Related Experiment Video
Updated: Jan 18, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
Quality-of-Life Outcomes in Adults and Children With Chiari 1 Malformation and in Those Managed Without Surgery: A
Rory J Piper1,2,3, Fardad T Afshari4, Wai C Soon5
1Department of Neurosurgery, John Radcliffe Hospital, Oxford , UK.
Insights
Quality of life remained stable for adults and children with Chiari 1 malformation (CM1) managed non-surgically over 12 months. Some adults experienced improvements in social functioning and pain.
Area of Science:
- Neurosurgery
- Quality of Life Research
- Clinical Cohort Studies
Background:
- Chiari 1 malformation (CM1) is a common condition often leading to neurosurgical consultation.
- Outcomes for non-surgically managed CM1 patients are less studied than surgical outcomes.
- The UK Chiari 1 Study focuses on quality of life in non-surgically treated CM1 patients.
Purpose of the Study:
- To evaluate the quality of life in adults and children with CM1 managed without surgery.
- To report findings 12 months after the initial neurosurgical clinic visit.
- To provide data on the natural history of CM1 in non-surgically managed cohorts.
Main Methods:
- Prospective, multicenter observational cohort study.
- Inclusion of adults (≥16 years) and children (<16 years) diagnosed with CM1.
- Collection of quality-of-life data using SF-36 (adults) and PedsQL™ (children) at baseline and 12 months.
Main Results:
- Baseline quality of life was significantly lower in all domains compared to normative data for both age groups.
- No significant decrease in quality-of-life subscores was observed at 12 months for non-surgically managed CM1 patients.
- Adult patients showed statistically significant improvements in social functioning and bodily pain scores at 12 months.
Conclusions:
- Non-surgical management of CM1 appears to stabilize quality of life over a 12-month period.
- Further research is needed to identify factors influencing quality of life in CM1 patients.
- Comparative studies of surgical versus non-surgical interventions for CM1 are warranted.
Background And Objectives:
Chiari 1 malformation (CM1) is a common MRI finding and a frequent reason for neurosurgical consultation. Although many studies have investigated surgical outcomes for patients with CM1, outcomes for those treated without surgery have been less frequently reported. The UK Chiari 1 Study reports the quality of life of adults and children with CM1 treated without surgery, 12 months after the first neurosurgical clinic visit.
Methods:
The UK Chiari 1 Study was a prospective, multicenter cohort study of adults (≥16 years) and children (<16 years) with CM1. This was an observational study that did not alter the course of clinical care. Symptoms and quality-of-life data (using Short-Form 36 in adults and the Pediatric Quality of Life Inventory™ in children) were collected at baseline and 12 months after the first clinical review for all participants.
Results:
One hundred ninety-two patients with CM1 (146 females; 148 adults) were studied at baseline, and 113 patients with CM1 treated without surgery were studied at a 12-month follow-up. Baseline quality-of-life scores in the study cohort were significantly lower in every domain compared with normative control data, in both adults and children. There were no decreases in quality-of-life subscores after 12 months in this cohort of adults and children with CM1 treated without surgery. Social functioning ( t = -40, P < .001) and bodily pain (t = -2.9; P = .03) Short-Form 36 scores showed improvements at 12 months in adult patients treated without surgery.
Conclusion:
This study demonstrates the stability of quality-of-life domains in adults and children with CM1 after 12 months who have been managed without surgery. Further studies are required to understand the determinants of poor quality of life in patients with CM1 and to investigate interventions for improving quality of life. There is a further need for robust comparison of surgical and nonsurgical management for patients with CM1.

