Skip to content

Nutritional and Metabolic Management of Toxidermia Patients Requiring Intensive Care (TEN Metabolism)

Nutritional and Metabolic Characteristics of Critically Ill Patients Admitted for Severe Toxidermia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05320653
Acronym
TEN metabolism
Enrollment
35
Registered
2022-04-11
Start date
2006-01-01
Completion date
2022-05-31
Last updated
2022-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum

Keywords

Critical care, Metabolism, Nutrition, Protein

Brief summary

Retrospective observational cohort study including all patients admitted for toxidermia (Lyell syndrome, Stevens-Johnson Syndrome (SJS), or other extensive skin destruction) to the Burn unit of the adult ICU of the Lausanne burn center between 2006 and 2020. Inclusion criteria: age \>18 years and admission to the burn-ICU for toxidermia whatever body surface affected. Exclusion criteria: to have declined access to the medical record, a stay shorter than 24 hours, and major burns. The observation period will be limited to the first 31 days of the ICU stay. All variables related to nutritional and metabolic management will be recorded

Detailed description

There are yet no description of the metabolic characteristics of patients admitted for Toxic epidermal necrolysis (TEN) or Stevens-Johnson Syndrome (SJS) which are a rare condition, often assimilated to major burns in terms of metabolic requirements. We will conduct a retrospective observational cohort study including all patients admitted for toxidermia (general term including TEN or Lyell syndrome, SJS, and other extensive skin destruction) to the Burn unit of the adult ICU of the Lausanne burn center between 2006 and 2020. The primary outcome will be compliance with the ICU's feeding protocol (feeding route, early start of enteral feeding, ), and secondary outcomes will include the adequacy of energy and protein delivery, and use of indirect calorimetry, and the comparison with both general and burn critically ill patients from prior studies in the ICU. Inclusion criteria: age \>18 years and admission to the burn-ICU for toxidermia whatever body surface affected. Exclusion criteria: to have declined access to the medical record, and a stay shorter than 24hours, and major burns. The observation period will be limited to the first 31 days of the ICU stay. The recorded variables will include demographic characteristics, severity scores (SAPSII, SCORe of Toxic Epidermal Necrosis (SCORTEN for SJS/TEN), Nutrition risk screening (NRS) score), body surface area (BSA) affected by the disease, fluid intakes and balance (exudate volume estimation not included) of the first 10 days, body weight during the stay, renal function, length of mechanical ventilation and of ICU stay. Nutritional variables include the route of feeding, the 24hr energy prescription and delivery, protein, glucose, and lipid intakes, propofol, insulin, indirect calorimetry (IC) studies. Laboratory blood results include glucose, prealbumin, albumin, C-reactive protein (CRP), triglycerides, creatinine, and trace elements (Cu, Se, Zn). Descriptive statistics: Wilcoxon rank test, while Chi2 test, changes over time with one-way ANOVA .

Interventions

DIETARY_SUPPLEMENTMedical nutrition

Nutrition therapy of the critically ill patients

Sponsors

Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum

Inclusion criteria

* age \>18 years * admission to the burn-ICU

Exclusion criteria

* declined access to the medical record * stay shorter than 24hours

Design outcomes

Primary

MeasureTime frameDescription
Compliance with ICU feeding protocolICU stay, but maximum 30 daysProportion of ICU days with covered needs

Secondary

MeasureTime frameDescription
Protein deliveryICU stay but maximum 30 daysDelivery of at least 1.1 g/kg day of protein
Energy deliveryICU stay but maximum 30 daysDelivery of at least 25 kcal/kg/day

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026