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1.
Approximately 10%-20% of the cases of acute pancreatitis have acute necrotizing pancreatitis. The infection of pancreatic necrosis is typically associated with a prolonged course and poor prognosis. The multidisciplinary, minimally invasive “step-up” approach is the cornerstone of the management of infected pancreatic necrosis (IPN). Endosonography-guided transmural drainage and debridement is the preferred and minimally invasive technique for those with IPN. However, it is technically not feasible in patients with early pancreatic/peripancreatic fluid collections (PFC) (< 2-4 wk) where the wall has not formed; in PFC in paracolic gutters/pelvis; or in walled off pancreatic necrosis (WOPN) distant from the stomach/duodenum. Percutaneous drainage of these infected PFC or WOPN provides rapid infection control and patient stabilization. In a subset of patients where sepsis persists and necrosectomy is needed, the sinus drain tract between WOPN and skin-established after percutaneous drainage or surgical necrosectomy drain, can be used for percutaneous direct endoscopic necrosectomy (PDEN). There have been technical advances in PDEN over the last two decades. An esophageal fully covered self-expandable metal stent, like the lumen-apposing metal stent used in transmural direct endoscopic necrosectomy, keeps the drainage tract patent and allows easy and multiple passes of the flexible endoscope while performing PDEN. There are several advantages to the PDEN procedure. In expert hands, PDEN appears to be an effective, safe, and minimally invasive adjunct to the management of IPN and may particularly be considered when a conventional drain is in situ by virtue of previous percutaneous or surgical intervention. In this current review, we summarize the indications, techniques, advantages, and disadvantages of PDEN. In addition, we describe two cases of PDEN in distinct clinical situations, followed by a review of the most recent literature.  相似文献   
2.
目的探讨改良张力支具对肱骨髁间骨折患者术后功能康复的临床效果评价。 方法回顾性分析本院采用切开复位内固定术治疗的40例肱骨髁间骨折患者的资料。单纯采用普通固定支具进行功能锻炼的为对照组(21例),采用改良张力支具进行功能锻炼的为观察组(19例)。比较两组患者术后去除支具和末次随访时肘关节屈曲度、肘关节背伸度、前臂旋前度、前臂旋后度和Mayo肘关节功能评分,以评定改良张力支具的疗效。 结果所有患者术后均获得随访,平均随访13.79个月。观察组与对照组相比,术后去除支具时肘关节屈伸活动度[(104.47±12.37)° vs.(88.85±8.10)°,P<0.001],差异有统计学意义;肘关节旋转活动度[(140.31±16.87)° vs.(135.66±12.86)°,P=0.331],差异无统计学意义;肘关节Mayo评分[(78.84±5.04)分vs.(73.80±4.46)分,P=0.002],差异有统计学意义。末次随访时肘关节屈伸活动度[(107.52±12.30)° vs.(93.00±8.47)°,P<0.001],差异有统计学意义;肘关节旋转活动度[(141.42±17.02)° vs.(137.19±12.80)°,P=0.37],差异无统计学意义;肘关节Mayo评分[(80.15±5.24)分vs.(74.95±4.18)分,P=0.001],差异有统计学意义。 结论术后使用改良张力支具可以改善肱骨髁间骨折患者的屈伸活动度和肘关节功能。  相似文献   
3.
4.
目的分析垂体后叶素联合酚妥拉明治疗支气管扩张大咯血的临床效果。方法回顾性选取100例支气管扩张大咯血患者,依据治疗方法不同分为常规治疗组和联合治疗组,各50例。常规治疗组患者给予常规治疗,联合治疗组在常规治疗基础上给予垂体后叶素联合酚妥拉明治疗。比较两组患者的临床疗效,治疗前后的生命体征、经皮血氧饱和度,出血天数、总出血量,不良反应发生情况。结果联合治疗组患者的治疗总有效率92.0%(46/50)显著高于常规治疗组的74.0%(37/50),差异具有统计学意义(P<0.05)。联合治疗组患者治疗前体温、呼吸频率、心率、舒张压、收缩压、经皮血氧饱和度分别为(38.6±1.4)℃、(43.5±7.2)次/min、(115.2±14.3)次/min、(55.2±9.2)mm Hg(1 mm Hg=0.133 kPa)、(85.2±11.2)mm Hg、(60.5±14.7)%,治疗后分别为(36.8±1.2)℃、(29.6±5.5)次/min、(85.2±10.1)次/min、(80.5±10.5)mm Hg、(110.3±10.3)mm Hg、(95.3±13.5)%;常规治疗组患者治疗前体温、呼吸频率、心率、舒张压、收缩压、经皮血氧饱和度分别为(38.3±1.9)℃、(44.3±7.5)次/min、(114.4±13.7)次/min、(55.0±9.5)mm Hg、(86.3±11.5)mm Hg、(61.5±14.9)%,治疗后分别为(37.3±1.2)℃、(34.2±5.6)次/min、(94.3±11.8)次/min、(66.5±9.7)mm Hg、(95.3±10.4)mm Hg、(85.5±12.6)%。两组患者治疗前体温、呼吸频率、心率、舒张压、收缩压、经皮血氧饱和度比较差异均无统计学意义(P>0.05);治疗后,两组患者的体温、呼吸频率、心率均低于本组治疗前,舒张压、收缩压、经皮血氧饱和度均高于本组治疗前,差异具有统计学意义(P<0.05);治疗后,联合治疗组患者体温、呼吸频率、心率均低于常规治疗组,舒张压、收缩压、经皮血氧饱和度均显著高于常规治疗组,差异具有统计学意义(P<0.05)。联合治疗组患者的出血天数(7.0±1.2)d显著短于常规治疗组的(10.4±1.5)d,总出血量(730.7±156.5)ml显著少于常规治疗组的(906.8±140.0)ml,差异具有统计学意义(P<0.05)。联合治疗组患者的不良反应发生率8.0%(4/50)显著低于常规治疗组的24.0%(12/50),差异具有统计学意义(P<0.05)。结论垂体后叶素联合酚妥拉明治疗支气管扩张大咯血的临床效果好。  相似文献   
5.
摘要:目的 通过评估经鼻导管高流量湿化氧疗在肺部感染患者中的临床疗效,为肺部感染尤其是重症肺炎的患者呼吸道管理策略提供一定的参考依据。方法 2015年9月至2017年9月,采用方便抽样方法选取收治于复旦大学附属华山医院感染科的375例肺部感染患者作为研究对象。依据时间将2015年9月1日至2016年8月31日、2016年9月1日至2017年8月31日入院的患者分别纳入对照组和观察组,对照组患者接受常规治疗,观察组患者在对照组的基础上根据病情接受经鼻导管高流量湿化氧疗。比较两组患者的住院时长、气管插管(包括无创/有创气管切开)人数比例以及预后转归。在对照组和观察组的重症肺炎患者中评估接受经鼻导管高流量湿化氧疗的患者预后情况。结果 观察组重症肺炎的患者比例较对照组高,预后较对照组好,均有统计学差异(P < 0.05)。与未使用HFNC治疗的患者比较,发现接受HFNC的重症肺炎患者预后更好,有统计学差异(P < 0.05)。使用HFNC治疗后,重症肺炎患者的多个指标如呼吸频率、心率、氧饱和度、氧分压均有显著改善,均有统计学差异(P < 0.05)。结论 近年来,我院感染科收治患者的肺部感染患者人数越来越多,重症化比例也越来越高。在此情况下,医院的管理、医生的诊疗、护士的护理到位,使整体肺部感染患者的住院天数、预后转归与既往病情较轻的时候并无差异。同时,接受HFNC的重症肺炎患者,预后明显好转,表明HFNC对改善肺部感染患者预后有明显疗效。  相似文献   
6.
PurposeTo study, from a U.S. payer’s perspective, the economic consequences of drug-coated balloon (DCB) versus standard percutaneous transluminal angioplasty (PTA) use for the treatment of stenotic lesions in dysfunctional hemodialysis arteriovenous fistulae.Materials and MethodsCost differences between DCBs and PTA at year 1 and beyond were calculated via 2 methods. The first approach used the mean absolute number of trial-observed access circuit reinterventions through 12 months (0.65 ± 1.05 vs 1.05 ± 1.18 events per patient for DCBs and PTA, respectively) and projected treatment outcomes to 3 years. The second approach was based on the trial-observed access circuit primary patency rates at 12 months (53.8% vs 32.4%) and calculated the cost difference on the basis of previously published Medicare cost for patients who maintained or did not maintain primary patency. Assumptions regarding DCB device prices were tested in sensitivity analyses, and the numbers needed to treat were calculated.ResultsUsing the absolute number of access circuit reinterventions approach, the DCB strategy resulted in an estimated per-patient savings of $1,632 at 1 year and $4,263 at 3 years before considering the DCB device cost. The access circuit primary patency approach was associated with a per-patient cost savings of $2,152 at 1 year and $3,894 at 2.5 years of follow-up. At the theoretical DCB device reimbursement of $1,800, savings were $1,680 and $2,049 at 2.5 and 3 years, respectively. The one-year NNT of DCB compared to PTA was 2.48.ConclusionsEndovascular therapy for arteriovenous access stenosis with the IN.PACT AV DCB can be expected to be cost-saving if longer follow-up data confirm its clinical effectiveness.  相似文献   
7.
ObjectiveTo determine the long-term cardiovascular disease risk of astronauts with spaceflight exposure compared with a well-matched cohort.MethodsNational Aeronautics and Space Administration (NASA) astronauts are selected into their profession based upon education, unique skills, and health and are exposed to cardiovascular disease risk factors during spaceflight. The Cooper Center Longitudinal Study (CCLS) is a generally healthy cohort from a preventive medicine clinic in Dallas, Texas. Using a matched cohort design, astronauts who were selected beginning April 1, 1959, (and each subsequent selection class through 2009) and exposed to spaceflight were matched to CCLS participants who met astronaut selection criteria; 1514 CCLS participants matched to 303 astronauts in a 5-to-1 ratio on sex, date of birth, and age. The outcome of cardiovascular mortality through December 31, 2016, was determined by death certificate or National Death Index.ResultsThere were 11 deaths caused by cardiovascular disease (CVD) among astronauts and 46 among CCLS participants. There was no evidence of increased mortality risk in astronauts (hazard ratio [HR]=1.10; 95% confidence interval [CI], 0.50 to 2.45) with adjustment for baseline cardiovascular covariates. However, the secondary outcome of CVD events showed an increased adjusted risk in astronauts (HR=2.41; 95% CI, 1.26 to 4.63).ConclusionNo increased risk of CVD mortality was observed in astronauts with spaceflight exposure compared with a well-matched cohort, but there was evidence of increased total CVD events. Given that the duration of spaceflight will increase, particularly on missions to Mars, continued surveillance and mitigation of CVD risk is needed to ensure the safety of those who venture into space.  相似文献   
8.
目的探讨超微经皮肾镜取石术(UMP)应用于直径1.5~2.5 cm肾及输尿管上段结石患者中的安全性和有效性。方法回顾性分析2018年6月-2020年6月宿迁市第一人民医院收治的60例直径为1.5~2.5 cm肾及输尿管上段结石患者的临床资料,均采用UMP治疗,分析患者手术时间、住院时间、手术成功率、结石清除率、并发症发生率及额外镇痛药使用情况。结果60例患者均一期建立通道并顺利完成手术。所有患者均未行单通道手术,未接受输血,无毗邻脏器损伤(肠道、肝脏和脾脏等),无血气胸发生;存在尿外渗或者有明显症状的腹膜后灌注液患者3例(5.0%),均行保守治疗好转;发热(体温高于38℃)5例(8.3%),均对症治疗后好转;无感染性休克患者。手术时间为35~98 min,平均(56.1±21.3)min;术后住院天数为3~8 d,平均(4.1±1.8)d;术后立即评估结石清除率为85.0%(51/60),术后1个月评估结石清除率为91.7%(55/60);术后镇痛药使用率为15.0%(9/60)。结论UMP是治疗直径1.5~2.5 cm肾及输尿管上段结石安全、有效的治疗方法之一,值得临床推广。  相似文献   
9.
PurposeTo report the 5-year results from the Pivotal Multicenter Trial of Ultrasound-Guided Percutaneous Arteriovenous Fistula (pAVF) Creation for Hemodialysis Access.Materials and MethodsThe retrospective review of 107 intent-to-treat (ITT) patients from the pivotal trial provided a long-term follow-up population (LTP) of 85 patients with a median follow-up duration of 50 months (range, 12–60 months). Data evaluated in the LTP group were fistula maturation and usage, secondary procedures, and complications. The Kaplan-Meier analysis of primary patency, assisted primary patency, cumulative patency, and functional patency (time from 2-needle cannulation to abandonment) were performed for the ITT population.ResultsIn the LTP, 99% (84 of 85) of fistulae were mature, with 99% (78 of 79) of patients requiring hemodialysis using their pAVF. Sustained fistula use (2-needle cannulation at the prescribed rate, 2 of 3 sessions) was achieved in 92% (78 of 85) of patients, with 7 patients not using their pAVF because they were not on dialysis (n = 4), were on peritoneal dialysis (n = 2), and refused to use fistula (n = 1). Fistula maintenance was required in 31.8% (27 of 85) of patients and included fistula dysfunction (21.2%), thrombosis (5.9%), cannulation injury (12.9%), and arm swelling (4.7%). The number of procedures performed per patient per year to maintain function and patency was 0.32 (91 of 288) for years 2–5. The cumulative patency rates were 89.5%, 88.4%, 88.4%, 85.6%, and 82.0% for years 1, 2, 3, 4, and 5, respectively. The functional patency was 91.8% at the end of the study. There were no major complications related to pAVF during the long-term follow-up.ConclusionsPercutaneous fistulae have provided clinically effective and durable access for hemodialysis with low complications. The continued use and evaluation of pAVF are warranted.  相似文献   
10.
PurposeTo evaluate the midterm outcomes of percutaneous transluminal renal angioplasty (PTRA) for pediatric renovascular hypertension (RVH).Materials and MethodsThe clinical data of patients who underwent PTRA for RVH in the authors’ hospital from 2012 to 2019 were retrospectively analyzed. Postprocedural blood pressure, glomerular filtration rate (GFR) of the affected kidney, restenosis, and complications were closely monitored.ResultsPTRA was performed in a total of 30 children (20 boys and 10 girls), with a mean age of 7.3 years ± 0.7 (range, 40 days to 13.9 years) and a mean weight of 25.0 kg ± 2.3 (range, 3.4–53 kg). The median follow-up period was 26.5 months (range, 1 month to 7.5 years). Technical success was achieved in 26 (86.7%) of the 30 patients. Restenosis developed in 3 patients (10.0%). Only 1 patient underwent stent implantation, and the stent fractured 8 months later, requiring further intervention. There were no other complications. In terms of clinical benefit of blood pressure control after the initial PTRA procedure, 15 patients (50%) were cured and 7 patients (23.3%) showed improvement. There was no significant difference in the etiology, lesion location, and lesion length between patients with clinical benefit and failure (P = .06, P = .202, and P = .06, respectively). GFR of the affected kidney was significantly improved from 19.9 mL/min ± 11.2 to 38.1 mL/min ± 11.9 at the 6-month follow-up after PTRA (P < .001).ConclusionsThe overall results of PTRA for pediatric RVH caused by different etiologies are promising. PTRA not only provided a clinical benefit of blood pressure control in 73.3% of the patients but also significantly improved the function of the affected kidney.  相似文献   
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