Wang Qiang, Wu Yuanxing, Chen Biyao, Zhou Jianxin
Intensive Care Unit, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100050 PR China.
Department of Emergency, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100050 PR China.
BMC Anesthesiol. 2015 Mar 13;15:33. doi: 10.1186/s12871-015-0012-1. eCollection 2015.
To identify changes in cefoperazone/sulbactam penetration into cerebrospinal fluid (CSF) after craniotomy and to investigate preliminarily whether cefoperazone/sulbactam CSF concentration can reach therapeutic level when administered intravenously after neurosurgical operation.
Neurosurgical patients with an indwelling ventricular drainage pipe who received prophylactic cefoperazone/sulbactam for the treatment of intracranial infection were received a cefoperazone/sulbactam 2:1, 3.0-g infusion for 3 hours every 6 hours for 24 h. Venous blood and CSF specimens were collected to determine cefoperazone/sulbactam concentrations.
The cefoperazone and sulbactam concentrations in serum were highest at the second hour (237.54 ± 336.72 mg/L and 66.52 ± 80.38 mg/L, respectively) and then decreased. The cefoperazone and sulbactam concentrations in CSF were highest at the 4th hour (39.22 ± 75.55 mg/L and 6.24 ± 8.35 mg/L, respectively) and then decreased. CSF penetration measured by the ratio of peak concentrations (CSF/serum) was 8.6% ± 7.2% for cefoperazone and 13.5% ± 11.9% for sulbactam, CSF penetration measured by the ratio of trough concentrations (CSF/serum) was 13.4% ± 5.3% for cefoperazone and 106.5% ± 87.5% for sulbactam. CSF penetration represented by the ratio of area under the curve (AUC) of CSF and serum was 14.5% for cefoperazone and 22.6% for sulbactam. Neurosurgical impairment of the blood-brain barrier may improve the CSF penetration of these drugs, but it is difficult to reach the MIC90 of resistant bacteria. If single intravenous administration time was extended to 3 hours, the serum concentrations of drugs were able to meet the PK/PD standard (T> MIC%> 50%) for treating common, highly resistant bacteria.
The CSF penetration of cefoperazone/sulbactam may be enhanced after neurosurgical impairment of the blood-brain barrier. This study is a pilot research of cefoperazone/sulbactam using in neurosurgical individuals, However, it needs to be confirmed by further large-scale studies.
确定开颅术后头孢哌酮/舒巴坦透过血脑屏障进入脑脊液(CSF)的变化情况,并初步探讨神经外科手术后静脉给药时头孢哌酮/舒巴坦的脑脊液浓度能否达到治疗水平。
对留置脑室引流管且接受预防性头孢哌酮/舒巴坦治疗颅内感染的神经外科患者,每6小时静脉滴注2:1的头孢哌酮/舒巴坦3.0 g,持续3小时,共24小时。采集静脉血和脑脊液标本以测定头孢哌酮/舒巴坦浓度。
血清中头孢哌酮和舒巴坦浓度在第2小时最高(分别为237.54±336.72 mg/L和66.52±80.38 mg/L),随后下降。脑脊液中头孢哌酮和舒巴坦浓度在第4小时最高(分别为39.22±75.55 mg/L和6.24±8.35 mg/L),随后下降。以峰浓度比值(脑脊液/血清)衡量的脑脊液透过率,头孢哌酮为8.6%±7.2%,舒巴坦为13.5%±11.9%;以谷浓度比值(脑脊液/血清)衡量的脑脊液透过率,头孢哌酮为13.4%±5.3%,舒巴坦为106.5%±87.5%。以脑脊液和血清曲线下面积比值表示的脑脊液透过率,头孢哌酮为14.5%,舒巴坦为22.6%。血脑屏障的神经外科损伤可能会提高这些药物的脑脊液透过率,但难以达到耐药菌的MIC90。若单次静脉给药时间延长至3小时,药物血清浓度能够满足治疗常见高耐药菌的PK/PD标准(T>MIC%>50%)。
血脑屏障发生神经外科损伤后,头孢哌酮/舒巴坦的脑脊液透过率可能会提高。本研究是头孢哌酮/舒巴坦在神经外科患者中应用的初步研究,然而,尚需进一步大规模研究予以证实。