Current pathways of care for whiplash follow a "stepped care model," result in modest treatment outcomes and fail to offer efficient management solutions. This study aimed to evaluate the effectiveness of a risk-stratified clinical pathway of care (CPC) compared with usual care (UC) in people with acute whiplash. We conducted a multicentre, 2-arm, parallel, randomised, controlled trial in primary care in Australia. Participants with acute whiplash (n = 216) were stratified for risk of a poor outcome (low vs medium/high risk) and randomised using concealed allocation to either the CPC or UC. In the CPC group, low-risk participants received guideline-based advice and exercise supported by an online resource, and medium-risk/high-risk participants were referred to a whiplash specialist who assessed modifiable risk factors and then determined further care. The UC group received care from their primary healthcare provider who had no knowledge of risk status. Primary outcomes were neck disability index (NDI) and Global Rating of Change (GRC) at 3 months. Analysis blinded to group used intention-to-treat and linear mixed models. There was no difference between the groups for the NDI (mean difference [MD] [95% confidence interval (CI)] -2.34 [-7.44 to 2.76]) or GRC (MD 95% CI 0.08 [-0.55 to 0.70]) at 3 months. Baseline risk category did not modify the effect of treatment. No adverse events were reported. Risk-stratified care for acute whiplash did not improve patient outcomes, and implementation of this CPC in its current form is not recommended.

Implementation of a risk-stratified, guideline-based clinical pathway of care to improve health outcomes following whiplash injury (Whiplash ImPaCT): A multicentre, randomized, controlled trial / Rebbeck T.; Bandong A.N.; Leaver A.; Ritchie C.; Armfield N.; Arora M.; Cameron I.D.; Connelly L.B.; Daniell R.; Gillett M.; Ingram R.; Jagnoor J.; Kenardy J.; Mitchell G.; Refshauge K.; Scotti Requena S.; Robins S.; Sterling M.. - In: PAIN. - ISSN 0304-3959. - ELETTRONICO. - 164:10(2023), pp. 2216-2227. [10.1097/j.pain.0000000000002940]

Implementation of a risk-stratified, guideline-based clinical pathway of care to improve health outcomes following whiplash injury (Whiplash ImPaCT): A multicentre, randomized, controlled trial

Connelly L. B.;Robins S.;
2023

Abstract

Current pathways of care for whiplash follow a "stepped care model," result in modest treatment outcomes and fail to offer efficient management solutions. This study aimed to evaluate the effectiveness of a risk-stratified clinical pathway of care (CPC) compared with usual care (UC) in people with acute whiplash. We conducted a multicentre, 2-arm, parallel, randomised, controlled trial in primary care in Australia. Participants with acute whiplash (n = 216) were stratified for risk of a poor outcome (low vs medium/high risk) and randomised using concealed allocation to either the CPC or UC. In the CPC group, low-risk participants received guideline-based advice and exercise supported by an online resource, and medium-risk/high-risk participants were referred to a whiplash specialist who assessed modifiable risk factors and then determined further care. The UC group received care from their primary healthcare provider who had no knowledge of risk status. Primary outcomes were neck disability index (NDI) and Global Rating of Change (GRC) at 3 months. Analysis blinded to group used intention-to-treat and linear mixed models. There was no difference between the groups for the NDI (mean difference [MD] [95% confidence interval (CI)] -2.34 [-7.44 to 2.76]) or GRC (MD 95% CI 0.08 [-0.55 to 0.70]) at 3 months. Baseline risk category did not modify the effect of treatment. No adverse events were reported. Risk-stratified care for acute whiplash did not improve patient outcomes, and implementation of this CPC in its current form is not recommended.
2023
Implementation of a risk-stratified, guideline-based clinical pathway of care to improve health outcomes following whiplash injury (Whiplash ImPaCT): A multicentre, randomized, controlled trial / Rebbeck T.; Bandong A.N.; Leaver A.; Ritchie C.; Armfield N.; Arora M.; Cameron I.D.; Connelly L.B.; Daniell R.; Gillett M.; Ingram R.; Jagnoor J.; Kenardy J.; Mitchell G.; Refshauge K.; Scotti Requena S.; Robins S.; Sterling M.. - In: PAIN. - ISSN 0304-3959. - ELETTRONICO. - 164:10(2023), pp. 2216-2227. [10.1097/j.pain.0000000000002940]
Rebbeck T.; Bandong A.N.; Leaver A.; Ritchie C.; Armfield N.; Arora M.; Cameron I.D.; Connelly L.B.; Daniell R.; Gillett M.; Ingram R.; Jagnoor J.; Kenardy J.; Mitchell G.; Refshauge K.; Scotti Requena S.; Robins S.; Sterling M.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/954373
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