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Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue最新文献

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[The research progress on acute lung injury following liver transplantation]. 肝移植术后急性肺损伤的研究进展。
Yu Wang, Yi-he Liu
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引用次数: 0
[Effects of PNU282987 on organ function and survival in dogs with lethal burn shock]. [PNU282987对致死性烧伤休克犬器官功能及存活的影响]。
Ming-hua Du, Quan Hu, Hong-min Luo, Zhi-long Lin, Li Ma, Huan Wang, Sen Hu

Objective: To investigate the effects of PNU282987, a α7 nicotinic acetylcholine receptor agonist (α7nAChR), on organ function and survival rate in dogs with lethal burn shock.

Methods: Twelve adult male Beagle dogs were subjected to 50% total body surface area (TBSA) full-thickness flame injury, and then they were randomly divided into a burn group and a PNU282987 group (PNU group), each n=6. The dogs in PNU group received PNU282987 (0.38 mg/kg, venous pumping) and the dogs in burn group received equal amount of normal saline solution as the control group. The mean arterial pressure (MAP) and the plasma levels of tumor necrosis factor-α (TNF-α), alanine aminotransferase (ALT), MB isoenzyme of creatine kinase (CK-MB), creatinine (Cr), blood urea nitrogen (BUN) were continuously determined before and 0.5, 2, 4, 8, 12, 24 hours after burn. All the above measurements were performed with animals in conscious and cooperative state. At the end of 24-hours-period experiment, the survival rate was recorded.

Results: The MAP significantly decreased after burn compared with the baseline data before-injury. The level of MAP in PNU group were significantly higher than those of the burn group from 4 hours after burn, and it returned to 83.6% of baseline level at 24 hours. In contrast, those in the burn group progressively decreased with time till death. The plasma levels of TNF-α in PNU group were significantly lower than those of burn group at each time points post injury. The ALT, Cr, BUN and CK-MB of the burn group increased persistently, while those of the PNU group increased at first and decreased subsequently except for ALT increased persistently, and they were all significantly lower than those of the burn group till to the time point of 12 hours (ALT:51.2±7.0 U/L vs. 104.8±7.4 U/L, Cr:42.7±5.4 μmol/L vs. 88.5±4.8 μmol/L, BUN:4.9±1.2 mmol/L vs. 14.7±1.4 mmol/L, CK-MB:564.0±39.1 U/L vs. 734.0±35.9 U/L, all P<0.05). At the end of 24-hours-period experiment, the survival rate of the PNU group was 50% (3/6) and significantly higher than that of the burn group 0(0/6).

Conclusions: The results indicated that PNU282987 decrease the levels of inflammatory cytokine, improve the organ functions and increase 24-hour survival rate in dogs with lethal burn injury. And PNU282987 may have potential clinical application.

目的:探讨α7烟碱乙酰胆碱受体激动剂(α7nAChR) PNU282987对致死性烧伤休克犬器官功能及存活率的影响。方法:将12只成年雄性Beagle犬进行50%体表面积(TBSA)全层火焰损伤,随机分为烧伤组和PNU282987组(PNU组),每组n=6。PNU组给予PNU282987 (0.38 mg/kg,静脉泵送),烧伤组给予等量生理盐水溶液作为对照组。连续测定烧伤前及烧伤后0.5、2、4、8、12、24 h的平均动脉压(MAP)和血浆肿瘤坏死因子-α (TNF-α)、丙氨酸转氨酶(ALT)、肌酸激酶MB同工酶(CK-MB)、肌酐(Cr)、血尿素氮(BUN)水平。上述所有测量均在有意识和合作状态下进行。24小时试验结束时,记录成活率。结果:与伤前基线数据相比,烧伤后MAP显著降低。烧伤后4 h, PNU组MAP水平显著高于烧伤组,24 h时恢复到基线水平的83.6%。而烧伤组则随时间逐渐减少,直至死亡。PNU组损伤后各时间点血浆TNF-α水平均显著低于烧伤组。烧伤组ALT、Cr、BUN、CK-MB持续升高,PNU组除ALT持续升高外先升高后降低,且至12 h均显著低于烧伤组(ALT:51.2±7.0 U/L vs. 104.8±7.4 U/L, Cr:42.7±5.4 μmol/L vs. 88.5±4.8 μmol/L, BUN:4.9±1.2 mmol/L vs. 14.7±1.4 mmol/L, CK-MB:564.0±39.1 U/L vs. 734.0±35.9 U/L)。结果表明,PNU282987可降低致死性烧伤犬炎性细胞因子水平,改善脏器功能,提高24小时存活率。PNU282987具有潜在的临床应用价值。
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引用次数: 0
[Clinical observation of the role of Chenxia Sijunzi decoction in promoting the recovery of gastrointestinal function in critically ill patients]. [晨霞四君子汤促进危重患者胃肠功能恢复的临床观察]。
Jian-hong Guo, Gai Chen, Sheng-quan Yang, Mao-hua Wei, Xiao Chen

Objective: To observe the clinical effects of Chenxia Sijunzi decoction on promoting gastrointestinal function recovery in severe patients.

Methods: A prospective randomized controlled study was conducted. Eighty severe patients feeding with enteral nutrition from September 2011 to March 2012 were divided into three groups according to the method of random number table. The traditional Chinese medicine group and western medicine group were consisted of 35 cases respectively, and 10 cases were control group. Control group was routine symptomatically treated without any medicines for promoting gastrointestinal power function, helping the lower extremities to move and enhancing the turn over, letting the gastrointestinal function recover by its self. Chinese medicine group was tube fed with Chenxia Sijunzi decoction on the basis of control group, western medicine group was tube fed with the multienzyme tablets and mosapride dispersible tablets on the basis of control group. Then the differences in bowel sound recovery time and the time for passage of gas by anus and the bowel movement time and length of stay in hospitals within three groups were observed.

Results: The time of bowel sound recovery (41.02±7.52 hours, 44.02±6.23 hours), gas passage time by anus (49.90±6.95 hours, 51.32±5.12 hours) and the bowel movement time (58.22±6.71 hours, 60.91±3.72 hours) in both traditional Chinese medicine and the western medicine group were significantly reduced compared with the control group (54.62±5.51 hours, 64.68±9.47 hours, 78.20±7.11 hours, all P<0.01), and the days in hospital (5.1±1.7 days, 5.0±1.5 days) were shortened significantly compared with the control group (8.9±1.4 days, both P<0.01). However, results did not demonstrate any significant differences in each testing index between traditional Chinese medicine and western medicine group (all P>0.05).

Conclusion: Chenxia Sijunzi decoction can promote severe patient's gastrointestinal function recovery and reduce hospitalization days.

目的:观察陈夏四君子汤促进重症患者胃肠功能恢复的临床疗效。方法:采用前瞻性随机对照研究。采用随机数字表法将2011年9月至2012年3月80例经肠内营养喂养的重症患者分为3组。中药组35例,西药组10例为对照组。对照组常规对症治疗,不加任何促进胃肠动力功能、帮助下肢活动、增强翻身等药物,使胃肠功能自行恢复。中药组在对照组基础上灌胃晨霞四君子汤,西药组在对照组基础上灌胃多酶片和莫沙必利分散片。然后观察三组患者肠声恢复时间、肛门通气时间、排便时间和住院时间的差异。结果:中药组和西药组患儿的肠声恢复时间(41.02±7.52 h, 44.02±6.23 h)、肛门通气时间(49.90±6.95 h, 51.32±5.12 h)、排便时间(58.22±6.71 h, 60.91±3.72 h)均显著低于对照组(54.62±5.51 h, 64.68±9.47 h, 78.20±7.11 h,均p < 0.05)。结论:晨霞四君子汤能促进重症患者胃肠功能恢复,缩短住院天数。
{"title":"[Clinical observation of the role of Chenxia Sijunzi decoction in promoting the recovery of gastrointestinal function in critically ill patients].","authors":"Jian-hong Guo,&nbsp;Gai Chen,&nbsp;Sheng-quan Yang,&nbsp;Mao-hua Wei,&nbsp;Xiao Chen","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Objective: </strong>To observe the clinical effects of Chenxia Sijunzi decoction on promoting gastrointestinal function recovery in severe patients.</p><p><strong>Methods: </strong>A prospective randomized controlled study was conducted. Eighty severe patients feeding with enteral nutrition from September 2011 to March 2012 were divided into three groups according to the method of random number table. The traditional Chinese medicine group and western medicine group were consisted of 35 cases respectively, and 10 cases were control group. Control group was routine symptomatically treated without any medicines for promoting gastrointestinal power function, helping the lower extremities to move and enhancing the turn over, letting the gastrointestinal function recover by its self. Chinese medicine group was tube fed with Chenxia Sijunzi decoction on the basis of control group, western medicine group was tube fed with the multienzyme tablets and mosapride dispersible tablets on the basis of control group. Then the differences in bowel sound recovery time and the time for passage of gas by anus and the bowel movement time and length of stay in hospitals within three groups were observed.</p><p><strong>Results: </strong>The time of bowel sound recovery (41.02±7.52 hours, 44.02±6.23 hours), gas passage time by anus (49.90±6.95 hours, 51.32±5.12 hours) and the bowel movement time (58.22±6.71 hours, 60.91±3.72 hours) in both traditional Chinese medicine and the western medicine group were significantly reduced compared with the control group (54.62±5.51 hours, 64.68±9.47 hours, 78.20±7.11 hours, all P<0.01), and the days in hospital (5.1±1.7 days, 5.0±1.5 days) were shortened significantly compared with the control group (8.9±1.4 days, both P<0.01). However, results did not demonstrate any significant differences in each testing index between traditional Chinese medicine and western medicine group (all P>0.05).</p><p><strong>Conclusion: </strong>Chenxia Sijunzi decoction can promote severe patient's gastrointestinal function recovery and reduce hospitalization days.</p>","PeriodicalId":23992,"journal":{"name":"Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue","volume":"24 11","pages":"674-6"},"PeriodicalIF":0.0,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31030189","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Analysis on the clinical pulmonary infection score on the detection of multidrug resistance organisms in lower respiratory tract in ventilated patients in intensive care unit]. [重症监护病房通气患者下呼吸道多药耐药菌检测临床肺部感染评分分析]。
Huan Liu

Objective: To investigate the characteristics of multidrug resistance (MDR) organisms from the lower respiratory tract in ventilated patients, and the constitution, detection time and mortality of the intensive care unit (ICU) patients with different clinical pulmonary infection scores (CPIS).

Methods: A retrospective study was conducted. The clinical data of 72 cases with lower respiratory tract MDR on ventilation more than 48 hours were collected from April 2010 to December 2011. CPIS were calculated at the same time. Thirty-three patients with CPIS>6 were diagnosed as ventilation associated pneumonia (VAP), while 39 having CPIS ≤6 (non-VAP). The characteristics of MDR, the detection time and mortality of the patients were compared between the two groups.

Results: The first five MDR were Baumannii [49.5%(34/74)], Klebsiella pneumoniae [24.3%(18/74)], Escherichia coli [20.3%(15/74)], Pseudomonas aeruginosa [5.4%(4/74)] and Methicillin-resistant Staphylococcus aureus [MRSA, 4.1%(3/74)] in VAP group, while the first five were Escherichia coli [40.2%(37/92)], Pseudomonas aeruginosa [33.7%(31/92)], Klebsiella pneumoniae [13.1%(12/92)], Baumannii [8.7%(8/92)] and MRSA [4.3%(4/92)] in non-VAP group. There was no significant difference in average detection time between VAP group and non-VAP group (10.7±1.5 days vs. 9.4±1.8 days, P>0.05). The mortality rate in VAP group was significantly higher than that in non-VAP group (39.4% vs. 23.1%, P<0.05).

Conclusions: Different MDR may be detected in lower respiratory tracts no matter the ventilated patients having VAP or not, which influence the patients prognosis and should be monitored intensively. Antibiotics should be empirically prescribed and adjusted dynamically.

目的:探讨通气患者下呼吸道多药耐药(MDR)菌的特点,以及不同临床肺部感染评分(CPIS)重症监护病房(ICU)患者的体质、检出时间和死亡率。方法:回顾性研究。收集2010年4月至2011年12月通气超过48 h的72例下呼吸道MDR患者的临床资料。同时计算cpi。CPIS>6的33例诊断为通气相关性肺炎(VAP), CPIS≤6(非VAP)的39例诊断为通气相关性肺炎。比较两组患者的耐多药特点、检测时间及病死率。结果:VAP组MDR前5位分别为鲍曼尼菌[49.5%(34/74)]、肺炎克雷伯菌[24.3%(18/74)]、大肠埃希菌[20.3%(15/74)]、铜绿假单胞菌[5.4%(4/74)]和耐甲氧西林金黄色葡萄球菌[MRSA, 4.1%(3/74)],非VAP组MDR前5位分别为大肠埃希菌[40.2%(37/92)]、铜绿假单胞菌[33.7%(31/92)]、肺炎克雷伯菌[13.1%(12/92)]、鲍曼尼菌[8.7%(8/92)]和MRSA[4.3%(4/92)]。VAP组与非VAP组的平均检测时间(10.7±1.5 d∶9.4±1.8 d, P>0.05)差异无统计学意义。VAP组的死亡率明显高于非VAP组(39.4% vs. 23.1%)。结论:通气患者下呼吸道有无VAP均存在不同程度的MDR,影响患者预后,应加强监测。抗生素应经验性处方并动态调整。
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引用次数: 0
[Neonatal rat cerebral cortical neurons culture method]. [新生大鼠大脑皮层神经元培养方法]。
Na Yao, Di-fen Wang, Xi Song, Xian-lin Liu
{"title":"[Neonatal rat cerebral cortical neurons culture method].","authors":"Na Yao,&nbsp;Di-fen Wang,&nbsp;Xi Song,&nbsp;Xian-lin Liu","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":23992,"journal":{"name":"Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue","volume":"24 11","pages":"685-6"},"PeriodicalIF":0.0,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31030193","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[The relationship between the level of N-terminal pro-B-type natriuretic peptide and prognosis in patients with sepsis]. 脓毒症患者n端前b型利钠肽水平与预后的关系。
Pub Date : 2012-11-01 DOI: 10.3760/CMA.J.ISSN.1003-0603.2012.11.007
Jian Liu, Hong-Xia Wang, K. Men
OBJECTIVETo detect the relationship between the level of N-terminal pro-B-type natriuretic peptide (NT-proBNP) and prognosis in patients with sepsis.METHODSA prospective controlled study was conducted. Sixty cases, including 39 sepsis and 21 severe sepsis, were enrolled from May 2010 to October 2011 in intensive care unit (ICU) of Second Hospital of Tianjin Medical University. The serum level of NT-proBNP was determined and acute physiology and chronic health evaluation II (APACHEII) score was calculated on the 1st and 3rd day. The receiver operator characteristic curve (ROC curve) was draw. According to the 28-day prognosis, all patients were divided into the survival group (n=42) or the death group (n=18). At the same time 30 healthy people were enrolled as control group.RESULTSThe level of NT-proBNP in the sepsis patients on the 1st and 3rd day were significantly higher than those of healthy controls (65.77±34.78 ng/L, 74.23±42.12 ng/L vs. 48.36±35.53 ng/L, P<0.05 and P<0.01). The level on 1st day of the severe sepsis group was higher than sepsis group (71.69±32.86 ng/L vs. 50.11±36. 98 ng/L, P<0.05), but there was no statistically significance on the 3rd day. The level of NT-proBNP in death group was increased gradually and significantly higher than that of survival group on the 3rd days (99.20±44.34 ng/L vs. 66.79±39.28 ng/L, P<0.05), but no difference was found on the 1st day. The APACHEII score of severe sepsis group were much higher than those of sepsis group on the 1st and 3rd day (1st day:23.92±7.57 vs. 14.87±6.50, 3rd day:19.28±8.80 vs. 10.43±7.27, both P<0.01). The APACHEII score of death group were also much higher than those of survival group on the 1st and 3rd day (1st day:26.71±6.72 vs. 18.83±7.84, 3rd day:31.11±5.06 vs. 13.80±7.27, both P<0.01). The cut point for the evaluation of sepsis prognosis were NT-proBNP≥63.5 ng/L and APACHEII score≥20, which sensitivity were 65.4% and 88.5%, and specificity were 62.5% and 69.4% respectively.CONCLUSIONSerum NT-proBNP levels elevation imply the poor prognosis in patients with sepsis.
目的探讨脓毒症患者n端前b型利钠肽(NT-proBNP)水平与预后的关系。方法采用前瞻性对照研究。选取2010年5月至2011年10月在天津医科大学第二医院重症监护室(ICU)收治的60例患者,其中脓毒症39例,严重脓毒症21例。测定血清NT-proBNP水平,并于第1天和第3天计算急性生理和慢性健康评估II (APACHEII)评分。绘制受试者操作者特征曲线(ROC曲线)。根据28天预后将所有患者分为生存组(n=42)和死亡组(n=18)。同时选取30名健康人作为对照组。结果脓毒症患者第1、3天NT-proBNP水平均显著高于健康对照组(65.77±34.78 ng/L、74.23±42.12 ng/L、48.36±35.53 ng/L, P<0.05、P<0.01)。严重脓毒症组第1天血药浓度高于脓毒症组(71.69±32.86 ng/L∶50.11±36 ng/L)。98 ng/L, P<0.05),但在第3天无统计学意义。死亡组NT-proBNP水平逐渐升高,第3天显著高于生存组(99.20±44.34 ng/L vs. 66.79±39.28 ng/L, P<0.05),第1天差异无统计学意义。严重脓毒症组APACHEII评分在第1天、第3天明显高于脓毒症组(第1天:23.92±7.57比14.87±6.50,第3天:19.28±8.80比10.43±7.27,P均<0.01)。死亡组APACHEII评分在第1天、第3天明显高于生存组(第1天:26.71±6.72比18.83±7.84,第3天:31.11±5.06比13.80±7.27,P均<0.01)。评价脓毒症预后的切入点为NT-proBNP≥63.5 ng/L, APACHEII评分≥20,敏感性分别为65.4%和88.5%,特异性分别为62.5%和69.4%。结论血清NT-proBNP水平升高提示脓毒症患者预后不良。
{"title":"[The relationship between the level of N-terminal pro-B-type natriuretic peptide and prognosis in patients with sepsis].","authors":"Jian Liu, Hong-Xia Wang, K. Men","doi":"10.3760/CMA.J.ISSN.1003-0603.2012.11.007","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1003-0603.2012.11.007","url":null,"abstract":"OBJECTIVE\u0000To detect the relationship between the level of N-terminal pro-B-type natriuretic peptide (NT-proBNP) and prognosis in patients with sepsis.\u0000\u0000\u0000METHODS\u0000A prospective controlled study was conducted. Sixty cases, including 39 sepsis and 21 severe sepsis, were enrolled from May 2010 to October 2011 in intensive care unit (ICU) of Second Hospital of Tianjin Medical University. The serum level of NT-proBNP was determined and acute physiology and chronic health evaluation II (APACHEII) score was calculated on the 1st and 3rd day. The receiver operator characteristic curve (ROC curve) was draw. According to the 28-day prognosis, all patients were divided into the survival group (n=42) or the death group (n=18). At the same time 30 healthy people were enrolled as control group.\u0000\u0000\u0000RESULTS\u0000The level of NT-proBNP in the sepsis patients on the 1st and 3rd day were significantly higher than those of healthy controls (65.77±34.78 ng/L, 74.23±42.12 ng/L vs. 48.36±35.53 ng/L, P<0.05 and P<0.01). The level on 1st day of the severe sepsis group was higher than sepsis group (71.69±32.86 ng/L vs. 50.11±36. 98 ng/L, P<0.05), but there was no statistically significance on the 3rd day. The level of NT-proBNP in death group was increased gradually and significantly higher than that of survival group on the 3rd days (99.20±44.34 ng/L vs. 66.79±39.28 ng/L, P<0.05), but no difference was found on the 1st day. The APACHEII score of severe sepsis group were much higher than those of sepsis group on the 1st and 3rd day (1st day:23.92±7.57 vs. 14.87±6.50, 3rd day:19.28±8.80 vs. 10.43±7.27, both P<0.01). The APACHEII score of death group were also much higher than those of survival group on the 1st and 3rd day (1st day:26.71±6.72 vs. 18.83±7.84, 3rd day:31.11±5.06 vs. 13.80±7.27, both P<0.01). The cut point for the evaluation of sepsis prognosis were NT-proBNP≥63.5 ng/L and APACHEII score≥20, which sensitivity were 65.4% and 88.5%, and specificity were 62.5% and 69.4% respectively.\u0000\u0000\u0000CONCLUSION\u0000Serum NT-proBNP levels elevation imply the poor prognosis in patients with sepsis.","PeriodicalId":23992,"journal":{"name":"Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue","volume":"36 1","pages":"662-4"},"PeriodicalIF":0.0,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73365691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[The relationship between the level of N-terminal pro-B-type natriuretic peptide and prognosis in patients with sepsis]. 脓毒症患者n端前b型利钠肽水平与预后的关系。
Jian Liu, Hong-xia Wang, Kun Men

Objective: To detect the relationship between the level of N-terminal pro-B-type natriuretic peptide (NT-proBNP) and prognosis in patients with sepsis.

Methods: A prospective controlled study was conducted. Sixty cases, including 39 sepsis and 21 severe sepsis, were enrolled from May 2010 to October 2011 in intensive care unit (ICU) of Second Hospital of Tianjin Medical University. The serum level of NT-proBNP was determined and acute physiology and chronic health evaluation II (APACHEII) score was calculated on the 1st and 3rd day. The receiver operator characteristic curve (ROC curve) was draw. According to the 28-day prognosis, all patients were divided into the survival group (n=42) or the death group (n=18). At the same time 30 healthy people were enrolled as control group.

Results: The level of NT-proBNP in the sepsis patients on the 1st and 3rd day were significantly higher than those of healthy controls (65.77±34.78 ng/L, 74.23±42.12 ng/L vs. 48.36±35.53 ng/L, P<0.05 and P<0.01). The level on 1st day of the severe sepsis group was higher than sepsis group (71.69±32.86 ng/L vs. 50.11±36. 98 ng/L, P<0.05), but there was no statistically significance on the 3rd day. The level of NT-proBNP in death group was increased gradually and significantly higher than that of survival group on the 3rd days (99.20±44.34 ng/L vs. 66.79±39.28 ng/L, P<0.05), but no difference was found on the 1st day. The APACHEII score of severe sepsis group were much higher than those of sepsis group on the 1st and 3rd day (1st day:23.92±7.57 vs. 14.87±6.50, 3rd day:19.28±8.80 vs. 10.43±7.27, both P<0.01). The APACHEII score of death group were also much higher than those of survival group on the 1st and 3rd day (1st day:26.71±6.72 vs. 18.83±7.84, 3rd day:31.11±5.06 vs. 13.80±7.27, both P<0.01). The cut point for the evaluation of sepsis prognosis were NT-proBNP≥63.5 ng/L and APACHEII score≥20, which sensitivity were 65.4% and 88.5%, and specificity were 62.5% and 69.4% respectively.

Conclusion: Serum NT-proBNP levels elevation imply the poor prognosis in patients with sepsis.

目的:探讨脓毒症患者n端前b型利钠肽(NT-proBNP)水平与预后的关系。方法:采用前瞻性对照研究。选取2010年5月至2011年10月在天津医科大学第二医院重症监护室(ICU)收治的60例患者,其中脓毒症39例,严重脓毒症21例。测定血清NT-proBNP水平,并于第1天和第3天计算急性生理和慢性健康评估II (APACHEII)评分。绘制受试者操作者特征曲线(ROC曲线)。根据28天预后将所有患者分为生存组(n=42)和死亡组(n=18)。同时选取30名健康人作为对照组。结果:脓毒症患者血清NT-proBNP水平在第1、3天显著高于健康对照组(65.77±34.78 ng/L, 74.23±42.12 ng/L vs 48.36±35.53 ng/L)。结论:血清NT-proBNP水平升高提示脓毒症患者预后较差。
{"title":"[The relationship between the level of N-terminal pro-B-type natriuretic peptide and prognosis in patients with sepsis].","authors":"Jian Liu,&nbsp;Hong-xia Wang,&nbsp;Kun Men","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Objective: </strong>To detect the relationship between the level of N-terminal pro-B-type natriuretic peptide (NT-proBNP) and prognosis in patients with sepsis.</p><p><strong>Methods: </strong>A prospective controlled study was conducted. Sixty cases, including 39 sepsis and 21 severe sepsis, were enrolled from May 2010 to October 2011 in intensive care unit (ICU) of Second Hospital of Tianjin Medical University. The serum level of NT-proBNP was determined and acute physiology and chronic health evaluation II (APACHEII) score was calculated on the 1st and 3rd day. The receiver operator characteristic curve (ROC curve) was draw. According to the 28-day prognosis, all patients were divided into the survival group (n=42) or the death group (n=18). At the same time 30 healthy people were enrolled as control group.</p><p><strong>Results: </strong>The level of NT-proBNP in the sepsis patients on the 1st and 3rd day were significantly higher than those of healthy controls (65.77±34.78 ng/L, 74.23±42.12 ng/L vs. 48.36±35.53 ng/L, P<0.05 and P<0.01). The level on 1st day of the severe sepsis group was higher than sepsis group (71.69±32.86 ng/L vs. 50.11±36. 98 ng/L, P<0.05), but there was no statistically significance on the 3rd day. The level of NT-proBNP in death group was increased gradually and significantly higher than that of survival group on the 3rd days (99.20±44.34 ng/L vs. 66.79±39.28 ng/L, P<0.05), but no difference was found on the 1st day. The APACHEII score of severe sepsis group were much higher than those of sepsis group on the 1st and 3rd day (1st day:23.92±7.57 vs. 14.87±6.50, 3rd day:19.28±8.80 vs. 10.43±7.27, both P<0.01). The APACHEII score of death group were also much higher than those of survival group on the 1st and 3rd day (1st day:26.71±6.72 vs. 18.83±7.84, 3rd day:31.11±5.06 vs. 13.80±7.27, both P<0.01). The cut point for the evaluation of sepsis prognosis were NT-proBNP≥63.5 ng/L and APACHEII score≥20, which sensitivity were 65.4% and 88.5%, and specificity were 62.5% and 69.4% respectively.</p><p><strong>Conclusion: </strong>Serum NT-proBNP levels elevation imply the poor prognosis in patients with sepsis.</p>","PeriodicalId":23992,"journal":{"name":"Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue","volume":"24 11","pages":"662-4"},"PeriodicalIF":0.0,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31031324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Analysis on the clinical pulmonary infection score on the detection of multidrug resistance organisms in lower respiratory tract in ventilated patients in intensive care unit]. [重症监护病房通气患者下呼吸道多药耐药菌检测临床肺部感染评分分析]。
Pub Date : 2012-11-01 DOI: 10.3760/CMA.J.ISSN.1003-0603.2012.11.013
Huan Liu
OBJECTIVETo investigate the characteristics of multidrug resistance (MDR) organisms from the lower respiratory tract in ventilated patients, and the constitution, detection time and mortality of the intensive care unit (ICU) patients with different clinical pulmonary infection scores (CPIS).METHODSA retrospective study was conducted. The clinical data of 72 cases with lower respiratory tract MDR on ventilation more than 48 hours were collected from April 2010 to December 2011. CPIS were calculated at the same time. Thirty-three patients with CPIS>6 were diagnosed as ventilation associated pneumonia (VAP), while 39 having CPIS ≤6 (non-VAP). The characteristics of MDR, the detection time and mortality of the patients were compared between the two groups.RESULTSThe first five MDR were Baumannii [49.5%(34/74)], Klebsiella pneumoniae [24.3%(18/74)], Escherichia coli [20.3%(15/74)], Pseudomonas aeruginosa [5.4%(4/74)] and Methicillin-resistant Staphylococcus aureus [MRSA, 4.1%(3/74)] in VAP group, while the first five were Escherichia coli [40.2%(37/92)], Pseudomonas aeruginosa [33.7%(31/92)], Klebsiella pneumoniae [13.1%(12/92)], Baumannii [8.7%(8/92)] and MRSA [4.3%(4/92)] in non-VAP group. There was no significant difference in average detection time between VAP group and non-VAP group (10.7±1.5 days vs. 9.4±1.8 days, P>0.05). The mortality rate in VAP group was significantly higher than that in non-VAP group (39.4% vs. 23.1%, P<0.05).CONCLUSIONSDifferent MDR may be detected in lower respiratory tracts no matter the ventilated patients having VAP or not, which influence the patients prognosis and should be monitored intensively. Antibiotics should be empirically prescribed and adjusted dynamically.
目的探讨不同临床肺部感染评分(CPIS)的重症监护病房(ICU)患者下呼吸道多药耐药(MDR)菌的特点及体质、发现时间和死亡率。方法采用回顾性研究。收集2010年4月至2011年12月通气超过48 h的72例下呼吸道MDR患者的临床资料。同时计算cpi。CPIS>6的33例诊断为通气相关性肺炎(VAP), CPIS≤6(非VAP)的39例诊断为通气相关性肺炎。比较两组患者的耐多药特点、检测时间及病死率。结果VAP组MDR前5位分别为鲍曼尼菌[49.5%(34/74)]、肺炎克雷伯菌[24.3%(18/74)]、大肠埃希菌[20.3%(15/74)]、铜绿假单胞菌[5.4%(4/74)]和耐甲氧西林金黄色葡萄球菌[MRSA, 4.1%(3/74)],非VAP组MDR前5位分别为大肠埃希菌[40.2%(37/92)]、铜绿假单胞菌[33.7%(31/92)]、肺炎克雷伯菌[13.1%(12/92)]、鲍曼尼菌[8.7%(8/92)]和MRSA[4.3%(4/92)]。VAP组与非VAP组的平均检测时间(10.7±1.5 d∶9.4±1.8 d, P>0.05)差异无统计学意义。VAP组病死率明显高于非VAP组(39.4% vs. 23.1%, P<0.05)。结论通气患者下呼吸道有无VAP均可出现不同程度的多药耐药,影响患者预后,应加强监测。抗生素应经验性处方并动态调整。
{"title":"[Analysis on the clinical pulmonary infection score on the detection of multidrug resistance organisms in lower respiratory tract in ventilated patients in intensive care unit].","authors":"Huan Liu","doi":"10.3760/CMA.J.ISSN.1003-0603.2012.11.013","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1003-0603.2012.11.013","url":null,"abstract":"OBJECTIVE\u0000To investigate the characteristics of multidrug resistance (MDR) organisms from the lower respiratory tract in ventilated patients, and the constitution, detection time and mortality of the intensive care unit (ICU) patients with different clinical pulmonary infection scores (CPIS).\u0000\u0000\u0000METHODS\u0000A retrospective study was conducted. The clinical data of 72 cases with lower respiratory tract MDR on ventilation more than 48 hours were collected from April 2010 to December 2011. CPIS were calculated at the same time. Thirty-three patients with CPIS>6 were diagnosed as ventilation associated pneumonia (VAP), while 39 having CPIS ≤6 (non-VAP). The characteristics of MDR, the detection time and mortality of the patients were compared between the two groups.\u0000\u0000\u0000RESULTS\u0000The first five MDR were Baumannii [49.5%(34/74)], Klebsiella pneumoniae [24.3%(18/74)], Escherichia coli [20.3%(15/74)], Pseudomonas aeruginosa [5.4%(4/74)] and Methicillin-resistant Staphylococcus aureus [MRSA, 4.1%(3/74)] in VAP group, while the first five were Escherichia coli [40.2%(37/92)], Pseudomonas aeruginosa [33.7%(31/92)], Klebsiella pneumoniae [13.1%(12/92)], Baumannii [8.7%(8/92)] and MRSA [4.3%(4/92)] in non-VAP group. There was no significant difference in average detection time between VAP group and non-VAP group (10.7±1.5 days vs. 9.4±1.8 days, P>0.05). The mortality rate in VAP group was significantly higher than that in non-VAP group (39.4% vs. 23.1%, P<0.05).\u0000\u0000\u0000CONCLUSIONS\u0000Different MDR may be detected in lower respiratory tracts no matter the ventilated patients having VAP or not, which influence the patients prognosis and should be monitored intensively. Antibiotics should be empirically prescribed and adjusted dynamically.","PeriodicalId":23992,"journal":{"name":"Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue","volume":"12 1","pages":"680-2"},"PeriodicalIF":0.0,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88212310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Effect of ulinastatin in traumatic brain injury with multiple injuries]. [乌司他丁治疗创伤性脑损伤合并多发伤的疗效]。
Pub Date : 2012-11-01 DOI: 10.3760/CMA.J.ISSN.1003-0603.2012.11.012
Y. Tu, Yun-feng Diao, Xiping Yang, HongTao Sun, Sai Zhang
OBJECTIVETo investigate the effect of ulinastatin (UTI) in traumatic brain injury (TBI) with multiple injuries.METHODSA prospective analysis of TBI patients with multiple injuries was performed. Sixty cases of cranial trauma with multiple injuries patients were randomly divided into two groups. There were 28 cases in control group while 32 cases in treatment group. Control group underwent conventional treatment while intravenous infusion of UTI was performed in treatment group. The dose of UTI was 200 kU every 8 hours. Patients' intracranial cerebral pressure (ICP) were monitored at admission and 10 days after treatment. At the same time levels of white blood cell (WBC), C-reactive protein (CRP), procalcitonin (PCT), alanine aminotransferase (ALT), aspartate amino transfer enzymes (AST), creatinine (Cr), blood urea nitrogen (BUN), tumor necrosis factor-α (TNF-α), interleukin (IL-2, IL-6) were detected.RESULTSICP was down trend after treatment in UTI group, but there was no statistical difference compared with the control group. Hepatic and renal function and inflammation factor levels were significantly decreased in both groups. WBC, CRP, PCT, ALT, AST, Cr, BUN, TNF-α, IL-2, IL-6 were significantly lower in UTI group than those in control group (WBC:12.3±4.5×10(9)/L vs. 15.9±6.3×10(9)/L, CRP:46.12±11.47 mg/L vs. 64.24±18.31 mg/L, PCT:4.51±1.27 μg/L vs. 10.51±4.27 μg/L, ALT:47.26±8.23 U/L vs. 60.94±8.39 U/L, AST:42.67±7.63 U/L vs. 68.51±10.17 U/L, Cr:79.62±15.36 μmol/L vs. 102.36±16.82 μmol/L, BUN:6.35±2.36 mmol/L vs. 8.39±1.67 mmol/L, TNF-α:93.6±31.5 μg/L vs. 195.8±23.9 μg/L, IL-2:12.3±4.5 μg/L vs. 15.9±6.3 μg/L, IL-6:52.36±12.46 μg/L vs. 69.34±26.13 μg/L, all P<0.05). The incidence of systemic inflammatory response syndrome (SIRS) and multiple organ dysfunction syndrome (MODS) in UTI group were significantly lower than those in control group (21.88% vs. 46.43%, 9.38% vs. 28.57%, both P<0.05).CONCLUSIONApplication of UTI treatment in TBI with multiple trauma patients can potentially protect the brain, liver and other organ function, thus significantly reduce incidence rate of SIRS and MODS by reducing the release of inflammatory mediators and systemic reaction to the trauma invasion.
目的探讨乌司他丁(ulinastatin, UTI)治疗多发创伤性脑损伤的疗效。方法对多发损伤的TBI患者进行前瞻性分析。将60例颅脑外伤合并多发伤患者随机分为两组。对照组28例,治疗组32例。对照组给予常规治疗,治疗组给予尿路感染静脉滴注。尿路感染剂量为200 kU / 8 h。入院时及治疗后10 d监测患者颅内压(ICP)。同时检测白细胞(WBC)、c反应蛋白(CRP)、降钙素原(PCT)、丙氨酸转氨酶(ALT)、天冬氨酸氨基转移酶(AST)、肌酐(Cr)、血尿素氮(BUN)、肿瘤坏死因子-α (TNF-α)、白细胞介素(IL-2、IL-6)水平。结果UTI组治疗后icp有下降趋势,但与对照组比较差异无统计学意义。两组患者肝肾功能及炎症因子水平均显著降低。WBC、CRP、PCT、ALT、AST Cr、包子,TNF -α,2、il - 6在泌尿道感染组比对照组显著降低(白细胞:12.3±4.5×10 (9)/ L和15.9±6.3×10 (9)/ L, c反应蛋白:46.12±11.47 mg / L和64.24±18.31 mg / L, PCT: 4.51±1.27μg / L和10.51±4.27μg / L, ALT: 47.26±8.23 U / L和60.94±8.39 U / L, AST: 42.67±7.63 U / L和68.51±10.17 U / L, Cr: 79.62±15.36μmol / L和102.36±16.82μmol / L,包:6.35±2.36更易/ L和8.39±1.67更易/ L, TNF -α:93.6±31.5μg / L和195.8±23.9μg / L, IL-2:12.3±4.5μg / L和15.9±6.3μg / L,IL-6:52.36±12.46μg / L和69.34±26.13μg / L,所有P < 0.05)。UTI组全身炎症反应综合征(SIRS)和多器官功能障碍综合征(MODS)发生率显著低于对照组(21.88%比46.43%,9.38%比28.57%,P均<0.05)。结论应用UTI治疗多发创伤TBI患者,可潜在地保护脑、肝等脏器功能,通过减少炎症介质的释放和对创伤侵袭的全身反应,显著降低SIRS和MODS的发生率。
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引用次数: 3
[Plasma D-dimer changes and prognostic implication in severe acute pancreatitis]. [重症急性胰腺炎患者血浆d -二聚体变化及其预后意义]。
Pub Date : 2012-11-01 DOI: 10.3760/CMA.J.ISSN.1003-0603.2012.11.006
Hong-jun Wu, Rongqing Li, Yi Li, Xue-zhong Yu
OBJECTIVETo study the role of plasma D-dimer in human severe acute pancreatitis (SAP) and its relationship with disease severity.METHODSA prospective study was performed. From February 2010 to June 2011, plasma concentration of D-dimer and the results of other routine laboratory tests were measured in 32 SAP inpatients at admission immediately and 24, 48, 72 hours after admission. Ranson scores were also recorded. The relationship between plasma concentration of D-dimer and the results of other routine laboratory tests, Ranson scores were analyzed, and so did the relationship between plasma concentration of D-dimer and severity of patient's condition.RESULTS(1) There were no obvious changes for plasma concentration of D-dimer and the results of other routine laboratory index in 32 SAP inpatients at each time points after admission. (2) Plasma concentration of D-dimer of SAP was positively related to white blood count (WBC), creatinine (Cr), prothrombin time (PT) and activated partial thromboplastin time (APTT) and negatively related to hematocrit (Hct), albumin and calcium (P<0.05 or P<0.01). Plasma concentration of D-dimer of SAP at 48 hours after admission had positive relationship with Ranson scores (r=0.729, P=0.001). (3) Plasma concentration of D-dimer of SAP inpatients in CT grade D, E stage were significantly higher than that in CT grade B, C stage (1.18±0.02 mg/L, 1.23±0.01 mg/L vs. 0.90±0.02 mg/L, 0.93±0.01 mg/L, all P<0.05). (4) Plasma concentration of D-dimer of SAP in inpatients with multiple organ failure (MOF) at 24 hours and 48 hours were significantly higher than that in inpatients without MOF (24 hours: 1.26±0.02 mg/L vs. 0.93±0.02 mg/L, 48 hours:1.25±0.02 mg/L vs. 0.93±0.02 mg/L, both P<0.05).CONCLUSIONPlasma concentration of the D-dimer is significantly increased in SAP patients, and is related to the severity. The first plasma concentration of D-dimer of SAP after admission can well reflect severity of patient's condition.
目的探讨血浆d -二聚体在重症急性胰腺炎(SAP)中的作用及其与病情严重程度的关系。方法采用前瞻性研究。2010年2月至2011年6月,测定32例SAP住院患者入院时及入院后24、48、72 h血浆d -二聚体浓度及其他常规实验室检查结果。Ranson评分也被记录下来。分析血浆d -二聚体浓度与其他常规实验室检查结果、Ranson评分的关系以及血浆d -二聚体浓度与患者病情严重程度的关系。结果(1)32例SAP住院患者入院后各时间点血浆d -二聚体浓度及其他常规实验室指标均无明显变化。(2) SAP血浆d -二聚体浓度与白细胞计数(WBC)、肌酐(Cr)、凝血酶原时间(PT)、活化部分凝血活素时间(APTT)呈正相关,与血细胞比容(Hct)、白蛋白、钙呈负相关(P<0.05或P<0.01)。入院后48 h血浆SAP d -二聚体浓度与Ranson评分呈正相关(r=0.729, P=0.001)。(3) SAP患者CT分级D、E期血浆D-二聚体浓度显著高于CT分级B、C期(1.18±0.02 mg/L、1.23±0.01 mg/L vs. 0.90±0.02 mg/L、0.93±0.01 mg/L, P均<0.05)。(4)住院多器官功能衰竭患者24小时、48小时血浆SAP d -二聚体浓度显著高于非多器官功能衰竭患者(24小时:1.26±0.02 mg/L vs. 0.93±0.02 mg/L, 48小时:1.25±0.02 mg/L vs. 0.93±0.02 mg/L, P均<0.05)。结论SAP患者血浆d -二聚体浓度明显升高,且与病情严重程度相关。入院后第一次血浆SAP d -二聚体浓度可以很好地反映患者病情的严重程度。
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引用次数: 2
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Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue
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