| Literature DB >> 26442789 |
Yen-Fu Chen1, Karla Hemming2, Andrew J Stevens2, Richard J Lilford1.
Abstract
Evaluations of service delivery interventions with contemporaneous controls often yield null results, even when the intervention appeared promising in advance. There can be many reasons for null results. In this paper we introduce the concept of a 'rising tide' phenomenon being a possible explanation of null results. We note that evaluations of service delivery interventions often occur when awareness of the problems they intend to address is already heightened, and pressure to tackle them is mounting throughout a health system. An evaluation may therefore take place in a setting where the system as a whole is improving - where there is a pronounced temporal trend or a 'rising tide causing all vessels to rise'. As a consequence, control sites in an intervention study will improve. This reduces the difference between intervention and control sites and predisposes the study to a null result, leading to the conclusion that the intervention has no effect. We discuss how a rising tide may be distinguished from other causes of improvement in both control and intervention groups, and give examples where the rising tide provides a convincing explanation of such a finding. We offer recommendations for interpretation of research findings where improvements in the intervention group are matched by improvements in the control group. Understanding the rising tide phenomenon is important for a more nuanced interpretation of null results arising in the context of system-wide improvement. Recognition that a rising tide may have predisposed to a null result in one health system cautions against generalising the result to another health system where strong secular trends are absent. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/Entities:
Keywords: Cluster trials; Evaluation methodology; Health services research; Quality improvement; Randomised controlled trial
Mesh:
Year: 2015 PMID: 26442789 PMCID: PMC4853562 DOI: 10.1136/bmjqs-2015-004372
Source DB: PubMed Journal: BMJ Qual Saf ISSN: 2044-5415 Impact factor: 7.035
Issues to be considered for assessing a rising tide phenomenon and results of assessment for the four case studies*
| SPI2 | Critical pathways | EQHIV | MERIT | |
|---|---|---|---|---|
| Direct evidence | ||||
| Improvement in process and/or outcome measures observed in external sites: | Yes | Yes | Yes | Yes |
| Timing: before or during evaluation study | Before and during | Before and during | Before | During |
| System-wide or specific external site(s) | System-wide | Specific external sites | System-wide | System-wide (but 30% participation) |
| Qualitative evidence showing behaviour changes driven by external factors in both study groups | Yes | Yes | Yes | Yes |
| Suggestive evidence | ||||
| Baseline measures better than expected, or already showing high standards or improving trend | Yes | Yes | Yes | Yes |
| Circumstantial evidence | ||||
| Heightened awareness of the problems | Yes | Yes | Yes | Yes |
| Contamination within study | No | No | Unlikely | Unlikely |
| Other potential sources of biases‡ | Not apparent | Not apparent | Attrition bias cannot be ruled out | Not apparent |
*Improvement in process and/or outcome measures were observed in both intervention and control groups in these studies during the evaluation period.
†Factors of which the impact on study findings could resemble a rising tide phenomenon.
‡Including selection bias (eg, control group being a selective sample of highly motivated units or having more headroom for improvement), bias in outcome assessment (eg, changes in methods of data collection or coding over time) and attrition bias (eg, poor-performing units dropping out and being excluded from analysis).
Figure 1Key characteristics and findings of the Safer Patients Initiatives phase 2 (SPI2). This controlled before-and-after study evaluated a multi-component intervention using an organisation-wide approach to improve patient safety. The key components included interventions to facilitate generic improvement in the hospital system to reduce adverse events (such as building a good leadership to support a culture of safety as well as interventions targeting specific clinical processes that carry a relatively high risk of adverse events (such as procedures aiming to enhance infection control). Various outcomes were measured, including staff morale, culture and opinion, the quality of acute medical care and perioperative care, use of consumables for hand hygiene, adverse events and hospital mortality in older patients with acute respiratory disease, intensive care unit mortality, infection rates associated with healthcare and patients satisfaction. SPI2 was preceded by a pilot phase (SPI1) that provides data on the pre-implementation phase for certain end-points, including the two outcomes illustrated here.
Figure 2Key characteristics and findings of the Critical Pathways Intervention. This controlled before-and-after study compared the effects of a quality improvement initiative utilising critical pathway framework on post-operative length of stay in a large teaching hospital with concurrent data from 2-3 similar neighbouring hospitals without the intervention. Multidisciplinary teams identified critical steps in the care process and specified required actions and desirable outcomes for each step. Patients entered into critical pathways were monitored and various methods of benchmarking and feedback were used in pathway management. The primary outcome was post-operative length of stay. Hospital charges and other process and clinical outcomes were also examined.
Figure 3Key characteristics and findings of the EQHIV study. This controlled before-and-after study evaluated the effectiveness of the ‘Breakthrough Series’, a multi-institutional quality improvement collaborative led by Institute for Healthcare Improvement, on improving the quality of case for clinics treating HIV infected patients. The 16-month intervention involved a series of meetings (learning sessions) covering the theory and practice of quality improvement in the intervention clinics and sharing ideas and progress between them. The primary outcome measures were rates of optimal antiretroviral therapy use and control of HIV viral load.
Figure 4Key characteristics and findings of the MERIT study. This cluster randomised controlled trial (RCT) investigated the effectiveness of introducing a medical emergency team (MET) that could be summoned when non-terminal hospital patients showed signs of physiological instability and deterioration. Staff in the intervention hospitals were trained over 4-months to identify and respond to patients requiring the attention of the team. The primary outcome was the combined incidence of cardiac arrests without a pre-existing not-for-resuscitation order. unplanned intensive care unit admissions and unexpected deaths measured before and after implementation.