Threshold Effects of Rehabilitation Intensity on Functional Recovery After Ischaemic Stroke: A Panel Threshold Regression Analysis of Australian Hospital Data

Abstract

Background Optimal rehabilitation dosing after ischaemic stroke remains contested. Linear assumptions underlying conventional regression models may mask clinically important threshold effects, whereby functional gains accelerate or plateau beyond specific intensity thresholds. This study applied panel threshold regression to Australian hospital administrative data to identify endogenous breakpoints in the dose-response relationship between rehabilitation intensity and functional recovery.

Methods We used a retrospective longitudinal cohort derived from the Australian Stroke Clinical Registry (AuSCR) and the National Hospital Cost Data Collection (NHCDC) for fiscal years 2018-2019 to 2022-2023. The analytical sample comprised 18,742 hospitalised ischaemic stroke patients across 48 public hospitals in five Australian states. The primary exposure was daily rehabilitation intensity (minutes of physiotherapy, occupational therapy, and speech pathology per inpatient day). The primary outcome was change in the modified Rankin Scale (mRS) score from admission to discharge. We employed Hansen’s (1999) panel threshold regression framework to test for single, double, and triple threshold effects, using bootstrap p-values (n=500) to establish statistical significance. Fixed-effects estimation controlled for unobserved hospital heterogeneity. Secondary outcomes included acute length of stay and discharge destination. Cost-related parameters were benchmarked against published Australian cost-effectiveness data.

Results The panel threshold model identified two statistically significant breakpoints in the intensity-recovery relationship (p<0.001 for both). Below the first threshold (27.4 minutes/day; 95% CI: 24.8-29.6), each additional minute of daily rehabilitation was associated with a 0.008-point reduction in mRS score (beta = -0.008, 95% CI: -0.011 to -0.005, p<0.001). Between the two thresholds (27.4 to 54.7 minutes/day; 95% CI: 51.2-58.9), the marginal benefit approximately doubled (beta = -0.018, 95% CI: -0.022 to -0.013, p<0.001). Above the upper threshold (>54.7 minutes/day), the marginal effect diminished substantially (beta = -0.004, 95% CI: -0.009 to 0.002, p=0.186), suggesting a ceiling effect. These dose-response patterns were consistent across age subgroups, stroke severity strata, and hospital volume tertiles.

Conclusions Rehabilitation intensity thresholds exist in stroke inpatient recovery and are non-linear. Patients receiving between 27 and 55 minutes of daily multidisciplinary therapy derive disproportionate functional benefit per unit of resource investment. Scheduling rehabilitation below the lower threshold represents a clinically and economically suboptimal allocation of inpatient resources. These findings have direct implications for workforce planning, clinical pathway design, and value-based commissioning in Australian public hospitals.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics approval was obtained from the Australian Institute of Health and Welfare Ethics Committee (EO2023/4-1088) and from the human research ethics committees of each of the five participating state health departments.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

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Data Availability

All data produced in the present work are contained in the manuscript

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