Evidence map›Paper›PMID 31717467›Full record

ArticlePharmaceutics2019

Extended Release Combination Antibiotic Therapy from a Bone Void Filling Putty for Treatment of Osteomyelitis.

Raquib Hasan, Kambri Schaner, Meredith Schroeder, Abbey Wohlers, Jacob Shreffler, Codi Schaper, Hariharaputhiran Subramanian, Amanda Brooks

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Raquib HasanDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58102, USA.
Kambri SchanerDepartment of Biological Sciences, North Dakota State University, Fargo, ND 58102, USA.
Meredith SchroederDepartment of Microbiological Sciences, North Dakota State University, Fargo, ND 58102, USA.
Abbey WohlersDepartment of Pharmacy, North Dakota State University, Fargo, ND 58102, USA.
Jacob ShrefflerDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58102, USA.
Codi SchaperDepartment of Animal Sciences, North Dakota State University, Fargo, ND 58102, USA.
Hariharaputhiran SubramanianDepartment of Chemistry and Biochemistry, North Dakota State University, Fargo, ND 58102, USA.
Amanda BrooksDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58102, USA.
North Dakota State University · US

Funding

ND EPSCoR Doctoral Dissertation FellowshipNorth Dakota Department of Commerce Phase I Venture Grant
6 · The paper itself

Abstract

In spite of advances in Total Joint Replacements (TJR), infection remains a major concern and a primary causative factor for revision surgery. Current clinical standards treat these osteomyelitis infections with antibiotic-laden poly(methyl methacrylate) (PMMA)-based cement, which has several disadvantages, including inadequate local drug release kinetics, antibiotic leaching for a prolonged period and additional surgical interventions to remove it, etc. Moreover, not all antibiotics (e.g., rifampicin, a potent antibiofilm antibiotic) are compatible with PMMA. For this reason, treatment of TJR-associated infections and related complications remains a significant concern. The objective of this study was to develop a polymer-controlled dual antibiotic-releasing bone void filler (ABVF) with an underlying osseointegrating substrate to treat TJR implant-associated biofilm infections. An ABVF putty was designed to provide sustained vancomycin and rifampicin antibiotic release for 6 weeks while concurrently providing an osseointegrating support for regrowth of lost bone. The reported ABVF showed efficient antibacterial and antibiofilm activity both in vitro and in a rat infection model where the ABVF both showed complete bacterial elimination and supported bone growth. Furthermore, in an in vivo k-wire-based biofilm infection model, the ABVF putty was also able to eliminate the biofilm infection while supporting osseointegration. The retrieved k-wire implants were also free from biofilm and bacterial burden. The ABVF putty delivering combination antibiotics demonstrated that it can be a viable treatment option for implant-related osteomyelitis and may lead to retention of the hardware while enabling single-stage surgery.

Indexed as

biofilmbone void fillercombination antibiotic deliverydrug releaseinfectionosteomyelitisrifampicintotal joint replacementvancomycin

Identifiers

PMID31717467
PMCPMC6920883
OpenAlexW2983183717

What OpenQuestion 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 OpenQuestion graph.