Dose Optimization of Colistin: A Systematic Review
Colistin is considered a last treatment option for multi-drug and extensively resistant Gram-negative infections. We aimed to assess the available data on the dosing strategy of colistin. A systematic review was performed to identify all published studies on the dose optimization of colistin. Grey l...
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Published in | Antibiotics (Basel) Vol. 10; no. 12; p. 1454 |
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Main Authors | , , , , , , , , , , , , |
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26.11.2021
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Abstract | Colistin is considered a last treatment option for multi-drug and extensively resistant Gram-negative infections. We aimed to assess the available data on the dosing strategy of colistin. A systematic review was performed to identify all published studies on the dose optimization of colistin. Grey literature and electronic databases were searched. Data were collected in a specified form and the quality of the included articles was then assessed using the Newcastle-Ottawa scale for cohort studies, the Cochrane bias tool for randomized clinical trials (RCT), and the Joanna Briggs Institute (JBI) critical checklist for case reports. A total of 19 studies were included, of which 16 were cohort studies, one was a RCT, and two were case reports. A total of 18 studies proposed a dosing regimen for adults, while only one study proposed a dosing schedule for pediatric populations. As per the available evidence, a loading dose of 9 million international units (MIU) of colistin followed by a maintenance dose of 4.5 MIU every 12 h was considered the most appropriate dosing strategy to optimize the safety and efficacy of treatment and improve clinical outcomes. This review supports the administration of a loading dose followed by a maintenance dose of colistin in severe and life-threatening multi-drug Gram-negative bacterial infections. |
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AbstractList | Colistin is considered a last treatment option for multi-drug and extensively resistant Gram-negative infections. We aimed to assess the available data on the dosing strategy of colistin. A systematic review was performed to identify all published studies on the dose optimization of colistin. Grey literature and electronic databases were searched. Data were collected in a specified form and the quality of the included articles was then assessed using the Newcastle-Ottawa scale for cohort studies, the Cochrane bias tool for randomized clinical trials (RCT), and the Joanna Briggs Institute (JBI) critical checklist for case reports. A total of 19 studies were included, of which 16 were cohort studies, one was a RCT, and two were case reports. A total of 18 studies proposed a dosing regimen for adults, while only one study proposed a dosing schedule for pediatric populations. As per the available evidence, a loading dose of 9 million international units (MIU) of colistin followed by a maintenance dose of 4.5 MIU every 12 h was considered the most appropriate dosing strategy to optimize the safety and efficacy of treatment and improve clinical outcomes. This review supports the administration of a loading dose followed by a maintenance dose of colistin in severe and life-threatening multi-drug Gram-negative bacterial infections.Colistin is considered a last treatment option for multi-drug and extensively resistant Gram-negative infections. We aimed to assess the available data on the dosing strategy of colistin. A systematic review was performed to identify all published studies on the dose optimization of colistin. Grey literature and electronic databases were searched. Data were collected in a specified form and the quality of the included articles was then assessed using the Newcastle-Ottawa scale for cohort studies, the Cochrane bias tool for randomized clinical trials (RCT), and the Joanna Briggs Institute (JBI) critical checklist for case reports. A total of 19 studies were included, of which 16 were cohort studies, one was a RCT, and two were case reports. A total of 18 studies proposed a dosing regimen for adults, while only one study proposed a dosing schedule for pediatric populations. As per the available evidence, a loading dose of 9 million international units (MIU) of colistin followed by a maintenance dose of 4.5 MIU every 12 h was considered the most appropriate dosing strategy to optimize the safety and efficacy of treatment and improve clinical outcomes. This review supports the administration of a loading dose followed by a maintenance dose of colistin in severe and life-threatening multi-drug Gram-negative bacterial infections. Colistin is considered a last treatment option for multi-drug and extensively resistant Gram-negative infections. We aimed to assess the available data on the dosing strategy of colistin. A systematic review was performed to identify all published studies on the dose optimization of colistin. Grey literature and electronic databases were searched. Data were collected in a specified form and the quality of the included articles was then assessed using the Newcastle-Ottawa scale for cohort studies, the Cochrane bias tool for randomized clinical trials (RCT), and the Joanna Briggs Institute (JBI) critical checklist for case reports. A total of 19 studies were included, of which 16 were cohort studies, one was a RCT, and two were case reports. A total of 18 studies proposed a dosing regimen for adults, while only one study proposed a dosing schedule for pediatric populations. As per the available evidence, a loading dose of 9 million international units (MIU) of colistin followed by a maintenance dose of 4.5 MIU every 12 h was considered the most appropriate dosing strategy to optimize the safety and efficacy of treatment and improve clinical outcomes. This review supports the administration of a loading dose followed by a maintenance dose of colistin in severe and life-threatening multi-drug Gram-negative bacterial infections. |
Author | Obaid, Najla A. Mahrous, Ahmad Jamal Alghamdi, Saleh Faidah, Hani Saleh Algethamy, Manal Elrggal, Mahmoud Essam Saleem, Zikria AlQarni, Abdullmoin Khogeer, Asim A. Sheikh, Aziz Haseeb, Abdul Alotaibi, Amal F. Almarzoky Abuhussain, Safa S. |
AuthorAffiliation | 10 Usher Institute, The University of Edinburgh, Teviot Place, Edinburgh EH16 4UX, UK; aziz.sheikh@ed.ec.uk 5 Alnoor Specialist Hospital, Department of Infection Prevention & Control Program, Makkah 24382, Saudi Arabia; mmalgethamy@moh.gov.sa 7 Plan and Research Department, General Directorate of Health Affairs of Makkah Regiona, Ministry of Health, Makkah 24382, Saudi Arabia; akhogeer@moh.gov.sa 3 Department of Clinical Pharmacy, Faculty of Clinical Pharmacy, Al Baha University, Al Baha 65779, Saudi Arabia; saleh.alghamdi@bu.edu.sa 8 Medical Genetics Unit, Maternity & Children Hospital, Makkah Healthcare Cluster, Ministry of Health, Makkah 24382, Saudi Arabia 6 Alnoor Specialist Hospital, Infectious Diseases Department, Makkah 24382, Saudi Arabia; al-qrni@hotmail.com 2 Department of Microbiology, Faculty of Medicine, Umm Al Qura University, Makkah 24382, Saudi Arabia; hsfaidah@uqu.edu.sa 4 Department of Pharmaceutics, College of Pharmacy, Umm Al Qura University, Makkah 24382, Saudi Arabia; n |
AuthorAffiliation_xml | – name: 5 Alnoor Specialist Hospital, Department of Infection Prevention & Control Program, Makkah 24382, Saudi Arabia; mmalgethamy@moh.gov.sa – name: 8 Medical Genetics Unit, Maternity & Children Hospital, Makkah Healthcare Cluster, Ministry of Health, Makkah 24382, Saudi Arabia – name: 6 Alnoor Specialist Hospital, Infectious Diseases Department, Makkah 24382, Saudi Arabia; al-qrni@hotmail.com – name: 10 Usher Institute, The University of Edinburgh, Teviot Place, Edinburgh EH16 4UX, UK; aziz.sheikh@ed.ec.uk – name: 9 Department of Pharmacy Practice, Faculty of Pharmacy, The University of Lahore, Lahore 54000, Pakistan; xikria@gmail.com – name: 1 Department of Clinical Pharmacy, College of Pharmacy, Umm Al Qura University, Makkah 24382, Saudi Arabia; afotaibi@uqu.edu.sa (A.F.A.); merggal@uqu.edu.sa (M.E.E.); ajmahrous@uqu.edu.sa (A.J.M.); ssmarzoky@uqu.edu.sa (S.S.A.A.) – name: 7 Plan and Research Department, General Directorate of Health Affairs of Makkah Regiona, Ministry of Health, Makkah 24382, Saudi Arabia; akhogeer@moh.gov.sa – name: 3 Department of Clinical Pharmacy, Faculty of Clinical Pharmacy, Al Baha University, Al Baha 65779, Saudi Arabia; saleh.alghamdi@bu.edu.sa – name: 4 Department of Pharmaceutics, College of Pharmacy, Umm Al Qura University, Makkah 24382, Saudi Arabia; naobaid@uqu.edu.sa – name: 2 Department of Microbiology, Faculty of Medicine, Umm Al Qura University, Makkah 24382, Saudi Arabia; hsfaidah@uqu.edu.sa |
Author_xml | – sequence: 1 givenname: Abdul orcidid: 0000-0003-2455-5054 surname: Haseeb fullname: Haseeb, Abdul – sequence: 2 givenname: Hani Saleh surname: Faidah fullname: Faidah, Hani Saleh – sequence: 3 givenname: Saleh orcidid: 0000-0002-7975-933X surname: Alghamdi fullname: Alghamdi, Saleh – sequence: 4 givenname: Amal F. surname: Alotaibi fullname: Alotaibi, Amal F. – sequence: 5 givenname: Mahmoud Essam surname: Elrggal fullname: Elrggal, Mahmoud Essam – sequence: 6 givenname: Ahmad Jamal orcidid: 0000-0002-7140-741X surname: Mahrous fullname: Mahrous, Ahmad Jamal – sequence: 7 givenname: Safa S. orcidid: 0000-0003-2513-5043 surname: Almarzoky Abuhussain fullname: Almarzoky Abuhussain, Safa S. – sequence: 8 givenname: Najla A. orcidid: 0000-0001-7094-0813 surname: Obaid fullname: Obaid, Najla A. – sequence: 9 givenname: Manal surname: Algethamy fullname: Algethamy, Manal – sequence: 10 givenname: Abdullmoin surname: AlQarni fullname: AlQarni, Abdullmoin – sequence: 11 givenname: Asim A. orcidid: 0000-0002-6508-7747 surname: Khogeer fullname: Khogeer, Asim A. – sequence: 12 givenname: Zikria orcidid: 0000-0003-3202-6347 surname: Saleem fullname: Saleem, Zikria – sequence: 13 givenname: Aziz surname: Sheikh fullname: Sheikh, Aziz |
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Keywords | dose optimization nephrotoxicity Gram-negative infections colistin |
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SubjectTerms | Antibiotics Bacterial diseases Bacterial infections Case reports Clinical outcomes Clinical trials Colistin Data search Dosage dose optimization Drug dosages Drug resistance Gram-negative bacteria Gram-negative infections Infections Maintenance nephrotoxicity Optimization Patients Pediatrics Pharmacokinetics Plasma Regulatory approval Reviews Systematic Review |
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Title | Dose Optimization of Colistin: A Systematic Review |
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