Open-access Overprediction of mortality with the Hunt and Hess score in aneurysmal subarachnoid hemorrhage: retrospective multicenter study

INTRODUCTION

Aneurysmal subarachnoid hemorrhage (aSAH) accounts for 5% of strokes and is still associated with high morbidity and mortality, with case fatality approaching 50%.(1) Clinical prediction models are essential for outcome estimation.(2) The Hunt and Hess (HH) and World Federation of Neurosurgical Societies (WFNS) scales are widely used to determine severity and prognosis at admission.(3,4) However, their predictive accuracy in contemporary neurocritical care is uncertain, as early aneurysm repair and improved intensive care unit (ICU) management have significantly modified survival patterns.(5,6) This study evaluated the predictive performance of the HH score for predicting in-hospital mortality and described neurological outcomes at discharge and 6 months in a multicenter Latin American cohort.

METHODS

A retrospective cohort study was performed from 2011 to 2022 across three high-complexity hospitals in Argentina (Hospital Alemán, Hospital Universitario Austral, and Hospital Italiano de Buenos Aires).

Adults (≥ 18 years) admitted to the ICU with angiographically confirmed non-traumatic aSAH were included. Patients with SAH secondary to neurosurgical manipulation or without aneurysmal confirmation were excluded. Inclusion occurred at ICU admission following aSAH diagnosis. Collected data included demographics, Acute Physiology and Chronic Health Evaluation II (APACHE II), HH grade, treatment modality, and neurological outcomes using the modified Rankin Scale (mRS) at discharge and 6 months. Discrimination was evaluated by the area under the Receiver Operating Characteristic curve (AUROC), and calibration was assessed by comparing predicted versus observed mortality and by Cox-based calibration statistics. Statistical analyses are detailed in the Supplementary Material.

RESULTS

Of 222 screened patients, 175 met inclusion criteria (mean age 59 ± 14 years; mean APACHE II 13 ± 8.4). The most frequent HH grade was 2 (n = 64; 36.6%). Overall, in-hospital mortality was 21% (n = 37). The HH score showed acceptable discrimination for mortality prediction (AUROC 0.74; 95%CI 0.66 - 0.82) but poor calibration (calibration-in-the-large −3.6; slope 0.3), systematically overestimating mortality across all grades. Predicted mortality was 10% for HH grade 1 (observed 0%) and 99% for grade 5 (observed 46%).

Baseline characteristics and outcomes by HH grade are summarized in table 1. The calibration curve demonstrated overestimation across all categories (Figure 1). At discharge, 49% achieved mRS ≤ 3, increasing to 54% at 6 months. Among HH four and five patients, the favorable outcome increased from 9% to 22% at 6 months. Differences between ICU survivors and non-survivors, including functional outcomes and treatment strategies, are summarized in table 2. The 1-year and 5-year survival rates were 72% and 70%, respectively. Additional results are presented in the Supplementary Material.

Table 1
Demographic characteristics
Figure 1
Calibration plot with the relation between expected and observed mortality probability.
Table 2
Differences between intensive care unit survivors and non-survivors

DISCUSSION

The HH score demonstrated good discrimination but poor calibration for in-hospital mortality prediction, substantially overestimating mortality, especially in high-grade cases. These findings align with recent international cohorts reporting acceptable discrimination but weak calibration. Nguyen et al. and Rojas-Panta et al. reported good discrimination of the HH scale (AUROC 0.84 - 0.71).(7,8) However, calibration was not assessed in these studies, and predicted mortality differed from observed mortality despite good discrimination.

The overprediction likely reflects contemporary improvements in aneurysm repair and neurocritical care, which have reduced mortality even in severe cases.(5,9) Comparison with WFNS and Glasgow coma scale (GCS) suggests that HH performs similarly in discrimination but tends to overestimate risk, particularly in poor neurological grades, consistent with prior studies.(7) Patient-level factors, including age, sex, and APACHE II, not captured by the HH score, may partly explain the poor calibration observed. However, formal meta-regression was not feasible due to sample size limitations. Neurological recovery, particularly among patients with HH grades 4 - 5, continues beyond ICU discharge, supporting cautious prognostication and avoiding early withdrawal-of-care decisions.(10)

This study is one of the first multicenter prognostic evaluations of aSAH in Latin America. Limitations include its retrospective design, limited follow-up, and modest sample size.

In conclusion, although widely used, the HH score overpredicts mortality in contemporary aSAH care and should not be used as the sole parameter for clinical decision-making.

  • Publisher's note

AVAILABILITY OF DATA AND MATERIALS

Data is available on demand from referees.

Supplementary Material

Supplementary Material

REFERENCES

  • 1 Lawton MT, Vates GE. Subarachnoid Hemorrhage. N Engl J Med. 2017;377(3):257-66.
  • 2 van Smeden M, Reitsma JB, Riley RD, Collins GS, Moons KG. Clinical prediction models: diagnosis versus prognosis. J Clin Epidemiol. 2021;132:142-5.
  • 3 World Federation of Neurosurgical Societies Committee. Report of a universal subarachnoid hemorrhage grading scale. J Neurosurg. 1988;68(6):985-6.
  • 4 Hunt WE, Hess RM. Surgical risk as related to time of intervention in the repair of intracranial aneurysms. J Neurosurg. 1968;28(1):14-20.
  • 5 Konczalla J, Seifert V, Beck J, Güresir E, Vatter H, Raabe A, et al. Outcome after Hunt and Hess Grade V subarachnoid hemorrhage: a comparison of pre-coiling era (1980-1995) versus post-ISAT era (2005-2014). J Neurosurg. 2018;128(1):100-10.
  • 6 Samuels OB, Sadan O, Feng C, Martin K, Medani K, Mei Y, et al. Aneurysmal subarachnoid hemorrhage: trends, outcomes, and predictions from a 15-year perspective of a single neurocritical care unit. Neurosurgery. 2021;88(3):574-83.
  • 7 Nguyen TA, Mai TD, Vu LD, Dao CX, Ngo HM, Hoang HB, et al. Validation of the accuracy of the modified World Federation of Neurosurgical Societies subarachnoid hemorrhage grading scale for predicting the outcomes of patients with aneurysmal subarachnoid hemorrhage. PLoS One. 2023;18(8):e0289267.
  • 8 Rojas-Panta G, Reyes-Narro GF, Toro-Huamanchumo C, Choque-Velasquez J, Saal-Zapata G. Prognostic value of scales for aneurysmal subarachnoid hemorrhage: report of a reference center in Peru. Neurocirugia (Engl Ed). 2024;35(1):1-5.
  • 9 Nieuwkamp DJ, Setz LE, Algra A, Linn FH, de Rooij NK, Rinkel GJ. Changes in case fatality of aneurysmal subarachnoid haemorrhage over time, according to age, sex, and region: a meta-analysis. Lancet Neurol. 2009;8(7):635-42.
  • 10 Mocco J, Ransom ER, Komotar RJ, Schmidt JM, Sciacca RR, Mayer SA, et al. Preoperative prediction of long-term outcome in poor-grade aneurysmal subarachnoid hemorrhage. Neurosurgery. 2006;59(3):529-38.

Edited by

Publication Dates

  • Publication in this collection
    17 July 2026
  • Date of issue
    2026

History

  • Received
    03 Nov 2025
  • Accepted
    23 Dec 2025
location_on
Associação de Medicina Intensiva Brasileira - AMIB Rua Arminda, 93 - 7º andar - Vila Olímpia, CEP: 04545-100, Tel.: +55 (11) 5089-2642 - São Paulo - SP - Brazil
E-mail: ccs@amib.org.br
rss_feed Stay informed of issues for this journal through your RSS reader
Go to top Report error