TableĀ 3

Associations between study characteristics and the incidence of the composite outcome (death, non-fatal ICH or new or worsened persistent focal neurological deficit attributed to CCM or its treatment)

All cohorts (n=63)Neurosurgery (n=49)Stereotactic radiosurgery (n=14)
Study characteristicCohortsEventsRR (95% CI)CohortsEventsRR (95% CI)CohortsEventsRR (95% CI)
Midyear, y*131780.91 (0.85 to 0.98)8621.03 (0.96 to 1.11)
Age, y222441.01 (0.98 to 1.05)141820.99 (0.95 to 1.03)8620.96 (0.65 to 1.41)
Female, %222441.01 (0.99 to 1.03)141821.00 (0.98 to 1.02)8621.03 (0.87 to 1.21)
Brainstem, %222441.02 (1.01 to 1.03)141821.03 (1.01 to 1.05)8621.03 (0.95 to 1.11)
ICH as presenting symptom, %222441.00 (0.99 to 1.01)141820.98 (0.96 to 1.00)8621.04 (0.96 to 1.13)
Children, %81251.03 (0.98 to 1.09)61221.08 (0.98 to 1.21)23Not estimable
  • All analyses are adjusted for patient age, sex, proportion of brainstem CCM and proportion of patients presenting with haemorrhage, unless stated otherwise. The RRs are expressed per 1% increase in the proportion of patients with a study characteristic or per 1-year increase in age or midyear.

  • *We did not analyse the effect of midyear on the composite outcome in all cohorts together because there was a significant interaction between midyear and treatment modality (p=0.003).

  • CCM, cerebral cavernous malformation; ICH, intracranial haemorrhage; RR, rate ratio.