Evidence map›Paper›PMID 37706420›Full record

ArticleSaudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association2024

Clinical and laboratory features of biliary atresia and patterns of management practices: Saudi national study (2000-2018).

Homoud Alhebbi, Mohammed El-Edreesi, Mohammed Abanemai, Omar Saadah, Maher Alhatlani, Hana Halabi, Razan Bader, Ahmed Al Sarkhy, Ahmed Aladsani, Sami Wali and 5 more

Open access · diamondAbstract readMulticenter Study
In one paragraph

Article in Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Use of percutaneous cholecysto-cholangiogram in the evaluation of neonatal cholestasis.Journal of pediatric gastroenterology and nutrition · 2026
    Article
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

15 authors at 8 institutions in 1 country.

Homoud AlhebbiDivision of Pediatric Gastroenterology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Mohammed El-EdreesiDivision of Pediatric Gastroenterology, Johns Hopkins Aramco Healthcare, Dhahran, Saudi Arabia.
Mohammed AbanemaiDepartment of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Omar SaadahDivision of Pediatric Gastroenterology, King Abdulaziz University, Jeddah, Saudi Arabia.
Maher AlhatlaniAl Imam Abdulrahman Bin Faisal Hospital, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.
Hana HalabiMaternity and Children's Hospital, Makkah, Saudi Arabia.
Razan BaderMulti-organ Transplant Center, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Ahmed Al SarkhyDepartment of Pediatrics, Gastroenterology Division, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.
Ahmed AladsaniDepartment of Pediatrics, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Sami WaliDivision of Pediatric Gastroenterology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Talal AlguofiOrgan Transplant Centre, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Nawaf AlkhathranDivision of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Amira NasserAllahCollege of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Muhammed Salman BashirDepartment of Biostatistics, Research Services Administration, Research Center, King Fahad Medical City, Riyadh, Saudi Arabia.
Abdulrahman Al-HussainiDivision of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Riyadh Armed Forces Hospital · SAKing Faisal Specialist Hospital & Research Centre · SAKing Saud University · SAImam Abdulrahman Bin Faisal University · SAKing Fahad Specialist Hospital · SAKing Fahd Medical City · SAMaternity and Children's Hospital · SANational Guard Health Affairs · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe utilized the data from the Saudi national biliary atresia (BA) study (2000-2018) to describe the clinical, biochemical, imaging, and histopathological features of BA and the perioperative clinical practices among local pediatric gastroenterologists.

methodsThis is a retrospective, multicenter, nationwide study that included 10 tertiary care governmental hospitals including the four liver transplant (LT) centers in different regions across Saudi Arabia.

resultsBA was diagnosed in 204 infants (106 females; 10% preterm). The median age at referral was 65 days. Congenital anomalies were present in 68 patients (33%); 22 were splenic malformation (10.8%). The medians of laboratory investigations were total bilirubin (189 μmol/l), direct bilirubin (139 μmol/l), ALT (164 u/l), and GGT (472 u/l). The level of serum GGT was normal in 26 cases (12.7%). The ultrasound findings included hypoplastic or atrophic gall bladder (GB) (65%), normal GB (30%), and cord sign (5%). A HIDA scan was performed in 99 cases (48.52%). Magnetic resonance cholangiopancreatography (MRCP) was performed in 27 cases (13%). A total of 179 liver biopsies (88%) were obtained. The most common histopathologic findings were bile duct proliferation (92%), canalicular cholestasis (96%), bile plugs (84%), and portal fibrosis (95%). Cholangiography was performed in 139 cases (68%): operative in 122 (60%) and percutaneous in 17 (8%). A total of 143 children (70%) underwent Kasai portoenterostomy (KPE) at a median age of 70 days. After KPE, steroid was used in 37% of the cases and 100 cases (70%) were prescribed prophylactic antibiotics for variable duration (ranging between 3 and 12 months).

conclusionOur data show marked variation in the diagnostic evaluation and perioperative management of BA cases among the different tertiary centers. There is a need to establish a national BA registry in Saudi Arabia aiming to standardize pre- and postoperative clinical practices. Additionally, normal serum GGT level, normal GB size on ultrasound, and being a premature baby should not preclude the diagnostic workup for BA.

Indexed as

Bile Duct DiseasesBiliary AtresiaBilirubinChildFemaleHumansInfantInfant, NewbornRetrospective StudiesSaudi ArabiaBilirubin

Identifiers

PMID37706420
PMCPMC10980299
OpenAlexW4386543706

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.