Evidence map›Paper›PMID 35625345›Full record

ReviewAntibiotics (Basel, Switzerland)2022

Ways to Improve Insights into Clindamycin Pharmacology and Pharmacokinetics Tailored to Practice.

Laura Armengol Álvarez, Greet Van de Sijpe, Stefanie Desmet, Willem-Jan Metsemakers, Isabel Spriet, Karel Allegaert, Jef Rozenski

Open access · goldAbstract readReview
In one paragraph

Review in Antibiotics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Oral clindamycin for peritonitis due toJAC-antimicrobial resistance · 2024
    Article
  11. Increasing Rate of FatalMicroorganisms · 2024
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. 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

7 authors at 3 institutions in 2 countries.

Laura Armengol ÁlvarezRega Institute for Medical Research, KU Leuven, B-3000 Leuven, Belgium.
Greet Van de SijpeDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, B-3000 Leuven, Belgium.
Stefanie DesmetDepartment of Laboratory Medicine, University Hospitals Leuven, B-3000 Leuven, Belgium.
Willem-Jan MetsemakersDepartment of Development and Regeneration, KU Leuven, B-3000 Leuven, Belgium.ORCID 0000-0002-4114-9093
Isabel SprietDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, B-3000 Leuven, Belgium.
Karel AllegaertDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, B-3000 Leuven, Belgium.ORCID 0000-0001-9921-5105
Jef RozenskiRega Institute for Medical Research, KU Leuven, B-3000 Leuven, Belgium.ORCID 0000-0001-9624-5536
KU Leuven · BERega Institute for Medical Research · BEErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the increase in bacterial resistance and the decrease in the development of new antibiotics, the appropriate use of old antimicrobials has become even more compulsory. Clindamycin is a lincosamide antibiotic approved for adults and children as a drug of choice for systemic treatment of staphylococcal, streptococcal, and gram-positive anaerobic bacterial infections. Because of its profile and high bioavailability, it is commonly used as part of an oral multimodal alternative for prolonged parenteral antibiotic regimens, e.g., to treat bone and joint or prosthesis-related infections. Clindamycin is also frequently used for (surgical) prophylaxis in the event of beta-lactam allergy. Special populations (pediatrics, pregnant women) have altered cytochrome P450 (CYP)3A4 activity. As clindamycin is metabolized by the CYP3A4/5 enzymes to bioactive N-demethyl and sulfoxide metabolites, knowledge of the potential relevance of the drug's metabolites and disposition in special populations is of interest. Furthermore, drug-drug interactions derived from CYP3A4 inducers and inhibitors, and the data on the impact of the disease state on the CYP system, are still limited. This narrative review provides a detailed survey of the currently available literature on pharmacology and pharmacokinetics and identifies knowledge gaps (special patient population, drug-drug, and drug-disease interactions) to describe a research strategy for precision medicine.

Indexed as

antibioticbacterial infectionsclindamycinCYP450 enzymesdrug–drug interactionspharmacokineticsspecial patient populations

Identifiers

PMID35625345
PMCPMC9137603
OpenAlexW4281254473

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.