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Replacing protein via enteral nutrition in a stepwise approach in critically ill patients: the REPLENISH randomized clinical trial protocol.
Arabi, Yaseen M; Al-Dorzi, Hasan M; Sadat, Musharaf; Muharib, Dina; Algethamy, Haifa; Al-Hameed, Fahad; Mady, Ahmed; AlGhamdi, Adnan; Almekhlafi, Ghaleb A; Al-Fares, Abdulrahman A; Kharaba, Ayman; Al Bshabshe, Ali; Maghrabi, Khalid; Al Ghamdi, Khalid; Rasool, Ghulam; Chalabi, Jamal; AlHumedi, Haifaa Ibrahim; Sakkijha, Maram Hasan; Alamrey, Norah Khalid; Alhutail, Rabeah Hamad; Sifaoui, Kaouthar; Almaani, Mohammed; Alqahtani, Rakan; Qureshi, Ahmad S; Hejazi, Mohammed Moneer; Arishi, Hatim; AlQahtani, Samah; Ghazi, Amro Mohamed; Baaziz, Saleh T; Azhar, Abeer Othman; Alabbas, Sara Fahad; AlAqeely, Mohammed; AlOrabi, Ohoud; Al-Mutawa, Aliaa; AlOtaibi, Maha; Aldibaasi, Omar; Jose, Jesna; Starkopf, Joel; Preiser, Jean-Charles; Perner, Anders; Al-Dawood, Abdulaziz.
Afiliación
  • Arabi YM; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia. yaseenarabi@yahoo.com.
  • Al-Dorzi HM; Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia. yaseenarabi@yahoo.com.
  • Sadat M; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia. yaseenarabi@yahoo.com.
  • Muharib D; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia. yaseenarabi@yahoo.com.
  • Algethamy H; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Al-Hameed F; Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Mady A; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • AlGhamdi A; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Almekhlafi GA; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Al-Fares AA; Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Kharaba A; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • Al Bshabshe A; Intensive Care Department, King Saud Medical City, Riyadh, Saudi Arabia.
  • Maghrabi K; Department of Anesthesia and Critical Care, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Al Ghamdi K; Ministry of National Guard Health Affairs, Jeddah, Saudi Arabia.
  • Rasool G; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.
  • Chalabi J; King Abdullah International Medical Research Center, Jeddah, Saudi Arabia.
  • AlHumedi HI; Intensive Care Department, King Saud Medical City, Riyadh, Saudi Arabia.
  • Sakkijha MH; College of Medicine, Tanta University, Tanta, Egypt.
  • Alamrey NK; Department of Intensive Care Services, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Alhutail RH; Department of Intensive Care Services, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Sifaoui K; Department of Anesthesia, Critical Care Medicine and Pain Medicine, Al-Amiri Hospital, Ministry of Health, Kuwait City, Kuwait.
  • Almaani M; Pulmonary & Critical Care Departments, King Fahad Hospital, Medinah, Saudi Arabia.
  • Alqahtani R; Critical Care Units, Ministry of Health, Madinah, Saudi Arabia.
  • Qureshi AS; Department of Critical Care Medicine, King Khalid University, Aseer Central Hospital, Abha, Saudi Arabia.
  • Hejazi MM; Department of Critical Care Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Arishi H; Department of Critical Care Medicine, King Faisal Specialist Hospital and Research Centre, Jeddah, Saudi Arabia.
  • AlQahtani S; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • Ghazi AM; Ministry of National Guard Health Affairs, Jeddah, Saudi Arabia.
  • Baaziz ST; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.
  • Azhar AO; Intensive Care Department, King Abdulaziz Medical City, Jeddah, Saudi Arabia.
  • Alabbas SF; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • AlAqeely M; King Abdulaziz Hospital, Ministry of National Guard Health Affairs, AlAhsa, Saudi Arabia.
  • AlOrabi O; King Saud Bin Abdulaziz University for Health Sciences, AlAhsa, Saudi Arabia.
  • Al-Mutawa A; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • AlOtaibi M; Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Aldibaasi O; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • Jose J; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Starkopf J; Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Preiser JC; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • Perner A; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Al-Dawood A; Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Trials ; 24(1): 485, 2023 Jul 30.
Article en En | MEDLINE | ID: mdl-37518058
ABSTRACT

BACKGROUND:

Protein intake is recommended in critically ill patients to mitigate the negative effects of critical illness-induced catabolism and muscle wasting. However, the optimal dose of enteral protein remains unknown. We hypothesize that supplemental enteral protein (1.2 g/kg/day) added to standard enteral nutrition formula to achieve high amount of enteral protein (range 2-2.4 g/kg/day) given from ICU day 5 until ICU discharge or ICU day 90 as compared to no supplemental enteral protein to achieve moderate amount enteral protein (0.8-1.2 g/kg/day) would reduce all-cause 90-day mortality in adult critically ill mechanically ventilated patients.

METHODS:

The REPLENISH (Replacing Protein Via Enteral Nutrition in a Stepwise Approach in Critically Ill Patients) trial is an open-label, multicenter randomized clinical trial. Patients will be randomized to the supplemental protein group or the control group. Patients in both groups will receive the primary enteral formula as per the treating team, which includes a maximum protein 1.2 g/kg/day. The supplemental protein group will receive, in addition, supplemental protein at 1.2 g/kg/day starting the fifth ICU day. The control group will receive the primary formula without supplemental protein. The primary outcome is 90-day all-cause mortality. Other outcomes include functional and quality of life assessments at 90 days. The trial will enroll 2502 patients.

DISCUSSION:

The study has been initiated in September 2021. Interim analysis is planned at one third and two thirds of the target sample size. The study is expected to be completed by the end of 2025. TRIAL REGISTRATION ClinicalTrials.gov Identifier NCT04475666 . Registered on July 17, 2020.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Enfermedad Crítica Tipo de estudio: Clinical_trials / Guideline Aspecto: Patient_preference Límite: Adult / Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Enfermedad Crítica Tipo de estudio: Clinical_trials / Guideline Aspecto: Patient_preference Límite: Adult / Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita
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