JAMA· 2012Q1· Klinik çalışma
Yoğun Mekanik Ventilasyonda Sedasyon İçin Dekmedetomidin ve Midazolam veya Propofol Karşılaştırması
Dexmedetomidine vs Midazolam or Propofol for Sedation During Prolonged Mechanical Ventilation
- 970atıf
- Q1SCImago
- 2012yıl
Kısa özet
Yoğun bakımda uzun süreli mekanik ventilasyona bağlı hastalarda yapılan çalışmada, deksmedetomidinin hafif ila orta düzeyde sedasyonu sürdürmede midazolam ve propofol kadar etkili olduğu, midazolama kıyasla mekanik ventilasyon süresini azalttığı ve her iki ilaca kıyasla hastaların ağrı ile iletişimini iyileştirdiği bulundu.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- Dekmedetomidin, hafif ila orta düzeyde sedasyon sağlamada midazolam ve propofole göre yetersiz kalmadı.
- Dekmedetomidin ile mekanik ventilasyon süresi midazolama göre 41 saat daha kısaydı (P=.03).
- Hastaların ağrı ile iletişimi deksmedetomidin ile midazolama göre (19.7 VAS farkı) ve propofole göre (11.2 VAS farkı) iyileşti.
- Dekmedetomidin, midazolama kıyasla daha yüksek hipotansiyon (%20.6'ya karşı %11.6) ve bradikardi (%14.2'ye karşı %5.2) oranlarıyla ilişkilendirildi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
CONTEXT: Long-term sedation with midazolam or propofol in intensive care units (ICUs) has serious adverse effects. Dexmedetomidine, an α(2)-agonist available for ICU sedation, may reduce the duration of mechanical ventilation and enhance patient comfort. OBJECTIVE: To determine the efficacy of dexmedetomidine vs midazolam or propofol (preferred usual care) in maintaining sedation; reducing duration of mechanical ventilation; and improving patients' interaction with nursing care. DESIGN, SETTING, AND PATIENTS: Two phase 3 multicenter, randomized, double-blind trials carried out from 2007 to 2010. The MIDEX trial compared midazolam with dexmedetomidine in ICUs of 44 centers in 9 European countries; the PRODEX trial compared propofol with dexmedetomidine in 31 centers in 6 European countries and 2 centers in Russia. Included were adult ICU patients receiving mechanical ventilation who needed light to moderate sedation for more than 24 hours (midazolam, n = 251, vs dexmedetomidine, n = 249; propofol, n = 247, vs dexmedetomidine, n = 251). INTERVENTIONS: Sedation with dexmedetomidine, midazolam, or propofol; daily sedation stops; and spontaneous breathing trials. MAIN OUTCOME MEASURES: For each trial, we tested whether dexmedetomidine was noninferior to control with respect to proportion of time at target sedation level (measured by Richmond Agitation-Sedation Scale) and superior to control with respect to duration of mechanical ventilation. Secondary end points were patients' ability to communicate pain (measured using a visual analogue scale [VAS]) and length of ICU stay. Time at target sedation was analyzed in per-protocol population (midazolam, n = 233, vs dexmedetomidine, n = 227; propofol, n = 214, vs dexmedetomidine, n = 223). RESULTS: Dexmedetomidine/midazolam ratio in time at target sedation was 1.07 (95% CI, 0.97-1.18) and dexmedetomidine/propofol, 1.00 (95% CI, 0.92-1.08). Median duration of mechanical ventilation appeared shorter with dexmedetomidine (123 hours [IQR, 67-337]) vs midazolam (164 hours [IQR, 92-380]; P = .03) but not with dexmedetomidine (97 hours [IQR, 45-257]) vs propofol (118 hours [IQR, 48-327]; P = .24). Patients' interaction (measured using VAS) was improved with dexmedetomidine (estimated score difference vs midazolam, 19.7 [95% CI, 15.2-24.2]; P < .001; and vs propofol, 11.2 [95% CI, 6.4-15.9]; P < .001). Length of ICU and hospital stay and mortality were similar. Dexmedetomidine vs midazolam patients had more hypotension (51/247 [20.6%] vs 29/250 [11.6%]; P = .007) and bradycardia (35/247 [14.2%] vs 13/250 [5.2%]; P < .001). CONCLUSIONS: Among ICU patients receiving prolonged mechanical ventilation, dexmedetomidine was not inferior to midazolam and propofol in maintaining light to moderate sedation. Dexmedetomidine reduced duration of mechanical ventilation compared with midazolam and improved patients' ability to communicate pain compared with midazolam and propofol. More adverse effects were associated with dexmedetomidine. TRIAL REGISTRATION: clinicaltrials.gov Identifiers: NCT00481312, NCT00479661.
Yazarların özeti; kaynağından alınmıştır. JAMA, 2012 · DOI ↗
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