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Published on: September 10, 2018
The Seow Operative Score (SOS) as a decision-making adjunct for paediatric Chiari I malformation: a preliminary study
Sharon Y Y Low1,2,3, Lee Ping Ng4, Audrey J L Tan4
1Neurosurgical Service, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore. sharon.low.y.y@singhealth.com.sg.
Insights
The natural history of Chiari I malformation (C1M) in children is unclear. This study introduces the Seow Operative Score (SOS) to aid in managing paediatric C1M, showing its utility in guiding surgical decisions.
Area of Science:
- Neurosurgery
- Paediatric Neurology
- Medical Scoring Systems
Background:
- The natural history and management of Chiari I malformation (C1M) in children remain poorly understood.
- Conflicting reports exist regarding surgical indications, techniques, and prognostic indicators for paediatric C1M.
Purpose of the Study:
- To report institutional experience in managing paediatric Chiari I malformation (C1M).
- To discuss workflow processes including imaging, surgical techniques, and intervention indications.
- To introduce and evaluate the Seow Operative Score (SOS) for feasibility in neurosurgical intervention for paediatric C1M.
Main Methods:
- Retrospective review of paediatric C1M patients, divided into non-operated (10) and operated (19) groups.
- Application of the in-house designed Seow Operative Score (SOS) to stratify patients.
- Analysis of patient outcomes based on SOS and treatment decisions.
Main Results:
- Non-operated patients predominantly had a low SOS (0-1), with one patient (SOS 2.5) showing resolution of symptoms and syrinx under surveillance.
- Operated patients mostly had a high SOS (≥3).
- Two patients with SOS 2 underwent surgery due to progressive symptoms or extensive syrinx after surveillance.
Conclusions:
- The Seow Operative Score (SOS) demonstrates feasibility in guiding neurosurgical intervention decisions for paediatric Chiari I malformation (C1M).
- Institutional experience highlights the importance of tailored management based on individual patient factors and scoring systems.
- Further global research is advocated for enhanced understanding and management of paediatric C1M.
Purpose:
The natural history of Chiari I malformation (C1M) in the paediatric population is poorly understood. There are conflicting reports with regards to surgical indications, operative techniques and peri-operative prognostic indicators. In this paper, we report our institutional experience in the management of paediatric C1M.
Methods:
The workflow process which includes preferred imaging modalities, surgical techniques and indications for intervention is discussed. In particular, we describe one of our current projects-an in-house designed Seow Operative Score (SOS) as a feasibility scoring system for neurosurgical intervention in our local cohort of paediatric C1M patients.
Results:
In our series, we have 2 groups: 10 non-operated patients versus 19 operated patients. In the non-operated group, the majority of patients had a SOS of 0 to 1. One patient had a score of 2.5 and was kept under close surveillance. Follow-up imaging demonstrated resolution of the cerebellar herniation and intraspinal syrinx. In the operated group, 17 patients had a SOS of 3 or more. Two patients had a SOS of 2. For these 2, 1 developed progressive symptoms, and the other had an extensive cervico-thoracic syrinx. Decision was made for surgery after a period of surveillance.
Conclusions:
In this paper, we report our institutional experience in managing paediatric C1M and, at the same time, highlight salient points of our practices. Meanwhile, we advocate collective global efforts and in-depth research for better disease understanding of this challenging condition.
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