4.6 Article

Short-Term Organ Dysfunction Is Associated With Long-Term (10-Yr) Mortality of Septic Shock

期刊

CRITICAL CARE MEDICINE
卷 44, 期 8, 页码 E728-E736

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CCM.0000000000001843

关键词

long-term survival; organ dysfunction; renal replacement therapy; septic shock; vasopressors; ventilation

资金

  1. Region Skane
  2. Swedish Government
  3. Canadian Institutes of Health Research (CIHR) IMPACT Research Fellowship
  4. CIHR (SONRIS)
  5. Providence Health Care Research Scholarship
  6. Canadian Institutes of Health Research
  7. Ferring Pharmaceuticals
  8. La Jolla Pharmaceuticals
  9. CytoVale
  10. Merck
  11. Grifols
  12. Asahi Kesai Pharmaceuticals of America
  13. UBC/Providence Health Care

向作者/读者索取更多资源

Objectives: As mortality of septic shock decreases, new therapies focus on improving short-term organ dysfunction. However, it is not known whether short-term organ dysfunction is associated with long-term mortality of septic shock. Design: Retrospective single-center. Setting: Mixed medical-surgical ICU. Patients: One thousand three hundred and thirty-one patients with septic shock were included from 2000-2004. To remove the bias of 28-day nonsurvivors' obvious association with long-term mortality, we determined the associations of days alive and free of ventilation, 2vasopressors and renal replacement therapy in 28-day and 1-year survivors with 1-, 5- and 10-year mortality in unadjusted analyses and analyses adjusted for age, gender, Acute Physiology and Chronic Health Evaluation II and presence of chronic comorbidities. Interventions: None. Measurements and Main Results: Days alive and free of ventilation, vasopressors, and renal replacement therapy were highly significantly associated with 1-, 5-, and 10-year mortality (p < 0.0001). In 28-day survivors, using Bonferroni-corrected multiple logistic regression, days alive and free of ventilation (p < 0.0001, p = 0.0002, and p = 0.001), vasopressors (p < 0.0001, p < 0.0001, and p = 0.0004), and renal replacement therapy (p = 0.0008, p = 0.0008, and p = 0.0002) were associated with increased 1-, 5-, and 10-year mortality, respectively. In 1-year survivors, none of the acute organ support and dysfunction measures were associated with 5-and 10-year mortality. Conclusions: Days alive and free of ventilation, vasopressors, and renal replacement therapy in septic shock in 28-day survivors was associated with 1-, 5-, and 10-year mortality. These associations are nullified in 1-year survivors in whom none of the acute organ support measures were associated with 5-and 10-year mortality. This suggests that therapies that decrease short-term organ dysfunction could also improve long-term outcomes of 28-day survivors of septic shock.

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