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BioMed Research International
Volume 2014 (2014), Article ID 630835, 15 pages
Does Intraoperative Ulinastatin Improve Postoperative Clinical Outcomes in Patients Undergoing Cardiac Surgery: A Meta-Analysis of Randomized Controlled Trials
1Department of Anesthesiology, The First Affiliated Hospital of Sun Yat-sen University, No. 58 Zhongshan 2nd Road, Guangzhou, Guangdong 510080, China
2School of Public Health, Sun Yat-sen University, No. 74 Zhongshan 2nd Road, Guangzhou, Guangdong 510080, China
3Guangzhou Municipal Center for Disease Control and Prevention, Guangzhou 0086-510080, China
Received 1 July 2013; Revised 4 November 2013; Accepted 2 December 2013; Published 9 March 2014
Academic Editor: Sebastian Straube
Copyright © 2014 Qiu-Lan He et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Introduction. The systematic meta-analysis of randomized controlled trials (RCTs) evaluated the effects of intraoperative ulinastatin on early-postoperative recovery in patients undergoing cardiac surgery. Methods. RCTs comparing intraoperative ulinastatin with placebo in cardiac surgery were searched through PubMed, Cochrane databases, Medline, SinoMed, and the China National Knowledge Infrastructure (1966 to May 20th, 2013). The primary endpoints included hospital mortality, postoperative complication rate, length of stay in intensive care unit, and extubation time. The physiological and biochemical parameters illustrating postoperative cardiac and pulmonary function as well as inflammation response were considered as secondary endpoints. Results. Fifteen RCTs (509 patients) met the inclusion criteria. Ulinastatin did not affect hospital mortality, postoperative complication rate, or ICU length of stay but reduced extubation time. Ulinastatin also increased the oxygenation index on postoperative day 1 and reduced the plasma level of cardiac troponin-I. Additionally, ulinastatin inhibited the increased level of tumor necrosis factor-alpha, polymorphonuclear neutrophil elastase, interleukin-6, and interleukin-8 associated with cardiac surgery. Conclusion. Ulinastatin may be of value for the inhibition of postoperative increased inflammatory agents and most likely provided pulmonary protective effects in cardiac surgery. However, larger adequately powered RCTs are required to define the clinical effect of ulinastatin on postoperative outcomes in cardiac surgery.
The use of a cardiopulmonary bypass (CPB) during cardiac surgery leads to leukocyte (including neutrophil) activation, triggering a systemic inflammatory response , and inducing postoperative complications which include myocardial dysfunction [2, 3], acute lung injury , and multiorgan failure . This contributes to prolonged postoperative recovery, delayed extubation time, and an extended intensive care unit (ICU) stay [6, 7].
Ulinastatin, one of the Kunitz-type human protease inhibitors found in urine, has the capacity to inhibit the neutrophilic elastase and the activation of proinflammatory cytokines , where it is anticipated that it could suppress the systematic inflammatory response associated with cardiac surgery. Although ulinastatin has been tested in many small sample sized clinical trials in cardiac surgery since the 1990s, where it has demonstrated the clear inhibitory effects in attenuating the postoperative increase in proinflammatory cytokines, its impact on clinical outcomes and postoperative complications remains controversial [9–15]. As a consequence, ulinastatin is not currently part of routine treatment for patients undergoing cardiac surgery . We therefore undertook a systematic review and meta-analysis of randomized controlled trials (RCTs) which analyzed the effects of intraoperative ulinastatin treatment on postoperative clinical outcomes in patients undergoing cardiac surgery.
2. Materials and Methods
2.1. Literature Search, Inclusion, and Exclusion Criteria
We adopted the methods detailed in the Cochrane Handbook for Systematic Reviews version  and the guidelines of the PRISMA statement  for conduct of the meta-analysis. The search included the Cochrane Databases, Pubmed, Medline, SinoMed, and the China National Knowledge Infrastructure (CNKI) from 1966 to May 20th 2013, using the text words and medical subject headings (MeSH) comprising “ulinastatin” and “cardiac surgery”. The Cochrane Collaboration’s highly sensitive search strategy (HSSS) was used to identify the relevant articles in the Cochrane Databases and Medline . Text words and MeSH without HSSS were used to identify the relevant articles in Pubmed, SinoMed, and CNKI. ClinicalTrials.gov was also examined for relevant studies. Two reviewers (HQL and SHH) independently screened the titles and abstracts in order to select trials involving patients undergoing elective cardiac surgery who received intraoperative ulinastatin. Following the preliminary search, 253 articles were identified as potentially eligible and suitable for in-depth analysis.
Eligible inclusion criteria for the studies were that (1) prospective RCTs compare the ulinastatin group with the placebo group in cardiac surgery; (2) the baseline characteristics including age, sex, and type of operation were comparable between the groups; (3) the language of published studies was restricted to English, Chinese, and Japanese; (4) the period of follow-up was at least 24 hours after surgery. Exclusion criteria were that (1) the method of randomization was incorrect; (2) there were duplicate publications; (3) there was a lack of any data regarding the clinical endpoints; (4) studies were performed on a cohort of patients previously used for another trial. The full texts of highly relevant articles were thoroughly read and analyzed by the two reviewers.
2.2. Data Extraction and Outcome Measures
Descriptive data (e.g., patient population, type of surgery, intervention, and exclusion criteria) and markers of validity (e.g., methods of randomization, blinding) from all trials were extracted. Primary endpoints of interest were the hospital mortality, the early-postoperative complication rate, the length of stay in ICU, and extubation time. Secondary endpoints included the oxygenation index (OI), the cardiac index (CI) and the plasma levels of cardiac troponin-I (cTnI), creatine kinase MB isoenzyme (CK-MB), tumor necrosis factor-alpha (TNF-α), polymorphonuclear neutrophil elastase (PMNE), interleukin-6 (IL-6), and interleukin-8 (IL-8) on the postoperative first day (POD1). We accepted the authors’ definitions for clinical outcomes. An early-postoperative complication was defined as organ dysfunction or an infective complication during the hospital stay as well as excessive bleeding requiring reoperation. The extubation time was defined as the duration (in hours) of postoperative mechanical ventilation. Two independent investigators (HQL and YF) abstracted the relevant data and measured the outcomes. When a discrepancy occurred, a third reviewer (SHH) acted as a referee so that a final consensus decision could be made.
2.3. Quality Scoring and Risk of Bias Assessment
The Jadad score was used for the quality assessment of the included trials . Details of the quality assessment included the methodology of randomization, the adequacy of allocation concealment, whether a blind or double-blind method was used, whether an intention-to-treat analysis was utilized and descriptions of withdrawals, and follow-up. A risk of bias assessment was performed in accordance with guidelines outlined in the Cochrane handbook for Systematic Reviews or Interventions v.5.1.0. Two authors (HQL and ZF) reviewed all studies and subjectively assigned a value of “high”, “low”, or “unclear” to the following: (1) selection bias (was the randomization sequence adequate? was allocation concealment satisfactory?); (2) performance and detection bias (were participants, personnel, and outcome assessors blinded?); (3) attrition bias (were incomplete outcome data sufficiently assessed and dealt with?); (4) publication bias (was there evidence of selective outcome reporting?); and (5) any other sources of identifiable bias. The two trained reviewers (HQL and ZF) assessed the quality of the trials and the risk of bias independently resolving differences by consensus.
2.4. Statistical Analysis
An intention-to-treat analysis was used in the meta-analysis. The mean difference (MD) or odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated with the methods recommended by the Cochrane Collaboration . The Cochrane’s test was used to detect heterogeneity among the studies. If the value of Cochrane’s test was more than 0.05, a fixed effects model was employed and the Mantel-Haenszel method was performed to analyze the data. If the value was less than 0.05, heterogeneity was explored. Egger’s regression was used to detect publication bias . Meta-analysis was conducted using Review manager 5 (version 5.0.14; Copenhagen: the Nordic Cochrane Centre, the Cochrane Collaboration) and Egger’s regression was performed with the Stata 10.0 software (Stata Corp, USA).
3.1. Characteristics of Included Studies
Fifteen studies involving 509 participants were included in the meta-analysis [22–36]. Figure 1 depicts the flow chart of the selection process. The characteristics of included studies are shown in Table 1. None of the studies was a multicenter RCT. The median sample size of the RCTs was 30 patients (range 15–60). With regard to the types of surgery, one trial assessed only aortic arch replacements , four trials only evaluated coronary artery bypass grafts (CABG) [23, 25, 29, 30], five trials reported only valve surgery [26, 28, 33–35], three trials evaluated only repairs of atrial or ventricular septal defects [22, 24, 32], and two trails were mixed in nature [27, 31]. All trials except one  were conducted with CPB. Ulinastatin treatment protocols varied in their dosage and administration times. The risk of bias analysis (Figure 2) showed that eleven studies described their randomization methods [22, 25, 27–29, 31–36] and that five studies were double-blind [25, 28, 29, 35, 36]. Because all included studies were RCTs, the Jadad score for all studies was >2 with a mean overall Jadad score of . Table 1 shows that twelve of the studies with a Jadad score > 3 were considered high-quality RCTs  and that four studies had a Jadad score = 5 [28, 29, 33, 35].
3.2. Data Synthesis
Table 2 summarizes the results of the meta-analysis for each outcome.
3.3. Hospital Mortality
Nine RCTs reported data on hospital mortality [22, 24, 26, 27, 29, 30, 32, 34–36]. There were a total of 7 postoperative deaths (7/306, 2.3%). Two patients in the ulinastatin group died of coagulapathy  and cardiac infraction , respectively. Myocardial infarction and respiratory failure were the main causes of death in the control group. Since 6 of these trials did not present any hospital deaths, where all of the participants survived (“zero-sum” studies), the remaining 3 RCTs (126 patients) [27, 32, 36] were used to perform the meta-analysis. Ulinastatin treatment did not influence overall hospital mortality (OR = 0.48; 95% CI, 0.12 to 1.99; ; Cochrane’s test, ) (Figure 3).
3.4. Early-Postoperative Complication Rates
Twelve RCTs reported data on early-postoperative complications [22, 24, 26, 27, 29–36] with 6 trials being zero-sum studies which reported that there were no patient suffering postoperative complications due to operation or CPB procedures [22, 26, 30, 31, 33, 34]. In the ulinastatin groups of the remaining 6 RCTs, postoperative complications included 6 cases of myocardial ischemia [27, 29, 35], 1 wound infection , 1 reoperation for bleeding , 7 respiratory failures , and 4 renal failures , whilst in the control groups, there were 13 cases of myocardial ischemia [27, 29, 36], 3 patients with excessive bleeding [24, 36], 4 respiratory failures [32, 35], 1 wound infection , and 5 renal failures [35, 36] (Table 3). As only one trial  reported the number of comorbidities, which was more than the total number of patients, the remaining 5 RCTs (176 patients) [24, 27, 29, 32, 36] were estimable to perform the analysis showing that ulinastatin treatment did not influence early-postoperative complication rate (OR = 0.41; 95% CI, 0.16 to 1.08; ; Cochrane’s test, ) (Figure 4).
3.5. ICU Length of Stay
Eight RCTs (318 patients) evaluated the effect of ulinastatin on the length of stay in ICU [22, 27–30, 33, 34, 36]. Four of these trials reported a significantly shorter ICU length of stay in the ulinastatin treatment groups [27, 33, 34, 36]; however, meta-analysis using the random effects model showed that the ulinastatin treatment did not significantly decrease the length of stay in ICU (MD = −5.21 h; 95% CI, −11.64 h to 1.21 h; ; Cochrane’s test, ) (Figure 5).
3.6. Extubation Time
Eleven RCTs (385 patients) reported extubation time [22, 23, 25, 27–30, 33–36] with 5 of the trials recording a significantly reduced extubation time in the ulinastatin groups (27, 29, 30, 34, 36). Meta-analysis showed that ulinastatin treatment significantly reduced extubation time (MD = −4.18 h; 95% CI, −6.87 h to −1.49 h; ; Cochrane’s χ2 test, ) (Figure 6). Furthermore, to investigate the impact of total ulinastatin dosage on the outcome, we undertook an exploratory subgroup analysis and found that trials with a total dosage < 10,000 U/kg (206 patients) [23, 25, 27, 29, 33, 35] had a negative outcome (), whereas those with total dosage > 10,000 U/kg had a positive outcome (MD = −9.86 h; 95% CI, −16.58 h to −3.14 h, ). Similar subgroup analysis of the isolated CABG trials (104 patients) [23, 25, 29, 30] and isolated valve repair trials (156 patients) [28, 33–35] showed no difference between ulinastatin-treated and control groups ( and , resp.).
3.7. Postoperative OI and CI
Five trials (127 patients) reported the postoperative oxygenation indexes (OI) [22, 23, 29, 34, 35] which was increased by ulinastatin treatment (MD = 85.23; 95% CI, 59.75 to 110.72; ; Cochrane’s χ2 test, ) (Figure 7).
Four trials (138 patients) reported the postoperative cardiac indexes (CI) [28, 29, 34] showing no difference between the ulinastatin-treated and the control groups (MD = −0.17; 95% CI, −0.40 to 0.06; ; Cochrane’s χ2 test, ) (Figure 8).
3.8. Myocardial Damage Agents (cTnI and CKMB)
Six trials (206 patients) reported the levels of plasma cTnI on postoperative first day (POD1) [24, 25, 27, 32, 33, 35] and showed that ulinastatin treatment significantly reduced the level of cTnI (MD = −0.97 ng/mL; 95% CI, −1.66 ng/mL to −0.28 ng/mL; ; Cochrane’s χ2 test, ) (Figure 9).
Six trials (242 patients) reported the levels of plasma CKMB on POD1 [24, 27–29, 33, 35] with recording a significantly higher CKMB level in the ulinastatin group , whereas 3 trials reported significantly lower CKMB levels following ulinastatin therapy [24, 27, 35]. Overall, meta-analysis showed no difference between ulinastatin groups and control groups (MD = −3.86 ng/mL; 95% CI, −9.68 ng/mL to 1.95 ng/mL;; Cochrane’s χ2 test, ) (Figure 10).
3.9. Plasma Inflammatory Agents (TNF-α, PMNE, IL-6, and IL-8)
Seven RCTs (203 patients) reported the levels of plasma TNF-α on POD1 [22, 26, 30, 32, 34–36]. Meta-analysis showed that ulinastatin treatment significantly inhibited the increased level of TNF-α (MD = −49.04 pg/mL; 95% CI, −76.15 pg/mL to −21.92 pg/mL; ; Cochrane’s χ2 test, ) (Figure 11).
Six RCTs (161 patients) reported the levels of plasma PMNE on POD1 [23, 26, 29–31, 36] showing a decrease on POD 1 after ulinastatin treatment (MD = −6.86 μg/dL; 95% CI, −11.79 μg/dL to −1.94 μg/dL; ) (Figure 12). As 4 of these studies focused on CABG, an exploratory subgroup analysis was performed and showed no difference between the ulinastatin-treated and the control groups (MD = −6.55 μg/dL; 95% CI, −14.46 μg/dL to 1.35 μg/dL; ).
Eight RCTs (219 patients) reported the levels of plasma IL-6 on POD1 [22, 29–32, 34–36] where ulinastatin significantly decreased the level of IL-6 on POD 1 (MD = −28.02 pg/mL; 95% CI, −47.95 pg/mL to −8.08 pg/mL; ) (Figure 13). But when analyzing the CABG surgery subgroups (75 patients) [29–31], ulinastatin had no effect (MD = −41.78 pg/mL; 95% CI, −108.25 pg/mL to −24.68 pg/mL; ).
Six RCTs (165 patients) reported the levels of plasma IL-8 on POD1 [22, 29–31, 34] showing a significantly decrease with ulinastatin treatment (MD = −20.38 pg/mL; 95% CI, −32.48 pg/mL to −8.28 pg/mL; ) (Figure 14).
3.10. Sensitivity Analysis for Study Quality
We undertook subgroup meta-analysis including exclusively high-quality studies (Jadad score ≥ 3) in order to find how the quality of studies influenced the outcomes of our meta-analysis. Regarding the clinical and physiologic outcomes, our conclusion among high-quality RCTs remained consistent. But for biologic outcomes, the meta-analysis of 5 high-quality studies [22, 33–36] indicated that ulinastatin did not have inhibitory effect on plasma levels of TNF-α (); and meta-analysis of 3 high-quality studies [29, 31, 36] showed no difference in plasma levels of PMNE between the ulinastatin-treated and the control groups either ().
Our meta-analysis showed a significant decrease in the extubation time for ulinastatin-treated patients but no effect on hospital mortality, early postoperative complication rate, or ICU length of stay when compared with controls. In an assessment of secondary outcome measures, ulinastatin increased the oxygenation index (OI) but not the cardiac index (CI) and reduced the plasma levels of cTnI but not CK-MB measured on the first postoperative day. Additionally, ulinastatin significantly inhibited the increased postoperative level of PMNE, TNF-α, IL-6, and IL-8 associated with cardiac surgery.
The decrease in extubation time and the increased OI indicate that the intraoperative use of ulinastatin does provide some clinical benefits such as the improvement of early postoperative pulmonary function, a finding which has been reported previously [10, 23, 37–39].
Cardiopulmonary bypass (CPB) and cardiac surgery usually induce an activation and release of neutrophil and proinflammatory cytokines , most notably IL-6 and IL-8, which may be early prognosis factors for organ dysfunction following cardiac surgery . In this respect, it was reported that the removal by ultrafiltration of inflammatory substances from the circulation including inflammatory cytokines and scavenger toxins may improve early postoperative organ function after cardiac surgery [2, 42].
The transcription of IL-6, IL-8, and TNF-α is a secondary event induced by the bioactive IL-1 beta [43, 44], where it is anticipated that the protease inhibitor, ulinastatin which has inhibitory effects on neutrophilic elastase and on the conversion of prointerleukin 1 beta (pro-IL-1; 31 kDa peptide, inactive) to IL-1 beta (17 kDa peptide, active) [43, 45], will attenuate the acute phase response. Consistent with these results in animals [43–45] as well as in patients undergoing major operations (such as hepatectomy) or in those with mutitrauma [46–55], the finding of the present meta-analysis focusing on cardiac surgery would suggest that intraoperative ulinastatin inhibits the sequestration and activation of neutrophil and attenuates the normal postoperative rise in cytokines, reducing the systemic inflammatory response syndrome, pulmonary microvascular permeability, and postoperative lung edema [55–57]. These findings would correlate with a higher OI in ulinastatin-treated cases and a more rapid extubation time consequent upon a more aggressive policy by intensive care physicians to more rapidly wean their patients from mechanical ventilation. Moreover, a decreased extubation time may protect patients from ventilator-associated pneumonia and contribute to a reduction in the length of ICU stay and the hospital cost along with a diminution in psychosocial and physical risks to the patient and even death [58, 59]. Interestingly, in our study, subgroup analysis concerning the total dose of ulinastatin indicates that a higher dosage protocol significantly reduced extubation time which may suggest a dose-dependent effect of ulinastatin on pulmonary protection. High-quality RCTs comparing different dosages of ulinastatin are required in order to answer this question.
The reduced periods of intubation with ulinastatin impact on the length of ICU stay where 4 trials included in the analysis confirmed a lesser length of ICU stay with ulinastatin therapy [27, 33, 34, 36] (Figure 4), although meta-analysis on all 8 trials which reported the length of ICU stay did not show a significant effect. Concerning this point, the factors affecting the length of ICU stay in patients undergoing cardiac surgery are ambiguous, including the basic preoperative cardiac function of patient, the length of the CPB, the recovery of major organ function, new onset atrial fibrillation, a stuck mechanical valve, the presence of postoperative bleeding, and unknown iatrogenic factors [60–62]. It is expected that these factors should be equally distributed within the RCTs examined for this meta-analysis. It is further likely that conflicting reports on the postoperative effects of ulinastatin will affect the meta-analysis of ICU stay, reflecting the heterogeneity of RCTs, some of which did not define standards of ICU discharge [22, 33] or report on postoperative complications [29, 35].
Ulinastatin also significantly decreased the postoperative levels of cTnI. Normally, it has been shown that surgical procedures as well as CPB during cardiac surgery induce a systemic acute inflammatory response and regional myocardial I/R injury leading to increased endothelial permeability and free radical damage to vessels and parenchyma with coincident myocardial damage . Both cTnI and CK-MB are predictive factors which reflect myocardial injury where cTnI is the most sensitive indicator of minor myocardial damage with superior cardiac specificity when compared with CK-MB [64–66]. The decreased levels of cTnI would suggest a potential role for ulinastatin as a myocardial protective agent, although the observed clinical outcomes, (e.g. incidence of postoperative myocardial ischemia) could not be determined. Studies involving larger patient numbers are required; however, it may, well, be that there are more specific clinical outcome indicators worth assessing such as the occurrence of delayed myocardial ischemia up to 30 or 60 days after surgery.
Recently, an increasing body of evidence has highlighted the role of ulinastatin in postoperative mortality and morbidities with controversial results [22, 24, 26, 27, 29, 30, 32, 34, 35, 50, 52, 54, 67–69]. Interpretation of these trials is difficult since there is considerable heterogeneity, particularly regarding the type of surgery, the length of CPB, and the dosage of ulinastatin used. Further, the majority of the trials focused on low-risk patients, which may result in a much lower observed death rate (2.3%) than would normally be expected with CPB alone (3.2% to 12.8%) . Without clear definitions, tracking complication events such as myocardial infarction after cardiac surgery is likely to be underreported, limiting the value of the meta-analytic approach in the assessment of both hospital mortality and postoperative complication rates. Although our analysis showed a trend of favoring a decreased complication rate with ulinastatin, larger, adequately powered and well-designed RCTs are required to better elucidate the impact of perioperative ulinastatin.
Despite the rigorous nature of the analysis and a high agreement between observers, our study has several limitations. Firstly, the majority of studies focused on biochemical markers of inflammation with relatively poor descriptions of the secondary clinical outcomes, an effect likely to result in significant underreporting of perioperative adverse events. Secondly, the small sample size in many cases makes interpretation guarded where it cannot be assumed that variables like ICU stay and extubation times are normally distributed. Thirdly, the diversity of the surgeries performed, the ulinastatin doses utilized, and the timing of ulinastatin administration (intra- versus postoperative) [32, 34] are confounding factors. The analysis of studies over a 20-year period where there have been considerable changes in cardiac surgery and anesthesia as well as in CPB technology, myocardial protection, and antifibrinolytic therapies will also influence the overall results.
In conclusion, it remains insufficient evidence to support a beneficial effect of ulinastatin on mortality, the postoperative complication rate, or the length of ICU stay following cardiac surgery. Analysis shows, however, that intraoperative ulinastatin might provide protective effects on cardiac and pulmonary function, reducing plasma levels of cTnI, increasing the oxygenation index, and reducing the extubation time. These effects might be associated with a concomitant inhibition of neutrophilic elastase and an attenuation of the normal rise in proinflammatory cytokines normally detected on the first postoperative day after cardiac surgery.
Conflict of Interests
The authors declare no conflict of interests.
Qiu-Lan He and Hai-Hua Shu conceived the study, participated in study design, prepared data, collected data, performed statistical analysis, and wrote the paper. Fei Zhong participated in study design, performed statistical analysis, and wrote the paper. Fang Ye, Ming Wei, Wei-Feng Liu, and Mei-Na Li reviewed the eligible articles and then collected and prepared the data. Qiao-Bo Li, Wen-Qi Huang, and Lai-Bao Sun contributed to the writing and critical appraisal of the paper. All authors read and approved the final paper.
This work was supported by research funding offered by Techpool Biopharma Co. Ltd, China in 2012 (Fund no. 01200905). The authors would like to thank Professor Andrew Zbar and Benjamin Ross for language editing of the paper.
- J. Rossaint, C. Berger, H. van Aken et al., “Cardiopulmonary bypass during cardiac surgery modulates systemic inflammation by affecting different steps of the leukocyte recruitment cascade,” PLoS ONE, vol. 7, no. 9, Article ID e45738, 2012.
- M. A. Munger, B. Johnson, I. J. Amber, K. S. Callahan, and E. M. Gilbert, “Circulating concentrations of proinflammatory cytokines in mild or moderate heart failure secondary to ischemic or idiopathic dilated cardiomyopathy,” The American Journal of Cardiology, vol. 77, no. 9, pp. 723–727, 1996.
- C. Tentolouris, D. Tousoulis, C. Antoniades et al., “Endothelial function and proinflammatory cytokines in patients with ischemic heart disease and dilated cardiomyopathy,” International Journal of Cardiology, vol. 94, no. 2-3, pp. 301–305, 2004.
- Y. L. Yang, K. L. Huang, H. L. Liou, and H. I. Chen, “The involvement of nitric oxide, nitric oxide synthase, neutrophil elastase, myeloperoxidase and proinflammatory cytokines in the acute lung injury caused by phorbol myristate acetate,” Journal of Biomedical Science, vol. 15, no. 4, pp. 499–507, 2008.
- J. H. Holmes, N. C. Connolly, D. L. Paull et al., “Magnitude of the inflammatory response to cardiopulmonary bypass and its relation to adverse clinical outcomes,” Inflammation Research, vol. 51, no. 12, pp. 579–586, 2002.
- T. S. Sun, X. B. Chen, Z. Liu, Z. Y. Ma, and J. Z. Zhang, “Relationship between the operation time of multiple fractures with system inflammation changes and clinical outcomes,” Zhonghua Wai Ke Za Zhi, vol. 46, no. 13, pp. 961–965, 2008.
- L. F. Gentile, A. G. Cuenca, P. A. Efron et al., “Persistent inflammation and immunosuppression: a common syndrome and new horizon for surgical intensive care,” Journal of Trauma and Acute Care Surgery, vol. 72, no. 6, pp. 1491–1501, 2012.
- J. Hirose, T. Ozawa, T. Miura et al., “Human neutrophil elastase degrades inter-α-trypsin inhibitor to liberate urinary trypsin inhibitor related proteins,” Biological and Pharmaceutical Bulletin, vol. 21, no. 7, pp. 651–656, 1998.
- Q. Zhou, G. Wang, C. Gao, and T. Chen, “Effect of ulinastatin on perioperative inflammatory response to coronary artery bypass grafting with cardiopulmonary bypass,” Zhong Nan Da Xue Xue Bao Yi Xue Ban, vol. 35, no. 2, pp. 107–110, 2010.
- X. Y. Yu and L. L. Fan, “Effects of different doses of ulinastatin on inflammatory response and pulmonary function after cardiopulmonary bypass,” Zhongguo Wei Zhong Bing Ji Jiu Yi Xue, vol. 21, no. 11, pp. 664–667, 2009.
- J. M. Shen, L. Li, and X. J. He, “Effects of ulinastatin on erythrocyte lipid peroxidation in patients undergoing open heart surgery,” Zhong Nan Da Xue Xue Bao Yi Xue Ban, vol. 29, no. 2, pp. 187–189, 2004.
- T. Kawamura, K. Inada, O. Kimura, N. Akasaka, and R. Wakusawa, “The inhibitory effects of ulinastatin on the increase of interleukin 8 and 6 during open heart surgery,” Masui, vol. 43, no. 12, pp. 1818–1823, 1994.
- T. Kawai, Y. Wada, K. Nishiyama et al., “Usefulness of ulinastatin as a radical scavenger for protection of reperfusion injury after myocardial ischemia in open heart surgery,” Journal of the Japanese Association for Thoracic Surgery, vol. 39, no. 12, pp. 2157–2162, 1991.
- T. Kawamura, K. Inada, N. Akasaka, and R. Wakusawa, “Ulinastatin reduces elevation of cytokines and soluble adhesion molecules during cardiac surgery,” Canadian Journal of Anaesthesia, vol. 43, no. 5 I, pp. 456–460, 1996.
- K. Inoue and H. Takano, “Urinary trypsin inhibitor as a therapeutic option for endotoxin-related inflammatory disorders,” Expert Opinion on Investigational Drugs, vol. 19, no. 4, pp. 513–520, 2010.
- J. I. Han, “Urinary trypsin inhibitor: miraculous medicine in many surgical situations?” Korean Journal of Anesthesiology, vol. 58, no. 4, pp. 325–327, 2010.
- J. P. T. Higgins and S. Green, Cochrane Handbook for Systematic Reviews of Interventions Version 5.0.0, The Cochrane Collaboration, 2011.
- D. Moher, A. Liberati, J. Tetzlaff, et al., “Preferred reporting items for systematic reviews and meta-analysis: the PRISMA statement,” PLoS Medicine, vol. 6, no. 7, Article ID e1000097, 2009.
- L. Zhang, I. Ajiferuke, and M. Sampson, “Optimizing search strategies to identify randomized controlled trials in MEDLINE,” BMC Medical Research Methodology, vol. 6, article 23, 2006.
- A. R. Jadad, R. A. Moore, D. Carroll et al., “Assessing the quality of reports of randomized clinical trials: is blinding necessary?” Controlled Clinical Trials, vol. 17, no. 1, pp. 1–12, 1996.
- M. Egger, G. D. Smith, M. Schneider, and C. Minder, “Bias in meta-analysis detected by a simple, graphical test,” The British Medical Journal, vol. 315, no. 7109, pp. 629–634, 1997.
- Y. F. Jiang, W. W. Wang, W. L. Ye et al., “Effects of alprostadil and ulinastatin on inflammatory response and lung injury after cardiopulmonary bypass in pediatric patients with congenital heart diseases,” Zhonghua Yi Xue Za Zhi, vol. 88, no. 41, pp. 2893–2897, 2008.
- A. Mishima, Y. Takeuti, S. Usami, H. Kotani, Y. Suzuki, and J. Yura, “Effects of ulinastatin on plasma polymorphonuclear leukocyte elastase activity and respiratory function in patients undergoing cardiopulmonary bypass,” Nihon Kyobu Geka Gakkai Zasshi, vol. 38, no. 4, pp. 607–612, 1990.
- T. Y. Ren, X. W. Yang, Y. Ma, F. Wang, and W. D. Qiang, “Myocardial protective effect of ulinastatin against ischemia/reperfusion injury during open heart surgery with cardiopulmonary bypass,” Zhonghua Yi Xue Za Zhi, vol. 83, no. 16, pp. 1391–1393, 2003.
- G. Y. Wang, H. B. Qiu, S. G. Zhan, and L. H. Li, “Protection of ulinastatin against myocardial injury induced by off-pump coronary artery bypass graft surgery: report of 24 cases,” Zhonghua Yi Xue Za Zhi, vol. 87, no. 35, pp. 2502–2504, 2007.
- D. J. Wang, J. X. Liu, and B. L. Yin, “Protective effects of ulinastatin on the lung injury during cardiopulmonary bypass,” Zhong Nan Da Xue Xue Bao Yi Xue Ban, vol. 30, no. 6, pp. 670–672, 2005.
- X. Zhang and X. G. Qin, “Effect of ulinastatin on cardiac and lung function of patients with moderate and high risk in cardiac surgery under cardiopulmonary bypass,” Modern Preventive Medicine, vol. 7, pp. 1822–1824, 2012.
- S. Y. Oh, J. C. Kim, Y. S. Choi, W. K. Lee, Y. K. Lee, and Y. L. Kwak, “Effects of ulinastatin treatment on myocardial and renal injury in patients undergoing aortic valve replacement with cardiopulmonary bypass,” Korean Journal of Anesthesiology, vol. 62, no. 2, pp. 148–153, 2012.
- K. Nakanishi, S. Takeda, A. Sakamoto, and A. Kitamura, “Effects of ulinastatin treatment on the cardiopulmonary bypass-induced hemodynamic instability and pulmonary dysfunction,” Critical Care Medicine, vol. 34, no. 5, pp. 1351–1357, 2006.
- J. Bingyang, L. Jinping, L. Mingzheng, W. Guyan, and F. Zhengyi, “Effects of urinary protease inhibitor on inflammatory response during on-pump coronary revascularisation. Effect of ulinastatin on inflammatory response,” Journal of Cardiovascular Surgery, vol. 48, no. 4, pp. 497–503, 2007.
- Y. Sato, S. Ishikawa, A. Otaki et al., “Induction of acute-phase reactive substances during open-heart surgery and efficacy of ulinastatin. Inhibiting cytokines and postoperative organ injury,” The Japanese Journal of Thoracic and Cardiovascular Surgery, vol. 48, no. 7, pp. 428–434, 2000.
- H. Q. Tu and T. Ming, “Postoperative application of ulinastatin in infants with critical congenital heart disease,” Journal of Nanchang University (Medical Science), vol. 51, no. 2, pp. 37–40, 2011.
- J. E. Song, W. S. Kang, D. K. Kim et al., “The effect of ulinastatin on postoperative blood loss in patients undergoing open heart surgery with cardiopulmonary bypass,” Journal of International Medical Research, vol. 39, no. 4, pp. 1201–1210, 2011.
- J. Li, Z. Wang, Z. Xu, S. Huang, and F. Qiao, “The role of ulinastatin in management of systemic inflammatory response syndrome post—CPB,” Internationl Journal of Emergency and Critical Car, vol. 4, no. 4, pp. 1929–1933, 2007.
- J. Song, J. Park, J. Y. Kim et al., “Effect of ulinastatin on perioperative organ function and systemic inflammatory reaction during cardiac surgery: a randomized double-blinded study,” Korean Journal of Anesthesiology, vol. 64, no. 4, pp. 334–340, 2013.
- E. X. Chong, C. W. Zou, M. Y. Zhang, and L. Guo, “Effects of high-dose ulinastatin on inflammatory response and pulmonary function in patients with type-A aortic dissection after cardiopulmonary bypass under deep hypothermic circulatory arrest,” Journal of Cardiothoracic and Vascular Anesthesia, vol. 27, no. 3, pp. 479–484, 2013.
- A. Hiyama, J. Takeda, Y. Kotake, H. Morisaki, and K. Fukushima, “A human urinary protease inhibitor (ulinastatin) inhibits neutrophil extracellular release of elastase during cardiopulmonary bypass,” Journal of Cardiothoracic and Vascular Anesthesia, vol. 11, no. 5, pp. 580–584, 1997.
- N. Sato, K. Murakami, K. Ishida, K. Ikeda, and K. Saito, “Pulmonary hypertension and polymorphonuclear leukocyte elastase after esophageal cancer operations,” Annals of Thoracic Surgery, vol. 51, no. 5, pp. 754–758, 1991.
- A. Sato, Y. Kuwabara, N. Shinoda, M. Kimura, H. Ishiguro, and Y. Fujii, “Use of low dose dopamine, gabexate mesilate and ulinastatin reduces the water balance and pulmonary complication in thoracic esophagectomy patients,” Diseases of the Esophagus, vol. 18, no. 3, pp. 151–154, 2005.
- D. Paparella, T. M. Yau, and E. Young, “Cardiopulmonary bypass induced inflammation: pathophysiology and treatment,” European Journal of Cardio-Thoracic Surgery, vol. 21, no. 2, pp. 232–244, 2002.
- A. Sablotzki, M. G. Dehne, I. Friedrich et al., “Different expression of cytokines in survivors and non-survivors from MODS following cardiovascular surgery,” European Journal of Medical Research, vol. 8, no. 2, pp. 71–76, 2003.
- E. E. Apostolakis, E. N. Koletsis, N. G. Baikoussis, S. N. Siminelakis, and G. S. Papadopoulos, “Strategies to prevent intraoperative lung injury during cardiopulmonary bypass,” Journal of Cardiothoracic Surgery, vol. 5, no. 1, article 1, 2010.
- C. A. Dinarello, “Biologic basis for interleukin-1 in disease,” Blood, vol. 87, no. 6, pp. 2095–2147, 1996.
- P. Kelk, R. Claesson, L. Hänström, U. H. Lerner, S. Kalfas, and A. Johansson, “Abundant secretion of bioactive interleukin-1β by human macrophages induced by Actinobacillus actinomycetemcomitans leukotoxin,” Infection and Immunity, vol. 73, no. 1, pp. 453–458, 2005.
- K. Inoue, H. Takano, A. Shimada et al., “Urinary trypsin inhibitor protects against systemic inflammation induced by lipopolysaccharide,” Molecular Pharmacology, vol. 67, no. 3, pp. 673–680, 2005.
- Y. M. Shao, L. Q. Zhang, L. H. Deng, and H. G. Yao, “Clinical study on effects of ulinastatin on patients with systemic inflammatory response syndrome,” Zhongguo Wei Zhong Bing Ji Jiu Yi Xue, vol. 17, no. 4, pp. 228–230, 2005.
- X. Y. Lu, W. A. Zeng, W. Q. Lin, B. X. Chen, and W. X. He, “Effect of ulinastatin on inflammatory responses induced by oesophagectomy,” Nan Fang Yi Ke Da Xue Xue Bao, vol. 27, no. 1, pp. 81–83, 2007.
- T. Nishiyama and K. Hanaoka, “Do the effects of a protease inhibitor, ulinastatin, on elastase release by blood transfusion depend on interleukin 6?” Critical Care Medicine, vol. 29, no. 11, pp. 2106–2110, 2001.
- J. H. Park, S. H. Kwak, C. W. Jeong, H. B. Bae, and S. J. Kim, “Effect of ulinastatin on cytokine reaction during gastrectomy,” Korean Journal of Anesthesiology, vol. 58, no. 4, pp. 334–337, 2010.
- T. Tani, H. Abe, Y. Endo, K. Hanasawa, and M. Kodama, “Effects of a urinary trypsin inhibitor on acute circulatory insufficiency after surgical operation,” The American Journal of Surgery, vol. 175, no. 2, pp. 142–145, 1998.
- K. Hamazaki, N. Matsubara, Y. Yunoki, M. Mori, H. Mimura, and K. Orita, “Effects of ulinastatin on polymorphonuclear leukocyte elastase and interleukin 6 levels after hepatectomy,” Clinical Therapeutics, vol. 16, no. 4, pp. 680–685, 1994.
- N. Sato, S. Endo, Y. Kimura et al., “Influence of a human protease inhibitor on surgical stress induced immunosuppression,” Digestive Surgery, vol. 19, no. 4, pp. 300–305, 2002.
- Y. Huang, K. Xie, J. Zhang, Y. Dang, and Z. Qiong, “Prospective clinical and experimental studies on the cardioprotective effect of ulinastatin following severe burns,” Burns, vol. 34, no. 5, pp. 674–680, 2008.
- K. H. Park, K. H. Lee, H. Kim, and S. O. Hwang, “The anti-inflammatory effects of ulinastatin in trauma patients with hemorrhagic shock,” Journal of Korean Medical Science, vol. 25, no. 1, pp. 128–134, 2010.
- H. Chen, M. Y. He, and Y. M. Li, “Treatment of patients with severe sepsis using Ulinastatin and Thymosin α1: a prospective, randomized, controlled pilot study,” Chinese Medical Journal, vol. 122, no. 8, pp. 883–888, 2009.
- K. Inoue, H. Takano, R. Yanagisawa, and T. Yoshikawa, “Protective effects of urinary trypsin inhibitor on systemic inflammatory response induced by lipopolysaccharide,” Journal of Clinical Biochemistry and Nutrition, vol. 43, no. 3, pp. 139–142, 2008.
- Y. Fang, P. Xu, C. Gu et al., “Ulinastatin improves pulmonary function in severe burn-induced acute lung injury by attenuating inflammatory response,” Journal of Trauma—Injury, Infection and Critical Care, vol. 71, no. 5, pp. 1297–1304, 2011.
- B. Blackwood, M. Murray, A. Chisakuta, C. R. Cardwell, and P. O'Halloran, “Protocolized versus non-protocolized weaning for reducing the duration of invasive mechanical ventilation in critically ill paediatric patients,” Cochrane Database of Systematic Reviews, no. 7, Article ID CD009082, 2013.
- C. W. Tang, P. Y. Liu, Y. F. Huang et al., “Ventilator-associated pneumonia after pediatric cardiac surgery in southern Taiwan,” Journal of Microbiology, Immunology and Infection, vol. 42, no. 5, pp. 413–419, 2009.
- Y. Lin, X. Zhu, F. Liu et al., “Analysis of risk factors of prolonged intensive care unit stay of critically ill obstetric patients: a 5-year retrospective review in 3 hospitals in Beijing,” Chinese Critical Care Medicine, vol. 23, no. 8, pp. 449–453, 2011.
- S. Silberman, D. Bitran, D. Fink, R. Tauber, and O. Merin, “Very prolonged stay in the intensive care unit after cardiac operations: early results and late survival,” Annals of Thoracic Surgery, vol. 96, no. 1, pp. 15–21, 2013.
- D. Joskowiak, U. Kappert, K. Matschke, and S. Tugtekin, “Prolonged intensive care unit stay of patients after cardiac surgery: initial clinical results and follow-up,” Thoracic and Cardiovascular Surgeon, vol. 61, no. 8, pp. 701–707, 2013.
- R. P. Whitlock, S. Chan, P. J. Devereaux et al., “Clinical benefit of steroid use in patients undergoing cardiopulmonary bypass: a meta-analysis of randomized trials,” European Heart Journal, vol. 29, no. 21, pp. 2592–2600, 2008.
- C. Y. Jia, L. Wang, Z. G. Mao, J. L. Zhang, and L. Zhang, “Combined myocardial injury markers for diagnosis of acute myocardial infarction,” Sichuan Da Xue Xue Bao Yi Xue Ban, vol. 40, no. 6, pp. 1082–1085, 2009.
- J. Dawie, R. Chawla, Y. Worku, and A. Azazh, “Diagnosis of ischemic heart disease using CK-MB, troponin-i and ischemia modified albumin,” Ethiopian Medical Journal, vol. 49, no. 1, pp. 25–33, 2011.
- P. Collinson, S. Goodacre, D. Gaze, and A. Gray, “Very early diagnosis of chest pain by point-of-care testing: comparison of the diagnostic efficiency of a panel of cardiac biomarkers compared with troponin measurement alone in the RATPAC trial,” Heart, vol. 98, no. 4, pp. 312–318, 2012.
- J. W. Yoo, J. K. Ryu, S. H. Lee et al., “Preventive effects of ulinastatin on post-endoscopic retrograde cholangiopancreatography pancreatitis in high-risk patients: a prospective, randomized, placebo-controlled trial,” Pancreas, vol. 37, no. 4, pp. 366–370, 2008.
- K. Uemura, Y. Murakami, Y. Hayashidani et al., “Randomized clinical trial to assess the efficacy of ulinastatin for postoperative pancreatitis following pancreaticoduodenectomy,” Journal of Surgical Oncology, vol. 98, no. 5, pp. 309–313, 2008.
- H. Fujishiro, K. Adachi, T. Imaoka et al., “Ulinastatin shows preventive effect on post-endoscopic retrograde cholangiopancreatography pancreatitis in a multicenter prospective randomized study,” Journal of Gastroenterology and Hepatology, vol. 21, no. 6, pp. 1065–1069, 2006.
- R. Levin, M. Degrange, C. Del Mazo, E. Tanus, and R. Porcile, “Preoperative levosimendan decreases mortality and the development of low cardiac output in high-risk patients with severe left ventricular dysfunction undergoing coronary artery bypass grafting with cardiopulmonary bypass,” Experimental and Clinical Cardiology, vol. 17, no. 3, pp. 125–130, 2012.