MedPath

Impact of Comprehensive Rehabilitation Nursing Combined With Refined Airway Management and Nutritional Support on Prognosis and Care Delivery Models in Critically Ill Patients

Not Applicable
Completed
Conditions
Critically Ill Patients
Nutritional Support
Pulmonary Infections
Gastrointestinal Bleeding
Acute Kidney Injury (AKI)
Registration Number
NCT07025941
Lead Sponsor
Taizhou Hospital of Traditional Chinese Medicine
Brief Summary

This combined intervention protocol effectively improves the prognosis of critically ill patients and optimizes nursing management models

Detailed Description

To investigate the impact of comprehensive rehabilitation nursing combined with refined airway management and nutritional support on the prognosis of critically ill patients and nursing management models, and to develop a new care management protocol. Critically ill patients were divided into a control group (routine nursing) and an intervention group (comprehensive rehabilitation nursing combined with refined airway management and nutritional support). Complications such as pulmonary infection and gastrointestinal bleeding, as well as clinical indicators including oxygen saturation (SpO₂), mechanical ventilation time (MVT), and length of stay (LOS), were compared between the two groups. Logistic regression and XGBoost models were constructed to analyze key influencing factors.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
101
Inclusion Criteria
  • Fulfillment of ICU admission standards with critical illness confirmed by attending physicians or senior specialists
  • Age ≥ 18 years
  • Stable vital signs:

Systolic blood pressure ≥ 90 mmHg and ≤ 180 mmHg

Heart rate ≤ 120 beats/min

Oxygen saturation (SpO₂) ≥ 85% under ≤ 60% fraction of inspired oxygen (FiO₂)

  • Intact or tolerable gastrointestinal (GI) function for enteral nutrition
  • Informed consent from both patients and families
Exclusion Criteria

(1)

  • Terminal malignancies
  • Brain death
  • Irreversible organ failure (e.g., end-stage cirrhosis, advanced heart failure)
  • Comorbidities potentially confounding study outcomes
  • Contraindications to interventions (e.g., laryngeal edema, complete intestinal obstruction)
  • Pregnancy or lactation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
ICU Length of Stay (LOS)From randomization to ICU discharge, up to 60 days

Calendar days from ICU admission to discharge criteria met (APACHE II score ≤10, hemodynamic stability for ≥24h).

Secondary Outcome Measures
NameTimeMethod
Incidence of Pulmonary InfectionsFrom ICU admission to 48 hours post-extubation or 14-day intervention period

Rate of ventilator-associated pneumonia (VAP) and other pulmonary infections confirmed by clinical criteria (temperature \>38°C or \<36°C, purulent secretions, leukocytosis \>10×10⁹/L or leukopenia \<4×10⁹/L) plus microbiological evidence from sputum/BALF cultures.

Trial Locations

Locations (1)

Taizhou Hospital of Traditional Chinese Medicine

🇨🇳

Taizhou, Jiangsu, China

Taizhou Hospital of Traditional Chinese Medicine
🇨🇳Taizhou, Jiangsu, China

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.