Author/Authors :
Miroliaee, Amir Ebrahim Clinical Pharmacy Department - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Salamzadeh, Jamshid Clinical Pharmacy Department - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Shokouhi, Shervin Department of Infectious Diseases - Loghman Hospital - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Fatemi, Alireza Infectious Diseases and Tropical Medicine Research Center - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Ardehali, Hossein Department of Critical Care - Shohadaye-Tajrish Hospital - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Hajiesmaeili, Mohammad Reza Loghman Clinical Research Development Center - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Sahraei, Zahra Clinical Pharmacy Department - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Ventilator-associated pneumonia (VAP) is a common and serious problem that develops
after more than 48 h of mechanical ventilation. Improving the activity of immune system with
vitamin D, and its consequent impact on prognostic biomarkers of VAP was studied in the
current study.
A randomized double blind placebo controlled clinical trial was designed. A total of 46
patients with VAP, who were suffering from vitamin D deficiency, were randomly allocated
into the study groups of placebo (n=22) and treatment (n=24) The treatment group received
300,000 units of intramuscular vitamin D. Serum levels of procalcitonin and vitamin D along
with SOFA and CPIS scores were determined at baseline and on day 7 after intervention. The
mortality rate of patients was also monitored for the succeeding 28 days after the injection.
The administration of vitamin D significantly enhanced its levels (P<0.0001) in the treated
patients (12.28 ± 8.26) in comparison to placebo group (1.15 ± 1.50). The levels of PCT were
significantly decreased (p=0.001) in the treatment group (– 0.02 ± 0.59 ng/mL) compared to that
of placebo group (0.68 ± 1.03 ng/mL). However, changes in (SOFA) and CPIS scores were not
significantly different between study groups (p=0.63 and p=0.32, respectively). Interestingly,
the mortality rate of patients in the treatment group (5/24) was significantly lower (p=0.04) than
that of the placebo group (11/22).
In conclusion, our results indicate that vitamin D supplementation can significantly reduce
the procalcitonin in (VAP) patients, and must be considered as a preventive and/or therapeutic
strategy.
Keywords :
Vitamin D , SOFA score , CPIS score , VAP , Procalcitonin