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icu中血液凈化的應(yīng)用指南(參考版)

2024-10-04 05:47本頁(yè)面
  

【正文】 20(7):14161421.48. Tan HK, Baldwin I。Toole J, et al. Improving the delivery of continuous renal replacement therapy using regional citrate anticoagulation. Clin 2004。29(3):271277.45. Vargas Hein O, Kox WJ, Spies C. Anticoagulation in continuous renal replacement therapy. Contrib 。8(6):701707.43. KozekLangenecker SA, Kettner SC, Oismueller C, et al. Anticoagulation with prostaglandin E1 and unfractionated heparin during continuous venovenous hemofiltration. Crit Care 1998。30(4):301307.41. Reeves JH, Cumming AR, Gallagher L, et al. A controlled trial of lowmolecularweight heparin (dalteparin) versus unfractionated heparin as anticoagulant during continuous venovenous hemodialysis with filtration. Crit Care 1999。69(6):527534。20(2):155161.38. Oudemansvan Straaten HM, Wester JP, de Pont AC, et al. Anticoagulation strategies in continuous renal replacement therapy: can the choice be evidence based? Intensive Care 2006。30(2):260265.36. Hirsh J, Raschke R. 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A pilot study of highadsorption hemofiltration in human septic shock. Int J Artif 2007。65(1):3442.22. Morgera S, Haase M, Rocktaschel J, et al. High permeability haemofiltration improves peripheral blood mononuclear cell proliferation in septic patients with acute renal failure. Nephrol Dial 2003。58(4):17511757.20. Heering P, Ivens K, Thumer O, et al. The use of different buffers during continuous hemofiltration in critically ill patients with acute renal failure. Intensive Care 1999。156(287296.18. Maccariello E, Rocha E, Dalboni MA, et al. Customized bicarbonate buffered dialysate and replacement solutions for continuous renal replacement therapies: effect of crystallization on the measured levels of electrolytes and buffer. Artif 2001。62(5):18551863.16. Thomas CM, Zhang J, Lim TH, et al. Concentration of heparinlocking solution and risk of central venous hemodialysis catheter malfunction. Asaio 2007。45(5):315319.14. Canaud B, Chenine L, Henriet D, et al. Optimal management of central venous catheters for hemodialysis. Contrib 。49(1):99108.12. Canaud B, Desmeules S, Klouche K, et al. Vascular access for dialysis in the intensive care unit. Best Pract Res Clin 2004。156(275286.10. Parienti JJ, Thirion M, Megarbane B, et al. Femoral vs jugular venous catheterization and risk of nosoial events in adults requiring acute renal replacement therapy: a randomized controlled trial. 28 2008。9(3):R266273.8. Tordoir J, Canaud B, Haage P, et al. EBPG on Vascular Access. Nephrol Dial 2007。30(2):124132.6. Gotch FA. Kt/V is the best dialysis dose parameter. Blood 。6(5):429433.4. Ronco C, Bellomo R, Homel P, et al. Effects of different doses in continuous venovenous haemofiltration on outes of acute renal failure: a prospective randomised trial. 1 2000。13(6):385402.2. Rogiers P, Zhang H, Pauwels D, et al. Comparison of polyacrylonitrile (AN69) and polysulphone membrane during hemofiltration in canine endotoxic shock. Crit Care 2003。h)持續(xù)16~18h中、小分子溶質(zhì)清除能力強(qiáng)IHDF高高高通量100~2003510~20中、小分子溶質(zhì)清除能力強(qiáng)注: (Lp>20);低通量濾器(Lp<10). Lp即單位面積膜超濾系數(shù),單位為mL/⒉置換 (透析)液速率和血流速率可根據(jù)實(shí)際情況調(diào)整⒊Qb Qf Qd 表3各種CRRT模式的要點(diǎn)和主要特點(diǎn) 治療原理濾器超濾系數(shù)血流量置換 (透析)液速率主要特點(diǎn) 對(duì)流彌散Qb(mL/min)Qf(mL/kg抗生素在RRT過程中影響因素表2各種IRRT模式的要點(diǎn)和主要特點(diǎn) 治療原理濾器超濾系數(shù)血流量置換 (透析)液速率主要特點(diǎn) 對(duì)流彌散Qb(mL/min)Qf(mL/kg因此,疾病狀態(tài)、藥物和CRRT的機(jī)械因素顯著降低了常規(guī)藥代動(dòng)力學(xué)計(jì)算公式?jīng)Q定抗生素劑量應(yīng)用的可能性[133]。血流速率和透析液速率的升高可改變跨膜壓而增加藥物的清除率。同樣,容易穿透組織且與組織結(jié)合的抗生素具有較大容積分布,CRRT清除也較少;另外,全身感染本身也可以增加抗生素的容積分布而半衰期延長(zhǎng),從而改變多種抗生素的蛋白結(jié)合。接受CRRT治療的重癥患者,其藥代動(dòng)力學(xué)非常復(fù)雜,有多個(gè)因素影響清除率,而根據(jù)這些參數(shù)推薦一個(gè)統(tǒng)一的抗生素治療劑量也非常困難。IRRT持續(xù)時(shí)間較短,對(duì)藥物的影響較小,因此文獻(xiàn)報(bào)道較少。RRT過程中,動(dòng)脈和靜脈內(nèi)的藥物濃度不同,為更加精確計(jì)算SC,取動(dòng)脈和靜脈濃度的平均值。 ([A] + [V] ) 247。藥物的篩漏系數(shù)(Sieving coefficient, SC )在不同RRT模式下各異,而藥物的清除效率與滲漏系數(shù)相關(guān)。 主要介紹氨基酸和蛋白質(zhì)丟失量以及如何補(bǔ)充二、藥物劑量調(diào)整RRT過程中,藥物清除率與腎臟、CRRT、其他器官代謝等三個(gè)因素相關(guān)。~ g/kg/ d的蛋白,目的在于維持正氮平衡。一、蛋白質(zhì)和氨基酸。CRRT時(shí)可增加除脂肪以外的營(yíng)養(yǎng)素如氨基酸、糖及微量元素的丟失,丟失量報(bào)導(dǎo)不一,可能與超濾液中糖的含量、置換液與血漿濃度梯度、CRRT通透量諸因素有關(guān)。血流速率與血小板關(guān)系 第五部分CRRT過程中的藥物劑量調(diào)整及營(yíng)養(yǎng)支持血液凈化過程中,不但有害物質(zhì)被清除體外,而且機(jī)體原有的電解質(zhì)、蛋白質(zhì)或氨基酸以及藥物等也可被清除體外。感染的預(yù)防㈢ 血小板降低CRRT可引起血小板降低,嚴(yán)重者需中止RRT治療。導(dǎo)管穿刺處的血腫可并發(fā)感染,應(yīng)積極預(yù)防。低血壓原因和處理㈡ 感染管道連接、取樣、置換液和血濾器更換是外源性污染的主要原因;最為嚴(yán)重的是透析液或置換液被污染引起嚴(yán)重的血流感染。這可以采用生物相容性高的濾器或透析器加以避免。下述嚴(yán)重并發(fā)癥應(yīng)及時(shí)處理:常見并發(fā)癥描述:4大類㈠ 低血壓低血壓是血液透析模式下的常見并發(fā)癥,血液濾過時(shí)少見。而一項(xiàng)回顧性研究表明,采用碳酸氫鈉配方進(jìn)行血濾治療時(shí)可出現(xiàn)低血糖[126],因此,應(yīng)根據(jù)需要選擇恰當(dāng)?shù)难潜O(jiān)測(cè)和控制方案。RRT過程中凝血發(fā)生動(dòng)態(tài)變化而需檢測(cè):抗凝劑、HIT、無(wú)抗凝后凝血恢復(fù)㈣RRT中血電解質(zhì)和血糖監(jiān)測(cè)RRT過程中可能出現(xiàn)電解質(zhì)、酸堿紊亂,應(yīng)定期監(jiān)測(cè)。定期行凝血的化驗(yàn)檢查,以便及時(shí)調(diào)整抗凝方案和發(fā)現(xiàn)HIT綜合征。 正水平衡病人死亡率高㈢凝血功能監(jiān)測(cè)RRT應(yīng)用抗凝劑時(shí)易發(fā)生出血?;谝陨匣A(chǔ),該中心應(yīng)用利尿劑、小劑量多巴胺及RRT策略控制并發(fā)ARF的干細(xì)胞移植兒童的液體量,觀察發(fā)現(xiàn)有效糾正液體過負(fù)荷可降低病死率[125]。Vincent等在24個(gè)歐洲國(guó)家的198個(gè)ICU進(jìn)行的回顧性觀察顯示:ICU病死率除與sepsis的發(fā)生率相關(guān)外,還同年齡和正水平衡密切相關(guān)[123]。血液動(dòng)力學(xué)監(jiān)測(cè)的理由:IHD可有低血壓;負(fù)水治療㈡體液量監(jiān)測(cè)CRRT過程中監(jiān)測(cè)體液量的目的在于恢復(fù)患者體液的正常分布比率。重癥患者常伴有體液潴留而需負(fù)水平衡,但是在負(fù)水平衡開始過程中必需密切監(jiān)測(cè)血流動(dòng)力學(xué),防止引發(fā)醫(yī)源性有效容量缺乏導(dǎo)致組織器官的低灌注。多種毒物的清除模式 第四部分 治療過程中的監(jiān)測(cè)和并發(fā)癥處理一、監(jiān)測(cè)㈠血流動(dòng)力學(xué)重癥患者RRT過程中易發(fā)生血流動(dòng)力學(xué)不穩(wěn)定,特別是IHD治療時(shí)發(fā)生率更高??刹捎玫哪J接蠧VVH(毒鼠強(qiáng))[118]、低流量血液透析(如丙戊酸鈉中毒)[119]、血液透析序貫CVVHD(如金屬鋰中毒)[120]、高效血液透析(萬(wàn)古霉素過量)[121]、CAVHD(如乙二醇中毒)[122]等。血液灌流依賴于吸附劑、酶、活細(xì)胞等對(duì)血液某些成分進(jìn)行吸
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