Evidence map›Paper›PMID 36601502›Full record

ArticleSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society2022

The potential role of adjunctive ascorbic acid in the prevention of colistin-induced nephrotoxicity in critically ill patients: A retrospective study.

Khalid Al Sulaiman, Ohoud Aljuhani, Abdullah M Alhammad, Kholoud Al Aamer, Sara Alshehri, Abdulmohsen Alhuwahmel, Abdullah Kharbosh, Areej Alshehri, Hanan Alshareef, Ibrahim Al Sulaihim and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 55% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Voghera Sweet Pepper: A Potential Ally against Oxidative Stress and Aging.International journal of molecular sciences · 2023
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 12 institutions in 2 countries.

Khalid Al SulaimanPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Ohoud AljuhaniDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Abdullah M AlhammadDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Kholoud Al AamerPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Sara AlshehriPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Abdulmohsen AlhuwahmelCollege of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdullah KharboshDepartment of Clinical Pharmacy, College of Pharmacy, Taif University, Taif, Saudi Arabia.
Areej AlshehriFerring Pharmaceuticals, Jeddah, Saudi Arabia.
Hanan AlshareefDepartment of Pharmacy Practice, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.
Ibrahim Al SulaihimPharmaceutical Care Department, Presidency of State Security, Central Security Hospitals, Riyadh, Saudi Arabia.
Albandari AlghamdiDepartment of Pharmacy Practice, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O.Box 84428, Riyadh 11671, Saudi Arabia.
Shmeylan Al HarbiPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Ramesh VishwakarmaStatistics Department, European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
Numan AlabdanPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Yousef AlrajhiPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Abdulmalik Al KatheriPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Abeer A AlenaziPharmaceutical Care Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Mai AlalawiDepartment of Pharmaceutical Sciences, Fakeeh College of Medical Sciences, Jeddah, Saudi Arabia.
Ghassan Al GhamdiKing Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
King Abdulaziz Medical City · SAKing Saud bin Abdulaziz University for Health Sciences · SAKing Abdullah International Medical Research Center · SAEuropean Organisation for Research and Treatment of Cancer · BEKing Abdulaziz University · SAKing Saud University · SAPrincess Nourah bint Abdulrahman University · SARiyadh Armed Forces Hospital · SASecurity Forces Hospital · SASoliman Fakeeh Hospital · SATaif University · SAUniversity of Tabuk · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colistin is considered a valuable and last-resort therapeutic option for MDR gram-negative bacteria. Nephrotoxicity is the most clinically pertinent adverse effect of colistin. Vivo studies suggest that administering oxidative stress-reducing agents, such as ascorbic acid, is a promising strategy to overcome colistin-induced nephrotoxicity (CIN). However, limited clinical data explores the potential benefit of adjunctive ascorbic acid therapy for preventing CIN. Therefore, this study aims to assess the potential nephroprotective role of ascorbic acid as adjunctive therapy against CIN in critically ill patients. Method: This was a retrospective cohort study at King Abdulaziz Medical City (KAMC) for all critically ill adult patients who received IV colistin. Eligible patients were classified into two groups based on the ascorbic acid use as concomitant therapy within three days of colistin initiation. The primary outcome was CIN odds after colistin initiation, while the secondary outcomes were 30-day mortality, in-hospital mortality, ICU, and hospital LOS. Propensity score (PS) matching was used (1:1 ratio) based on the patient's age, SOFA score, and serum creatinine. Results: A total of 451 patients were screened for eligibility; 90 patients were included after propensity score matching based on the selected criteria. The odds of developing CIN after colistin initiation were similar between patients who received ascorbic acid (AA) as adjunctive therapy compared to patients who did not (OR (95 %CI): 0.83 (0.33, 2.10), p-value = 0.68). In addition, the 30-day mortality, in-hospital mortality, ICU, and hospital LOS were similar between the two groups. Conclusion: Adjunctive use of Ascorbic acid during colistin therapy was not associated with lower odds of CIN. Further studies with a larger sample size are required to confirm these findings.

Indexed as

AA, Ascorbic AcidAKI, Acute Kidney InjuryAscorbic AcidCIN, Colistin-induced NephrotoxicityCKD, Chronic kidney diseaseColistinColistin-induced nephrotoxicityHD, HemodialysisICU, Intensive Care UnitLOS, Length of StayMDR, Multiple drug resistanceMortalityNephrotoxicityPS, Propensity ScoreVitamin CXDR, Extensively drug-resistant

Identifiers

PMID36601502
PMCPMC9805966
OpenAlexW4303684641

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.