID-19: management and challenges. Lancet Gastroenterol Hepatol. 2020;5:428-430.
  • Referans12. Jonathan Kopel, Abhilash Perisetti, Mahesh Gajendra. Clinical Insights Into the Gastrointestinal Manifestations of COVID-19. Dig Dis Sci. 2020 May 23;1-8
  • Referans13. Xu L, Liu, J, Lu ML et al. Liver injury during highly pathogenic human coronavirus infections. Liver International. 2020;40:998–1004
  • Referans14. Kulkarni A.V., Kumar P., Tevethia H.V. Systematic review with meta-analysis: liver manifestations and outcomes in COVID-19. Aliment Pharmacol Ther. 2020;52:584–599.
  • Referans15. Cai Q, Huang D, Yu H, et al. COVID-19: Abnormal liver function tests. J Hepatol. 2020 Sep;73(3):566-574.
  • Referans16. Metawea MI, Yousif WI, Moheb I.. COVID 19 and liver: An A-Z literature review. Dig Liver Dis. 2021 Feb;53(2):146-152.
  • Referans17. Marjot T, Webb GJ, Barritt AS 4th et al. COVID-19 and liver disease: mechanistic and clinical perspectives. Nat Rev Gastroenterol Hepatol. 2021 May;18(5):348-364.
  • Referans18. Asselah T, Durantel D, Pasmant E et al. COVID-19: Discovery, diagnostics and drug development. J Hepatol. 2021 Jan;74(1):168-184.
  • Referans19. Saviano A, Wrensch F, Ghany MG et al. Liver Disease and Coronavirus Disease 2019: From Pathogenesis to Clinical Care. Hepatology. 2021 Aug;74(2):1088-1100.
  • ReferansReferans20. Amin M. COVID-19 and the liver: overview. Eur J Gastroenterol Hepatol. 2021 Mar 1;33(3):309-311.
  • Referans21. Alqahtani SA, Schattenberg JM. Liver injury in COVID-19: The current evidence. United European Gastroenterol J. 2020 Jun;8(5):509-519.
  • Referans22. Alexandre Olry, Lucy Meunier, Bénédicte Délire. Drug-Induced Liver Injury and COVID-19 Infection: The Rules Remain the Same. Editorial Drug Saf. 2020 Jul;43(7):615-617.
  • Referans23. Tian D, Ye Q. Hepatic complications of COVID-19 and its treatment. J Med Virol. 2020 May 21:10.1002
  • Referans24. Kumar-M P, Mishra S, Jha DK et al. Coronavirus disease (COVID-19) and the liver: a comprehensive systematic review and meta-analysis. Coronavirus disease (COVID-19) and the liver: a comprehensive systematic review and meta-analysis.
  • Referans25. Tai-Nin Chau, Kam-Cheong Lee, Hung Yao et al. SARS-associated viral hepatitis caused by a novel coronavirus: report of three cases. Hepatology. 2004 Feb;39(2):302-10.
  • Referans26. Chai X, Hu L, Zhang Y, et al. Specific ACE2 expression in cholangiocytes may cause liver damage after 2019-nCoV infection. bioRxiv;2020
  • Referans27. Yafei Zhang, Liang Zheng, Lan Liu et al. Liver impairment in COVID-19 patients: A retrospective analysis of 115 cases from a single centre in Wuhan city, China. Liver Int 2020 Sep;40(9):2095-2103.
  • Referans28. Parohan M, Yaghoubi S, Seraj A. Liver injury is associated with severe Coronavirus disease 2019 (COVID‐19) infection: a systematic review and meta‐analysis of retrospective studies. Hepatol Res. 2020 May 9:10.1111
  • Referans29. Lei F, Liu YM, Zhou F, et al. Longitudinal association between markers of liver injury and mortality in COVID-19 in China. Hepatology. 2020 May 2:10.1002
  • Referans29. Qin S., Li W., Shi X., et al. 3044 Cases reveal important prognosis signatures of COVID-19 patients. Comput. Struct. Biotechnol. J. 2021;19:1163–1175.
  • Referans30. Alqahtani SA, Schattenberg JM. Liver injury in COVID-19: The current evidence. United European Gastroenterol J. 2020 Jun;8(5):509-519
  • Referans31. Zhonghua Liu Xing Bing Xue Za Zhi. Novel Coronavirus Pneumonia Emergency Response Epidemiology T The epidemiological characteristics of an outbreak of 2019 novel coronavirus diseases (COVID-19) in China. 2020;41:145–151.
  • Referans32. Peckham H, de Gruijter NM, Raine C et al. Male sex identified by global COVID-19 meta-analysis as a risk factor for death and ITU admission. Nat Commun. 2020;11:6317.
  • Referans33. Fan Z., Chen L., Li J. et al. Clinical features of COVID-19 related liver damage. MedRxiv. 20
  • Referans34. Wang Q., Wang Q., Zhao H. Pattern of liver injury in adult patients with COVID-19: a retrospective analysis of 105 patients. Mil Med Res. 2020;7:28.
  • Referans35. Li W., Moore M.J., Vasilieva N. et al Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426:450–454
  • Referans36. Hisashi Kai, Mamiko Kai. Interactions of Coronaviruses With ACE2, Angiotensin II, and RAS Inhibitors-Lessons From Available Evidence and Insights Into COVID-19. Hypertens Res . 2020 Apr 27;1-7.
  • Referans37. Markus Hoffmann, Hannah Kleine-Weber, Simon Schroeder et al. SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor. Cell. 2020 Apr 16; 181(2): 271–280.
  • Referans38. Glowacka I., Bertram S., Müller M.A et al. Evidence that TMPRSS2 activates the severe acute respiratory syndrome coronavirus spike protein for membrane fusion and reduces viral control by the humoral immune response. J. Virol. 2011;85:4122–4134
  • Referans39. Qing Ye, Bili Wang, and Jianhua Mao. The pathogenesis and treatment of the `Cytokine Storm' in COVID-19. J Infect. 2020 Jun; 80(6): 607–613.
  • Referans40. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012.
  • Referans41. Ortiz GX, Lenhart G, Becker MW et al. Drug-induced liver injury and COVID-19: A review for clinical practice. 2021 Sep 27; 13(9): 1143–1153.
  • Referans42.Cavalcanti AB, Zampieri FG, Rosa RG et al. Hydroxychloroquine with or without Azithromycin in Mild-to-Moderate Covid-19. N Engl J Med. 2020; 383:2041–2052
  • Referans43.Sodeifian F, Seyedalhosseini ZS, Kian N et al. Suspected cholestatic liver injury induced by favipiravir in a patient with COVID-19. Infect Chemother . Feb;27(2):390-392.
  • Referans44.Yamazaki S, Suzuki T, Sayama M et al. Suspected cholestatic liver injury induced by favipiravir in a patient with COVID-19. J Infect Chemother. 2021 Feb;27(2):390-392.
  • Referans45. Avigan (favipiravir) Review Report. Pharmaceuticals and Medical Devices Agency, 2014
  • Referans46. Pilkington V., Pepperrell T., Hill A. A review of the safety of favipiravir — a potential treatment in the COVID-19 pandemic? J Virus Erad. 2020;6:45–51
  • Referans47. Lin Fu, Jun Fei, Shen Xu et al. Liver Dysfunction and Its Association with the Risk of Death in COVID-19 Patients: A Prospective Cohort StudyJ Clin Transl Hepatol. 2020 Sep 28; 8(3): 246–254.
There are 48 citations in total.

Details

Primary Language Turkish
Subjects Health Care Administration
Journal Section Research Articles
Authors

Berrin Yalınbaş Kaya 0000-0002-1414-4115

Yonca Yılmaz Ürün 0000-0001-6686-0300

İsmail Yenilmez 0000-0002-3357-3898

Yeliz Mert Kantar 0000-0001-7101-8943

Ali Türeyen 0000-0001-8991-720X

Hatice Hamarat 0000-0001-8694-5686

Zeynep Irmak Kaya 0000-0002-3954-1985

Serdar Efe 0000-0002-1229-0602

Cansu Demiral This is me 0000-0002-4576-0148

Pamir Çerçi 0000-0002-0844-6352

Muslih Ürün 0000-0002-9883-3398

Publication Date August 1, 2022
Published in Issue Year 2022 Volume: 3 Issue: 2

Cite

APA Yalınbaş Kaya, B., Yılmaz Ürün, Y., Yenilmez, İ., Mert Kantar, Y., et al. (2022). Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma. Eskisehir Medical Journal, 3(2), 157-166.
AMA Yalınbaş Kaya B, Yılmaz Ürün Y, Yenilmez İ, Mert Kantar Y, Türeyen A, Hamarat H, Irmak Kaya Z, Efe S, Demiral C, Çerçi P, Ürün M. Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma. Eskisehir Med J. August 2022;3(2):157-166.
Chicago Yalınbaş Kaya, Berrin, Yonca Yılmaz Ürün, İsmail Yenilmez, Yeliz Mert Kantar, Ali Türeyen, Hatice Hamarat, Zeynep Irmak Kaya, Serdar Efe, Cansu Demiral, Pamir Çerçi, and Muslih Ürün. “Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri Ve Klinik Özellikleri; Vaka-Kontrollü Çalışma”. Eskisehir Medical Journal 3, no. 2 (August 2022): 157-66.
EndNote Yalınbaş Kaya B, Yılmaz Ürün Y, Yenilmez İ, Mert Kantar Y, Türeyen A, Hamarat H, Irmak Kaya Z, Efe S, Demiral C, Çerçi P, Ürün M (August 1, 2022) Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma. Eskisehir Medical Journal 3 2 157–166.
IEEE B. Yalınbaş Kaya, “Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma”, Eskisehir Med J, vol. 3, no. 2, pp. 157–166, 2022.
ISNAD Yalınbaş Kaya, Berrin et al. “Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri Ve Klinik Özellikleri; Vaka-Kontrollü Çalışma”. Eskisehir Medical Journal 3/2 (August 2022), 157-166.
JAMA Yalınbaş Kaya B, Yılmaz Ürün Y, Yenilmez İ, Mert Kantar Y, Türeyen A, Hamarat H, Irmak Kaya Z, Efe S, Demiral C, Çerçi P, Ürün M. Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma. Eskisehir Med J. 2022;3:157–166.
MLA Yalınbaş Kaya, Berrin et al. “Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri Ve Klinik Özellikleri; Vaka-Kontrollü Çalışma”. Eskisehir Medical Journal, vol. 3, no. 2, 2022, pp. 157-66.
Vancouver Yalınbaş Kaya B, Yılmaz Ürün Y, Yenilmez İ, Mert Kantar Y, Türeyen A, Hamarat H, Irmak Kaya Z, Efe S, Demiral C, Çerçi P, Ürün M. Sars-Cov-2 Enfeksiyonunun Hepatobiliyer Sisteme Etkileri ve Klinik Özellikleri; Vaka-Kontrollü Çalışma. Eskisehir Med J. 2022;3(2):157-66.