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      Predictive nomogram models for unfavorable prognosis after aneurysmal subarachnoid hemorrhage: Analysis from a prospective, observational cohort in China

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          Abstract

          Aim

          The aim of the study was to identify predictors for 3‐month poor functional outcome or death after aSAH and develop precise and easy‐to‐use nomogram models.

          Methods

          The study was performed at the department of neurology emergency in Beijing Tiantan Hospital. A total of 310 aSAH patients were enrolled between October 2020 and September 2021 as a derivation cohort, while a total of 208 patients were admitted from October 2021 to March 2022 as an external validation cohort. Clinical outcomes included poor functional outcome defined as modified Rankin Scale score (mRS) of 4–6 or all‐cause death at 3 months. Least absolute shrinkage and selection operator (LASSO) analysis, as well as multivariable regression analysis, were applied to select independent variables associated with poor functional outcome or death and then to construct two nomogram models. Model performance were evaluated through discrimination, calibration, and clinical usefulness in both derivation cohort and external validation cohort.

          Results

          The nomogram model to predict poor functional outcome included seven predictors: age, heart rate, Hunt‐Hess grade on admission, lymphocyte, C‐reactive protein (CRP), platelet, and direct bilirubin levels. It demonstrated high discrimination ability (AUC, 0.845; 95% CI: 0.787–0.903), satisfactory calibration curve, and good clinical usefulness. Similarly, the nomogram model combining age, neutrophil, lymphocyte, CRP, aspartate aminotransferase (AST) levels, and treatment methods to predict all‐cause death also revealed excellent discrimination ability (AUC, 0.944; 95% CI: 0.910–0.979), satisfactory calibration curve, and clinical effectiveness. Internal validation showed the bias‐corrected C‐index for poor functional outcome and death was 0.827 and 0.927, respectively. When applied to the external validation dataset, both two nomogram models exhibited high discrimination capacity [poor functional outcome: AUC = 0.795 (0.716–0.873); death: AUC = 0.811 (0.707–0.915)], good calibration ability, and clinical usefulness.

          Conclusions

          Nomogram models constructed for predicting 3‐month poor functional outcome or death after aSAH are precise and easily applicable, which can help physicians to identify patients at risk, guide decision‐making, and provide new directions for future studies to explore the novel treatment targets.

          Abstract

          We constructed precise and easily applicable nomogram models to predict 3‐month poor functional outcome or death after aSAH. These prediction models can help physicians to identify patients at risk, guide decision‐making, and provide new directions for future studies to explore the novel treatment targets.

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          Most cited references47

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          Nomograms in oncology: more than meets the eye.

          Nomograms are widely used as prognostic devices in oncology and medicine. With the ability to generate an individual probability of a clinical event by integrating diverse prognostic and determinant variables, nomograms meet our desire for biologically and clinically integrated models and fulfill our drive towards personalised medicine. Rapid computation through user-friendly digital interfaces, together with increased accuracy, and more easily understood prognoses compared with conventional staging, allow for seamless incorporation of nomogram-derived prognosis to aid clinical decision making. This has led to the appearance of many nomograms on the internet and in medical journals, and an increase in nomogram use by patients and physicians alike. However, the statistical foundations of nomogram construction, their precise interpretation, and evidence supporting their use are generally misunderstood. This issue is leading to an under-appreciation of the inherent uncertainties regarding nomogram use. We provide a systematic, practical approach to evaluating and comprehending nomogram-derived prognoses, with particular emphasis on clarifying common misconceptions and highlighting limitations.
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            Guidelines for the management of aneurysmal subarachnoid hemorrhage: a guideline for healthcare professionals from the American Heart Association/american Stroke Association.

            The aim of this guideline is to present current and comprehensive recommendations for the diagnosis and treatment of aneurysmal subarachnoid hemorrhage (aSAH). A formal literature search of MEDLINE (November 1, 2006, through May 1, 2010) was performed. Data were synthesized with the use of evidence tables. Writing group members met by teleconference to discuss data-derived recommendations. The American Heart Association Stroke Council's Levels of Evidence grading algorithm was used to grade each recommendation. The guideline draft was reviewed by 7 expert peer reviewers and by the members of the Stroke Council Leadership and Manuscript Oversight Committees. It is intended that this guideline be fully updated every 3 years. Evidence-based guidelines are presented for the care of patients presenting with aSAH. The focus of the guideline was subdivided into incidence, risk factors, prevention, natural history and outcome, diagnosis, prevention of rebleeding, surgical and endovascular repair of ruptured aneurysms, systems of care, anesthetic management during repair, management of vasospasm and delayed cerebral ischemia, management of hydrocephalus, management of seizures, and management of medical complications. aSAH is a serious medical condition in which outcome can be dramatically impacted by early, aggressive, expert care. The guidelines offer a framework for goal-directed treatment of the patient with aSAH.
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              International subarachnoid aneurysm trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: a randomised comparison of effects on survival, dependency, seizures, rebleeding, subgroups, and aneurysm occlusion.

              Two types of treatment are being used for patients with ruptured intracranial aneurysms: endovascular detachable-coil treatment or craniotomy and clipping. We undertook a randomised, multicentre trial to compare these treatments in patients who were suitable for either treatment because the relative safety and efficacy of these approaches had not been established. Here we present clinical outcomes 1 year after treatment. 2143 patients with ruptured intracranial aneurysms, who were admitted to 42 neurosurgical centres, mainly in the UK and Europe, took part in the trial. They were randomly assigned to neurosurgical clipping (n=1070) or endovascular coiling (n=1073). The primary outcome was death or dependence at 1 year (defined by a modified Rankin scale of 3-6). Secondary outcomes included rebleeding from the treated aneurysm and risk of seizures. Long-term follow up continues. Analysis was in accordance with the randomised treatment. We report the 1-year outcomes for 1063 of 1073 patients allocated to endovascular treatment, and 1055 of 1070 patients allocated to neurosurgical treatment. 250 (23.5%) of 1063 patients allocated to endovascular treatment were dead or dependent at 1 year, compared with 326 (30.9%) of 1055 patients allocated to neurosurgery, an absolute risk reduction of 7.4% (95% CI 3.6-11.2, p=0.0001). The early survival advantage was maintained for up to 7 years and was significant (log rank p=0.03). The risk of epilepsy was substantially lower in patients allocated to endovascular treatment, but the risk of late rebleeding was higher. In patients with ruptured intracranial aneurysms suitable for both treatments, endovascular coiling is more likely to result in independent survival at 1 year than neurosurgical clipping; the survival benefit continues for at least 7 years. The risk of late rebleeding is low, but is more common after endovascular coiling than after neurosurgical clipping.
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                Author and article information

                Contributors
                zxq@vip.163.com
                Journal
                CNS Neurosci Ther
                CNS Neurosci Ther
                10.1111/(ISSN)1755-5949
                CNS
                CNS Neuroscience & Therapeutics
                John Wiley and Sons Inc. (Hoboken )
                1755-5930
                1755-5949
                08 June 2023
                November 2023
                : 29
                : 11 ( doiID: 10.1002/cns.v29.11 )
                : 3567-3578
                Affiliations
                [ 1 ] Department of Neurology, Beijing Tiantan Hospital Capital Medical University Beijing China
                [ 2 ] China National Clinical Research Center for Neurological Diseases Beijing China
                [ 3 ] Research Unit of Artificial Intelligence in Cerebrovascular Disease Chinese Academy of Medical Sciences Beijing China
                [ 4 ] Center of Stroke, Beijing Institute of Brain Disorders Capital Medical University Beijing China
                Author notes
                [*] [* ] Correspondence

                Xingquan Zhao, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, No.119 South 4th Ring West Road, Fengtai District, Beijing 100070, China.

                Email: zxq@ 123456vip.163.com

                Author information
                https://orcid.org/0000-0002-0944-7613
                https://orcid.org/0000-0003-2169-4462
                https://orcid.org/0000-0001-6836-0705
                https://orcid.org/0000-0001-8345-5147
                Article
                CNS14288 CNSNT-2022-1092.R2
                10.1111/cns.14288
                10580355
                37287438
                f0b29c55-965c-415e-aeb7-dd9e9f77b34d
                © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 14 May 2023
                : 08 December 2022
                : 23 May 2023
                Page count
                Figures: 4, Tables: 3, Pages: 12, Words: 6535
                Funding
                Funded by: Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences
                Award ID: 2019‐I2M‐5‐029
                Funded by: Beijing Municipal Committee of Science and Technology
                Award ID: Z201100005620010
                Funded by: Beijing Hospitals Authority Innovation Studio of Young Staff Funding Support
                Award ID: 202112
                Funded by: Ministry of Finance of the People's Republic of China
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                November 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.4 mode:remove_FC converted:17.10.2023

                Neurosciences
                aneurysmal subarachnoid hemorrhage,nomogram,prediction,prognosis
                Neurosciences
                aneurysmal subarachnoid hemorrhage, nomogram, prediction, prognosis

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