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DOI 10.1016/j.jsps.2022.03.013

Медицинская библиотека · Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022

Incidence, patterns, risk factors and clinical outcomes of intravenous acyclovir induced nephrotoxicity.

Al-Alawi Abdullah M, Al-Maqbali Juhaina Salim, Al-Adawi Maria, Al-Jabri Anan, Falhammar Henrik

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Аннотация

OBJECTIVES

Acyclovir is approved to treat herpes simplex virus (HSV) type 1, type 2 and varicella-zoster virus. It is mainly eliminated via the kidneys, for which drug crystals accumulation might lead to nephrotoxicity. This study aimed to determine the incidence, risk factors, preventive measures, and clinical outcomes of acyclovir induced-nephrotoxicity.

METHODS

This is a retrospective cohort study of patients >12 years of age at Sultan Qaboos University Hospital (SQUH) receiving IV acyclovir therapy between January 2016 and December 2020.

RESULTS

Out of 191 included patients, 40 (20.1%) developed acyclovir induced-nephrotoxicity. Age (per year older: OR 1.04, 95 %CI 1.01-1.07), total duration of treatment (per day OR1.19, 95 %CI 1.06-1.33), and concomitant use of vancomycin (OR 5.96, 95 %CI 1.87-19.01) were significant independent risk factors for acyclovir induced-nephrotoxicity development. Nine patients (4.5%) died during the same hospitalization, including those three patients who required renal replacement therapy (1.5%).

CONCLUSION

Frequent monitoring of kidney function for older patients with concurrent use of vancomycin and IV hydration is essential to prevent IV acyclovir induced-nephrotoxicity. Antimicrobial stewardship is a crucial method to reduce the duration of treatment with IV acyclovir as appropriate.

Для цитирования: Al-Alawi Abdullah M, Al-Maqbali Juhaina Salim, Al-Adawi Maria, Al-Jabri Anan, Falhammar Henrik. Incidence, patterns, risk factors and clinical outcomes of intravenous acyclovir induced nephrotoxicity.. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society. 2022. DOI: 10.1016/j.jsps.2022.03.013.
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