ReviewChild and adolescent psychiatric clinics of North America2010
Developmental and psychosocial issues in cystic fibrosis.
Review in Child and adolescent psychiatric clinics of North America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled 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.
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.
Who cites it
16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 72 citations in OpenAlex.
- Anxiety in Children with Cystic Fibrosis and Their Parents: A Systematic Review.Clinical child and family psychology review · 2021Pooled it
- Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosis.The Cochrane database of systematic reviews · 2015Pooled it
- Mapping Perceived Impact, Facilitators and Barriers of Cystic Fibrosis Management in Children and Adolescents: A Qualitative Study From the Parents' Perspective.Scandinavian journal of caring sciences · 2025Article
- Translation, cross-cultural adaptation, and evaluation of psychometric properties of the cystic fibrosis stigma scale.Scientific reports · 2025Article
- Navigating Pediatric Cor Pulmonale: A Comprehensive Review of Diagnosis and Management.Cureus · 2024Review
- Telerehabilitation in Children and Adolescents with Cystic Fibrosis: A Scoping Review.Healthcare (Basel, Switzerland) · 2024Article
- Development of a Cystic Fibrosis Primary Palliative Care Intervention: Qualitative Analysis of Patient and Family Caregiver Preferences.Journal of patient experience · 2023Article
- Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosis.The Cochrane database of systematic reviews · 2018Review
- A Prototype Exercise-Empowerment Mobile Video Game for Children With Cancer, and Its Usability Assessment: Developing Digital Empowerment Interventions for Pediatric Diseases.Frontiers in pediatrics · 2018Article
- The Epidemiological Characteristics of Epilepsy in the Province of Khyber Pakhtunkhwa, Pakistan.Frontiers in neurology · 2018Article
- Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population.Tuberculosis and respiratory diseases · 2016Article
- Association Between Outcomes and Demographic Factors in an Azeri Turkish Population With Cystic Fibrosis: A Cross-Sectional Study in Iran From 2001 Through 2014.Iranian Red Crescent medical journal · 2016Article
- Assessment of stigma in patients with cystic fibrosis.BMC pulmonary medicine · 2014Observational
- European Cystic Fibrosis Society Standards of Care: Framework for the Cystic Fibrosis Centre.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2014Review
- Health-related quality of life of Spanish children with cystic fibrosis.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2012Article
- Spirometry-related pain and distress in adolescents and young adults with cystic fibrosis: the role of acceptance.Pain research & managementArticle
Corrections and comments
- Reprinted as
Authors and funding
3 authors at 2 institutions in 1 country.
Funding
Abstract
Cystic fibrosis (CF) is a multisystemic life-limiting genetic disorder, primarily affecting respiratory functioning. Most patients with CF are diagnosed by 2 years of age, and the current median predicted survival rate is 37.4 years old, with 95% of patients dying from complications related to pulmonary infection. Given the chronic, progressive, and disabling nature of CF, multiple treatments are prescribed, most on a daily basis. Thus, this illness requires children, with the aid of their families, to adopt multiple health-related behaviors in addition to managing more typical developmental demands. The morbidity and mortality factors pose cognitive, emotional, and behavioral challenges for many children with CF and their families. This article applies a developmental perspective to describing the psychosocial factors affecting psychological adjustment and health-related behaviors relevant to infants, preschool and school-age children, and adolescents with CF. Topics particularly pertinent to developmental periods and medical milestones are noted, with clinical implications highlighted.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.