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1.
目的:探讨G6PD缺陷引起新生儿胆红素脑病的诊疗规律.方法:回顾2006年6月至2008年5月收治12例G6PD缺陷引起新生儿胆红素脑病临床资料.结果:男11例,女1例,均为足月儿,住院日龄为(8.0±4.7)d,<7d3例,≥7d9例.症状以嗜睡或反应差、发热、抽搐最常见.体征有手足心发黄,颈后仰或角弓反张、四肢肌张力增高及脑性尖叫.血清胆红素峰值(486.25±153.2)μmol/L,9例血清总胆红素>340μmol/L.9例G6PD活性重度缺陷(<0.3IU/L),其中3例G6PD活性为0.治愈8例,好转2例,自动出院1例,死亡1例.结论:G6PD缺陷致胆红素脑病特点为男性足月儿多见,75%入院≥7d,症状以嗜睡或反应差、发热最常见,1/2有抽搐,体征以手足心发黄、颈后仰或角弓反张、四肢肌张力增高常见.9例血清总胆红素>340μmol/L,多伴有贫血和G6PD活性严重缺陷.  相似文献   

2.
新生儿高胆红素血症病因及转归分析   总被引:3,自引:0,他引:3  
林娜娜 《广西医学》2004,26(7):960-962
目的 了解本地区足月新生儿高胆红素血症的病因与转归情况 ,以及影响转归的因素 ,以提高高胆红素血症的临床诊治水平。方法 对 2 39例血清总胆红素 (TBIL)≥ 2 2 0 6 μmol L的足月新生儿高胆红素血症病例的病因 ,胆红素水平、转归及影响转归的一些因素进行前瞻回顾性分析。结果 病因以G 6 PD缺陷居首位 (2 9 7% ) ,其它依次为感染因素 (18 4 % )、ABO溶血 (17 2 % )、母乳性黄疸 (8 4 % )、喂养不足 (7 9% )、G 6 PD并ABO溶血 (4 2 % )、少数为CROTCHS感染 (1 7% ) ;TBIL2 2 0 6 μmol L~ 342 μmol L14 8例 ,343μmol L~ 4 2 7 5 μmol L5 1例 ,>4 2 7 5 μmol L4 0例 ,最高达 779 4 μmol L ;大部分病例转归良好 (2 14 2 39) ,发生核黄疸 2 2例 ,其中以G 6 PD缺陷占多数 (14 2 2 ) ,TBIL >4 5 0 μmol L时近 5 0 % (17 35 )发生核黄疸 ,当TBIL >6 0 0 μmol L时近 90 %(7 8)发生核黄疸。 1例入院时TBIL >5 0 0 μmol L无核黄疸症状的病例随访 4个月时诊断为核黄疸后遗症。 结论 本地区高胆病因以G 6 PD缺陷为主 ,合并感染时胆红素水平明显升高 ,易发生核黄疸 ,尽早积极治疗感染是防治G 6 PD缺陷儿高胆红素血症的重要措施 ;控制胆红素水平有利于减少核黄疸的发生 ;无核黄疸症状的严重  相似文献   

3.
目的了解横县ABO溶血、G6PD缺陷及ABO溶血合并G6PD缺陷所致新生儿黄疸的发生率及临床特点.方法回顾2008年1月-2010年1月我院收治的新生儿黄疸病例.检测G6PD缺陷采用NBT法,ABO溶血病采用免疫学三项试验.黄疸干预标准采用2001年全国新生儿黄疸推荐方案.结果98例可明确病因,以G6PD缺陷最多见.42例(42.9%)在生后24小时内出现黄疸.78.3%ABO溶血病合并G6PD缺陷在24小时内出现黄疸,与其他组相比,p<0.001.70.6%ABO溶血病在生后48小时内住院,与其他两组比较p<0.05.血清总胆红素浓度的峰值在<72小时也以ABO溶血病合并G6PD缺陷最高,p<0.05.11例并发核黄疸,9例为G6PD缺陷,1例为G6PD缺陷合并ABO溶血病.结论横县新生儿病理性黄疸的病因49.6%为G6PD缺陷所致.11例核黄疸中10例与G6PD缺陷有关.72%G6PD缺陷时黄疸多在48小时内出现.但生后两日内住院率低.36例ABO溶血病中,19例合并G6PD缺陷,ABO溶血合并G6PD缺陷时黄疸出现早,24小时内显黄占78.9%,小于72小时血胆红素值226.71±103.19μmol/L.ABO溶血病出现黄疸早,但黄疸程度不如ABO溶血病合并G6PD缺陷.  相似文献   

4.
目的 比较ABO溶血病与红细胞葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症致足月新生儿高胆红素血症的临床特点.方法 对2013年3月至2015年2月入住海南省妇幼保健院新生儿科的104例足月新生儿ABO溶血病(ABO组)与51例G6PD缺乏症(G6PD组)所致高胆红素血症的临床特点进行病例对照分析.结果 72 h内ABO组97例(93.27%),G6PD组47例(92.16%)出现黄疸并达峰值;ABO组黄疸出现时间为(1.28±0.78)d,明显短于G6PD组的(1.83±1.01)d,差异具有统计学意义(P<0.05);ABO组与G6PD组血清总胆红素峰值分别为(326.54±91.05)μmol/L和(360.23±128.34)μmol/L,两组比较差异无统计学意义(P>0.05);ABO组与G6PD组黄疸平均消退时间分别为(5.58±1.24)d和(5.94±1.65)d,两组比较差异无统计学意义(P>0.05).两组共3例存在急性胆红素脑病表现,其中ABO组2例,G6PD组1例.结论 ABO溶血病与G6PD缺乏症是足月新生儿早期高胆的常见原因;新生儿ABO溶血病较G6PD缺乏症所致新生儿黄疸发生时间早,黄疸程度及消退时间等差异无统计学意义.  相似文献   

5.
目的 探讨G6PD缺陷症对新生儿高胆红素血症病程的影响.方法 确诊高胆红素血症新生儿77例,分为两组:G6PD缺陷症组37例,G6PD正常组40例.全部病例均给予双面蓝光光疗,对比两组新生儿治疗前血清总胆红素(Total serum bilirubin,TSB)、血红蛋白和治疗后TSB、血红蛋白、总光疗时间、住院天数.结果 G6PD缺陷症组和G6PD正常组新生儿治疗前TSB分别为(278.43±15.26) μmol/L和(276.68±12.15) μmol/L(P>0.05),血红蛋白分别为(165.58+10.90) g/L和(160.95±9.76) g/L (P>0.05).G6PD缺陷症组和G6PD正常组新生儿治疗后TSB分别为(168.70±9.79) μmol/L和(162.68±12.09) μmol/L (P<0.05),血红蛋白分别为(150.59±7.82) g/L和(153.63±7.80) g/L(P>0.05).G6PD缺陷症组和G6PD正常组新生儿总光疗时间分别为(65.51 ±16.87)h和(45.00±12.67)h (P<0.01),住院天数分别为(7.22±1.60)d和(5.58±1.45)d (P<0.01).结论 G6PD缺陷症新生儿虽无明显溶血发生,但G6PD缺乏也会延缓高胆红素血症的消退,增加光疗时间和住院天数.  相似文献   

6.
新生儿高胆红素血症是新生儿早期常见症状 ,足月儿血总胆红素 >2 0 5 .2 μm ol/ L,早产儿 >2 5 6 .5 μmol/ L,称高胆红素血症。未结合胆红素 >342 μmol/ L 可引起胆红素脑病 ,损害中枢神经系统 ,甚至危及生命 ,我院新生儿科在应用药物治疗的同时 ,结合使用蓝光治疗 ,以降低血胆红素 ,取得较好的疗效。现将护理体会介绍如下。1 临床资料  本组共 16 7例 ,其中男 10 5例 ,女 6 2例 ,病因 :红细胞酶 (G- 6 - PD)缺陷引起 36例 ,感染引起 5 5例 ,其他原因引起 76例 ,结果 :病愈 142例 ,好转 2 1例 ,死亡 2例 ,放弃治疗 2例。2 光疗指…  相似文献   

7.
1目的 探讨新生儿 ABO溶血症和 G6 PD缺陷症所致新生儿高胆红素血症的早期鉴别诊断和治疗。 2方法 对比分析84例 ABO溶血症和 6 2例 G6 PD缺陷症的临床表现和实验室检查。3结果 ABO溶血症在黄疸出现时间和高峰时间上早于 G6 PD缺陷症 (P<0 .0 0 1,P<0 .0 1) ,但相差时间不超过 1d。两组在黄疸程度上差异无统计学意义。G6 PD缺陷症组核黄疸发生率为 9.7%。 4结论  ABO溶血症和 G6 PD缺陷症鉴别诊断有赖于实验室检查。对有 G6 PD缺陷症产妇所分娩的新生儿进行重点监护、早期积极治疗是防止核黄疸的关键  相似文献   

8.
107例新生儿高胆红素血症病因分析及预防对策   总被引:4,自引:0,他引:4  
新生儿高胆红素血症 (简称高胆 )是新生儿时期最常见病症之一 ,可由不同病因引起 ,阐明本病的有关因素对其防治具有重要意义。本文对我院从 1 991~ 1 999年收治的 1 0 7例新生儿高胆进行病因分析 ,为其防治提供依据。1 临床资料1 .1 一般资料  1 0 7例新生儿高胆中 ,符合新生儿高胆红素血症诊断标准 [1] (足月儿血清胆红素 >2 2 0 .6μmol/L,早产儿≥ 2 56.5μmol/L) ,且以未结合胆红素为主 ,足月儿 1 0 4例 ,早产儿 3例 ,男 79例 ,女 2 8例 ,男女比例为 2 .62∶ 1 ;年龄 1 d~ 2 8d,<7d 75例 ,>7d 32例。1 .2 病因分析 G- 6PD缺陷 …  相似文献   

9.
陈俊  田鸾英  黄璐  常利利  宋艳 《海南医学》2012,23(13):13-14
目的探讨G6PD缺陷症对新生儿高胆红素血症病程的影响。方法确诊高胆红素血症新生儿77例,分为两组:G6PD缺陷症组37例,G6PD正常组40例。全部病例均给予双面蓝光光疗,对比两组新生儿治疗前血清总胆红素(Total serum bilirubin,TSB)、血红蛋白和治疗后TSB、血红蛋白、总光疗时间、住院天数。结果 G6PD缺陷症组和G6PD正常组新生儿治疗前TSB分别为(278.43±15.26)μmol/L和(276.68±12.15)μmol/L(P>0.05),血红蛋白分别为(165.58±10.90)g/L和(160.95±9.76)g/L(P>0.05)。G6PD缺陷症组和G6PD正常组新生儿治疗后TSB分别为(168.70±9.79)μmol/L和(162.68±12.09)μmol/L(P<0.05),血红蛋白分别为(150.59±7.82)g/L和(153.63±7.80)g/L(P>0.05)。G6PD缺陷症组和G6PD正常组新生儿总光疗时间分别为(65.51±16.87)h和(45.00±12.67)h(P<0.01),住院天数分别为(7.22±1.60)d和(5.58±1.45)d(P<0.01)。结论 G6PD缺陷症新生儿虽无明显溶血发生,但G6PD缺乏也会延缓高胆红素血症的消退,增加光疗时间和住院天数。  相似文献   

10.
目的:探讨新生儿胆红素脑病警告期诊断的临床依据与标准,以利早期诊治此症。方法:回顾性分析13例诊断胆红素脑病警告期的新生儿发病因素、临床特点及诊治经过。结果:13例新生儿发病均有明显的病理因素,包括病理溶血、感染、缺氧及早产等,血清总胆红素>340μmol/L8例,206μmol/L<总胆红素<340μmol/L 5例,全部病例具有嗜睡、拒食等抑制症状,经早期积极治疗,病情均无进一步发展。结论:新生儿胆红素脑病警告期的诊断的确立,不仅要参照血清总胆红素值,更要意识到临床表现才是最有价值的诊断依据。  相似文献   

11.
Objective: To evaluatel the value of D-dimers in patients with acute aortic dissection (AAD). Methods: This study consisted of 16 patients with AAD and 27 non-AAD patients. Serum D-dimets were measured by Sta-Liatest D-DI immunoturbidimetric assay. Results: D-dimer level was higher (P < 0.001) in patients with AAD(7.91 ± 5.52 μg/ml) than that in non- AAD group(1.57±1.24 μg/ml). D-dimer was positive (>0.4 μg/ml) in all patients with AAD and in 10 control group patients (37%). Among patients with acute AAD, D-dimers tended to be higher in Stanford A than in Stanford B (8.67 ± 4.31 μg/ml vs. 3.24±1.27 μg/ml, P <0.01). D-dimer values tended to be higher in more extended disease(3.84 ± 1.65 μg/ml, 8.57 ± 3.58 μg/ml and 11.87 ± 5.69 μg/ml in thoracic aorta, thoracic and abdominal aorta, thoracic and abdominal aorta and iliacal arteries, respectively, P < 0.05 for both 8.57 ± 3.58 and 11.87 ± 5.69 vs. 3.84 ± 1.65 ). Including the control group into the analysis, we found a sensitivity of 100%, a negative predictive value of 100%, and a specificity of 66% and a positive predictive value of 64% for D-dimer in diagnosis of AAD in our patients with suspected AAD. Conclusion: D-dimer was elevated in patients with AAD. A negative D-dimer test result could be useful in excluding AAD.  相似文献   

12.
Objective: To set up a simple and reliable rat model of combined liver-kidney transplantation. Methods: SD rats served as both donors and recipients. 4℃ sodium lactate Ringer's was infused from portal veins to donated livers,and from abdominal aorta to donated kidneys, respectively. Anastomosis of the portal vein and the inferior vena cava (IVC) inferior to the right kidney between the graft and the recipient was performed by a double cuff method, then the superior hepatic vena cava with suture. A patch of donated renal artery was anastomosed to the recipient abdominal aorta. The urethra and bile duct were reconstructed with a simple inside bracket. Results: Among 65 cases of combined liver-kidney transplantation, the success rate in the late 40 cases was 77.5%. The function of the grafted liver and kidney remained normal. Conclusion: This rat model of combined liver-kidney transplantation can be established in common laboratory conditions with high success rate and meet the needs of renal transplantation experiment.  相似文献   

13.
Objective To observe blood pressure change with age in salt-sensitive teenagers whose salt sensitivity were determined by repeated testing.Methods Salt sensitivity was determined through intravenous infusion of normal saline combined with volume-depletion by oral diuretic furosemide in 55 teenagers. After five years, salt sensitivity was re-examined and subject blood pressure was followed up. Blood pressure changes in salt-sensitive teenagers were compared to that of non-salt sensitive teenagers over five years.Results After 5 years, the repetition rate of salt sensitivity determined by intravenous saline loading is 92.7%. In teenagers with salt sensitivity on the baseline, both the systolic blood pressure increments and increment rates were much higher than non-salt sensitive teenagers (12.7±12.1 mmHg vs. 2.8±5.2 mmHg, P< 0.01; 12.2%± 12.0% vs. 2.5% ±4.4%, P< 0.001,respectively). There was a similar trend for diastolic blood pressure (8.4 ± 6.4 mmHg vs. 3.7 ± 6.4 mmHg, P = 0.052; 13.2% ±10.6 % vs. 6.8%± 10.1%, P = 0.053, respectively).Conclusions Salt sensitivity determined by intravenous saline loading showed good reproducibility. Blood pressure increments with age were much higher in salt-sensitive teenagers than non-salt sensitive teenagers, especially in terms of systolic blood pressure.  相似文献   

14.
目的:评价使用安心颗粒对急诊经皮冠状动脉介入术(PPCI)术后生活质量的影响.方法:将160例接受PPCI的急性ST段抬高型心肌梗死患者随机分为安心颗粒组(术前顿服安心颗粒8.8g,术后安心颗粒4.4 g/次,每日2次)和对照组(仅接受基础药物治疗).所有患者均服用阿司匹林、氯吡格雷和阿托伐他汀.分别在入院时、出院前1d、出院后180 d时,应用心肌梗死多维度量表(MIDAS)、中文版SF-36评价量表对患者生活质量评分.并观察术后30 d以内的出血并发症、血小板减少症发生情况.结果:入院时和出院前1d,两组患者的心肌梗死MIDAS、SF-36量表评分比较无差异(P>0.05);出院后180 d时,与对照组比较,安心颗粒组MIDAS、SF-36评分明显减低(P<0.05);组内与入院时比较,两组出院前1d、出院后180 d时,MIDAS、SF-36评分均降低(P<0.05).两组患者在随访期间均无大量出血、少量出血、重度和极重度血小板减少症发生,安心颗粒组有4例、对照组有7例发生不明显出血(P>0.05).两组发生轻度血小板减少症的患者数比较无差异(P>0.05).结论:PPCI使用安心颗粒,能改善急性ST段抬高型心肌梗死患者的生活质量,且不增加出血风险.  相似文献   

15.
Objective:To investigate the influences of urapidil and nicardipine on rabbit sinus function,atrio-ventricular node function and hemodynamics.Methods:Thirty-two Angora's rabbits were selected and randomly divided into four groups.U1 group:urapidil 0.25 mg/kg;U2 group:urapidil 0.5 mg/kg;N1 group:nicardipine 10 μg/kg;N2 group:nicardipine 20 μg/kg.All these medicine were administrated within 30 seconds.Measurements were taken before and after the administration of urapidil or nicardipine for the following data:mean blood pressure(MAP),heart rate(HR),sino-atrial conduction time(SACT),maximal sinoatrial recovery time(SNRTmax)corrected sinus node recovery time(CSNRT),index of sinus node recovery time(SNRTI),Wenckebach A-V conduction frequency (WB),and P-R interval.Results:Significant MAP and HR changes were identified in all of the four groups before and after administration of both urapidil and nicardipine.No significant changes could be found in the rest of the parameters.Intergroup analysis showed that SACT and CSNRT of N1 and N2 groups were shorter than those of the U2 group(P<0.01);the MAP decreased(P<0.01)and the HR increased drastically(P<0.01).Conclusions:Neither urapidil(0.25 mg/kg,0.5 mg/kg)nor nicardipine(10μg/kg,20μg/kg)has any significant influence on rabbit sinus function or rabbit atrio-ventricular node function.Nicardipine could be a better choice than urapidil for parafunctional sinus node patients.  相似文献   

16.
Objective:To investigate the gene expression of osteoprotegerin(OPG) and osteoclast differentiation factor(ODF) in the bone tissue of patients with hip fracture due to osteoporosis. Methods:OPGmRNA and ODFmRNA in the bone tissue in 50 cases of osteoporosis sufferers(over 50 years old) with hip fracture(Observer Group) and 30 cases of hip facture sufferers with no osteoporosis(Control group) were analyzed with the Semi-Quantitative RT-PCR method. Results:The mRNA expressed of ODF, OPG were both high in the patients with hip fracture. In the control group, the expression of OPG mRNA was observed, while the expression of ODF mRNA was very slight. Conclusion:Aged patients contained all signals including OPG, ODF that are essential for inducing osteoclastogenesis and promoting bone resorption.  相似文献   

17.
Objective:To investigate the clinical features, pathological characteristics and immunophenotype of solid-pseudopapillary tumor of the pancreas(SPTP). Methods:Nine surgically treated cases of SPTP were retrospectively reviewed. Hematoxylin and Eosin(HE) staining and immunohistochemical staining were used to analyze all cases, and the general clinical data was collected. Results:Six patients were asymptomatic except for a palpable mass. Two patients complained of vague-epigastric pain. One patient appeared jaundice. The tumor was encapsulated and solid tissues alternately with cystic tissues. Histologically, the histological structure of solid portion was pseudopapillary with a fibrovascular core. Tumor cells were uniform and medium-sized which were arranged in sheets ets or nests or pseudopapillary patterns. Immunohistochemical studies demonstrated that SPTP proved positive in vimentin(9/9 cases), AAT(9/9 cases), NSE(9/9 cases), ACT(7/9 cases), CK20(2/9 cases), CgA(1/9 cases), S-100(3/gcases), PR(4/gcases), Syn(3/9 cases) and CD56(5/9cases), negative in CEA and ER. Conclusion:SPTP is a tumor predominantly occurring in young women frequently without special symptoms. This tumor has various characteristical histological patterns with different immunophenotype.  相似文献   

18.
Objective:To probe into the influence of changes of ovarian hormones on the pathogenesis of the specific sub-type premenstrual syndrome(PMS)and reveal partial microcosmic mechanisms of adverse flow of liver-qi.Methods:Estradiol(E2)and progesterone(P)levels in serum were determined at different phases of menstrual cycle by radioimmunoassay.Results:In the group of PMS with adverse flow of liver-qi.the secretive peak value Of E2 and P at the follicular phase significantly decreased,and the secretive peak value at the luteal phase did not come into being.Conclusions:Low E2 and P secretive peak at the follicular phase and absence of secretive peak at the luteal phase is one of the microcosmic mechanisms of PMS with adverse flow of liver-qi.One of the pathophysiologic mechanisms of specific sub-type PMS is probably the continuous low level of E2and P.  相似文献   

19.
Real-time three-dimensional echocardiography (RT3DE)is a new ultrasound technique that enables dynamic threedimensional visualization and quantification of the heart in real time. Investigation of feasibility and methodology of RT3DE in determining left ventricular (LV) and right ventricular (RV) volumes, RT3DE was performed in 35 normal adults using Philips SONOS 7500 system with a 2-4 MHz matrix array transducer. The 60°×60° "pyramid" volume database was obtained and analyzed on a TomTec echo workstation. Both LV and RV volumes were calculated with four 3DE methods (i.e. apical 2, 4, 8, and 16-plane) through manually tracing ventricular endocardial borders in end diastole and end systole. Stroke volumes were then calculated. LV volume was also measured by 2DE Simpson's rule using GE VIVID 7 ultrasound machine.  相似文献   

20.
Increasing maternal age is the only etiological factor unequivocally linked to Down's syndrome in humans. The occurrence rate of newborns with Down's syndrome is about 1/220 in women over 35 years old. However, the occurrence rate in embryos fertilized in vitro, of the elder woman is unclear. Using FISH we screened the number of chromosome 21 in preimplanted embryos of 5 elderly women (average age, 38.4 years) to study the feasibility and necessity of screening trisomy 21 in embryos in patients over 35 years old at the in vitro fertilization (IVF) center.  相似文献   

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