Handoffs and Transitions in Critical Care - Understanding Scalability
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Customized handoff.
- Кому может быть актуально
- Состояния в реестре: Patient Handoff, Healthcare Team, Communication, Patient Safety. Базовые параметры: от 18 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
The investigators will leverage implementation science and engineering to adapt, implement, and rigorously evaluate tailored postoperative handoff protocols and implementation strategies. In doing so, the investigators will develop a vital understanding of the factors needed for successful and sustained use of evidence-based interventions in acute care. This knowledge will inform approaches to bridge the evidence-to-practice gap that prevents effective interventions from realizing the promise of improved patient outcomes in acute care settings.
Подробное описание
Surgical patients who require post-surgical critical care are usually transferred from the operating room (OR) to the intensive care unit (ICU) for ongoing care. The process of transferring the patient from the OR to the ICU is called a "handoff." Handoffs involve the transfer of patient information and transfer of patient care responsibilities from the OR team to the ICU team. Multiple studies suggest that these handoffs can expose patients to preventable harm, which can be avoided with standardization of the handoff. The Handoffs and Transitions in Critical Care (HATRICC; IRB #819726) study, started in 2014, developed and implemented a standardized OR to ICU handoff process in two Penn surgical ICUs (SICUs) that did not have a standardized handoff process.
Four clinicians (surgeon, anesthetist, ICU provider, and ICU nurse) from two teams (surgical and intensive care) usually take part in handoff communication. During the HATRICC study, the investigators evaluated handoff communication between the OR and ICU teams before and after implementation of the new standardized handoff process (the "HATRICC process") in multiple ways, using observations, interviews, focus groups, and surveys. The investigators demonstrated a 20% improvement in information exchange after implementation of the HATRICC standardized handoff process, a process tailored to meet the needs of the different clinicians participating in OR to ICU handoffs.
Prior studies have indicated short-term success in standardizing OR to ICU handoffs, but sustainability of these improvement interventions has been less well studied. Two studies have demonstrated sustained or improved information exchange following the institution of structured OR to ICU handoff processes, but the factors influencing sustainability remain to be elucidated.
The aims of this study are to:
1. Ascertain determinants of OR-to-ICU handoff protocol adoption and use in 12 adult and pediatric ICUs in five health systems. 2. Adapt handoff protocols using engineering approaches and select tailored implementation strategies with implementation mapping. 3. Test the effectiveness of tailored, multifaceted, multilevel implementation strategies. 4. Design and create a digital toolkit for other ICUs to identify implementation determinants, customize OR-to-ICU handoff protocol, and select appropriate implementation strategies.
Вмешательства
- Поведенческое Customized handoff
A customized handoff will be implemented that consists of choreographed handoffs utilizing a structured handoff tool to facilitate information exchange.
Первичные конечные точки
- Adherence to standardized handoff intervention (Fidelity) measured by number of handoff steps followed. [Срок оценки: This outcome will be measured at monthly intervals starting Year 1, Quarter 2 and continuing until the end of Year 5.]
- New-onset organ failure [Срок оценки: This outcome will be measured at monthly intervals starting Year 1, Quarter 2 and continuing until the end of Year5]
Вторичные конечные точки (12)
- Perception among implementation stakeholders that a given treatment, service, practice, or innovation is agreeable, palatable, or satisfactory (Acceptability) [Срок оценки: Baseline (Year 1); within 2months of implementation; within 2 months of beginning sustainment]
- Perceived fit, relevance, or compatibility of the innovation in a practice setting or to address a particular issue (Appropriateness), measured by the Intervention Appropriateness Measure [Срок оценки: Baseline (Year 1); within 2months of implementation; within 2 months of beginning sustainment]
- Feasibility of treatment or innovation to be carried out in a practice setting, measured using the Feasibility of Intervention Measure. [Срок оценки: Baseline (Year 1); within 2months of implementation; within 2 months of beginning sustainment]
- Fidelity over time (Sustainment) [Срок оценки: This outcome will be measured at monthly intervals starting 2 years after implementation, up to 5 years.]
- Monetary and non-monetary costs measured using the line item classification system [Срок оценки: This outcome will be measured within 2 months of implementation; within2 months of beginning sustainment]
- Teamwork (effectiveness) measured using the Team Emergency Assessment Measure. [Срок оценки: This outcome will be measured at quarterly intervals starting Year 1, Quarter 2 and continuing until the end of Year 5]
- Clinician satisfaction measured at the individual level. [Срок оценки: This outcome will be measured annually from Years 1 to 5.]
- Workload measured using the NASA Task Load Index. [Срок оценки: This outcome will be measured at quarterly intervals starting Year 1, Quarter 2 and continuing until the end of Year 5.]
- Completeness of information exchange (Information Omissions) measured using a structured observation form. [Срок оценки: This outcome will be measured at monthly intervals starting Year 1, Quarter 2 and continuing until the end of Year5]
- Weighted average of the reliability-adjusted observed-to-expected ratios for component indicators of adverse events [Срок оценки: This outcome will be measured at quarterly intervals starting Year 1, Quarter 2 and continuing until the end of Year 5.]
- AHRQ PSI 9: Perioperative hemorrhage or hematoma rate(effectiveness) [Срок оценки: This outcome will be measured at monthly intervals starting Year 1, Quarter 2 and continuing until the end of Year 5]
- AHRQ PSI 10: Postoperative physiologic or metabolic derangement rate (effectiveness) [Срок оценки: This outcome will be measured at monthly intervals starting Year 1, Quarter 2 and continuing until the end of Year 5.]
Критерии участия
Inclusion Criteria for Clinicians:
- Age ≥ 18 years
- Cares for patients at any point in the surgical continuum of care, including pre-operative, intra-operative, or post-operative care, OR has administrative responsibilities relevant to patient care at the study hospitals
- Fluency in English
Inclusion Criteria for Patients:
- Patient admitted for inpatient care at the study hospitals and experiences a post-operative handoff from the operating room to the intensive care unit.
Exclusion Criteria for Clinicians:
- Being a member of research staff
Exclusion Criteria for Patients:
- (none)
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Не применимо
- Модель
- Одна группа
- Маскирование
- Открытое
- Основная цель
- Организация здравоохранения
Центры проведения
США · 5 центров
- Johns Hopkins — Baltimore
- Cooper Health — Camden
- Temple Health — Philadelphia
- University of Pennsylvania — Philadelphia
- UT Southwestern Medical Center — Dallas
Публикации
- Ashcraft LE, Watson MA, Vaughan C, Lee S, Yang S, Lane-Fall MB. Rapid and pragmatic implementation mapping for pre-implementation contextual analysis in multisite implementation trials. Front Health Serv. 2026 Jul 3;6:1782980. doi: 10.3389/frhs.2026.1782980. eCollection 2026. PMID 42490896
- Lane-Fall MB, Christakos A, Russell GC, Hose BZ, Dauer ED, Greilich PE, Hong Mershon B, Potestio CP, Pukenas EW, Kimberly JR, Stephens-Shields AJ, Trotta RL, Beidas RS, Bass EJ. Handoffs and transitions in critical care-understanding scalability: study protocol for a multicenter stepped wedge type 2 hybrid effectiveness-implementation trial. Implement Sci. 2021 Jun 15;16(1):63. doi: 10.1186/s13012 PMID 34130725
Идентификаторы
NCT: NCT04571749 · 843670 · R01HL153735