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Identifying Critically-ill Patients With COVID-19 Who Will Benefit Most From Nutrition Support Therapy: Validation of the NUTRIC Nutritional Risk Assessment Tool

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StatusActive, not recruiting
Sponsors
Peking University Third Hospital
Collaborators
School of Pharmaceutical Sciences, Peking University, Beijing, China
Department of Medicine, Queen's University, Kingston, Ontario, Canada

Keywords

Abstract

There was an interaction between mortality, nutritional intake and the Nutrition Risk in Critically ill (NUTRIC) score suggesting that those with higher NUTRIC scores benefited the most from increasing nutritional intake. Yet limited data were in Chinese patients. The current outbreak of novel coronavirus, named COVID-19, was first reported from Wuhan, China on Dec ember 31 , 2019. There are about 16% patients need ICU admission. The objective of this study is to validation of the "NUTRIC" nutritional risk assessment tool in Chinese ICU patients diagnosed as COVID-19.

Description

Heyland et al. previously proposed a novel scoring tool, the Nutrition Risk in Critically ill (NUTRIC) score, which is the first nutritional risk assessment tool developed and validated specifically for intensive care unit (ICU) patients. Many other risk scores and assessment tools exist to quantify nutrition risk but none have been specifically designed for ICU patients. Indeed, they generally consider all critically ill patients to be at high nutritional risk. However, the recognition that not all ICU patients will respond the same to nutritional interventions was the critical concept behind the NUTRIC score. There was an interaction between mortality, nutritional intake and NUTRIC score suggesting that those with higher NUTRIC scores benefited the most from increasing nutritional intake. However, the inferences about the validity of the NUTRIC score are limited in Chinese patients because of no data.

The current outbreak of novel coronavirus was first reported from Wuhan, China on Dec ember 31 , 2019 . This virus was named as 2019 nCoV by World Health Organization ( on Jan uary 12 , 2020). Following the advice of the Emergency Committee, the WHO declared the outbreak of 2019 nCoV a Public Health Emergency of International Concern . Patients show fever and / or respiratory symptoms, with the imaging characteristics of pneumonia, and other symptoms include hemoptysis muscle pain, headache, confusion, chest pain, and diarrhea. About 16% patients need ICU admission.

The objective of this study is to validation of the "NUTRIC" nutritional risk assessment tool in Chinese ICU patients diagnosed as COVID-19. This is a single-center, prospective cohort study of ICU patients with COVID-19. Data for all variables of the NUTRIC score will be collected. These include age, APACHE II score, SOFA score, number of co-morbidities, days from hospital admission to ICU admission. A logistic model including the NUTRIC score, the nutritional adequacy and their interaction will be estimated to assess if the NUTRIC score modified the association between nutritional adequacy and 28-day mortality.

Dates

Last Verified: 03/31/2020
First Submitted: 02/15/2020
Estimated Enrollment Submitted: 02/15/2020
First Posted: 02/17/2020
Last Update Submitted: 04/06/2020
Last Update Posted: 04/07/2020
Actual Study Start Date: 02/18/2020
Estimated Primary Completion Date: 04/03/2020
Estimated Study Completion Date: 06/30/2020

Condition or disease

Critically Ill
Coronavirus Infections

Intervention/treatment

Other: Nutrition support

Phase

-

Arm Groups

ArmIntervention/treatment
Cohort 1
High NUTRIC score
Cohort 2
low NUTRIC score

Eligibility Criteria

Ages Eligible for Study 18 Years To 18 Years
Sexes Eligible for StudyAll
Sampling methodProbability Sample
Accepts Healthy VolunteersYes
Criteria

Inclusion Criteria:

- Admitted to intensive care unit (ICU), Peking University Third Hospital since Feb 2020

- Adult (aged over 18 years)

- Anticipate a length of ICU stay (LOS) of more than 48 hours

- Diagnosed as 2019 coronavirus disease (COVID-19)

- With food intake difficulties (can't intake food by oneself)

Exclusion Criteria:

- aged under 18 years

- Actual ICU LOS of less than 48 hours

- Using medications of IL-6 or IL-6R

- Overdose

- Written informed consent not obtained in the prospective cohort

Outcome

Primary Outcome Measures

1. 28-day all cause mortality [from admission to 28-day/discharge, an average of length of ICU stay is 28-day]

Secondary Outcome Measures

1. All cause infection [from admission to 28-day/discharge, an average of length of ICU stay is 28-day]

2. The rate of complications [from admission to 28-day/discharge, an average of length of ICU stay is 28-day]

3. Length of ICU stay [from admission to 28-day/discharge, an average of length of ICU stay is 28-day]

4. Duration of mechanical ventilation [from admission to 28-day/discharge, an average of length of ICU stay is 28-day]

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