Evidence map›Paper›PMID 35754286›Full record

ReviewJournal of neuromuscular diseases2022

A Multidisciplinary Perspective Addressing the Diagnostic Challenges of Late-Onset Pompe Disease in the Arabian Peninsula Region Developed From an Expert Group Meeting.

Ali Al Shehri, Abdullah Al-Asmi, Abdullah Mohammed Al Salti, Abubaker Almadani, Ali Hassan, Ahmed K Bamaga, Edward J Cupler, Jasem Al-Hashel, Majed M Alabdali, Mohammed H Alanazy and 1 more

Abstract readReview
In one paragraph

Review in Journal of neuromuscular diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

11 authors.

Ali Al ShehriNeuromuscular Integrated Practice Unit, Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Abdullah Al-AsmiNeurology Unit, Medicine Department, College of Medicine and Health Sciences and Sultan Qabos University Hospital, Sultan Qaboos University, Muscat, Oman.
Abdullah Mohammed Al SaltiHead of Department Neurology, Khoula Hospital, Neuroscience, Muscat, Oman.
Abubaker AlmadaniHead of Neurology Department, Rashid Hospital, Dubai, UAE.
Ali HassanHead of Neurology Department, Tawam Hospital, AlAin, Abu Dhabi, UAE.
Ahmed K BamagaPediatric Department, Neuromuscular Medicine Unit, Faculty of Medicine, King Abdulaziz University Hospital, King Abdulaziz University, Jeddah, Saudi Arabia.
Edward J CuplerKing Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
Jasem Al-HashelConsultant Neurologist, Ibn Sina Hospital, Kuwait.
Majed M AlabdaliDepartment of Neurology, College of Medicine, Imam Abdulrahman bin Faisal University, Saudi Arabia.
Mohammed H AlanazyDepartment of Internal Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Suzan NooriHead of Department Neurology, University Hospital of Sharjah (UHS), Maliha, UAE.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pompe disease is a rare, metabolic, autosomal recessive disorder. Early diagnosis is critical for progressive Pompe disease as delays can significantly alter the clinical course of the disease. Diagnostic modalities, including dried blood spot testing and genetic testing, are available and are effective for diagnosing patients with late-onset Pompe disease (LOPD). However, clinicians face numerous clinical challenges related to the diagnosis of the disease. Two expert group committee meetings, involving 11 experts from the United Arab Emirates, Kuwait, the Kingdom of Saudi Arabia, and Oman, were convened in October 2019 and November 2020 respectively to develop a uniform diagnostic algorithm for the diagnosis of pediatric and adult LOPD in the Arabian Peninsula region. During the first meeting, the specialty-specific clinical presentation of LOPD was defined. During the second meeting, a diagnostic algorithm was developed after a thorough validation of clinical presentation or symptoms, which was performed with the aid of existing literature and expert judgement. A consensus was reached on the diagnostic algorithm for field specialists, such as neurologists, rheumatologists, general practitioners/internal medicine specialists, orthopedic specialists, and pulmonologists. This specialty-specific diagnostic referral algorithm for pediatric and adult LOPD will guide clinicians in the differential diagnosis of LOPD.

Indexed as

Glycogen Storage Disease Type IIAdultChildConsensusGroup ProcessesHumansacid alpha-glucosidaseArabian Peninsula regiondried blood spotLate-onset Pompe disease

Identifiers

PMID35754286
PMCPMC9535603

What OpenQuestion holds

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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.