| Literature DB >> 35202464 |
Yannick Tousignant-Laflamme1,2, Catherine Houle1,2, Chad Cook3,4,5, Florian Naye1,2, Annie LeBlanc6, Simon Décary1,2.
Abstract
In health care, clinical decision making is typically based on diagnostic findings. Rehabilitation clinicians commonly rely on pathoanatomical diagnoses to guide treatment and define prognosis. Targeting prognostic factors is a promising way for rehabilitation clinicians to enhance treatment decision-making processes, personalize rehabilitation approaches, and ultimately improve patient outcomes. This can be achieved by using prognostic tools that provide accurate estimates of the probability of future outcomes for a patient in clinical practice. Most literature reviews of prognostic tools in rehabilitation have focused on prescriptive clinical prediction rules. These studies highlight notable methodological issues and conclude that these tools are neither valid nor useful for clinical practice. This has raised the need to open the scope of research to understand what makes a quality prognostic tool that can be used in clinical practice. Methodological guidance in prognosis research has emerged in the last decade, encompassing exploratory studies on the development of prognosis and prognostic models. Methodological rigor is essential to develop prognostic tools, because only prognostic models developed and validated through a rigorous methodological process should guide clinical decision making. This Perspective argues that rehabilitation clinicians need to master the identification and use of prognostic tools to enhance their capacity to provide personalized rehabilitation. It is time for prognosis research to look for prognostic models that were developed and validated following a comprehensive process before being simplified into suitable tools for clinical practice. New models, or rigorous validation of current models, are needed. The approach discussed in this Perspective offers a promising way to overcome the limitations of most models and provide clinicians with quality tools for personalized rehabilitation approaches. IMPACT: Prognostic research can be applied to clinical rehabilitation; this Perspective proposes solutions to develop high-quality prognostic models to optimize patient outcomes.Entities:
Keywords: Clinical Rehabilitation; Decision Making; Outcome Assessment (Health Care); Patient-Centered Care; Prognosis
Mesh:
Year: 2022 PMID: 35202464 PMCID: PMC9155156 DOI: 10.1093/ptj/pzac023
Source DB: PubMed Journal: Phys Ther ISSN: 0031-9023
Types of Prognostic-Related Factors
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| Individuals who are healthy |
| Clinicians’ roles in preventive medicine might need to tackle screening tools designed with risk factors. Yet, in most circumstances, physical rehabilitation aims to improve the outcomes for patients with a health condition, meaning that they need to leverage prognostic factors instead. |
| People with a health condition |
| A recent Cochrane review on prognostic factors in low back pain found that patients who have positive recovery expectations are more likely to return to work. |
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| A patient with low back pain who has an occupation with low physical demands and uses pain medication is expected to have a better response to an exercise therapy program compared with a patient who does not exhibit these characteristics (positive treatment-effect modifiers). | |
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| When an individual’s physical function improves following exercises, the treatment mediator might be the decrease of fear-avoidance behaviors or kinesiophobia. |
Figure 1Prognostic factors and treatment-effect modifiers can be integrated into prognostic tools that can be used to personalize rehabilitation approaches.
Figure 2Representation of the PROGnosis RESearch Strategy (PROGRESS) framework.,
Main Characteristics of the Development and Validation Processes of Prognostic Models
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| 1. Model development | Prospective cohort (longitudinal); multivariate analysis of predictors | Provide an accurate estimate of risk of a future outcome for a patient |
| 2. Model internal validation | Prospective cohort (longitudinal); usually performed with data from the development sample | Quantify predictive performance of the model |
| 3. External validation | Prospective cohort (longitudinal); performed with data from a different sample | Allow adjusting for optimistic predictive performance found in internal validation (ie, overfitting) |
| 4. Development of prognostic tool | If not pragmatic, the prognostic model is translated into simple clinical prediction rules (CPRs) and clinical decision rules (CDRs) intended for clinical use (ie, prognostic tool); typically involves choosing a relevant threshold for clinical practice | Makes it possible to provide a simple tool for clinicians while taking advantage of the precision of statistical models for prediction in the development phase |
| 5. Impact analysis | Randomized trial in a clinical setting; performed with data from a different sample | Assess the impact of the implementation of the model on clinical outcomes or health care costs |
Methodological Characteristics of Clinical Decision Rule or Prescriptive Clinical Prediction Rule
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| 1. Development | Prospective cohort (longitudinal); multivariate analysis of predictors | Randomized controlled trial design: exploratory studies of association and confirmatory studies of validation of models predicting response to treatment might use through randomized controlled trial design. This will confirm that the model is predictive of response to treatment instead of predictive of the natural course of the disease. |
| 2. Internal validation | Prospective cohort (longitudinal); usually performed with data from the development sample | |
| 3. External validation | Prospective cohort (longitudinal); performed with data of a different sample |
CDR = clinical decision rule; pCPR = prescriptive clinical prediction rule.
Key Elements of Statistical Analysis to Consider When Selecting a Prognostic Tool
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| Performance | Calibration (reliability): | Calibration slope | The external validation of the WORRK model showed that its calibration was good, demonstrated by CIs of the observed probabilities, which covered the line of ideal calibration |
| Discrimination (accuracy): | C-statistics or c-index: | The WORRK model external validation showed an area under the receiver operating characteristic (ROC) curve (c-index) of 0.73 (95% CI = 0.70–0.77), which was considered sufficient by the authors | |
| Classification | Sensitivity | Classification measures are calculated when 1 or more probability thresholds have been set, leading to a dichotomization of scores that can negatively affect model performance. It is important to ensure that the chosen threshold is relevant for clinical practice | The WORRK model external validation showed a sensitivity of 72.4% (95% CI = 69.3–75.4) and a specificity of 61.2% (95% CI = 57.9–64.6) to predict the risk of not returning to work when the threshold was set to 0.5. |
WORRK = Wallis Occupational Rehabilitation RisK.