Critical Care, Department of Pharmacy Services, Virginia Commonwealth University Health System, Richmond, VA, USA.
Ann Pharmacother. 2013 Jun;47(6):e25. doi: 10.1345/aph.1R707. Epub 2013 May 14.
To report a case of subtherapeutic linezolid concentrations in a patient with morbid obesity.
A 34-year-old male with morbid obesity (265 kg, body mass index 82 kg/m(2)) was admitted for severe sepsis due to respiratory failure requiring emergent intubation and treatment of community-acquired pneumonia. Admission tracheal aspirate culture revealed methicillin-resistant Staphylococcus aureus (MRSA) for which vancomycin was prescribed. Therapy subsequently was changed to linezolid, because the patient's clinical status worsened, with significant hypoxia (partial pressure of arterial oxygen/fraction of inspired oxygen [PaO2/FiO2] ratio 145), increasing leukocytosis (white blood cell count from 10,800/μL on admission to 15,400/μL on hospital day 6), and persistent fever (38.3 °C). After 48 hours of linezolid monotherapy, the patient remained febrile with continued leukocytosis, worsening hypoxemia, and a persistently positive MRSA culture from a repeat endotracheal aspirate. Linezolid serum concentrations were obtained and vancomycin was reinstituted, after which the patient began to improve (afebrile, improving PaO2/FiO2 ratio, decreasing leukocytosis). On hospital day 12, the patient removed his endotracheal tube, and a sputum sample was obtained for culture. The patient's clinical status subsequently declined, prompting addition of cefepime to his antibiotic regimen. This sputum culture revealed not only MRSA, but also quinolone-resistant Escherichia coli. After completing treatment for both organisms the patient was discharged home.
Limited data on linezolid dosing in the morbidly obese population show lower serum drug concentrations than those in nonobese patients, but no clinical failure has been reported when treating MRSA skin and soft tissue infections or MRSA tracheitis. In our patient, low steady-state linezolid serum concentrations (peak 4.13 μg/mL [reference 15-27] and trough 1.27 μg/mL [reference 2-9]) were thought to contribute to his poor clinical response.
To our knowledge, this is the first report of subtherapeutic linezolid concentrations correlated with decreased clinical effectiveness when during treatment of MRSA pneumonia in a patient with morbid obesity.
报告 1 例病态肥胖患者出现利奈唑胺治疗浓度低于最低有效治疗浓度的情况。
1 例 34 岁男性,病态肥胖(体重 265 kg,体重指数 82 kg/m²),因呼吸衰竭导致严重脓毒症,需紧急插管,并治疗社区获得性肺炎。入院时的气管抽吸培养显示耐甲氧西林金黄色葡萄球菌(MRSA),因此给予万古霉素治疗。随后由于患者的临床状况恶化,出现显著缺氧(动脉血氧分压/吸入氧分数 [PaO2/FiO2] 比值 145)、白细胞计数增加(入院时白细胞 10800/μL,入院第 6 天增至 15400/μL)和持续发热(38.3°C),将治疗方案改为利奈唑胺。利奈唑胺单药治疗 48 小时后,患者仍持续发热,白细胞计数持续增加,缺氧恶化,重复气管抽吸的 MRSA 培养仍为阳性。于是检测了利奈唑胺的血清浓度,重新给予万古霉素,此后患者开始好转(不发热,PaO2/FiO2 比值改善,白细胞计数减少)。入院第 12 天,患者拔管,留取痰培养。此后患者的临床状况恶化,加用头孢吡肟治疗。该痰培养不仅显示 MRSA,还显示对喹诺酮类药物耐药的大肠埃希菌。两种病原体的治疗完成后,患者出院回家。
在病态肥胖人群中,关于利奈唑胺剂量的有限数据显示,与非肥胖患者相比,血清药物浓度较低,但在治疗 MRSA 皮肤和软组织感染或 MRSA 气管炎时,尚未有临床治疗失败的报道。在我们的患者中,较低的稳态利奈唑胺血清浓度(峰浓度 4.13 μg/mL[参考范围 15-27],谷浓度 1.27 μg/mL[参考范围 2-9])被认为是导致其临床疗效不佳的原因。
据我们所知,这是首例在病态肥胖患者中,治疗 MRSA 肺炎时出现低于治疗有效浓度的利奈唑胺浓度,与临床疗效下降相关的病例报告。