Evidence map›Paper›PMID 32548024›Full record

ArticleJournal of orthopaedic case reports2020

Technical Considerations of Complex Primary Total Hip Arthroplasty in a Rare Case of Combined Achondroplasia and Hereditary Multiple Exostosis Syndromes.

E Kenanidis, G Paparoidamis, N Garantziotis, P Kakoulidis, M Potoupnis, E Tsiridis

Open access · greenAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of orthopaedic case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

E KenanidisDepartment of Orthopaedic, Academic Orthopaedic Unit, Papageorgiou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
G PaparoidamisDepartment of Orthopaedic, Academic Orthopaedic Unit, Papageorgiou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
N GarantziotisDepartment of Orthopaedic, Academic Orthopaedic Unit, Papageorgiou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
P KakoulidisDepartment of Orthopaedic, Academic Orthopaedic Unit, Papageorgiou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
M PotoupnisDepartment of Orthopaedic, Academic Orthopaedic Unit, Papageorgiou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
E TsiridisDepartment of Orthopaedic, Academic Orthopaedic Unit, Papageorgiou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Papageorgiou General Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCombined achondroplasia and hereditary multiple exostosis (HME) syndrome is a rare autosomal dominant inherited skeletal dysplasia. We report, for the 1sttime, a complex primary hip arthroplasty in a patient with combined achondroplasia and HME syndrome. We emphasize to the femoral and acetabular surgical concerns and difficulties of the surgical exposure and soft tissue balancing for this complex procedure. CASE REPORT: An ambulatory 66-year-old female Caucasian with achondroplasia and HME presented with the left hip pain, progressive walk disability and limited range of hip motion due to severe hip osteoarthritis. Full cemented primary total hip arthroplasty (THA) with an impaction grafting technique was performed; posterior lip augmentation device was implanted to improve stability. At 5 years follow-up, the patient remains ambulatory and pain-free with improved range of hip motion. No signs of aseptic loosening are present.

conclusionsCemented THA could be an efficient option to reconstruct the complex hip anatomy in patients with skeletal dysplasia.

Indexed as

achondroplasiahereditary multiple exostosisTotal hip arthroplasty

Identifiers

PMID32548024
PMCPMC7276594
OpenAlexW3034684203

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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.