Oami Takehiko, Hattori Noriyuki, Matsumura Yosuke, Watanabe Eizo, Abe Ryuzo, Oshima Taku, Takahashi Waka, Yamazaki Shingo, Suzuki Tatsuya, Oda Shigeto
Department of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Division of Pharmacy, Chiba University Hospital, Chiba, Japan.
Front Med (Lausanne). 2017 Jun 8;4:70. doi: 10.3389/fmed.2017.00070. eCollection 2017.
Although vancomycin (VCM) is not absorbed from healthy intestinal mucosa, elevations in the serum VCM concentrations have been reported in some cases. The aims of this study are to evaluate the necessity of therapeutic drug monitoring (TDM) during enteral VCM administration in critically ill patients.
In this retrospective study, we enrolled 19 patients admitted to our intensive care unit who were treated with enteral VCM from December 2006 to January 2014. Clinical factors were compared between two groups: Group E whose serum concentrations were detectable, and Group N whose concentrations were below the detection limit of the VCM assay.
Group E comprises 7 patients, and Group N comprises 12 patients. The fasting duration in Group E was significantly longer compared with that in Group N (17 vs. 8 days, = 0.023). Furthermore, there was a significant correlation between the serum VCM concentrations and the fasting duration ( = 0.79, < 0.0001), and the amount of diarrhea ( = 0.46, = 0.046). No difference was observed in the amount of diarrhea at the time of TDM (Group E; 1,850 mL vs. Group N; 210 mL, = 0.055) and in the Sequential Organ Failure Assessment subscore for the renal system at the time of TDM (Group E; 4.0 vs. Group N; 1.5, = 0.068).
Long durations of fasting and massive diarrhea were associated with elevations in the serum VCM concentrations, which suggested that TDM might be necessary during enteral VCM administration in critically ill patients.
UMIN Clinical Trials Registry identifier UMIN000016955.
尽管万古霉素(VCM)不会从健康的肠黏膜吸收,但在某些情况下血清VCM浓度会升高。本研究的目的是评估在重症患者肠内给予VCM期间进行治疗药物监测(TDM)的必要性。
在这项回顾性研究中,我们纳入了2006年12月至2014年1月在我们重症监护病房接受肠内VCM治疗的19例患者。比较了两组的临床因素:血清浓度可检测到的E组和浓度低于VCM检测限的N组。
E组有7例患者,N组有12例患者。E组的禁食时间明显长于N组(17天对8天,P = 0.023)。此外,血清VCM浓度与禁食时间(r = 0.79,P < 0.0001)以及腹泻量(r = 0.46,P = 0.046)之间存在显著相关性。在TDM时腹泻量(E组;1850 mL对N组;210 mL,P = 0.055)和TDM时肾脏系统的序贯器官衰竭评估子评分(E组;4.0对N组;1.5,P = 0.068)方面未观察到差异。
长时间禁食和大量腹泻与血清VCM浓度升高有关,这表明在重症患者肠内给予VCM期间可能需要进行TDM。
UMIN临床试验注册标识符UMIN000016955。