双腔中文说明书

半永久单针双腔置换操作记录
摘要：
1.半永久单针双腔置换操作简介
2.操作过程详解
3.操作注意事项
4.总结
正文：
1.半永久单针双腔置换操作简介
半永久单针双腔置换操作是一种在医疗领域中常见的手术操作，主要涉及到血管内导管的置入与取出。

这种操作对于患者的治疗与康复有着重要的作用。

通过本篇文章，我们将详细介绍半永久单针双腔置换操作的相关内容。

2.操作过程详解
半永久单针双腔置换操作的过程可以分为以下几个步骤：
（1）准备工作：在操作前，医生会对患者进行全面的检查，确保患者身体状况符合手术要求。

同时，医生还会向患者详细解释手术过程及注意事项。

（2）皮肤消毒：在操作部位进行皮肤消毒，以减少手术感染的风险。

（3）穿刺：医生会选择合适的穿刺点，进行穿刺操作。

穿刺成功后，将导管送入血管内。

（4）固定导管：将导管的另一端固定在患者的皮肤上，确保导管稳定。

（5）测试导管通畅性：进行导管通畅性测试，确保导管正常工作。

（6）术后处理：术后对患者进行护理，观察患者身体状况，确保手术成
功。

3.操作注意事项
在进行半永久单针双腔置换操作时，医生和患者都需要注意以下几点：（1）严格遵循无菌操作规程，防止感染。

（2）选择合适的穿刺点和导管尺寸，确保操作顺利进行。

（3）在操作过程中，密切关注患者的反应，及时处理可能出现的问题。

（4）术后护理要做好，防止并发症的发生。

4.总结
半永久单针双腔置换操作是一种在医疗领域中常见的手术操作，对于患者的治疗与康复具有重要意义。

双腔起搏器操作流程下载温馨提示:该文档是我店铺精心编制而成，希望大家下载以后，能够帮助大家解决实际的问题。

文档下载后可定制随意修改，请根据实际需要进行相应的调整和使用，谢谢!并且，本店铺为大家提供各种各样类型的实用资料，如教育随笔、日记赏析、句子摘抄、古诗大全、经典美文、话题作文、工作总结、词语解析、文案摘录、其他资料等等，如想了解不同资料格式和写法，敬请关注!Download tips: This document is carefully compiled by theeditor. I hope that after you download them,they can help yousolve practical problems. The document can be customized andmodified after downloading,please adjust and use it according toactual needs, thank you!In addition, our shop provides you with various types ofpractical materials,such as educational essays, diaryappreciation,sentence excerpts,ancient poems,classic articles,topic composition,work summary,word parsing,copy excerpts,other materials and so on,want to know different data formats andwriting methods,please pay attention!双腔起搏器操作流程一、术前准备阶段。

在进行双腔起搏器植入手术之前，需要进行全面细致的准备工作。

一次性使用无菌硅胶导尿管使用说明书环氧乙烷(Ethylene Oxide) 灭菌只限使用一次保持干燥包装若开启或损坏，切勿使用避免阳光直射使用前请仔细阅读所有说明、警告和注意事项。

生产许可证编号：鲁食药监械生产许20180066号医疗器械注册证编号：鲁械注准20182140383产品技术要求编号：鲁械注准20182140383产品型号规格：一次性使用无菌硅胶导尿管按导管外径不同划分为不同规格（见表 1），医生可以根据成人男女及儿童等具体情况选用不同导尿管。

表1 导尿管型号及规格型号规格标准型双腔 2.0mm(6Fr)/2.7mm(8Fr)/3.3mm(10Fr)/4.0mm(12Fr)/4.7mm(14Fr)/5.3mm(16Fr)/6.0mm(18Fr)/6.7mm(20Fr)/7.3mm(22Fr)/8.0mm(24Fr)/8.7mm(26Fr)/9.3mm(28Fr)/10.0mm(30Fr）三腔 4.7mm(14Fr)/5.3mm(16Fr)/6.0mm(18Fr)/6.7mm(20Fr)/7.3mm(22Fr)/8.0mm(24Fr)/8.7mm(26Fr)/9.3mm(28Fr)/10.0mm(30Fr）女用型双腔 2.0mm(6Fr)/2.7mm(8Fr)/3.3mm(10Fr)/4.0mm(12Fr)/4.7mm(14Fr)/5.3mm(16Fr)/6.0mm(18Fr)/6.7mm(20Fr)/7.3mm(22Fr)/8.0mm(24Fr)/8.7mm(26Fr)/9.3mm(28Fr)/10.0mm(30Fr）三腔 4.7mm(14Fr)/5.3mm(16Fr)/6.0mm(18Fr)/6.7mm(20Fr)/7.3mm(22Fr)/8.0mm(24Fr)/8.7mm(26Fr)/9.3mm(28Fr)/10.0mm(30Fr）标准型（双腔、三腔）：使用人群不分性别，推荐1-3岁儿童选用10Fr及以下规格，4-7岁儿童选用10-12Fr，8-10岁儿童选用12Fr，11-18岁儿童选用12-18Fr，建议成人选用14Fr及以上规格，操作人员还可根据实际情况选用合适规格。

For Single Use Only DescriptionDouble Lumen oximetry catheters arenon-balloon catheters that provide the means for monitoring hemodynamic pressures, taking blood samples, and for continuously monitoring venous oxygen saturation using an Edwards monitoring system and Model OM2 optical module.IndicationsDouble Lumen oximetry catheters are indicated for the assessment of a patient’s hemodynamic condition through blood sampling, hemodynamic pressure monitoring, and venous oxygen saturation measurement. ContraindicationsAlthough there are no absolute contraindications to the use of the Double Lumen oximetry catheters, relative contraindications may include patients with recurrent sepsis or ahyper-coagulable state where the catheter could serve as a focus for septic or bland thrombus formation. A patient with a left bundle branch block may develop a right bundle branch block during catheter insertion, resulting in complete heart block. In such patients, the ability fortemporary transvenous pacing should beimmediately available (or the use of aSwan-Ganz Paceport or Pacing-TD catheter). Theuse of this catheter is also not recommended inlow birth weight infants due to the increased riskof intracranial bleeding.WarningsThis device is designed, intended, anddistributed for single use only. Do notre-sterilize or reuse this device. There areno data to support the sterility,nonpyrogenicity, and functionality of thedevice after reprocessing.Recommended EquipmentWarning: Compliance to IEC 60601-1 is onlymaintained when the catheter or probe(Type CF applied part, de fi brillation proof)is connected to a patient monitor orequipment that has a Type CF de fi brillationproof rated input connector. If attemptingto use a third party monitor or equipment,check with the monitor or equipmentmanufacturer to ensure IEC 60601-1compliance and compatibility with thecatheter or probe. Failure to ensuremonitor or equipment compliance to IEC60601-1 and catheter or probecompatibility may increase the risk ofelectrical shock to the patient/operator.Warning: Do not modify or alter theproduct in any way. Alteration ormodi fi cation may a ff ect patient/operatorsafety or product performance.1. Double Lumen oximetry catheter2. Edwards monitoring system3. Model OM2 Optical Module4. Sterile flush system and pressuretransducers5. Bedside ECG and pressure monitor systemIn addition, the following items should beimmediately available: antiarrhythmic drugs,defibrillator, and respiratory assist equipment.Oximeter SetupRefer to the appropriate operations manual fordetailed setup procedures.1. Connect the optical module to the Edwardsmonitoring system.2. Turn on the power switch.3. Connect the blue optical module connectorto the optical module. Make certain that theside of the connector labelled “TOP” is up asit is placed into the optical module.CalibrationPrecaution:In vitro calibration cannot beperformed with these catheters. For propercalibration, the catheter must be inserted intothe patient and an in vivo calibration performed(see appropriate operations manual for in vivocalibration procedures).Double Lumen Oximetry Catheters: 040F4 and 015F4Edwards, Edwards Lifesciences, the stylizedE logo, Paceport, Swan, and Swan-Ganz aretrademarks of Edwards Lifesciences Corporation.All other trademarks are the property of theirrespective owners.of the catheter tip position by chest X-ray film, noting insertion depth immediately following insertion. Ideally, the catheter tip should be positioned parallel to the vessel wall and no farther than the junction of the superior vena cava and right atrium.Warning: If there is any doubt that the catheter tip may not be intravascular, further steps should be taken to identify the exact location of the catheter tip, see Complications for cardiac perforation and vessel perforation.HemorrhageThe use of heparin infusions to maintain the patency of vascular catheters has been associated with germinal matrix-intraventricular hemorrhage in infants with birth weights under 2000 grams.Other ComplicationsCentral venous pressure catheters have also been associated with pneumothorax, air embolism, catheter embolism, nitroglycerin absorption, hemomediastinum/hydromediastinum, thoraces, and heparin induced thrombocytopenia.How SuppliedContents sterile and nonpyrogenic if package is unopened and undamaged. Do not use if package is opened or damaged. Do not resterilize.The packaging is designed to avoid crushing of the catheter. It is therefore recommended that the catheter remain inside the package until use. StorageStore in a cool, dry place. Temperature/Humidity Limitations:0° - 40 °C, 5% - 90% RHOperating ConditionsIntended to operate under physiological conditions of the human body.Shelf LifeThe recommended shelf life is marked on each package. Storage beyond the recommended time may result in catheter deterioration. Note: Resterilization will not extend the shelf life.Technical AssistanceFor technical assistance, please call Edwards Technical Support at the following telephone numbers: Inside the U.S. and Canada(24 hours): ................... 800.822.9837 Outside the U.S. and Canada(24 hours): ................... 949.250.2222 In the UK: ..........***********-Option4 In Ireland: .............. 01 8211012 Option 4 Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. DisposalAfter patient contact, treat the device as biohazardous waste. Dispose of in accordance with hospital policy and local regulations. Prices, specifications, and model availability are subject to change without notice.Refer to the symbol legend at the end of this document.Sterilized Using Ethylene OxideManufacturerEdwardsOne Edwards Way Irvine, CA 92614 USA Made in USATelephone 949.250.2500 800.424.3278FAX949.250.2525Edisonstrasse 685716 UnterschleissheimGermany11/16©Copyright 2016, Edwards Lifesciences LLCAll rights reserved.WEB IFU 10016115001 ADOC-0053072 ASymbol Legend。

ReCrossVascular Intervention // Coronary Dual Lumen OTW MicrocatheterDesigned for effective guide wire support andlesion crossingUniquely versatile guide wire redirection possibilities from two OTW lumens and three exit portsLow profile, trappable in 6FA unique solution for guide wire redirection and supportManufacturer:IMDS Operations B.V. Ceintuurbaan Noord 1509301 NZ Roden, The NetherlandsTel +31 (0)50 8200230************Distributor:BIOTRONIK AG Ackerstrasse 68180 Bülach, Switzerland Tel +41 (0) 44 8645111Fax +41 (0) 44 8645005*********************© 2019 BIOTRONIK AG – All rights reserved.Specifications are subject to modification, revision and improvement.450799/B /S e p _2019R eCrossD ual Lumen OTW MicrocatheterIndicated to support guide wires during access of coronary vasculature.*Technical Data Guide wire Guide wire size 0.014"Shaft design Reinforced shaft Lesion entry profile 1.5FExit markers 95 cm and 105 cm Coating HydrophilicShaft profileOval shaft 2.3F x 3.3F Guide wire compatibility0.014"Ordering InformationOrdering number IMDS article number Guiding catheter compatibility Usable length 451671RC14140255F140 cmVascular InterventionCoronaryThe crossability of ReCross through occluded lesions is comparable to best in class antegrade single lumen microcatheters. Two completely separate over the wire (OTW) lumens and a total of three exit ports, provide physicians additional possibilities to resolve complex PCI.Radiopaque tipHub stylet lumenRemovable styletUsable length: 140 cmHydrophilic coatingHub tip lumenExit port stylet lumen 8 mmExit marker at 95 cm and 105 cmExit port tip lumen 12 mmReinforced shaftUniquely versatile dual lumen catheter*Indication as per IFU.。

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Widely used in the ceramics industry on dirty water, clays, grout etc General purpose for use on water, most hydrocarbons and mild chemicalsCaustic solutions and dilute acids. Poor on oils and solventsGeneral purpose for use on water, most hydrocarbons and mild chemicals Main Properties and UsesMin Optimum Operating TemperaturesDiaphragmPump Model/Size/Material -18F -28C -11F -24C 50 to 140F 10 to 60C 50 to 140F 10 to 60C 50 to 140F 10 to 60C 50 to 130F 10 to 54C 50 to 130F 10 to 54C 50 to 130F 10 to 54C 50 to 212F 10 to 100C 50 to 140F 10 to 60C-10F -23C -4F -20C -40F -40C -40F -40C 32F 0C -10F -23C N/A N/A Elastomer Buna-N EPDM Geolast Neoprene Polyester Polyurethane PTFE Santoprene Stainless Steel B06 - 1/4" Stainless Steel B25 - 1” Aluminium B40 - 1 1/2” Stainless Steel X75 - 3” Cast IronB15 - 1/2” Polypropylene B50 - 2” PVDFB25 - 1” Full Flow 2:1B50 - 2” Stainless SteelB15 - 1/2” AluminiumM e t a l l i c P u m p sN o n -M e t a l l i c P u m p sH y g i e n i c P u m p s F D A P u m p sH i g h P r e s s u r e P u m p sP T F E P u m p s B40 - 1 1/2” Aluminium B50 - 2” Stainless Steel B06 - 1/4" PVDFB25 - 1” PVDFB50 - 2” Hygienic B25 - 1” Stainless Steel B25 - 1” Conductive PTFE B25 - 1” Cast IronB50 - 2” Aluminium X75 - 3” Stainless Steel B15 - 1/2” PVDFB15 - 1/2” Hygienic B50 - 2” Full Flow 2:1B15 - 1/2” Conductive PTFE B15 - 1/2” Stainless Steel B40 - 1 1/2” Cast IronX75 - 3” Aluminium B10 - 3/8” Polypropylene B50 - 2” Polypropylene B25 - 1” Standard 2:1B40 - 1 1/2” Stainless Steel B25 - 1” Stainless Steel B50 - 2” Cast IronB06 - 1/4" Polypropylene B25 - 1” Polypropylene B25 - 1” Hygienic B15 - 1/2” Stainless Steel B15 - 1/2” Virgin PTFE !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!B25 - 1” Virgin PTFEFluid Contact MaterialsAir Chamber Materials!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!S t a i n l e s s S t e e lP o l i s h e d S t a i n l e s sA l u m i n i u mC a s t I r o nN i c k e l P l a t e d A l u m i n i u mP o l y p r o p y l e n eS t a i n l e s s S t e e lE p o x y C o a t e d A l u m i n i u mE p o x y C o a t e d S t a i n l e s s S t e e lC o n d u c t i v e P T F EB u n a -NE P D M (I n c .F o o dG r a d e )G e o l a s tP o l y e s t e r (H y t e l )N e o p r e n e!!!!!!!!!!!!!!!!!!!!!!!!!!!!C o n d u c t i v e P T F EV i r g i n P T F EA l u m i n i u mC a s t I r o nP V D FP o l y p r o p y l e n eC o n d u c t i v e P o l y p r o p y l e n eViscosity GuideThis table is a guide only – cps = centipoise70 O i l 40 c p st e r sa t o J u i c e c p s30 O i l c p sc e r i n e c p s50 O i l 1 c p se 0 c p so n n a i s e 0 c p sa s s e s B 0 c p sr C r e a m 00 c p s!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!Ball Valve S.G.Materials Ball Valve Materials Max. Flow Max. Op PressureAir Inlet Max. Solid Size (mm)Fluid Connections Max Standard Weighted B50 - 2” Pumps Maximum 12000X75 - 3” Pumps Maximum 25000B06 - 1/4” Pumps B10 - 3/8” Pumps Maximum 200012005001000200040001000015000Maximum 2000B40 - 1 1/2” Pumps Maximum 12000B15 - 1/2” Pumps Maximum 5000B25 - 1” Pumps Maximum 50007.80N/AN/A 0.98N/AN/A N/A N/A N/A N/A N/A 1.23 2.641.0N/A 1.23 2.641.23 2.64212F 100C 356F 180C 158F 70C 158F 70C 212F 100C 212F 100C 212F 100C 176F 80C 3434111112076401480282011431171201203434111164420220220212012012076767640404014144136136484853032018060350125865001367553053015215248482616168898898895305305303203203201801801806060182”1 1/2”1”1/2”2”1”1”3/8”1/4”1/4”3”3”3”2”2”2”1 1/2”1 1/2”1 1/2”1”1”1”1/2”1/2”1/4”2” 150 RF2” 150 RF 1” 150 RF 1” 150 RF 1/2” 150 RF 1/2” 150 RF 2”1”1”3/8”3/8”1/4”1/4”3/4”3/8”3/8”1/4”3/4”3/8”1/4”3/4”3/8”1/4”3/4”3/4”3/8”3/8”1/4”1/4”1/4”1/4”1/4”3/4”3/4”3/4”3/4”3/4”3/4”3/8”3/8”3/8”3/8”3/8”3/8”1/4”1/4”1/4”77778.68.68.68.61616168.68.68.68.68.688887558.68.68.68.68.68.68.68.68.68.68.68.68.68.68.61001001001001251251251252322322321251251251251251161161161161007272125125125125125125125125125125125125125125125332266326331032663322222101010666666333222P T F E (O n e P i e c e )P o l y u r e t h a n eS a n t r o p r e n eP T F EV i t o nB u n a -NE P D M (I n c .F o o dG r a d e )N e o p r e n eS a n t o p r e n eS t a i n l e s s S t e e lP T F EV i t o nU K G P ML /M i nB S P (F )A N S I F l a n g eR J T (M )B S P (F )B a rP S I1/2” 150 RF 1/2” 150 RF 1” 150 RF 1” 150 RFAn ink pumping and mixing plant at Amcor Packaging in Australia using Blagdon 15 moulded pumps.Fully automated Rexson ink manufacturing plant. Blagdon 25 metallic pumps are used for mixing and recirculation.Blagdon 75 pump transferring paint from dispenser to blending vessel.Moulded Non Metallic SeriesMetallic SeriesMoulded Non Metallic SeriesPTFE Non Metallic SeriesHygienic SeriesMoulded Non Metallic SeriesMetallic SeriesPTFE – Non Metallic SeriesFull Flow High PressureHygienic SeriesMetallic SeriesMoulded Non Metallic SeriesMetallic SeriesMetallic SeriesFull Flow High PressureHygienic SeriesMetallic SeriesSubmersible Centrifugal Pump1” Aluminium 4 Port Pump also available in Stainless Steel, Polypropylene and Kynar 1” Industrial Stainless Steel Pumpc/w Steam Jacket1” Stainless Steel 2:1 Pump c/w Custom Flange Design2” Hygienic on Trolleyc/w Stainless Steel Trolley 1” Hygienic Pumpc/w Steam Jackets1/2” Aluminium with Stroke Counter1” Stainless Steel 2:1 Pump 1” Stainless with Steam Jacket4 Port Pump1/2” Aluminiumwith StrokeCounter2” Hygienicon Trolley1” HygienicMaintains constant oil density with varying flow Remote installation for ease of maintenance Ensures clean, filtered airCan be controlled independently of other equipmentBatch ControlLinkage to control equipmentGreater process control 10 - 30v DC, PNP normally openVirtually pulsation free flows Steadier pressuresLess vibration and noise Simple installation Variety of sizes and materials Automatically self-chargingANSI 150 as standard - also available:-- ANSI 300- PN16- Food Industry - RJT, DIN, TRI-CLAMPEase of connections to pipework systemsPulsation DampenerValve Block with SensorsFilter RegulatorsFlangesOil Bottle AssemblyExclusive to Blagdon Pump Robust heavy duty design Suitable for arduous installations Safe forunderground use - no aluminiumPakistan Singapore ThailandUKIndonesia LatviaPhilippines South AfricaTurkey USA ItalyMalaysiaPolandSpain UAE Japan Netherlands Saudi Arabia Sweden VenezuelaIndia Korea NorwayGLOBAL NETWORKAt Blagdon we are committed to providing our Customers with an exceptional product.Along with our global network of Distributors, will endeavour at all times to provide unrivalled customer satisfaction.To find your local Distributor click onDISTRIBUTOR from the home page.Finding the pump you want couldn’t be easier...Product LiteratureProduct specific literature is available which includes:Technical dataPerformance curvesApplicable industries/applications Available optionsTo view this online go to – LITERATURETo order additional copies go to – OTHER ENQUIRIESWorldwide DistributionAustralia Austria BelgiumDenmarkGermany Eire Hong Kong Columbia Finland HungaryCzech Republic FranceChile ChinaCanada How do I get a quotation?Go to ContactsI’d like to speak to a member of staffGo to ContactsI’d like to download some sales materialGo to LiteratureI’d like to download some technical information Go to Technical DetailsCan the pump handle my process?Go to Technical DetailsWhat options do I have?Go to ProductsHow does an airoperated pump work?Go to Blagdon Pump TutorialWhy use an air operated pump?Go to About Our PumpsOther EnquiriesLinksHome Sitemap Website FAQ's Website FeedbackBLAGDON PUMP(EUROPEAN PUMP GROUP)E-mail:************************:IDEX APG (ASIA PACIFIC)IDEX Asia Pacific Pte. 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雙腔靜脈導管
自我照護
建佑醫院 護理部 衛教小組
關心您的健康 雙腔靜脈導管為暫時性血液透析之血管通路。

藉由皮膚穿刺插入內頸靜脈或股靜脈，一般可使用一之八週。

正確完善的照顧導管，可降低感染及再重覆穿刺的機會。

◆日常須知日常須知：： 1. 導管需固定牢靠，避免糾結、牽扯或滑脫，管夾應置適當處並 關緊。

2. 以無菌技術更換傷口敷料，若傷口有潮濕滲血時，需隨時更換敷料。

3. 超過三天未透析者，導管需以生理食鹽水沖洗，並以抗凝劑充注導管以防凝固。

4. 導管插上約二週左右，入針處若有發紅現象但無疼痛症狀，屬正常情況，保持傷口敷料乾淨即可。

5. 傷口若有腫脹、發紅、分泌物流出或有壓痛現象，應告訴醫護人員。

6. 在家若有呼吸短促、胸痛、咳嗽不止、發燒、發冷等情形，應立刻到醫院處置。

7. 任何尖銳物品如剪刀、安全別針不可靠近導管。

8. 平時禁止由導管給藥或抽血，除非緊急需要及經醫師醫囑同意以避免導管感染。