Evidence map›Paper›PMID 33195743›Full record

ArticleGlobal pediatric health2020

Cystic Fibrosis Diagnosed Using Indigenously Wrapped Sweating Technique: First Large-Scale Study Reporting Socio-Demographic, Clinical, and Laboratory Features among the Children in Bangladesh A Lower Middle Income Country.

Arm Luthful Kabir, Sudipta Roy, Rahat Bin Habib, Kazi Selim Anwar, Md Abid Hossain Mollah, Ruhul Amin, Al Amin Mridha, Jasim Uddin Majumder, Md Delwar Hossain, Nazmul Haque and 2 more

Open access · goldAbstract read
In one paragraph

Article in Global pediatric health, 2020. 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
0.9field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. A comprehensive review of cystic fibrosis in Africa and Asia.Saudi journal of biological sciences · 2023
    Review
  2. Sweat Testing and Recent Advances.Frontiers in pediatrics · 2021
    Review
  3. 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

12 authors at 8 institutions in 2 countries.

Arm Luthful KabirAd-din Women's Medical College Hospital, Dhaka, Bangladesh.
Sudipta RoyAd-din Women's Medical College Hospital, Dhaka, Bangladesh.
Rahat Bin HabibDirector General Health Services, Dhaka, Bangladesh.
Kazi Selim AnwarIUHW, Narita, Chiba, Japan.
Md Abid Hossain MollahDhaka Medical College, Dhaka, Bangladesh.
Ruhul AminInstitute of Child Health (BICH), Dhaka, Bangladesh.
Al Amin MridhaShaheed Shuhrawardy Medical College, Dhaka, Bangladesh.
Jasim Uddin MajumderEast West Medical College, Dhaka, Bangladesh.
Md Delwar HossainInstitute of Child and Mother Health (ICMH), Dhaka, Bangladesh.
Nazmul HaqueDhaka Medical College, Dhaka, Bangladesh.
Shakil AhmedShaheed Shuhrawardy Medical College, Dhaka, Bangladesh.
Mohammod Jobayer ChistiInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Dhaka Medical College and Hospital · BDShaheed Suhrawardy Medical College · BDChild Health Research Foundation · BDDirectorate General of Health Services · BDEast West University · BDInstitute of Child and Mother Health · BDInternational Centre for Diarrhoeal Disease Research · BDInternational University of Health and Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to lack of robust data on childhood cystic fibrosis (CF) in Bangladesh we sought to evaluate their clinico-epidemiology. A cross-sectional observation was conducted adopting CF-foundation consensus-panel-diagnostic criteria in 3 tertiary-care-hospitals in Bangladesh from 2000 to 2017. Clinically suspected 95 CF-cases were subjected to sweat-chloride testing using locally-developed a fast, cheap and effective indigenously body-wrapped sweating technique measured by US-Easy Lyte-automated microprocessor-controlled analyzer marking ≥60 mmol/L as positive. Mean-age of CF-cases at disease-onset was 16.9 ± 26.6 months that significantly differed with age-at-diagnosis (

Indexed as

BangladeshchildrenCystic fibrosisfirst large-scale reportindigenously wrapped sweating technique

Identifiers

PMID33195743
PMCPMC7607759
OpenAlexW3094673430

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.