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Predicting the presence of macrovascular causes in non-traumatic intracerebral haemorrhage: The DIAGRAM prediction score

  • Nina A Hilkens
  • , Charlotte J J van Asch
  • , David J Werring
  • , Duncan Wilson
  • , Gabriël J E Rinkel
  • , Ale Algra
  • , Birgitta K Velthuis
  • , Gérard A P de Kort
  • , Theo D Witkamp
  • , Koen M van Nieuwenhuizen
  • , Frank-Erik de Leeuw
  • , Wouter J. Schonewille
  • , Paul L M de Kort
  • , Diederik W J Dippel
  • , Theodora W M Raaymakers
  • , Jeannette Hofmeijer
  • , Marieke J H Wermer
  • , Henk Kerkhoff
  • , Korné Jellema
  • , Irene M. Bronner
  • Michel J M Remmers, Henri Paul Bienfait, Ron J G M Witjes, H Rolf Jäger, Jacoba P Greving, Catharina J M Klijn,

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

Objective: A substantial part of non-traumatic intracerebral haemorrhages (ICH) arises from a macrovascular cause, but there is little guidance on selection of patients for additional diagnostic work-up. We aimed to develop and externally validate a model for predicting the probability of a macrovascular cause in patients with non-traumatic ICH. Methods: The DIagnostic AngioGRAphy to find vascular Malformations (DIAGRAM) study (n=298; 69 macrovascular cause; 23%) is a prospective, multicentre study assessing yield and accuracy of CT angiography (CTA), MRI/magnetic resonance angiography (MRA) and intra-arterial catheter angiography in diagnosing macrovascular causes in patients with non-traumatic ICH. We considered prespecified patient and ICH characteristics in multivariable logistic regression analyses as predictors for a macrovascular cause. We combined independent predictors in a model, which we validated in an external cohort of 173 patients with ICH (78 macrovascular cause, 45%). Results: Independent predictors were younger age, lobar or posterior fossa (vs deep) location of ICH, and absence of small vessel disease (SVD). A model that combined these predictors showed good performance in the development data (c-statistic 0.83; 95% C I 0.78 to 0.88) and moderate performance in external validation (c-statistic 0.66; 95% CI 0.58 to 0.74). When CTA results were added, the c-statistic was excellent (0.91; 95% CI 0.88 to 0.94) and good after external validation (0.88; 95% CI 0.83 to 0.94). Predicted probabilities varied from 1% in patients aged 51-70 years with deep ICH and SVD, to more than 50% in patients aged 18-50 years with lobar or posterior fossa ICH without SVD. Conclusion: The DIAGRAM scores help to predict the probability of a macrovascular cause in patients with nontraumatic ICH based on age, ICH location, SVD and CTA.

Original languageEnglish
Pages (from-to)674-679
Number of pages6
JournalJournal of neurology, neurosurgery, and psychiatry
Volume89
Issue number7
Early online date18 Jan 2018
DOIs
Publication statusPublished - 1 Jul 2018

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