TY - JOUR
T1 - The impact of nUrsiNg DEliRium Preventive INterventions in the Intensive Care Unit (UNDERPIN-ICU): A study protocol for a multi-centre, stepped wedge randomized controlled trial
AU - Wassenaar, Annelies
AU - Rood, Paul
AU - Schoonhoven, Lisette
AU - Teerenstra, Steven
AU - Zegers, Marieke
AU - Pickkers, Peter
AU - van den Boogard, Mark
PY - 2016/12/8
Y1 - 2016/12/8
N2 - Background: Delirium is a common disorder in Intensive Care Unit (ICU) patients and is associated with serious short- and long-term consequences, including re-intubations, ICU readmissions, prolonged ICU and hospital stay, persistent cognitive problems, and higher mortality rates. Considering the high incidence of delirium and its consequences, prevention of delirium is imperative. This study focuses on a program of standardized nursing and physical therapy interventions to prevent delirium in the ICU, called UNDERPIN-ICU (nUrsiNg DEliRium Preventive INterventions in the ICU).Objective: To determine the effect of the UNDERPIN-ICU program on the number of delirium-coma-free days in 28 days and several secondary outcomes, such as delirium incidence, the number of days of survival in 28 and 90 days and delirium-related outcomes.Design and Setting: A multicenter stepped wedge cluster randomized controlled trial.Methods: Eight to ten Dutch ICUs will implement the UNDERPIN-ICU program in a randomized order. Every two months the UNDERPIN-ICU program will be implemented in an additional ICU following a two months period of staff training. UNDERPIN-ICU consists of standardized protocols focusing on several modifiable risk factors for delirium, including cognitive impairment, sleep deprivation, immobility and visual and hearing impairment.Participants: ICU patients aged ?18 years (surgical, medical, or trauma) and at high risk for delirium, E-PRE-DELIRIC ?35%, will be included, unless delirium was detected prior ICU admission, expected length of ICU stay is less then one day or when delirium assessment is not possible.Discussion: For every intervention the balance between putative benefit and potential unwanted side effects needs to be considered. In non-ICU patients, it has been shown that a similar program resulted in a significant reduction of delirium incidence and duration. Recent small studies using multi component interventions to prevent delirium in ICU patients have also shown beneficial effect, without unwanted side effects. We therefore feel that the proportionality of potential positive effects of the UNDERPIN-ICU program, weighed against potential unwanted side effects is favourable. Since this has not been rigorously proven in ICU patients, we will study the effects of this program in ICU patients using a stepped wedge design.Trial registration: Intended registry: https://clinicaltrials.gov/. This will be done when the final version of this manuscript is accepted.Reporting method: Standard Protocol Items: Recommendations for Interventional Trails (SPIRIT).
AB - Background: Delirium is a common disorder in Intensive Care Unit (ICU) patients and is associated with serious short- and long-term consequences, including re-intubations, ICU readmissions, prolonged ICU and hospital stay, persistent cognitive problems, and higher mortality rates. Considering the high incidence of delirium and its consequences, prevention of delirium is imperative. This study focuses on a program of standardized nursing and physical therapy interventions to prevent delirium in the ICU, called UNDERPIN-ICU (nUrsiNg DEliRium Preventive INterventions in the ICU).Objective: To determine the effect of the UNDERPIN-ICU program on the number of delirium-coma-free days in 28 days and several secondary outcomes, such as delirium incidence, the number of days of survival in 28 and 90 days and delirium-related outcomes.Design and Setting: A multicenter stepped wedge cluster randomized controlled trial.Methods: Eight to ten Dutch ICUs will implement the UNDERPIN-ICU program in a randomized order. Every two months the UNDERPIN-ICU program will be implemented in an additional ICU following a two months period of staff training. UNDERPIN-ICU consists of standardized protocols focusing on several modifiable risk factors for delirium, including cognitive impairment, sleep deprivation, immobility and visual and hearing impairment.Participants: ICU patients aged ?18 years (surgical, medical, or trauma) and at high risk for delirium, E-PRE-DELIRIC ?35%, will be included, unless delirium was detected prior ICU admission, expected length of ICU stay is less then one day or when delirium assessment is not possible.Discussion: For every intervention the balance between putative benefit and potential unwanted side effects needs to be considered. In non-ICU patients, it has been shown that a similar program resulted in a significant reduction of delirium incidence and duration. Recent small studies using multi component interventions to prevent delirium in ICU patients have also shown beneficial effect, without unwanted side effects. We therefore feel that the proportionality of potential positive effects of the UNDERPIN-ICU program, weighed against potential unwanted side effects is favourable. Since this has not been rigorously proven in ICU patients, we will study the effects of this program in ICU patients using a stepped wedge design.Trial registration: Intended registry: https://clinicaltrials.gov/. This will be done when the final version of this manuscript is accepted.Reporting method: Standard Protocol Items: Recommendations for Interventional Trails (SPIRIT).
KW - Adult
KW - Critical care
KW - Delirium
KW - Intensive care
KW - Intervention study
KW - Nurses
KW - Randomized controlled trial
U2 - 10.1016/j.ijnurstu.2016.11.018
DO - 10.1016/j.ijnurstu.2016.11.018
M3 - Article
SN - 0020-7489
VL - 68
SP - 1
EP - 8
JO - International Journal of Nursing Studies
JF - International Journal of Nursing Studies
ER -