Vitamin D Supplementation in Mechanically Ventilated Patients in the Medical Intensive Care Unit

被引:9
|
作者
Leclair, Timothy R. [1 ]
Zakai, Neil [2 ,3 ]
Bunn, Janice Y. [4 ]
Gianni, Michael [5 ]
Heyland, Daren K. [6 ]
Ardren, Sara S. [3 ,7 ]
Stapleton, Renee D. [7 ]
机构
[1] Intermt Healthcare, Pulm Med, Salt Lake City, UT USA
[2] Univ Vermont, Med Ctr, Div Hematol & Oncol, Dept Med, Burlington, VT USA
[3] Larner Coll Med, Burlington, VT USA
[4] Univ Vermont, Coll Engn & Math Sci, Burlington, VT USA
[5] Univ Vermont, Med Ctr, Jeffords Inst Qual Analyt, Burlington, VT USA
[6] Queens Univ, Dept Crit Care Med, Kingston, ON, Canada
[7] Univ Vermont, Med Ctr, Div Pulm & Crit Care Med, Dept Med, Burlington, VT USA
关键词
critical care; mechanical ventilation; research and diseases; vitamin D; SERUM 25-HYDROXYVITAMIN D; CRITICALLY-ILL PATIENTS; ACUTE KIDNEY INJURY; D DEFICIENCY; CHOLECALCIFEROL; ASSOCIATION; TARGETS; ADULTS; TRIAL;
D O I
10.1002/jpen.1520
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background The utility of vitamin D (VITD) supplementation during critical illness and whether it may alter outcomes, including mortality and ventilator-free days, is unclear. We performed a retrospective cohort study in a generalizable population to investigate this question. Methods We included all mechanically ventilated adults admitted to the medical intensive care unit (ICU) service at a tertiary center from 2009 to 2012 who were in the ICU for at least 72 hours. Patients were grouped as having received or not received VITD at any time during the first 7 days of their ICU stay, and we adjusted for the following covariates with multivariable analyses: simplified acute physiology score, age, gender, admission diagnosis, race/ethnicity, admission season, admission day of the week, and VITD supplementation prior to admission. Results Among the 610 included patients, 281 received VITD, and 329 did not. There were no differences in outcomes between these groups. However, we did find significantly more ventilator-free days (21.0 +/- 2.6 [adjusted mean days +/- standard error] vs 17.6 +/- 2.4, P=0.04) and ICU-free days (18.5 +/- 2.5 vs 16.3 +/- 2.3, P=0.03) in patients who were taking VITD prior to admission (n=91) vs those who were not (n=519). No patients who were taking VITD before admission died vs 34.5% of those who were not (estimated odds ratio=4.9x10(-7), 95% CI=3.1x10(-7) to 7.5x10(-7), P<0.0001). Conclusion These results suggest that VITD supplementation during critical illness may not provide benefit and that further research investigating potential supplementation in ambulatory patients at high risk of ICU admission (eg, severe underlying chronic disease) is warranted.
引用
收藏
页码:1037 / 1043
页数:7
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