Evidence map›Paper›PMID 41798823›Full record

ArticleFrontiers in neurology

A parsimonious nomogram for individualized prediction of 1-year functional outcome after STN-DBS in Parkinson's disease: a single-center retrospective study.

Yiming Zhang, Qiushi Zhu, Baojun Fang, Fengyang Geng

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Article in Frontiers in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yiming ZhangDepartment of Neurosurgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Qiushi ZhuDepartment of Neurosurgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Baojun FangDepartment of Neurosurgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Fengyang GengDepartment of Neurosurgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In the context of Parkinson's disease (PD), subthalamic nucleus deep brain stimulation (STN-DBS) has been shown to alleviate motor symptoms; nevertheless, functional outcomes at follow-up continue to be inconsistent. Patients who are at a higher risk of unsatisfactory functional recovery could be identified with the use of a personalized risk stratification tool, which would also provide information for perioperative treatment. Methods: We retrospectively reviewed consecutive PD patients who underwent STN-DBS at the Department of Functional Neurosurgery, Liaocheng People's Hospital, from January 1, 2015 to August 1, 2024, with 1-year follow-up. The outcome was defined using the medication-off Schwab and England Activities of Daily Living Scale (S&E) at 1 year: good outcome (S&E > 70) versus poor outcome (S&E ≤ 70). Candidate predictors were prespecified and collected from three domains: general clinical characteristics, perioperative indicators, and preoperative specialist assessments. Through the use of multivariable logistic regression, independent predictors of poor outcomes were found, and a nomogram was produced. Bootstrap resampling was utilized in order to carry out the internal validation process. The area under the receiver operating characteristic curve [AUC (C-index)] was used to quantify the discrimination of the model, the calibration was investigated using a calibration plot and the Hosmer-Lemeshow test, and the clinical utility was evaluated using decision curve analysis (DCA). Results: 184 people were included in the study, with 109 having a positive outcome and 75 having a negative outcome. Out of the 195 patients that were eligible, 11 were lost to follow-up. Independently, worse outcome was linked with older age (odds ratio 1.08, 95% confidence interval 1.03-1.14), a lower score on the Mini-Mental State Examination (MMSE) (odds ratio 0.66, 95% confidence interval 0.56-0.79), and postoperative electrolyte disorder (odds ratio 2.97, 95% confidence interval 1.28-6.91). There was a low level of optimism on the internal validation (optimism-corrected C-index 0.841), despite the fact that the nomogram shown decent discrimination (AUC 0.846; bootstrap 95% confidence interval 0.781-0.905). In general, the calibration revealed that the projected risks and the observed hazards were in agreement. The results of the DCA indicated that the model had a positive net benefit across a wide range of threshold probabilities (0.20-0.99). Conclusion: For the purpose of predicting the functional prognosis of a patient with Parkinson's disease 1 year after receiving STN-DBS, we constructed a parsimonious nomogram that included age, MMSE, and postoperative electrolyte imbalance. In the event that our model is validated by an external source, it may be able to facilitate individualized perioperative risk assessment and collaborative decision-making.

Indexed as

calibrationdecision curve analysisdeep brain stimulationfunctional outcomenomogramParkinson’s diseaserisk predictionsubthalamic nucleus

Identifiers

PMID41798823
PMCPMC12962900

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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.