- Research article
- Open Access
A cluster randomized trial to assess the effect of clinical pathways for patients with stroke: results of the clinical pathways for effective and appropriate care study
BMC Medicine volume 10, Article number: 71 (2012)
Clinical pathways (CPs) are used to improve the outcomes of acute stroke, but their use in stroke care is questionable, because the evidence on their effectiveness is still inconclusive. The objective of this study was to evaluate whether CPs improve the outcomes and the quality of care provided to patients after acute ischemic stroke.
This was a multicentre cluster-randomized trial, in which 14 hospitals were randomized to the CP arm or to the non intervention/usual care (UC) arm. Healthcare workers in the CP arm received 3 days of training in quality improvement of CPs and in use of a standardized package including information on evidence-based key interventions and indicators. Healthcare workers in the usual-care arm followed their standard procedures. The teams in the CP arm developed their CPs over a 6-month period. The primary end point was mortality. Secondary end points were: use of diagnostic and therapeutic procedures, implementation of organized care, length of stay, re-admission and institutionalization rates after discharge, dependency levels, and complication rates.
Compared with the patients in the UC arm, the patients in the CP arm had a significantly lower risk of mortality at 7 days (OR = 0.10; 95% CI 0.01 to 0.95) and significantly lower rates of adverse functional outcomes, expressed as the odds of not returning to pre-stroke functioning in their daily life (OR = 0.42; 95 CI 0.18 to 0.98). There was no significant effect on 30-day mortality. Compared with the UC arm, the hospital diagnostic and therapeutic procedures were performed more appropriately in the CP arm, and the evidence-based key interventions and organized care were more applied in the CP arm.
CPs can significantly improve the outcomes of patients with ischemic patients with stroke, indicating better application of evidence-based key interventions and of diagnostic and therapeutic procedures. This study tested a new hypothesis and provided evidence on how CPs can work.
ClinicalTrials.gov ID: [NCT00673491].
Stroke represents one of the major public-health issues worldwide [1–4]. The American Stroke Association has reported that obstacles in translating scientific advances into clinical practice are often related to fragmentation caused by inadequate integration of facilities and professionals that should closely collaborate . This potentially contributes to the high morbidity, mortality, and economic cost of stroke [5–7]. Other studies have suggested that establishing well-organized, multidisciplinary care can help improve the quality of the service delivered and reduce the mortality rates associated with stroke [8, 9]. According to the Helsingborg Declaration of 2006 on European Stroke Strategies, all patients should have access to a continuum of care, from stroke units in the acute phase to appropriate rehabilitation and secondary prevention measures . Consequently, to improve the outcome, research and development priorities were identified: the optimization of the use of multidisciplinary teams, the development of better ways to deliver education to professionals and the public, the implementation of evidence-based care, and the evaluation of different models of stroke services .
The Australian National Stroke Foundation suggests that all patients with stroke who are admitted to the hospital should be managed using a clinical pathway (CP) . This recommendation was made using a body of evidence from the Cochrane Collaboration but care should be taken in its application [11–13]. Despite continuing interest in implementing CPs, the evidence base for their effectiveness remains inconclusive . Therefore, the purpose of the Clinical Pathways for Effective and Appropriate Care (CPEAC) Study (ClinicalTrials.gov number: NCT00673491) was to determine whether CPs can improve quality of care. The main objective was to determine whether CPs are more effective than usual care in treating patients with stroke, and whether CPs reduce both patient mortality and improve patient outcomes. The secondary objectives were to determine whether CPs increase the appropriateness of the care provided and to determine whether CPs help in implementing organized care in stroke-care facilities.
Ethics approval and funding
The project received ethical clearance as a prerequisite of approval for funding from the Italian Ministry of Health. The CPEAC study was approved by the ethics committe of Ancona, Marche Region, Italy, and the research was carried out in compliance with the Declaration of Helsinki. The managers in each unit consented to their clinic taking part in the trial. Patient consent to be randomized to the intervention or control arms was not obtained, because the study design required randomization to occur at the unit level. However, all individual patients gave consent to participate in the study and had the opportunity to withdraw from the study at any time. All patient data were managed in accordance with the Italian Data Protection Act . The CPEAC Study was promoted and funded by the Italian Ministry of Health (Special Programs art. 12 bis D.lgs 229/99) and Marche Region .
The CPEAC Study was designed as a multicenter cluster randomized controlled trial (cRCT), in which patients with stroke were randomized either to the experimental (CP) group or to the non-intervention (usual care; UC) group . The study was designed in accordance with the CONSORT statement for cRCTs . It was carried out during the period July 2005 to May 2007, and involved a sample of Italian hospitals. A cluster design was used because of the ethical and logistical issues associated with the implementation of CPs, which involves a series of complex actions at the institutional level [17–23]. A pilot study to define baseline levels of performance has been described previously .
Thirty-four units based in nine Italian regions were invited to participate in the study (Figure 1); of these, twenty-nine units expressed interest in implementing stroke CPs, and were assessed for eligibility . The selection of the units and the final randomization was based on the comparability of their location, patient population and volume, facilities, and teaching status. To participate in the study, the administrators of the units had to allow the institution to be allocated to either of the two research groups (CP or current practice) for a period of 1 year, and had to agree not to implement a CP for the acute care and/or rehabilitation of stroke if their institution was assigned to the UC group. Nine units were excluded because they did not meet the inclusion criteria, and five units withdrew after the project commenced, following a decision from their management (three units withdrew after the project pre-test and two units withdrew after the project began). One unit could not provide reassurance that they would not implement a CP if assigned to the control group, and therefore were excluded from the study sample. The remaining 14 units were stratified according to the availability of a stroke unit and to the teaching status of the unit, and the strata were randomized to one of the two arms. A simple randomization procedure was carried out in each stratification sample before the intervention, and patient randomization was carried out using a computer-generated sequence with allocation concealment. Blinding of patients and clinicians was not possible . The CP and UC groups each had seven hospitals assigned to them; both groups contained hospitals with a stroke unit, and both included one teaching hospital. The mean number of beds was 405 in the CP group, and 409 in the UC group.
Calculation of study sample
A calculation was made to identify the sample size needed to detect a significant difference in the 30-day mortality rate . Because of the mortality of patients with ischemic stroke has been reported to range from 8% to 17%, we expected that a similar difference in our sample would be required to evaluate CP as effective [3, 25, 26]. We consider this estimate reasonable because in the pilot study that we performed previously to the main trial, we observed an overall in-hospital mortality of 19.76%, which is consistent with the higher levels of mortality reported in the literature . Therefore, as the expected mortality rate of patients with ischemic stroke would be 8% to 17%, within 30 days of the incident we expected that the CP intervention would succeed in limiting mortality to 8%, and would therefore be clinically relevant. Based on this goal, a sample size of 476 patients (238 in each group) was required for the study to have 80% power at the 5% significance level. The sample-size calculation was performed in accordance with standard criteria for a cRCT [16, 19, 22, 27]. The sample size was adjusted using an inflation factor of 1.43 to account for cluster randomization: seven clusters per trial arm, with a cluster size of thirty-four patients and an intra-cluster correlation coefficient (ICC) of 0.018 [15, 28–30].
The sample included all consecutive patients admitted to the hospitals during the experimental period with a principal diagnosis of acute ischemic stroke (International Classification Diseases, Ninth Revision. Clinical Modification (ICD-9CM) code 434.91). To be included, patients had to be at least 18 years of age and admitted within 24 hours of stroke onset. Patients with hemorrhagic strokes (all ICD-9CM codes included in code 431) or transient ischemic attacks (ICD-9CM code 435.9) were excluded. Baseline was verified by comparing the two groups on admission both at the individual level (patient demographics and characteristics) and at the institutional/cluster level (availability of healthcare facilities, technologies, and human resources).
Randomization and interventions
The project started at each unit with a grand round that outlined the project protocol. To facilitate project implementation, a healthcare worker experienced in CPs was assigned to each unit in the experimental group. The teams included internal-medicine physicians, neurologists, physiatrists, epidemiologists, physiotherapists, occupational therapists, nurses, speech therapists, hospital pharmacists, psychologists, social workers, and support staff. The teams were formed on a voluntary basis; they received 3 days of training in quality improvement and in the development of CPs. To ensure the intervention was standardized, the teams also received a package including evidence-based key interventions and indicators provided by senior investigators of the Evidence-Based Medicine (EBM) unit of the Regional Healthcare Agency of Marche and the University of Eastern Piedmont [31–34]. The teams developed their CPs over a 6-month period (for examples of CPs, see Additional file 1, Additional file 2). All groups analyzed their care processes, reviewed best evidence, defined the appropriate goals of the pathways, and compiled the results into protocols and documentation [14, 35–37]. After development, the CPs were analyzed by the EBM unit of the Regional Healthcare Agency of Marche, and were judged consistent with current recommendations for the diagnosis and treatment of stroke. After validation of the CPs, each unit team educated its staff in the use of the CP and monitored its use. This meant that the CPs used in the study were not completely identical because of organizational adaptations at some sites ; however, all adhered substantially to existing Italian guidelines on the hospital treatment and rehabilitation of stroke, as described by Gensini et al.  and Provinciali .
Outcomes and follow-up
The primary outcome measure was 30-day mortality after stroke  defined as the proportion of ischemic stroke events that were fatal within 30 days of onset. Stroke fatality was chosen as the main outcome because it is clinically relevant, objectively measured, and reliably coded . The effect of CP intervention was analyzed with respect to 7-day mortality, length of in-hospital stay, hospital re-admission rates, institutionalization rates after hospital discharge, dependency levels, and complication rates along the entire continuum of care . The quality of the care provided to the patients was assessed by monitoring the implementation of evidence-based practice. The implementation of organized care at the cluster level was also evaluated. The list of indicators has been described previously in detail .
Local staff prospectively collected the data for both the intervention and the control groups. The staff were not given an incentives for data collection. Staff members were trained in data collection at two educational events. Data were collected using a standardized data-extraction tool that used web technology, and were anonymously entered into a secure database housed at the University of Eastern Piedmont. Mortality data were extracted from the Italian National Register of Mortality, which is based on local registers that are completed and used in each Health Authority at the Healthcare District level. These registers are uploaded in real time when a death occurs, and are matched monthly with the Municipality register for births and deaths. Completion of these registers is compulsory by the doctor certifying the death (deaths both at home or in medical institutions) and there is a national procedure for monitoring the quality and reliability of diagnosis data. In the current study, we did not have any particular problems about reliability of diagnosis of death because we followed up two cohorts of people affected by ischemic stroke, and when a death occurred, we verified the concordance of the cause of death recorded in the register with the pre-existing diagnosis of stroke.; the concordance of the two was 100%.
The study design was based on that described previously by Campbell et al.,  and on the Consort Statement for cRTCs, and the statistical analysis was performed accordingly  by the research team. The Fisher exact and Kruskal-Wallis tests for categorical and continuous variables, respectively, were performed at the cluster level. In addition, differences in the rates of 7-day and 30-day mortality and of return to pre-stroke functioning in daily life between groups and according to each variable under study were evaluated at the individual level using random-effects logistic regression, accounting for the clustering effect [15, 39, 40]. Variables were included if significant at the 0.10 level (backward approach), with the exception of gender, which was forced to entry. The presence of multicollinearity, interaction, and higher power terms was assessed to check final model validity. Patient outcomes were described according to gender (male); comorbidities (based on their Charlson-Deyo index, patients were categorized as having 0 to 1 or > 1 comorbidities) ; medical complications (at least one complication); admission to stroke unit (yes/no); access to organized care (based on organized care index as having 0 to1 or > 1 score) ; management by a stroke team (yes/no); use of antithrombotic drugs (antiplatelet or anticoagulant during the stay); and assessment of rehabilitation needs (yes/no). Because the assessment of rehabilitation needs does not have any effect on mortality, it was not included in the model for explaining mortality, but was included in the model for return to functional pre-stroke status. Significance was defined as P < 0.05 (two-sided). All analyses were intention-to-treat and were carried out using the software programs Statistica 7.1 (StatSoft, USA) and Stata (version 10; StataCorp LP, College Station, TX, USA).
The final sample consisted of 476 patients (238 in each group). As shown in Table 1, patients in the CP group had higher rates of hypertension, peripheral vasculopathy, and dementia rates, and a higher male prevalence, whereas the UC group had higher rates of diabetes and chronic obstructive pulmonary disease. No overall differences were found at the cluster level (Table 2).
Outcomes and estimation
Table 3 shows the discharge status of all patients according to the type of treatment received and various outcomes of care. The 7-day and 30-day mortality rates were lower in the CP group, but the difference was not significant, although there was a trend towards significance for the 7-day death rates. There were better results in the CP group for most of the secondary outcomes (rates of return to pre-stroke functioning in daily life, pressure-sore rates, and overall and in-hospital complication rates), except for the average length of stay, which was shorter in the UC group.
With regard to implementation of evidence-based key interventions into daily practice through the continuum of care, these were much more frequently used for the CP than for the UC groups (Table 4). Similarly, organized care was more frequently used for the CP group (Table 5). The proportion of patients receiving organized care was also significantly higher in the CP group than in the UC group.
The results of the multivariate random-effect logistic models predicting the 7-day and 30-day mortality and the rates of return to pre-stroke functioning in daily life are shown in Table 6. After adjusting for gender, comorbidities, complications, use of stroke unit, organized care, stroke team, and antithrombotic therapy, patients in the CP group had a significantly lower risk of 7-day in-hospital death (OR = 0.10; 95% CI 0.01 to 0.95) and a significantly higher probability of returning to pre-stroke functioning in their daily life (0.42; 0.18 to 0.98) compared with patients in the UC group.
The main finding of this study is that care delivered using CPs to patients with stroke was significantly more evidence-based than that delivered to patients with stroke receiving UC, and this seemed to translate to more effective treatment, because implementation of CPs resulted in a significant improvement of the outcomes.
There are several potential (and not mutually exclusive) explanations for these results, ranging from selection bias to improved performance. Selection bias may have occurred both at the individual and cluster levels. At the cluster level, no differences emerged; however, after randomization, some differences were seen between the CP and non-CP groups at the individual level. Therefore, interpretation of the outcomes before randomization could have been biased. Moreover, we could not use the National Institute of Health Stroke Scale (NHISS), because the study started before validation of this instrument in 2009 . Patient assessment before admission was partly performed, therefore the severity of stroke was not properly assessed. Except for mortality measures, we found a significant drop in sample size for certain outcomes in the non-intervention group. Thus, this may limit our findings regarding outcome improvement. However, CP use remained a significant determinant of the improved patient outcomes even after adjusting for potential confounders, including comorbidities at baseline and complications during the hospital stay. Therefore, the influence of selection bias, if any, is likely to be minor .
A second possible explanation for our findings is the different use of organized care in the two groups. The use of organized care and the access to the stroke units was were significantly higher in the CP group. Because use of organized care and stroke units are integrated approaches to managing stroke and are strong evidence-based independent predictors of in-hospital mortality, they were used as 'active components' promoted by the implementation of the CP [8, 24]. Therefore, the observed improvements in organized care and in use of stroke units and their positive effect on patient outcome were expected as part of the intervention.
With regard to outcomes, our results show how evidence-based care can be effectively implemented in real-world settings [6, 11]. Indeed, the use of evidence-based care was significantly improved in the CP group, which also made better use of the organized care, as mentioned above. These findings were apparent despite the complexity of objective evaluation of stroke, as has been reported by the primary stroke center certification program and the performance measurements of the Joint Commission [44–46]. Our findings were mostly based on short-term outcomes. Long-term and/or more qualitative outcomes, such as patient satisfaction and quality of life, were not evaluated. This was mainly due to the information system, especially in the method of documenting and collecting data (clinical records, paper-based abstraction tools), and could also be a limitation of our findings [12, 47].
In the study, we found a significant reduction only in 7-day mortality, whereas 30-day mortality was not significantly affected by the use of CPs. The 7-day mortality depends more on the early treatment of patients, but no specific protocol for factors influencing early arrival was implemented in the CP. Therefore, it is possible that the CP hospitals might have admitted patients earlier, and this would have artificially reduced their short-term in-hospital mortality rate. Although we did not have specific data on the events before admission, it is reasonable to assume that the randomization process would have controlled for this possible bias. However, after risk adjustment, the CP method remained a significant determinant of reduced 7-day mortality. Moreover, at discharge, patients in the CP group had a significantly higher rate of return to pre-stroke functioning compared with the UC group, and the process of care was significantly more consistent with evidence-based care. Based on our findings and those of other authors, we consider it reasonable to believe that the better outcomes observed for the CP group are attributable to an improvement in the quality of care achieved with the use of CPs [11, 44, 48, 49].
A limitation of our findings is that we could not examine the effect of CPs on the use of reperfusion therapy (tissue plasminogen activator; tPA), because in Italy the non-experimental use of this procedure was authorized only after the conclusion of this study. Early treatment based on tPA involves the expertise of several professionals, which can result in poor coordination or inefficiencies in the care process. Indeed, several studies have shown that tPA use in acute ischemic strokes can be enhanced by organized care, routine use of protocols, and multidisciplinary teamwork, which the current study also showed identified as active components of the implemented CP [48, 50]. Therefore, our findings suggest that the use of CPs through the implementation of better care might also be helpful for the effective use of tPA, but specific studies are required.
Because CPs are quality improvement initiatives it was not possible to blind the intervention or the assessment of the outcomes. Therefore it could have been that the awareness and attention associated with receiving a new intervention (Hawthorne effect) was responsible, in part, for the improved outcomes associated with the CPs. Given the type of intervention, a cluster randomized design was the most appropriate design to use [19, 22, 27, 40]. However, these studies have some limitations when applied to CPs . Indeed, context level adaptation, which is essential for the pathways to succeed, may be perceived as inappropriate in the trial design. Also, it may be difficult to replicate and maintain the original intervention. To reduce such issues, we implemented pathways that combined local standards with evidence-based indicators to maintain the integrity of the intervention at each site [21, 52].
This study adds evidence in favor of the notion that, compared with UC, CPs can help to provide better, comprehensive, and more specialized care to patients affected by stroke. However, additional studies are needed to further understand the cost-effectiveness of CPs and how to pass the critical point at which adherence to a pathway decreases [53–55].
Conflict of interests
The authors declare that they have no competing interests.
Donnan GA, Fisher M, Macleod M, Davis SM: Stroke. Lancet. 2008, 371: 1612-1623. 10.1016/S0140-6736(08)60694-7.
Bejot Y, Benatru I, Rouaud O, Fromont A, Besancenot JP, Moreau T, Giroud M: Epidemiology of stroke in Europe: geographic and environmental differences. J Neurol Sci. 2007, 262: 85-8. 10.1016/j.jns.2007.06.025.
American Heart Association American Stroke Association: Heart disease and stroke statistics 2008 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. 2008, 117: e25-146.
Lloyd-Jones D, Adams RJ, Brown TM, Carnethon M, Dai S, de SG, Ferguson TB, Ford E, Furie K, Gillespie C, et al: Executive summary: heart disease and stroke statistics--2010 update: a report from the American Heart Association. Circulation. 2010, 121: 948-954.
Schwamm LH, Pancioli A, Acker JE, Goldstein LB, Zorowitz RD, Shephard TJ, Moyer P, Gorman M, Johnston SC, Duncan PW, et al: Recommendations for the establishment of stroke systems of care: recommendations from the American Stroke Association's Task Force on the Development of Stroke Systems. Stroke. 2005, 36: 690-703.
Fonarow GC, Reeves MJ, Smith EE, Saver JL, Zhao X, Olson DW, Hernandez AF, Peterson ED, Schwamm LH: Characteristics, performance measures, and in-hospital outcomes of the first one million stroke and transient ischemic attack admissions in get with the guidelines-stroke. Circ Cardiovasc Qual Outcomes. 2010, 3: 291-302. 10.1161/CIRCOUTCOMES.109.921858.
Fonarow GC, Smith EE, Saver JL, Reeves MJ, Bhatt DL, Grau-Sepulveda MV, Olson DM, Hernandez AF, Peterson ED, Schwamm LH: Timeliness of tissue-type plasminogen activator therapy in acute ischemic stroke: patient characteristics, hospital factors, and outcomes associated with door-to-needle times within 60 minutes. Circulation. 2011, 123: 750-758. 10.1161/CIRCULATIONAHA.110.974675.
Saposnik G, Fang J, O'Donnell M, Hachinski V, Kapral MK, Hill MD: Escalating levels of access to in-hospital care and stroke mortality. Stroke. 2008, 39: 2522-2530. 10.1161/STROKEAHA.107.507145.
Kalra L, Evans A, Perez I, Knapp M, Swift C, Donaldson N: A randomised controlled comparison of alternative strategies in stroke care. Health Technol Assess. 2005, 9: iii-79.
Kjellstrom T, Norrving B, Shatchkute A: Helsingborg Declaration 2006 on European stroke strategies. Cerebrovasc Dis. 2007, 23: 231-241.
National Stroke Foundation: Clinical guidelines for stroke management 2010. 2010, Melbourne: National Stroke Foundation
Kwan J, Sandercock P: In-hospital care pathways for stroke. Cochrane Database Syst Rev. 2004, CD002924.
Kwan J: Care pathways for acute stroke care and stroke rehabilitation: from theory to evidence. J Clin Neurosci. 2007, 14: 189-200. 10.1016/j.jocn.2006.01.026.
Vanhaecht K, Ovretveit J, Elliott MJ, Sermeus W, Ellershaw JE, Panella M: Have we drawn the wrong conclusions about the value of care pathways? Is a Cochrane review appropriate?. Eval Health Prof. 2011, 35: 28-42.
Panella M, Marchisio S, Barbieri A, Di Stanislao F: A cluster randomized trial to assess the impact of clinical pathways for patients with stroke: rationale and design of the Clinical Pathways for Effective and Appropriate Care Study [NCT00673491]. BMC Health Serv Res. 2008, 8: 223-10.1186/1472-6963-8-223.
Schulz KF, Altman DG, Moher D: CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials. BMC Med. 2010, 8: 18-10.1186/1741-7015-8-18.
Campbell M, Fitzpatrick R, Haines A, Kinmonth AL, Sandercock P, Spiegelhalter D, Tyrer P: Framework for design and evaluation of complex interventions to improve health. BMJ. 2000, 321: 694-696. 10.1136/bmj.321.7262.694.
Loeb MB: Application of the development stages of a cluster randomized trial to a framework for valuating complex health interventions. BMC Health Serv Res. 2002, 2: 13-10.1186/1472-6963-2-13.
Medical Research Council (MRC): Cluster randomised trials: Methodological and ethical considerations. 2002, Medical Research Trials Series. London: MRC
Panella M, Marchisio S, Gardini A, Di Stanislao F: A cluster randomized controlled trial of a clinical pathway for hospital treatment of heart failure: study design and population. BMC Health Serv Res. 2007, 7: 179-10.1186/1472-6963-7-179.
Panella M, Marchisio S, Demarchi ML, Manzoli L, Di Stanislao F: Reduced in-hospital mortality for heart failure with clinical pathways: the results of a cluster randomised controlled trial. Qual Saf Health Care. 2009, 18: 369-373. 10.1136/qshc.2008.026559.
Craig P, Dieppe P, Macintyre S, Michie S, Nazareth I, Petticrew M: Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ. 2008, 337 (Suppl A): 1655.
De Luca A, Toni D, Lauria L, Sacchetti ML, Giorgi RP, Ferri M, Puca E, Prencipe M, Guasticchi G: An emergency clinical pathway for stroke patients--results of a cluster randomised trial (isrctn41456865). BMC Health Serv Res. 2009, 9: 14-10.1186/1472-6963-9-14.
Panella M, Brambilla R, Marchisio S, Di Stanislao F: Reducing stroke in-hospital mortality: organized care is a complex intervention. Stroke. 2008, 39: e186-10.1161/STROKEAHA.108.533877.
Fisher M: Stroke and TIA: epidemiology, risk factors, and the need for early intervention. Am J Manag Care. 2008, 14 (Suppl 2): S204-S211.
van der Worp HB, van GJ: Clinical practice. Acute ischemic stroke. N Engl J Med. 2007, 357: 572-579. 10.1056/NEJMcp072057.
Medical Research Council: A framework for development and evaluation of RCTs for complex interventions to improve health. London: Medical Research Council. 2000, 1: 19.
Ukoumunne OC, Gulliford MC, Chinn S, Sterne JA, Burney PG: Methods for evaluating area-wide and organisation-based interventions in health and health care: a systematic review. Health Technol Assess. 1999, 3: iii-92.
Campbell MK, Mollison J, Grimshaw JM: Cluster trials in implementation research: estimation of intracluster correlation coefficients and sample size. Stat Med. 2001, 20: 391-399. 10.1002/1097-0258(20010215)20:3<391::AID-SIM800>3.0.CO;2-Z.
Yudkin PL, Moher M: Putting theory into practice: a cluster randomized trial with a small number of clusters. Stat Med. 2001, 20: 341-349. 10.1002/1097-0258(20010215)20:3<341::AID-SIM796>3.0.CO;2-G.
Inzitari D: The Italian Guidelines for stroke prevention. The Stroke Prevention and Educational Awareness Diffusion (SPREAD) Collaboration. Neurol Sci. 2000, 21: 5-12. 10.1007/s100720070112.
Inzitari D, Carlucci G: Italian Stroke Guidelines (SPREAD): evidence and clinical practice. Neurol Sci. 2006, 27 (Suppl 3): S225-S227.
Gensini GF, Dilaghi B, Zaninelli A: Italian SPREAD Guidelines: from past to future. Neurol Sci. 2006, 27 (Suppl 3): S254-S257.
Gensini GF, Gusinu R: The systematic review of organised stroke care: a model for an unbiased assessment of trials on the effects of service organisation. The clinician's point of view. Intern Emerg Med. 2006, 1: 77-78. 10.1007/BF02934728.
Pearson SD, Goulart-Fisher D, Lee TH: Critical pathways as a strategy for improving care: problems and potential. Ann Intern Med. 1995, 123: 941-948.
Panella M, Marchisio S, Di Stanislao F: Reducing clinical variations with clinical pathways: do pathways work?. Int J Qual Health Care. 2003, 15: 509-521. 10.1093/intqhc/mzg057.
Vanhaecht K, Panella M, Van Zelm RT, Sermeus W: An overview on the concept and history of care pathways as complex interventions. Int J of Care Pathw. 2010, 14: 117-123. 10.1258/jicp.2010.010019.
Provinciali L: Role of scientific societies in implementation of stroke guidelines and clinical pathways promotion. Neurol Sci. 2006, 27 (Suppl 3): S284-S286.
Twisk J: Applied Multilevel Analysis. A practical guide. 2006, Cambridge. Cambridge University Press
Campbell MJ, Donner A, Klar N: Developments in cluster randomized trials and statistics in medicine. Stat Med. 2007, 26: 2-19. 10.1002/sim.2731.
Needham DM, Scales DC, Laupacis A, Pronovost PJ: A systematic review of the Charlson comorbidity index using Canadian administrative databases: a perspective on risk adjustment in critical care research. J Crit Care. 2005, 20: 12-19. 10.1016/j.jcrc.2004.09.007.
Pezzella FR, Picconi O, De LA, Lyden PD, Fiorelli M: Development of the Italian version of the National Institutes of Health Stroke Scale: It-NIHSS. Stroke. 2009, 40: 2557-2559. 10.1161/STROKEAHA.108.534495.
Hahn S, Puffer S, Torgerson DJ, Watson J: Methodological bias in cluster randomised trials. BMC Med Res Methodol. 2005, 5: 10-10.1186/1471-2288-5-10.
Fonarow GC, Gregory T, Driskill M, Stewart MD, Beam C, Butler J, Jacobs AK, Meltzer NM, Peterson ED, Schwamm LH, et al: Hospital certification for optimizing cardiovascular disease and stroke quality of care and outcomes. Circulation. 2010, 122: 2459-2469. 10.1161/CIR.0b013e3182011a81.
The Joint Commission website. 2011, [http://www.jointcommission.org/certification/primary_stroke_centers.aspx]
Lichtman JH, Jones SB, Wang Y, Watanabe E, Leifheit-Limson E, Goldstein LB: Outcomes after ischemic stroke for hospitals with and without Joint Commission-certified primary stroke centers. Neurology. 2011, 6: 1976-1982.
Loeb M, Carusone SC, Goeree R, Walter SD, Brazil K, Krueger P, Simor A, Moss L, Marrie T: Effect of a clinical pathway to reduce hospitalizations in nursing home residents with pneumonia: a randomized controlled trial. JAMA. 2006, 295: 2503-2510. 10.1001/jama.295.21.2503.
Gorelick AR, Gorelick PB, Sloan EP: Emergency department evaluation and management of stroke: acute assessment, stroke teams and care pathways. Neurol Clin. 2008, 26: 923-942. 10.1016/j.ncl.2008.05.008.
Middleton S, McElduff P, Ward J, Grimshaw JM, Dale S, D'Este C, Drury P, Griffiths R, Cheung NW, Quinn C, et al: Implementation of evidence-based treatment protocols to manage fever, hyperglycaemia, and swallowing dysfunction in acute stroke (QASC): a cluster randomised controlled trial. Lancet. 2011, 378: 1699-1706. 10.1016/S0140-6736(11)61485-2.
Moser DK, Kimble LP, Alberts MJ, Alonzo A, Croft JB, Dracup K, Evenson KR, Go AS, Hand MM, Kothari RU, et al: Reducing delay in seeking treatment by patients with acute coronary syndrome and stroke: a scientific statement from the American Heart Association Council on cardiovascular nursing and stroke council. Circulation. 2006, 114: 168-182. 10.1161/CIRCULATIONAHA.106.176040.
Donner A, Klar N: Pitfalls of and controversies in cluster randomization trials. Am J Public Health. 2004, 94: 416-422. 10.2105/AJPH.94.3.416.
Hawe P, Shiell A, Riley T: Complex interventions: how "out of control" can a randomised controlled trial be?. BMJ. 2004, 328: 1561-1563. 10.1136/bmj.328.7455.1561.
Vanhaecht K, De Witte K, Panella M, Sermeus W: Do pathways lead to better organized care processes?. J Eval Clin Pract. 2009, 15: 782-788. 10.1111/j.1365-2753.2008.01068.x.
Savitz LA, Kaluzny AD: Assessing the implementation of clinical process innovations: a cross-case comparison. J Healthc Manag. 2000, 45: 366-379.
Wolfe CD, Rudd AG: Improvement of care in acute stroke units. Lancet. 2011, 378: 1679-1680. 10.1016/S0140-6736(11)61545-6.
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We thank the CPEAC Study Steering Committee and the coordinators of the EQCP Study Unit Group for their contribution to the conception and coordination of the study, to the definition of the contents of the CP, and to the acquisition of data. The CPEAC Study was promoted and funded by the Italian Ministry of Health (Special Programs art. 12 bis D.lgs 229/99) and Marche Region. The funding sources played no role in the design, conduct, analysis, interpretation, reporting, writing of the study, or in the decision to submit the manuscript for publication.
MP conceived and developed this study, managed the project, and wrote the manuscript. MP had full access to all of the data in the study, and takes responsibility for the integrity of the data and the accuracy of the data analysis. SM helped to design the study in defining the indicator set and contributed to the manuscript. RB assisted in cluster creation and performed the statistical analysis. KV contributed to the evaluation of the findings and to the development of the manuscript. FDS provided input in the project, overviewed all steps of the study design, and undertook the final review of the manuscript. All authors have read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Flow chart of clinical pathway activities before, during, and after hospitalization of patients. This file contains a graphical representation of clinical pathway activities to be applied before, during, and after hospitalization, at discharge, and at follow-up, as defined by the working teams. (PPT 272 KB)
Additional file 2: List of clinical pathway activities to be applied before, during, and after patient hospitalization as defined by the working teams. This file contains detailed descriptions of of clinical pathway activities for application before, during, and after the hospitalization, at discharge, and at follow-up, as defined by the working teams. (DOC 84 KB)
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Panella, M., Marchisio, S., Brambilla, R. et al. A cluster randomized trial to assess the effect of clinical pathways for patients with stroke: results of the clinical pathways for effective and appropriate care study. BMC Med 10, 71 (2012). https://doi.org/10.1186/1741-7015-10-71
- Acute Ischemic Stroke
- Clinical Pathway
- Stroke Unit
- Stroke Team
- Marche Region