Intensive Care Unit, Department of Anaesthesiology and Intensive Care, University Hospital of Modena, L.go del Pozzo, 71, 41100, Modena, Italy.
Intensive Care Med. 2014 Dec;40(12):1888-96. doi: 10.1007/s00134-014-3474-6. Epub 2014 Sep 13.
To determine whether there was an association between adjunctive therapy with IgM-enriched immunoglobulin (IgM) and the 30-day mortality rate in patients with septic shock.
In 2008 we introduced IgM as a possible adjunctive therapy to be provided within 24 h after shock onset in the management protocol for patients with septic shock. In this retrospective study we included the adult patients suitable for IgM therapy admitted to our ICU from January 2008 to December 2011. An unadjusted comparison between patients who did or did not receive IgM therapy, a multivariate logistic model adjusted for confounders and propensity score-based matching were used to evaluate the association between early IgM treatment and mortality.
One hundred and sixty-eight patients were included in the study. Of these, 92 (54.8%) received IgM therapy. Patients who did or did not receive IgM were similar with regards to infection characteristics, severity scores and sepsis treatment bundle compliance. Patients who received IgM were more likely to have blood cultures before antibiotics and to attain a plateau inspiratory pressure less than 30 cmH2O (p < 0.05). The 30-day mortality rate was reduced by 21.1% (p < 0.05) in the group that received IgM compared to the group that did not. The multivariate adjusted regression model (OR 0.17; CI 95% 0.06-0.49; p = 0.001) and the propensity score-based analysis (OR 0.35; CI 95% 0.14-0.85; p = 0.021) confirmed that IgM therapy was associated with reduced mortality at 30 days after the onset of septic shock.
Our experience indicates that early adjunctive treatment with IgM may be associated with a survival benefit in patients with septic shock. However, additional studies are needed to better evaluate the role of IgM therapy in the early phases of septic shock.
确定在感染性休克患者中,辅助使用富含免疫球蛋白 M(IgM)的免疫球蛋白(IgM)与 30 天死亡率之间是否存在关联。
2008 年,我们在感染性休克患者的管理方案中引入了 IgM,作为在休克发作后 24 小时内可能的辅助治疗方法。在这项回顾性研究中,我们纳入了 2008 年 1 月至 2011 年 12 月期间我院 ICU 收治的适合 IgM 治疗的成年患者。通过对接受和未接受 IgM 治疗的患者进行未经调整的比较、调整混杂因素的多变量逻辑模型和基于倾向评分的匹配,评估早期 IgM 治疗与死亡率之间的关联。
本研究共纳入 168 例患者,其中 92 例(54.8%)接受了 IgM 治疗。接受或未接受 IgM 治疗的患者在感染特征、严重程度评分和脓毒症治疗包依从性方面相似。接受 IgM 治疗的患者在使用抗生素前更有可能进行血培养,并且达到平台吸气压力低于 30cmH2O 的可能性更大(p<0.05)。与未接受 IgM 治疗的患者相比,接受 IgM 治疗的患者在 30 天内的死亡率降低了 21.1%(p<0.05)。多变量调整后的回归模型(OR 0.17;95%CI 0.06-0.49;p=0.001)和基于倾向评分的分析(OR 0.35;95%CI 0.14-0.85;p=0.021)均证实,在感染性休克发作后 30 天内,IgM 治疗与降低死亡率相关。
我们的经验表明,早期辅助使用 IgM 可能与感染性休克患者的生存获益相关。然而,还需要更多的研究来更好地评估 IgM 治疗在感染性休克早期阶段的作用。