腹膜透析治疗小儿先天性心脏病术后急性肾功能衰竭

目的：探讨腹膜透析（ＰＤ）对小儿先天性心脏病（先心病）术后急性肾功能衰竭（ＡＲＦ）的治疗效果。方法：对３６例先心病术后ＡＲＦ行ＰＤ治疗患儿的临床资料作回顾性调查。结果：全组经ＰＤ治疗后的病死率为３０．６％,其中单纯ＡＲＦ的病死率１２．５％,显著低于合并其他系统器官衰竭组的４５％（Ｐ〈０．０５）。ＰＤ３～３０ｄ内肾功能恢复,其中１～２ｄ内血Ｋ＾＋恢复正常,２～５ｄ内血碳酸氢根（ＨＣＯ３＾－）恢复正常,４～６ｄ内血尿素氮下降４９．２％,血肌酐下降４２．６％。结论：对小儿先心病术后ＡＲＦ及早进行ＰＤ具有较好的治疗效果。     

腹膜透析对可溶性细胞间粘附分子-1水平的影响及其意义

目的：探讨腹膜透析对可溶性细胞间粘附分子－１（ｓＩＣＡＭ－１）水平的影响及其在长期透析患者免疫功能下降中的作用。方法：采用夹心ＥＬＩＳＡ方法分别检测感染期、非感染期连续不卧床腹膜透析（ＣＡＰＤ）患者血清及腹膜透析液中ｓＩＣＡＭ－１水平的变化。结果：与非感染期ＣＡＰＤ患者相比,感染期ＣＡＰＤ患者血清ｓＩＣＡＭ－１水平显著降低,腹透液ｓＩＣＡＭ－１水平明显升高（Ｐ〈０．０１）;治疗后血清及腹透液ｓＩＣＡＭ－１水平,均较治疗前显著升高或降低（Ｐ〈０．０１）。结论：ｓＩＣＡＭ－１在感染期ＣＡＰＤ患者血清及腹透液中的变化,可能损害了巨噬细胞的正常粘附能力,从而降低机体的免疫能力。     

Gastrointestinal absorption of phenytoin from an oil-in-water microemulsion

The absorption profile of phenytoin Na emulsion were examined compared to that of phenytoin suspension after oral administration in the rat. The corn oil-in-water emulsion, particle size of 184±57.8 nm, was prepared using a microfludizer, and phenytoin Na added by shaft homogenizer. The phenytoin emulsion or suspension, 100 mg/kg, were intubated intragastrically using oral dosing needle and blood samples were withdrawn via an indwelling cannula from the conscious rat. Plasma concentrations of phenytoin were measured with HPLC using phenacetin as an internal standard. The plasma concentration versus time data were fitted to a one compartment open model and the pharmacokinetic parameters were calculated using the computer program, Boomer. The phenytoin plasma concentrations from the emulsion at each observed time were about 1.5–2 times higher than those from the suspension, significantly at time of 5, 6 and 7 hr after administration. The absorption (k_a) and elimination rate constant (k_e) were not altered significantly, however the AUC increased from 65.6 to 106.7 μg·hr/ml after phenytoin suspension or emulsion oral administration, respectively. From an equilibrium dialysis study, the diffusion rate constant (k_IE) was considerably higher from the phenytoin Na emulsion (0.0439 hr⁻¹) than phenytoin suspension (0.0014 hr⁻¹).     

Evolution of renal replacement therapy in East Germany from 1989 to 1992

Diminished availability of facilities for renal replacementtherapy is known to cause spuriously low acceptance and treatmentrates. In this context the evolution of renal replacement therapyin the former German Democratic Republic is a useful model tostudy and to quantify some of the relevant factors. We performed a survey in all dialysis units for adults in EastGermany (excluding East Berlin) by questionnaire, achievinga response rate of 97%. From December 1989 to December 1992the number of dialysis centres increased from 53 to 96 (+81%),reaching 6.7 centres p.m.p. Of these facilities, 45% were hospitalunits, 29% private units, and 26% dialysis units run by non-profithealth care organizations. The number of dialysis stations forregular dialysis treatment increased from 602 to 1276 (+112%),i.e. 89 stations p.m.p. In parallel, the number of chronic dialysispatients increased from 2127 to 3848 (+81%), i.e. 267 patientsp.m.p. A more detailed survey was carried out in Thüringen andpart of Sachsen, in a region covering 5 million inhabitants.The acceptance rate for chronic dialysis treatment has increasedfrom 49 to 107 patients p.m.p. (+115%). The average age of newpatients increased from 49 to 59 years, the proportion of patientsaged 65 years increased from 16 to 42% and the proportion ofdiabetics from 13 to 35%. Introduction of alternative treatmentmodalities became possible, with 2.3% of the patients receivinghaemofiltrations and 3% CAPD. The proportion of HBs-antigen-positivepatients decreased from 14.2% to 5%. At the end of 1989 in the former GDR (excluding East Berlin),773 patients and, at the end of 1992, 1153 patients were alivewith functioning renal transplants (+49%). The annual rate oftransplantations was 254 in 1989, and 283 in 1992 (+11%), i.e.18 transplantations p.m.p. (including East Berlin). At the end of 1989 2900 patients (193 p.m.p.), and at the endof 1992 5001 patients (347 p.m.p.), werealive on renal replacementtherapy (dialysis or functioning renal transplant) in East Germany,excluding East Berlin; this represents a 72% increase. The figures in East Germany are now almost equivalent to thosein West Germany regarding the number of admissions (incidence),whereas the number of patients on renal replacement therapyis still lower (prevalence).     

Chronic dialysis in the infant less than 1 year of age

Dialysis in the infant carries a mortality rate of 16%. Institution of dialysis may be the result of adequate nutritional intake, but avoidance of nutritional intake should never be seen as a way to prevent dialysis. Increased caloric intake, usually via enteral feeding tubes, is needed for optimal growth in the infant with end-stage renal disease (ESRD) in order to attain adequate nutrition with resulting good growth. Renal formulae may be constituted as dilute (as in thepolyuric infant) or concentrated (as in theanuric infant) to fit the infants needs. Peritoneal dialysis (PD) is the usual mode of renal replacement therapy (97%), with access via a surgically placed cuffed catheter with attention to the placement of the exit site in order to avoid fecal or urinary contamination. PD volumes of 30–40 ml/kg per pass or 800–1,200 ml/m² per pass usually result in dialysis adequacy. Additional dietary sodium (3–5 mEq/kg per day) and protein (3–4 g/kg per day) are needed, due to sodium and protein losses in the dialysate. Protein losses are associated with significant infectious morbidity and nonresponsiveness to routine immunizations. Hemodialysis (HD) can be performed either as single- or dual-needle access that have minimal dead space (less then 2 ml) and recirculation rate (less then 5%). Attnetion to extracorporeal blood volume (<10% of=" intravascular=" volume),=" blood=" flow=" rates=" (3–5=" ml/kg=" per=" min),=" heparinization=" (activated=" clotting=" times),=" ultrafiltration=" (ultrafiltration=" monitor),=" and=" temperature=" control=" is=" imperative=" during=" each=" treatment.=" because=" infants'=" nutrition=" is=" mostly=" fluid,=" hd=" may=" be=" needed=" 4–6=" days/week=" (especially=" in=" the=" oligoanuric=" infant)=" to=" avoid=" excessive=" volume=" overload=" between=" treatments.=" at=" the=" end=" of=" the=" treatment=" a=" slow=" blood=" return=" with=" minimal=" saline=" rinse=" is=" needed=" to=" avoid=" hemodynamic=" compromise.=" infant=" dialysis,=" although=" technically=" challenging=" with=" a=" significant=" morbidity=" and=" mortality=" rate,=" can=" be=" safely=" carried=" out=" in=" the=" infant=" with=" esrd=" but=" requires=" infant-specific=" equipment=" and=" trained=">     

Higher Kt/V is needed for adequate dialysis if the treatment time is reduced

The widely used Kt/V concept for quantitating haemodialysis(HD) and ensuring adequate dialysis is based on several assumptions.In order to simplify the urea kinetic modelling, the body isassumed to be a single well-mixed compartment. Previously, morephysiological two-compartment or blood flow distribution modelshave been used to explain the phenomenon of blood urea reboundafter dialysis. This study attempts to evaluate the effectsof a multi compartment model on the removal of urea, i.e. onthe adequacy of dialysis. Four different tissue compartmentsof similar size are used, with flow rates between 40 and 3600ml/min for a bodyweight around 70 kg, allowing for blood flowheterogeneity within and between skeletal muscles. Dialysisis simulated by removing blood containing urea and replacingit with blood free of urea, during isovolumetric conditionsand assuming no diffusion barriers for urea. Several importantconclusions can be drawn from the model. Firstly the removalof urea is dependent both on the time of dialysis and on thenumber of HD treatments per week despite constant Kt/V. Secondlythe blood urea concentration is increased after dialysis—‘urearebound’—in accordance with clinical data. Thirdlythe concept of blood flow distribution can fully explain thedifference between haemodialysis and peritoneal dialysis interms of Kt/V needed for adequate dialysis. Thus a weekly Kt/Vof 3.6 for HD 4 h 3 times per week removes the same amount ofurea as CAPD and a Kt/V of 2.1. Also, nightly intermittent PDrequires similar Kt/Vs (0.1 higher) as CAPD to obtain equivalentremoval of urea. Finally the crucial point is that the Kt/Vrequired for adequate dialysis must be increased if the dialysistreatment time is reduced. If not, the patient with renal insufficiencysuffers the risk of being under-dialysed.     

Imbalance between intraperitoneal coagulation and fibrinolysis during peritonitis of CAPD patients: the role of mesothelial cells

We compared peritoneal dialysis effluents from 18 CAPD patientswho had not suffered from peritonitis during the last 6 months(group 1) with the effluents from five patients with acute peritonitis(group 2), measuring activation markers of coagulation and fibrinolysis.These markers included prothrombin fragment F1+2 (F1+2), thrombin-antithrombinIII complex (TAT), fibrin monomer (FM), and fibrin degradationproducts (FbDP). In the dialysate of group 1 we found remarkablyhigh levels of F1+2, TAT and FM concomitant with a high concentrationof FbDP, indicating a high rate of intraperitoneal fibrin turnover.The balance between peritoneal generation and degradation offibrin was disturbed in untreated patients of group 2, who hadsignificantly higher levels of coagulation markers and a higherratio between FM and FbDP. Seven days after treatment with intraperitonealadministration of antibiotics and heparin, F1+2, TAT, FM andFbDP decreased significantly. To evaluate the role of mesothelial cells (MC) in the high peritonealfibrin turnover we investigated the expression of tissue-typeplasminogen activator (t-PA), urokinase-type plasminogen activator(u-PA), plasminogen activator inhibitor type-1 (PAI-1), andtissue factor in cultured human peritoneal MC under basal conditionsand after exposure to tumour necrosis factor (TNF) interleukin-1(IL-1), or bacterial lipopolysaccharide (LPS). The exposureof MC to TNF or to a lesser extent IL-1 or LPS reduced theirfibrinolytic activity by decreasing t-PA production and increasingPAI-1 synthesis. Furthermore the addition of TNF resulted inactivation of the coagulation cascade by the expression of tissuefactor. These in-vitro findings explain the imbalance betweenintraperitoneal coagulation and fibrinolysis during peritonitisof CAPD patients.     

血清唾液酸含量诊断胃疾病探讨

测定慢性浅表性胃炎１５例,萎缩性胃炎５例,胃溃疡１５例,胃癌９例患者血唾液酸（ＳＡ）的含量。结果表明在４组胃疾病中,胃癌、胃溃疡ＳＡ比慢性浅表性胃炎高。经统计学处理（方差分析）差别有高度显著性（Ｆ＝９１７,Ｐ＜００１）。结论：定期测定ＳＡ含量,对胃部疾患的随访和病情变化有着重要意义。     

Penicillium peritonitis in an adolescent receiving chronic peritoneal dialysis

A 19-year-old female on chronic peritoneal dialysis developed acute peritonitis; multiple peritoneal fluid and catheter tip cultures yielded Penicillium species. She promptly responded to catheter removal and intravenous amphotericin B, followed by oral fluconazole, without further recurrences 1 year later. This is the first reported case of Penicillium peritonitis in the pediatric population. We review the microbiology and clinical spectrum of this disease, as well as the few previous reported cases in adults. Received: 2 November 1998 / Revised: 1 February 1999 / Accepted: 4 February 1999     

不同生物相容性的透析膜对红细胞免疫功能的影响

目的：了解血液透析病人透析过程中红细胞免疫功能指标的动态改变及不同生物相容性的透析膜对其变化的影响。方法：分别采用铜仿膜（Ｃｕ膜）、聚砜膜（ＰＳ膜）、聚甲基丙烯酸甲酯膜（ＰＭＭＡ膜）,观察了透析过程中不同时相的红细胞免疫功能指标ＲＢＣ－Ｃ３ｂ和ＲＢＣ－ＩＣ的变化。结果：尿毒症病人的 ＲＢＣ－Ｃ３ｂ显著下降, ＲＢＣ－ＩＣ显著增高。透析开始后,早期 ＲＢＣ－Ｃ３ｂ进一步下降,其后逐渐上升;而 ＲＢＣ－ＩＣ早期逐渐增加,其后逐渐稳定。结论：Ｃｕ膜能明显地影响红细胞的免疫功能; Ｐｓ膜次之; ＰＭＭＡ膜对其影响最小。