Sepsis
Conditions
Keywords
evidence based medicine, transition care, critical care, implementation science, pragmatic clinical trial
Brief summary
The purpose of this study is to evaluate if implementation of the Sepsis Transition and Recovery (STAR) program within a large healthcare system will improve outcomes for high-risk patients with suspected sepsis, while concurrently examining contextual factors related to STAR program delivery within routine care to generate knowledge of best practices for implementation and dissemination of post sepsis transitions of care. To address persistent morbidity and mortality for sepsis survivors, Atrium Health developed the Sepsis Treatment and Recovery (STAR) program which uses a nurse navigator to deliver a bundle of best-practice care elements for the delivery of longitudinal post-sepsis care for up to 90 days. These care elements are directed towards the specific challenges and sequelae following a sepsis hospitalization and include: 1) identification and treatment of new physical, mental, and cognitive deficits; 2) review and adjustment of medications; 3) surveillance of treatable conditions that commonly lead to poor outcomes including chronic conditions that may de-stabilize during sepsis and recovery; and 4) focus on palliative care when appropriate. ENCOMPASS (Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship) is an effectiveness-implementation hybrid type I trial, with the evaluation designed as a two-arm, pragmatic, stepped-wedge cluster randomized controlled trial conducted at eight regional hospitals in which each participating hospital begins in a usual care control phase and transitions to the STAR program intervention in a randomly assigned sequence. Patients are allocated to receive the treatment condition (i.e., usual care or STAR) assigned to their admission hospital at time of enrollment. ENCOMPASS will test the hypothesis that patients who receive care through the STAR program will have reduced mortality and hospital readmission assessed 90 days post index hospital discharge compared to patients who receive usual care.
Detailed description
BACKGROUND Sepsis is a common and life-threatening condition defined by organ dysfunction due to a dysregulated response to infection (Fleischmann, 2016). Aggressive early sepsis identification and treatment initiatives have decreased hospital mortality for patients with sepsis (Rhodes, 2017; Kaukonen, 2014). However, sepsis survivors continue to face challenges after the acute illness episode, experiencing new functional, cognitive, and psychological deficits, and high rates of hospital readmission and mortality in the 90-days after hospital discharge (Iwashyna, 2010; Borges, 2015; Annane, 2015; Prescott, 2015; Mayr, 2017). To address persistent morbidity and mortality for sepsis survivors, Atrium Health developed the Sepsis Treatment and Recovery (STAR) program which uses a nurse navigator to deliver a bundle of best-practice care elements for the delivery of longitudinal post-sepsis care for up to 90 days. These care elements are directed towards the specific challenges and sequelae following a sepsis hospitalization and include: 1) identification and treatment of new physical, mental, and cognitive deficits; 2) review and adjustment of medications; 3) surveillance of treatable conditions that commonly lead to poor outcomes including chronic conditions that may destabilize during sepsis and recovery; and 4) focus on palliative care when appropriate (Prescott, 2018) These care elements have good face-validity and have shown to be associated with improved outcomes for sepsis survivors in observational data (Taylor, 2020). However, they are not widely applied in real-world settings for this vulnerable population, likely hindered by a gap in understanding key contextual factors underlying how to best integrate this bundle of care elements into the complex and fragmented post-discharge setting (Brownson, 2012; Bodenheimer, 2008; Coleman, 2004; Kim, 2013) RATIONALE In randomized controlled trials (RCTs), successfully implemented care transition programs using nurse navigators have been shown to reduce hospital readmission and costs. To better enhance transitions of care for the highest risk, complex patients with suspected sepsis, the investigators propose extending this evidence using a nurse-facilitated care transition program for patients in the post-sepsis transition period to improve the implementation of recommended care practices and bridge care gaps. This approach, called the Sepsis Transition and Recovery (STAR) program, is the next step in the progression of the investigator team's work on improving discharge transitions and sepsis processes of care. A key aspect of this initiative includes the ability to identify sepsis survivors at the greatest risk for poor outcomes. For example, one-quarter of sepsis survivors account for three-quarters of hospital readmission and costs, indicating that identifying high-risk sepsis patients for targeted facilitation of best-practice care could efficiently impact quality and cost. The STAR program uses near real-time risk modeling to identify high-risk patients and a centrally located nurse, virtually connected to participating hospitals, to coordinate the application of evidence-based recommendations for post-sepsis care, overcome barriers to recommended care, and bridge gaps in service that can serve as points of failure for complex patients. During hospitalization, high-risk patients enter into a transition pathway integrated within Atrium Health Hospital Medicine's Transition Services program and includes the following core components: i) Introduction to STAR process prior to discharge (confirm provider consults e.g., PT, ID, palliative); ii) Disease-specific education and discharge playbook; iii) Virtual hospital follow-up evaluation within 48 hours including medication reconciliation; iv) Second, post-acute virtual follow-up within 72-96 hours (symptom monitoring, confirm provider follow-up); v) Weekly contact with STAR team; vi) Referral to provider follow-up (e.g., primary care provider, transition clinic) as appropriate; vii) Coordinated transition to the next appropriate care location after 90 days from time of discharge. The STAR navigator also meets weekly with the Medical Director of the Atrium Health Transition Services program who provides additional clinical oversight of ongoing cases. The ENCOMPASS (Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship) evaluation will examine if implementation of the STAR program within a large healthcare system will improve outcomes for high-risk sepsis patients. This cluster randomized program evaluation is designed to be a seamless part of routine care in a real-world setting to generate knowledge of best practices for implementation and dissemination of post-sepsis transitions of care. INVESTIGATIONAL PLAN Overall Study Design ENCOMPASS is an effectiveness-implementation hybrid type I trial. The evaluation component is designed as a two-arm, pragmatic, stepped-wedge cluster randomized controlled trial conducted at eight regional hospitals in which each participating hospital begins in a usual care control phase and transitions to the STAR program intervention in a randomly assigned sequence, with one of eight hospitals assigned to transition at each four-month interval (i.e., step). During the time that a hospital is allocated to usual care, all eligible patients will receive usual care. Once a hospital has been allocated to the STAR arm, all eligible patients will receive STAR during their index hospitalization and extending through 90 days from discharge or date of death. The ENCOMPASS trial will compare the effectiveness of the Sepsis Transition And Recovery (STAR) program versus usual care on post-sepsis care and patient outcomes. The STAR program is informed by existing evidence and designed using the Chronic Care Model to increase best-practice adherence and care coordination, resulting in improved transitions between hospitals and post-acute care during sepsis recovery. ENCOMPASS will test the STAR program intervention within the course of providing usual care among a large and diverse population of post-sepsis patients admitted to eight hospitals within Atrium Health, one of the largest, vertically integrated health systems in the US. The eight acute care hospitals participating in this study use the same EHR, which connects across all points of care, including outpatient practices, urgent care locations, emergency departments and hospitals. Consistent with the pragmatic study design concept, eligibility criteria are broad, the sample size is large and diverse, and study procedures are embedded into the context of routine care. To be objective in patient selection and allow for program evaluation, a data driven approach will be used to identify patients as eligible for program referral. Each weekday morning actively admitted patients at eight study hospitals will be identified from the electronic health record and Enterprise Data Warehouse and output into daily eligibility lists based on the study's inclusion/exclusion criteria. Primary analyses will be conducted using an intent-to-treat approach such that all eligible patients will be included. Planned enrollment is 4032 patients and STAR program follow-up will be completed 90 days after hospital discharge. Outcomes data will be tracked for 90 days and captured from routinely collected data from the Atrium Health Enterprise Data Warehouse. Given this evaluation protocol relies on using evidence-based interventions, only utilizes data collected as part of routine care, and is minimal risk to patients, the institutional review board granted the request for waiver of informed consent.
Interventions
In the STAR program intervention, a centrally located nurse navigator facilitates the application of four evidence-based core components of post-sepsis care (i.e., review of medications, new impairments, comorbidities, and palliative care) to patients prior to and during the 90 days after hospital discharge. The STAR navigator will provide telephone and EHR-based support within the hospitalization and to patients across all discharge settings with remote monitoring at specified intervals following hospital discharge. Patients will continue to receive STAR directed services for 90 days following their discharge and then will be transitioned back to the next appropriate care location.
Hospitals and their patients will not have access to the STAR program. Patients will continue to receive usual care throughout their stay and discharge, consisting of: patient education and follow-up instructions at discharge, which are not specific to sepsis; routine recommendations for follow-up visits with primary care providers; arrangements for home health services or care management follow-up based on each patient's needs but not specifically tailored to the sepsis population; discharge to post-acute setting with no sepsis-specific follow-up. All aspects of usual care will be determined by treating clinicians independent of trial assignment.
Sponsors
Study design
Intervention model description
Pragmatic, stepped-wedge cluster randomized controlled trial
Eligibility
Inclusion criteria
1. At least 18 years of age upon admission 2. Suspected infection 1. Oral/parenteral antibiotic or bacterial culture order within 24 hours of emergency department presentation; and 2. Evidence of systemic inflammatory response (i.e., at least two abnormal of temperature; heart rate; respiratory rate; and WBC count or bands) 3. Evidence of organ dysfunction (i.e., at least two points on either Quick Sepsis-related Organ Failure Assessment or Sepsis-related Organ Failure Assessment risk tools) 4. Deemed as high risk for 90-day readmission using risk-scoring models 5. Not discharged at the time of patient list generation
Exclusion criteria
1. Patients with a change in code status (i.e., do not resuscitate, do not intubate) within 24 hours after infection onset due to presumed limitation of aggressive treatment 2. Patients who reside \> 2.5 hours drive time from the treating hospital 3. Patients actively enrolled in a different care management program at time of admission 4. Patient has been randomized previously.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| All-cause Mortality and Hospital Readmission Rate | 90 days | Combined death or unplanned hospital readmission due to any cause, assessed 90 days after the index hospital discharge |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| All-cause Mortality Rate | 90 days | Patients with date of death prior to 90 days post discharge documented in the electronic health record or in linked national death records |
| All-cause Hospital Readmission Rate | 90 days | Any hospital readmission, including both inpatient and observation status hospitalizations, assessed 90 days post index hospital discharge. |
| Number of Outpatient Provider Visits | 90 days | Number of outpatient provider visits assessed 90 days post index hospital discharge |
| Number of Emergency Department Visits | 90 days | Number of emergency department visits assessed 90 days post index hospital discharge |
| Cause-specific Hospital Readmission Rate | 90 days | Any hospital readmission due to sepsis or other infection conditions assessed 90 days post index hospital discharge |
| Inpatient Functional Assessment or Physical Therapy Consult | Index hospital discharge | Documented inpatient functional assessment or physical therapy consult completed and captured from electronic health records |
| Inpatient Mental Health Assessment | Index hospital discharge | Documented inpatient mental health assessment completed and captured from electronic health records |
| Number of Days Alive and Outside the Hospital | 90 days | The total days alive without inpatient, observation, and emergency department care utilization beginning with the day of index hospital admission and ending 90 days after discharge or on the date of death if prior to 90 days. |
| Early Outpatient Provider Follow up | 7 days after discharge | The completion of hospital follow-up visit with an outpatient provider within 7 days of hospital discharge captured from electronic health records |
| Outpatient Medication Reconciliation | 90 days after hospital discharge | Completion of medication reconciliation in the electronic health record during the 90 days post hospital discharge |
| Palliative Care Consultation | Index hospital discharge | Documented completion of palliative care consult captured from electronic health records. |
| Completed Care Preferences | Index hospital discharge | Documented completion of patient care preferences form captured from electronic health records |
| Discharge to Hospice Care | Index hospital discharge | Discharge disposition of hospice care from initial sepsis hospitalization captured from electronic health records |
| Place of Death | 90 days after hospital discharge | In-hospital, hospice, and home or other location of death captured from electronic health records |
| Count of Participants With Support Service Referrals | 90 days after hospital discharge | Outpatient rehabilitation or physical, occupational, or speech therapy during follow-up |
Countries
United States
Participant flow
Recruitment details
This is a 36-month stepped-wedge cluster randomized trial. Each hospital begins enrolling patients under usual care and transitions to enrolling patients in STAR program one hospital at a time in a randomly determined sequence every 4 months. The randomization sequence was concealed to all hospitals until 1 month before each individual hospital transitioned to receive the STAR program. The trial was conducted at 7 hospitals in the Atrium Health system and one additional outside hospital.
Pre-assignment details
The outside hospital affiliated with a different health system withdrew from the trial after randomization but prior to receiving the intervention. The number of participants to start a Period is not equal to the number who completed the previous Period since this is a pragmatic trial with cross-sectional sampling of eligible patients in each step at each participating study site.
Participants by arm
| Arm | Count |
|---|---|
| Sepsis Transition and Recovery (STAR) Program In the STAR program intervention, a centrally located nurse navigator facilitates the application of four evidence-based core components of post-sepsis care (i.e., review of medications, new impairments, comorbidities, and palliative care) to patients prior to and during the 90 days after hospital discharge. The STAR navigator will provide telephone and EHR-based support within the hospitalization and to patients across all discharge settings with remote monitoring at specified intervals following hospital discharge. Patients will continue to receive STAR directed services for 90 days following their discharge and then will be transitioned back to the next appropriate care location. | 2,122 |
| Usual Care Hospitals and their patients will not have access to the STAR program. Patients will continue to receive usual care throughout their stay and discharge, consisting of: patient education and follow-up instructions at discharge, which are not specific to sepsis; routine recommendations for follow-up visits with primary care providers; arrangements for home health services or care management follow-up based on each patient's needs but not specifically tailored to the sepsis population; discharge to post-acute setting with no sepsis-specific follow-up. All aspects of usual care will be determined by treating clinicians independent of trial assignment. | 1,426 |
| Total | 3,548 |
Baseline characteristics
| Characteristic | Total | Sepsis Transition and Recovery (STAR) Program | Usual Care |
|---|---|---|---|
| Age, Continuous | 65.56 years STANDARD_DEVIATION 15.19 | 65.65 years STANDARD_DEVIATION 15.07 | 65.44 years STANDARD_DEVIATION 15.37 |
| Race (NIH/OMB) American Indian or Alaska Native | 12 Participants | 8 Participants | 4 Participants |
| Race (NIH/OMB) Asian | 30 Participants | 26 Participants | 4 Participants |
| Race (NIH/OMB) Black or African American | 867 Participants | 499 Participants | 368 Participants |
| Race (NIH/OMB) More than one race | 22 Participants | 12 Participants | 10 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 1 Participants | 1 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 48 Participants | 39 Participants | 9 Participants |
| Race (NIH/OMB) White | 2568 Participants | 1537 Participants | 1031 Participants |
| Sequential Organ Failure Assessment (SOFA) score | 4.637 units on a scale STANDARD_DEVIATION 2.464 | 4.635 units on a scale STANDARD_DEVIATION 2.521 | 4.647 units on a scale STANDARD_DEVIATION 2.378 |
| Sex: Female, Male Female | 1843 Participants | 1056 Participants | 787 Participants |
| Sex: Female, Male Male | 1705 Participants | 1066 Participants | 639 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 367 / 2,122 | 292 / 1,426 |
| other Total, other adverse events | 0 / 2,122 | 0 / 1,426 |
| serious Total, serious adverse events | 763 / 2,122 | 478 / 1,426 |
Outcome results
All-cause Mortality and Hospital Readmission Rate
Combined death or unplanned hospital readmission due to any cause, assessed 90 days after the index hospital discharge
Time frame: 90 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | All-cause Mortality and Hospital Readmission Rate | 1023 Participants |
| Usual Care | All-cause Mortality and Hospital Readmission Rate | 684 Participants |
All-cause Hospital Readmission Rate
Any hospital readmission, including both inpatient and observation status hospitalizations, assessed 90 days post index hospital discharge.
Time frame: 90 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | All-cause Hospital Readmission Rate | 763 Participants |
| Usual Care | All-cause Hospital Readmission Rate | 478 Participants |
All-cause Mortality Rate
Patients with date of death prior to 90 days post discharge documented in the electronic health record or in linked national death records
Time frame: 90 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | All-cause Mortality Rate | 367 Participants |
| Usual Care | All-cause Mortality Rate | 292 Participants |
Cause-specific Hospital Readmission Rate
Any hospital readmission due to sepsis or other infection conditions assessed 90 days post index hospital discharge
Time frame: 90 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Cause-specific Hospital Readmission Rate | 370 Participants |
| Usual Care | Cause-specific Hospital Readmission Rate | 222 Participants |
Completed Care Preferences
Documented completion of patient care preferences form captured from electronic health records
Time frame: Index hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Completed Care Preferences | 526 Participants |
| Usual Care | Completed Care Preferences | 309 Participants |
Count of Participants With Support Service Referrals
Outpatient rehabilitation or physical, occupational, or speech therapy during follow-up
Time frame: 90 days after hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Count of Participants With Support Service Referrals | 594 Participants |
| Usual Care | Count of Participants With Support Service Referrals | 374 Participants |
Discharge to Hospice Care
Discharge disposition of hospice care from initial sepsis hospitalization captured from electronic health records
Time frame: Index hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Discharge to Hospice Care | 97 Participants |
| Usual Care | Discharge to Hospice Care | 69 Participants |
Early Outpatient Provider Follow up
The completion of hospital follow-up visit with an outpatient provider within 7 days of hospital discharge captured from electronic health records
Time frame: 7 days after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Early Outpatient Provider Follow up | 468 Participants |
| Usual Care | Early Outpatient Provider Follow up | 348 Participants |
Inpatient Functional Assessment or Physical Therapy Consult
Documented inpatient functional assessment or physical therapy consult completed and captured from electronic health records
Time frame: Index hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Inpatient Functional Assessment or Physical Therapy Consult | 1768 Participants |
| Usual Care | Inpatient Functional Assessment or Physical Therapy Consult | 1196 Participants |
Inpatient Mental Health Assessment
Documented inpatient mental health assessment completed and captured from electronic health records
Time frame: Index hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Inpatient Mental Health Assessment | 2048 Participants |
| Usual Care | Inpatient Mental Health Assessment | 1385 Participants |
Number of Days Alive and Outside the Hospital
The total days alive without inpatient, observation, and emergency department care utilization beginning with the day of index hospital admission and ending 90 days after discharge or on the date of death if prior to 90 days.
Time frame: 90 days
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Number of Days Alive and Outside the Hospital | 72.2 Days |
| Usual Care | Number of Days Alive and Outside the Hospital | 71.9 Days |
Number of Emergency Department Visits
Number of emergency department visits assessed 90 days post index hospital discharge
Time frame: 90 days
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Number of Emergency Department Visits | 0.50 count of visits |
| Usual Care | Number of Emergency Department Visits | 0.46 count of visits |
Number of Outpatient Provider Visits
Number of outpatient provider visits assessed 90 days post index hospital discharge
Time frame: 90 days
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Number of Outpatient Provider Visits | 3.0 count of visits |
| Usual Care | Number of Outpatient Provider Visits | 3.6 count of visits |
Outpatient Medication Reconciliation
Completion of medication reconciliation in the electronic health record during the 90 days post hospital discharge
Time frame: 90 days after hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Outpatient Medication Reconciliation | 1590 Participants |
| Usual Care | Outpatient Medication Reconciliation | 866 Participants |
Palliative Care Consultation
Documented completion of palliative care consult captured from electronic health records.
Time frame: Index hospital discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Palliative Care Consultation | 430 Participants |
| Usual Care | Palliative Care Consultation | 234 Participants |
Place of Death
In-hospital, hospice, and home or other location of death captured from electronic health records
Time frame: 90 days after hospital discharge
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Sepsis Transition and Recovery (STAR) Program | Place of Death | In hospital deaths | 204 Participants |
| Sepsis Transition and Recovery (STAR) Program | Place of Death | Hospice deaths | 69 Participants |
| Sepsis Transition and Recovery (STAR) Program | Place of Death | Home or other deaths | 94 Participants |
| Usual Care | Place of Death | In hospital deaths | 150 Participants |
| Usual Care | Place of Death | Hospice deaths | 67 Participants |
| Usual Care | Place of Death | Home or other deaths | 75 Participants |