cholecalciferol has been researched along with Pneumonia--Ventilator-Associated* in 2 studies
1 trial(s) available for cholecalciferol and Pneumonia--Ventilator-Associated
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[Prevention Effect of Thymosin-alpha1 Aganist Early Ventilator-associated Pneumonia in Patients with Mechanical Ventilation].
To investigate the preventive effects of thymosin-alpha1 against early ventilator-associated pneumonia (VAP) in the patients with mechanical ventilation.. Fifty two patients with expectancy of mechanical ventilation over 48 h were divided into routine therapy group (n=26) and thymosin therapy group (n= 26) in random. The patients in routine therapy group were given intensive care unit (ICU) conventional treatment, and the patients in thymosin therapy group were given thymosin treatment additionally (1.6 mg subcutaneous injection, qd X 7 d). The incidence and occurrence time of VAP were observed, and the time of mechanical ventilation and ICU stay were recorded. The levels of CD3+, CD4+, CD4+ /CD8+ T lymphocyte, CD14+ mononuclear cell human leukocyte antigens-DR (CD14+ HLA-DR) and procalcitonin (PCT) were detected before mechanical ventilation and at the 3d and 7th d after mechanical ventilation.. The base line including the level of immunologic function had no difference between the two groups (P>0.05). The incidence of VAP in thymosin therapy group was lower than that in routine therapy group, but it was not significant difference (P>0.05). The durations of machine ventilation and ICU stay in thymosin therapy group were shorter than those in routine therapy group (P<0.05). The occurrence time of VAP in thymosin therapy group was significantly later than that in routine therapy group (P<0.05). At the 3rd and 7th d after mechanical ventilation, thymosin therapy group achived higher levels of CD3+, CD4+, CD4+ /CD8+ T lymphocyte and CD14+ HLA-DR than routine therapy group did (P<0.05).. Thymosinal may be able to improve immunologic function and prevent the incidence of early VAP in the patients with mechanical ventilation. Topics: Calcitonin; Calcitonin Gene-Related Peptide; Cholecalciferol; HLA-DR Antigens; Humans; Intensive Care Units; Lipopolysaccharide Receptors; Pneumonia, Ventilator-Associated; Protein Precursors; Respiration, Artificial; Thymalfasin; Thymosin | 2015 |
1 other study(ies) available for cholecalciferol and Pneumonia--Ventilator-Associated
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Serum vitamin D level was not associated with severity of ventilator associated pneumonia.
Vitamin D deficiency is considered one of the most common nutritional deficiencies associated with weakened immune system and increased likelihood of sepsis. The current study was conducted to investigate the association between serum vitamin D level and the severity and prognosis of ventilator associated pneumonia (VAP) in inpatients in intensive care unit (ICU).. Eighty-four consecutive patients with VAP were enrolled in this observational, prospective study conducted in the ICU of Besat Hospital, Hamadan. The patients were examined for serum 25-hydroxyvitamin D (vitD3) level and VAP severity and prognosis. Clinical pulmonary infection score was used for the diagnosis, and Sequential Organ Failure Assessment (SOFA) Score was used to determine the severity of VAP.. Low level serum vitD3 (under 30 ng/mL) was found in 66 (78.6%) patients. In this series of VAP patients, there were no significant differences in blood culture results, 14 and 28-day sepsis-associated mortality, mechanical ventilation duration, or SOFA Score on days 3, 7, and 14 between the low level and normal level vitD3 patients (p > 0.05).. Serum vitD3 level was not associated with mortality from VAP or complications due to sepsis in the inpatients in the ICU. Topics: Adolescent; Adult; Aged; Aged, 80 and over; Cholecalciferol; Female; Hospital Mortality; Humans; Intensive Care Units; Iran; Male; Middle Aged; Multiple Organ Failure; Pneumonia, Ventilator-Associated; Prospective Studies; Respiration, Artificial; Severity of Illness Index; Time Factors; Vitamin D; Young Adult | 2019 |