Association between prehospital vitamin D status and hospital-acquired bloodstream infections

被引:52
|
作者
Quraishi, Sadeq A. [1 ]
Litonjua, Augusto A. [3 ,4 ]
Moromizato, Takuhiro [5 ]
Gibbons, Fiona K. [3 ,4 ]
Camargo, Carlos A., Jr. [2 ]
Giovannucci, Edward [6 ,7 ]
Christopher, Kenneth B. [5 ]
机构
[1] Massachusetts Gen Hosp, Dept Anesthesia Crit Care & Pain Med, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Emergency Med, Boston, MA 02114 USA
[3] Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Pulm & Crit Care Div, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Med, Div Renal, Nathan Hellman Mem Lab, Boston, MA 02115 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[7] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
来源
关键词
CARE-ASSOCIATED INFECTIONS; LOCALLY WEIGHTED REGRESSION; D DEFICIENCY; HEALTH; RISK; INSUFFICIENCY; INITIATIVES; COMORBIDITY; PREVALENCE; MORTALITY;
D O I
10.3945/ajcn.113.058909
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: Alterations in immune function can predispose patients to nosocomial infections. Few studies have explored potentially modifiable host factors that may improve immune function and decrease risk of hospital-acquired bloodstream infection (HABSI). Vitamin D is a key regulator of innate and adaptive immune systems that may influence host susceptibility to infections. Objective: We investigated the association between prehospital serum 25-hydroxyvitamin D [25(OH)D] concentrations and risk of HABSI. Design: We performed a retrospective cohort study of 2135 adult patients from 2 Boston teaching hospitals. All patients had 25(OH)D concentrations measured before hospitalization between 1993 and 2010. The main outcome measure was HABSI, which was defined as positive blood cultures from samples drawn 48 h after hospital admission. Coagulase-negative Staphylococcus isolates were not considered to be bloodstream infections. Associations between 25(OH)D groups and HABSI were estimated by using bivariable and multivariable logistic regression models. Adjusted ORs were estimated with the inclusion of covariate terms thought to plausibly interact with both 25(OH)D concentration and HABSI. Results: Compared with patients with 25(OH)D concentrations >= 30 ng/mL, patients with concentrations <30 ng/mL had higher odds of HABSI. For 25(OH)D concentrations <10 ng/mL, the OR was 2.33 (95% CI: 1.45, 3.74); for 25(OH)D concentrations from 10 to 19.9 ng/mL, the OR was 1.60 (95% CI: 1.04, 2.46); and for 25(OH)D concentrations from 20 to 29.9 ng/mL, the OR was 1.13 (95% CI: 0.69, 1.84). After adjustment for age, sex, race (nonwhite compared with white), patient type (medical compared with surgical), and Deyo-Charlson index, the ORs of HABSI were 1.95 (95% CI: 1.22, 3.12), 1.36 (95% CI: 0.89, 2.07), and 0.98 (95% CI: 0.60, 1.62), respectively. Conclusions: The analysis of 2135 adult patients showed that 25(OH)D concentrations <10 ng/mL before hospitalization were associated with significantly increased odds of developing HABSI. These data support the initiation of randomized trials to test the role of vitamin D supplementation in HABSI prevention.
引用
收藏
页码:952 / 959
页数:8
相关论文
共 50 条
  • [41] The epidemiology of bloodstream infection contributing to mortality: the difference between community-acquired, healthcare-associated, and hospital-acquired infections
    Seok Jun Mun
    Si-Ho Kim
    Hyoung-Tae Kim
    Chisook Moon
    Yu Mi Wi
    BMC Infectious Diseases, 22
  • [42] The epidemiology of bloodstream infection contributing to mortality: the difference between community-acquired, healthcare-associated, and hospital-acquired infections
    Mun, Seok Jun
    Kim, Si-Ho
    Kim, Hyoung-Tae
    Moon, Chisook
    Wi, Yu Mi
    BMC INFECTIOUS DISEASES, 2022, 22 (01)
  • [43] Association Between Serum Albumin and Hospital-Acquired Infections After Aneurysmal Subarachnoid Hemorrhage
    Peng Wang
    Yu Zhang
    Xing Wang
    Liyuan Peng
    Lu Jia
    Tiangui Li
    Weelic Chong
    Yang Hai
    Chao You
    Fang Fang
    Neurocritical Care, 2022, 37 : 424 - 434
  • [44] Association Between Serum Albumin and Hospital-Acquired Infections After Aneurysmal Subarachnoid Hemorrhage
    Wang, Peng
    Zhang, Yu
    Wang, Xing
    Peng, Liyuan
    Jia, Lu
    Li, Tiangui
    Chong, Weelic
    Hai, Yang
    You, Chao
    Fang, Fang
    NEUROCRITICAL CARE, 2022, 37 (02) : 424 - 434
  • [45] A Prospective Observational Study Of Vitamin D And Hospital-Acquired Infections In A Medical Intensive Care Unit
    Kempker, J. A.
    West, K. G.
    Alvarez, J. A.
    Siwamogsatham, O.
    Ziegler, T. R.
    Tangpricha, V.
    Guidot, D. M.
    Martin, G. S.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2013, 187
  • [46] Different Epidemiology of Hospital-Acquired Bloodstream Infections Between Small Community Hospitals and Large Community Hospitals Reply
    Stenehjem, Edward
    Hersh, Adam L.
    Pavia, Andrew T.
    CLINICAL INFECTIOUS DISEASES, 2017, 64 (07) : 985 - 986
  • [47] Multicenter Evaluation of Computer Automated versus Traditional Surveillance of Hospital-Acquired Bloodstream Infections
    Lin, Michael Y.
    Woeltje, Keith F.
    Khan, Yosef M.
    Hota, Bala
    Doherty, Joshua A.
    Borlawsky, Tara B.
    Stevenson, Kurt B.
    Fridkin, Scott K.
    Weinstein, Robert A.
    Trick, William E.
    INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2014, 35 (12): : 1483 - 1490
  • [48] Hospital-acquired bloodstream infections in neurological and neurosurgical units in Hungary, 2005-2013
    R Szabó
    A Kurcz
    Antimicrobial Resistance and Infection Control, 4 (Suppl 1)
  • [49] RE: "RISK-SET MATCHING TO ASSESS THE IMPACT OF HOSPITAL-ACQUIRED BLOODSTREAM INFECTIONS"
    Ohneberg, Kristin
    Wolkewitz, Martin
    Schumacher, Martin
    AMERICAN JOURNAL OF EPIDEMIOLOGY, 2019, 188 (06) : 1192 - 1193
  • [50] Two-year prevalence study of hospital-acquired bloodstream infections in university hospital Trnava, Slovakia
    M Garabasova
    JS Brnova
    M Betkova
    A Streharova
    Antimicrobial Resistance and Infection Control, 4 (Suppl 1)