# Trends in research related to fetal therapy from 2012 to 2022: a bibliometric analysis

**Authors:** Yang Jia, Xiaoling Liang, Lini Liu, Huixi Ma, Chenhao Xu, Jingyuan Zeng, Rong Xu, Lu Ye, Linjun Xie

PMC · DOI: 10.3389/fped.2023.1288660 · Frontiers in Pediatrics · 2024-01-04

## TL;DR

This paper analyzes trends in fetal therapy research from 2012 to 2022, showing growth and shifts toward advanced treatments like gene and stem cell therapy.

## Contribution

The study provides a comprehensive bibliometric analysis of fetal therapy research trends and hotspots over the past decade.

## Key findings

- The number of fetal therapy publications increased significantly from 2012 to 2022.
- Research has shifted from traditional surgery to gene and stem cell therapies.
- Fetoscopic laser surgery and MRI are emerging as key research hotspots.

## Abstract

The development of prenatal diagnosis technology allows prompt detection of severe fetal diseases. To address adverse factors that threaten fetal survival, fetal therapy came into existence, which aims to preserve the function after birth to a higher degree and improve the quality of life.

To conduct a comprehensive bibliometric analysis of studies on fetal therapy in the past decade and explore the research trends and hotspots in this field.

We conducted a systematic search on the Web of Science Core Collection to retrieve studies related to fetal therapy published from 2012 to 2022. VOSviewer and CiteSpace were used to analyze the key features of studies, including annual output, countries/regions, institutions, authors, references, research hotspots, and frontiers.

A total of 9,715 articles were included after eliminating duplicates. The annual distribution of the number of articles showed that the number of articles published in fetal therapy had increased in the past decade. Countries and institutions showed that fetal therapy is more mature in the United States. Author analysis showed the core investigators in the field. Keyword analysis showed the clustering and emergence frequency, which helped summarize the research results and frontier hotspots in this field. The cocited references were sorted out to determine the literature with a high ranking of fetal therapy in recent years, and the research trend in recent years was analyzed.

This study reveals that countries, institutions, and researchers should promote wider cooperation and establish multicenter research cooperation in fetal therapy research. Moreover, fetal therapy has been gradually explored from traditional surgical treatment to gene therapy and stem cell therapy. In recent years, fetoscopic laser surgery, guideline, and magnetic resonance imaging have become the research hotspots in the field.

## Full-text entities

- **Genes:** FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}
- **Diseases:** aortic valve stenosis (MESH:D001024), chest mass (MESH:D013898), hindbrain herniation (MESH:D004677), TS (MESH:D005879), pulmonary valve (MESH:D011665), congenital heart disease (MESH:D006330), intracranial hemorrhage (MESH:D020300), hemophilia (MESH:D006467), placental abruption (MESH:D000037), chorionic angioma (MESH:D006391), premature membrane rupture (MESH:D005322), inclusion body cysts (MESH:C536816), hydrocephalus (MESH:D006849), placental insufficiency (MESH:D010927), urinary tract obstruction (MESH:D014552), osteogenesis imperfecta (MESH:D010013), heart failure (MESH:D006333), central nervous system disease (MESH:D002493), distal limb abnormalities (MESH:C565437), thoracic malformations (MESH:D013896), fetal anemia (MESH:D005315), brain injury (MESH:D001930), cystic fibrosis (MESH:D003550), Ebstein malformations (MESH:D004437), gestational diabetes mellitus (MESH:D016640), airway obstruction (MESH:D000402), laser coagulation (MESH:D001778), HIV (MESH:D015658), fetal distress (MESH:D005316), hypertension (MESH:D006973), congenital diaphragmatic hernia (MESH:D065630), sacrococcygeal teratoma (MESH:D013724), spina bifida (MESH:D016135), pulmonary hypoplasia (MESH:C562992), diaphragmatic hernia (MESH:D006548), premature delivery (MESH:C536271), bronchial or lung compression (MESH:D008171), fracture (MESH:D050723), pregnancy diseases (MESH:D011254), muscular dystrophy (MESH:D009136), tetralogy of Fallot (MESH:D013771), preterm birth (MESH:D047928), twin transfusion syndrome (MESH:D005330), myelomeningocele (MESH:D008591), infection (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10826513/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC10826513/full.md

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Source: https://tomesphere.com/paper/PMC10826513