Evidence map›Paper›PMID 29907913›Full record

ArticleInternational orthopaedics2019

Total hip arthroplasty in osteonecrosis secondary to sickle cell disease.

Mohamed Zubair Farook, Moji Awogbade, Karthik Somasundaram, Ines L H Reichert, Patrick L S Li

Open access · hybridAbstract read
In one paragraph

Article in International orthopaedics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Survival of total hip arthroplasty (THA) in sickle cell disease.Archives of orthopaedic and trauma surgery · 2023
    Article
  8. Review
  9. Sickle cell disease as an accelerated aging syndrome.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Osteonecrosis in sickle cell disease: an update on risk factors, diagnosis, and management.Hematology. American Society of Hematology. Education Program · 2019
    Review
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

5 authors at 3 institutions in 1 country.

Mohamed Zubair FarookDepartment of Trauma & Orthopaedics, King's College Hospital NHS Foundation Trust, King's College London, Denmark Hill, London, SE5 9RS, UK.
Moji AwogbadeDepartment of Haematological Medicine, Kings College Hospital NHS Foundation Trust, Denmark Hill, London, SE5 9RS, UK.
Karthik SomasundaramMorriston Hospital, Swansea, Wales, UK.
Ines L H ReichertDepartment of Trauma & Orthopaedics, King's College Hospital NHS Foundation Trust, King's College London, Denmark Hill, London, SE5 9RS, UK. ines.reichert@kcl.ac.uk.ORCID http://orcid.org/0000-0003-0192-9148
Patrick L S LiDepartment of Trauma & Orthopaedics, King's College Hospital NHS Foundation Trust, King's College London, Denmark Hill, London, SE5 9RS, UK.
King's College London · GBKing's College Hospital NHS Foundation Trust · GBMorriston Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) is a multisystem disease, and the predominant articular manifestation is osteonecrosis (ON). Total hip arthroplasty (THA) is technically challenging, and the complication rates are high. In this retrospective study, we have analysed the outcome of THA in a cohort of patients with SCD at our institution. MATERIALS AND

methodsWe identified 34 THAs between 1999 and 2016 in 30 patients (mean age 37 years) from our SCD database. Co-morbidities, both sickle and non-sickle-related, were documented. Complications and indications for revision surgery were analysed.

resultsAn uncemented prosthesis was predominantly used. The mean follow-up was 10.5 years (range 1-18). Six patients had revision surgery (17.6%), 2 (5.8%) for Prosthetic Joint Infection (PJI), and 4 (11.7%) for osteolysis of the acetabular component.

conclusionOur revision rates were comparable to the published literature. Our combined sickle cell clinic and the coordinated multidisciplinary management have been successful in reducing morbidity.

Indexed as

AcetabulumAdultAnemia, Sickle CellArthritis, InfectiousArthroplasty, Replacement, HipFemaleHip ProsthesisHumansMaleMiddle AgedOsteonecrosisReoperationRetrospective StudiesOsteonecrosisRevisionSickle cell diseaseTHA

Identifiers

PMID29907913
PMCPMC6399197
OpenAlexW2807732327

What OpenQuestion holds

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LicenceCC BY
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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.