Evidence map›Paper›PMID 37850770›Full record

ArticleActa bio-medica : Atenei Parmensis2023

Clinical and epidemiological features and therapeutic options of avascular necrosis in patients with sickle cell disease (SCD): a cross-sectional study.

Awni Alshurafa, Ashraf T Soliman, Vincenzo De Sanctis, Omar Ismail, Mohammad Abu-Tineh, Mohammad Khair Eddin Hemadneh, Farah Rahat Rashid, Khadra Yassin, Hana Qasim, Abdulqadir Jeprel Nashwan and 1 more

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In one paragraph

Article in Acta bio-medica : Atenei Parmensis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 9 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

11 authors at 8 institutions in 7 countries.

Awni AlshurafaHamad Medical Corporation. dr.a.shurafa@gmail.com.
Ashraf T Soliman. ATSOLIMAN56@gmail.com.
Vincenzo De Sanctis. vdesanctis@libero.it.
Omar Ismail. Oismail@hamad.qa.
Mohammad Abu-Tineh. abutineh90@gmail.com.
Mohammad Khair Eddin Hemadneh. Mhemadneh@hamad.qa.
Farah Rahat Rashid. Frashid2@hamad.qa.
Khadra Yassin. KYASSIN@hamad.qa.
Hana Qasim. Hanaa.qasem1@gmail.com.
Abdulqadir Jeprel Nashwan. anashwan@hamad.qa.
Mohamed A Yassin. Yassinmoha@gmail.com.
Hamad General Hospital · QAAdvanced BioNutrition (United States) · USAl-Qasemi Academic College of Education · ILAnsan University · KRHamad Medical Corporation · QAKing Hamad University Hospital · BHUniversity of the Philippines Diliman · PHYibin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAvascular necrosis (AVN) is a debilitating complication in sickle cell disease (SCD) patients, and its management is usually challenging. This study aims to evaluate the clinical and epidemiological features and therapeutic options of AVN in sickle cell patients in Qatar. PATIENTS AND

methodsA cross-sectional study was conducted on a 49 SCD patients who were diagnosed with AVN and attended the hematology clinic at the National Center for Cancer care & research, Hamad Medical Corporation, Qatar between Jan-2011 to Jan2021.  Results: Forty-nine adult patients with SCD who were diagnosed with AVN were studied. The median age of the study population is 32 years, and the median age at the first AVN diagnosis was 26 years (range: 11-44 yr.). 37 (75.5%) patients suffered from multiple joints AVN while 12(24.5%) had single joint involvement. 31 (63.3%) patients had bilateral hip AVN and 18 (36.7%) had shoulder involvement. 30 patients (61%) were on Hydroxyurea treatment. Based on FICAT and Alert classification of AVN, 57 % of patients had stage III and above at first diagnosis. 20 (40.8%) were managed with a conservative approach, 11 (22.4%) received hyperbaric oxygen with good response, 6(12.2%) underwent hip core decompression and 12(24.5%) underwent hip replacement surgery.

conclusionIn SCD patients, AVN occurred more during the 3rd and 4th decades of life. The majority of AVN represented with advanced stage and had multiple joint involvements. We recommend adopting a low threshold of joint imaging for early detection and prevention of further complications.

Indexed as

Anemia, Sickle CellOsteonecrosisAdolescentAdultChildCross-Sectional StudiesEarly Detection of CancerHumansQatarYoung Adult

Identifiers

PMID37850770
PMCPMC10644931
OpenAlexW4387728925

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.