Evidence map›Paper›PMID 30186329›Full record

ArticleStem cells international2018

Safety of Autologous Cord Blood Cells for Preterms: A Descriptive Study.

Jie Yang, Zhuxiao Ren, Chunyi Zhang, Yunbei Rao, Junjuan Zhong, Zhu Wang, Zhipeng Liu, Wei Wei, Lijuang Lu, Jiying Wen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

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  14. Autologous cord blood in children with cerebral palsy: a review.International journal of molecular sciences · 2019
    Review
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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

13 authors at 2 institutions in 1 country.

Jie YangDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.ORCID 0000-0002-7691-0241
Zhuxiao RenDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.
Chunyi ZhangDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.
Yunbei RaoDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.
Junjuan ZhongDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.
Zhu WangDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.
Zhipeng LiuGuangdong Cord Blood and Stem Cell Bank, Guangzhou, China.
Wei WeiGuangdong Cord Blood and Stem Cell Bank, Guangzhou, China.
Lijuang LuDepartment of Obstetrics, Guangdong Women and Children Hospital, Guangzhou, China.
Jiying WenDepartment of Obstetrics, Guangdong Women and Children Hospital, Guangzhou, China.
Guocheng LiuDepartment of Obstetrics, Guangdong Women and Children Hospital, Guangzhou, China.
Kaiyan LiuInstitute of Hematology, People's Hospital, Peking University, Beijing, China.ORCID 0000-0002-6751-7827
Qi WangDepartment of Neonatology, Guangdong Women and Children Hospital, Guangzhou, China.ORCID 0000-0001-8786-292X
Guangdong Province Women and Children Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreterm birth complications are one of the leading causes of death among children under 5 years of age. Despite advances in medical care, many survivors face a lifetime of disability, including mental and physical retardation, and chronic lung disease. More recently, both allogenic and autogenic cord blood cells have been applied in the treatment of neonatal conditions such as hypoxic-ischemic encephalopathy (HIE) and bronchopulmonary dysplasia (BPD).

objectiveTo assess the safety of autologous, volume- and red blood cell- (RBC-) reduced, noncryopreserved umbilical cord blood (UCB) cell infusion to preterm infants.

methodThis study was a phase I, open-label, single-arm, single-center trial to evaluate the safety of autologous, volume- and RBC-reduced, noncryopreserved UCB cell (5 × 10

resultsAfter processing, (22.67 ± 4.05) ml UCB cells in volume, (2.67 ± 2.00) × 10

conclusionsCollection, preparation, and infusion of fresh autologous UCB cells to preterm infants is feasible and safe. Adequately powered randomized controlled studies are needed.

Identifiers

PMID30186329
PMCPMC6114055
OpenAlexW2886357421

What OpenQuestion holds

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LicenceCC BY
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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.