CN1964752A - 盖尤其是消毒盖、用于腹膜透析的检测装置、用于腹膜透析的袋组件及其应用 - Google Patents
盖尤其是消毒盖、用于腹膜透析的检测装置、用于腹膜透析的袋组件及其应用 Download PDFInfo
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Abstract
本发明涉及一种盖尤其是消毒盖,用于保护和/或封闭腹膜透析用的腹部接口以及一种用于腹膜透析的检测装置。本发明还涉及一种用于腹膜透析的袋组件及其应用。考虑到在腹腔内输液顺序错误的部分严重的后果,本发明的目的在于,防止在腹膜透析中错误的输液顺序。按本发明上述目的通过以下技术方案实现,即:一种盖尤其是消毒盖具有有关相应地位于患者腹腔内的介质的信息。通过这种方法,在充满腹腔和移除袋组件后的任何时候都能得知目前在腹腔内的介质以及获得关于介质的量、浓度以及制造商的说明,这些说明在腹膜透析的接下来的步骤中需要注意。
Description
技术领域
本发明涉及一种盖,尤其是一种消毒盖,用于保护和/或封闭腹膜透析用的腹部接口以及一种用于腹膜透析的检测装置。本发明还涉及一种用于腹膜透析的袋组件及其应用。
背景技术
例如由EP0715860B1和DE19814047C1已知一种用于腹膜透析的患者连接器。它们使在腹膜透析治疗范围内无菌的连接和断开成为可能。在结束腹膜透析后,通过这样的患者连接器将封闭塞插入到进入患者腹腔内软管件的连接器中。除此之外,一般来说在腹部接口处安置一无菌的消毒盖,以便阻止细菌的侵入所述腹部接口内。因此通入患者腹腔的通道被消毒地封闭。
尽管在通常设计为袋的容器分别标出,在其中包含多少量的哪一种液体。但是这些信息在输完液体和移除袋后就不再存在。因为比如在CAPD(连续性非卧床腹膜透析)时,具有不同葡萄糖浓度的、渗透性的组分或者营养物的溶液必须按照一定顺序在一定的时间段由患者使用,这会容易地导致,他不再知道,目前在腹腔内存在哪一种液体以及多少量。更棘手的问题在于这种情况,即患者昏迷并且可能没有标出最后输入的溶液或者在具有轮班地更换人员的住院治疗中,可能导致在记录中的空白。
发明内容
考虑到在腹腔内输液顺序错误的部分严重的后果,本发明的目的在于,在腹膜透析中防止错误的输液顺序。
按本发明上述目的通过如下技术方案实现,即:盖尤其是一种消毒盖具有有关相应地位于患者腹腔内介质的信息。
通过这种方法,在充满腹腔和移除袋组件后的任何时候都能得知目前在腹腔内的介质以及得出其他如介质的量、浓度以及制造商的说明,这些说明在腹膜透析的接下来的步骤中需要注意。
在本发明的范围内规定,所述信息涉及到介质的种类。
所述信息可以不仅涉及到每次使用的溶液,例如用于区别是葡萄糖还是氨基酸溶液。
同样也规定,所述信息涉及介质的量。
此外,合适的是,所述信息还涉及到介质的浓度。
因为在腹膜透析中使用不同的介质浓度的溶液,例如含1.0%、1.25%或1.75%钙的钙溶液,有意义的是,也将浓度包括到编码中。
属于本发明的是,所述信息以色码、条形码、符号的形式或者可触摸的形式尤其是盲文的形式设置在盖上。
这些仅是一些例子,如信息可以设置在盖上,这些信息也可以任意补充。
有利的是,每一个盖都与相配的袋系统形成一个整体。
通过这种方式保证,对每一个袋系统提供标明其特征的盖,这样,一方面使用新的消毒盖,另一方面袋系统通过标有信息的盖可视地标示。
本发明的有利的扩展构造在于,一个与盖分离的、用来封闭相应盖的腹部接口的封闭塞具有相应的信息。
因为这样盖不仅同时可以作为封闭盖用于腹部接口,亦即封闭腹部接口和防止感染,也可以将两种功能分开,即作为封闭塞和盖使用,有意义的是,在后一种情况下两个部分都相应地标示出最后输入的液体。
在本发明范围内还有一种腹膜透析的检测装置,检测装置具有用于对在盖尤其是消毒盖上设置的、关于相应地位于患者腹腔内介质的信息进行处理的装置。
这种检测装置可以有利地与盖共同发生作用,防止在腹膜透析中错误的输液顺序。
此外还规定,设置输出信息的装置。
因此检测装置可以通过文本、语言的标记用于输出信息,使得除了使用者,第三者(例如医院中的医护人员)也可以获得目前使用溶液的信息。
本发明的有利的扩展构造还在于,检测装置具有在连接一不恰当的介质时触发报警的装置。
在检测装置中存贮待使用的溶液的顺序或者至少在接下来的溶液之间的不兼容性,从而检测装置可以在这种情形下触发报警,并且对错误的顺序做出警告。
此外,本发明还涉及一种用于腹膜透析的袋组件,其中袋组件包括至少一个装有液体的袋和一个盖尤其是消毒盖,其中盖具有有关所述袋的内含物的信息,特别是有关内含物的种类、量以及浓度的信息。
两个此类袋组件可以根据在盖上标示的信息进行区分。
在此所述盖可以用于保留在患者的腹部接口处。
在本发明的范围内,信息以色码、条形码、符号的形式或者可触摸的形式尤其是盲文的形式设置在盖上。
最后还包括袋组件在腹膜透析中的应用,袋组件包括至少一个装有液体的袋和一个盖尤其是消毒盖,其中盖具有袋的内含物的的信息,特别是内含物的种类、量以及浓度的信息,并且按本发明在用液体充满患者腹腔内后,所述盖保留在患者的腹部接口处。
本发明的优点在于,不仅使用者而且第三者,必要时借助于检测装置,可以获知在腹膜透析中所使用的溶液的相关信息,此外在输液顺序错误时能自动发出警报。
附图说明
以下借助于附图说明本发明的实施例。
图1示出带有按照本发明的盖的患者连接器。
具体实施方式
通过图1可以清楚地看出,一患者连接器1通过软管3与一腹膜透析用的袋系统2连接。患者连接器1具有盖4尤其是消毒盖4,它通过一个中间件5与患者连接器1相连。该中间件5中间分开,并且保持盖4和患者连接器1处于无菌状态。患者连接器1与患者的腹部接口连接,以便进行溶液的更换。紧接着,腹部接口又通过封闭塞和盖4或者通过同时承担封闭功能的盖4来封闭。
为了避免混淆出错和可以分别调出相应所使用溶液的信息,使用盖4,它具有例如以色码、条形码、符号的形式或者可触摸的编码(例如盲文)表示的信息。这些信息也可以通过一个具有颜色辨别、条形码读取器或者光传感器的相应的检测装置读取。
此类编码的例子通过以下的列表说明:
物质/浓度 | 颜色 | 可触摸的突起 |
1.5%葡萄糖 | 黄 | 1 |
2.3%葡萄糖 | 绿 | 2 |
4.25%葡萄糖 | 红 | 3 |
氨基酸 | 蓝 | 4 |
复合葡萄糖 | 紫 | 5 |
1.0%钙(Ca++) | 0-33%黑 | 无 |
1.25%钙(Ca++) | 34-66%黑 | 无 |
1.75%钙(Ca++) | 67-100%黑 | 无 |
对于腹膜透析中找到的其他物质,当然可以设置相应的编码。同样也可以设置编码组合,例如用于一定葡萄糖浓度和一定钙浓度。
在充满腹膜后,盖4保留在患者的腹部接口上,这样在相应所使用的消毒盖4上可以读出包含在腹膜内的液体。
通过这个方法,在患者昏迷时仍可以调出相关信息以及在输液顺序错误时获得警告提示。
Claims (14)
1.一种盖(4)尤其是消毒盖(4),用于保护和/或封闭腹膜透析用的腹部接口,其特征在于,所述盖(4)具有有关相应地位于患者腹腔内的介质的信息。
2.按照权利要求1所述的盖(4),其特征在于,所述信息涉及介质的种类。
3.按照权利要求1所述的盖(4),其特征在于,所述信息涉及介质的量。
4.按照权利要求1所述的盖(4),其特征在于,所述信息涉及介质的浓度。
5.按照权利要求1所述的盖(4),其特征在于,信息以色码、条形码、符号的形式或者可触摸的形式尤其是盲文的形式设置在盖(4)上。
6.按照权利要求1所述的盖(4),其特征在于,所述每个盖(4)都与相配的袋系统(2)形成一个整体。
7.按照权利要求1所述的盖(4),其特征在于,一与盖(4)分离的、用来封闭相应盖(4)的腹部接口的封闭塞具有相应的信息。
8.一种腹膜透析的检测装置,其特征在于,检测装置具有用于对在盖(4)尤其是消毒盖(4)上设置的、有关相应地位于患者腹腔内介质的信息进行处理的装置。
9.按照权利要求8所述的检测装置,其特征在于,设置用于输出信息的装置。
10.按照权利要求8所述的检测装置,其特征在于,所述检测装置具有在连接到一不恰当的介质时触发报警的装置。
11.一种腹膜透析的袋组件,其特征在于,袋组件包括至少一个装有液体的袋(2)和一个盖(4)尤其是消毒盖(4),其中盖(4)具有有关所述袋的内含物的信息,特别是有关内含物的种类、量以及浓度的信息。
12.按照权利要求11所述的袋组件,其特征在于,盖(4)用于保留在患者的腹部接口处。
13.按照权利要求11所述的袋组件,其特征在于,信息以色码、条形码、符号的形式或者可触摸的形式尤其是盲文的形式设置在盖(4)上。
14.袋组件在腹膜透析中的应用,袋组件包括至少一个装有液体的袋(2)和一个盖(4)尤其是消毒盖(4),其中盖(4)具有有关所述袋(2)的内含物的信息,特别是内含物的种类、量以及浓度的信息,并且在用液体充满患者腹腔内后,所述盖保留在患者的腹部接口处。
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DE102004027743.5 | 2004-06-07 | ||
DE102004027743A DE102004027743A1 (de) | 2004-06-07 | 2004-06-07 | Kappe, insbesondere Desinfektionskappe, Detektionsvorrichtung für die Peritonealdialyse, Beutelset für die Peritonealdialyse und dessen Verwendung |
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EP (1) | EP1753485B8 (zh) |
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CN (1) | CN100563733C (zh) |
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BR (1) | BRPI0511861B8 (zh) |
CA (1) | CA2566910C (zh) |
DE (1) | DE102004027743A1 (zh) |
EA (1) | EA012166B1 (zh) |
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-
2004
- 2004-06-07 DE DE102004027743A patent/DE102004027743A1/de not_active Ceased
-
2005
- 2005-06-03 AU AU2005251418A patent/AU2005251418B2/en not_active Ceased
- 2005-06-03 EA EA200602219A patent/EA012166B1/ru not_active IP Right Cessation
- 2005-06-03 KR KR1020077000271A patent/KR100892541B1/ko active IP Right Grant
- 2005-06-03 MX MXPA06014052A patent/MXPA06014052A/es active IP Right Grant
- 2005-06-03 US US11/628,371 patent/US8858493B2/en not_active Expired - Fee Related
- 2005-06-03 ES ES05753775T patent/ES2391023T3/es active Active
- 2005-06-03 JP JP2007526185A patent/JP4531814B2/ja not_active Expired - Fee Related
- 2005-06-03 EP EP05753775A patent/EP1753485B8/de not_active Not-in-force
- 2005-06-03 CN CNB2005800184748A patent/CN100563733C/zh not_active Expired - Fee Related
- 2005-06-03 CA CA2566910A patent/CA2566910C/en not_active Expired - Fee Related
- 2005-06-03 BR BRPI0511861A patent/BRPI0511861B8/pt not_active IP Right Cessation
- 2005-06-03 WO PCT/DE2005/001002 patent/WO2005120604A1/de active Application Filing
Also Published As
Publication number | Publication date |
---|---|
BRPI0511861B1 (pt) | 2018-04-17 |
EP1753485B8 (de) | 2012-10-24 |
EA200602219A1 (ru) | 2007-04-27 |
CA2566910A1 (en) | 2005-12-22 |
KR20070057762A (ko) | 2007-06-07 |
EP1753485A1 (de) | 2007-02-21 |
EA012166B1 (ru) | 2009-08-28 |
DE102004027743A1 (de) | 2006-01-05 |
EP1753485B1 (de) | 2012-08-01 |
JP4531814B2 (ja) | 2010-08-25 |
CA2566910C (en) | 2012-04-17 |
BRPI0511861B8 (pt) | 2021-06-22 |
CN100563733C (zh) | 2009-12-02 |
JP2008501449A (ja) | 2008-01-24 |
ES2391023T3 (es) | 2012-11-20 |
AU2005251418A1 (en) | 2005-12-22 |
US20080015492A1 (en) | 2008-01-17 |
AU2005251418B2 (en) | 2009-06-11 |
US8858493B2 (en) | 2014-10-14 |
KR100892541B1 (ko) | 2009-04-09 |
WO2005120604A8 (de) | 2007-03-08 |
MXPA06014052A (es) | 2007-05-09 |
BRPI0511861A (pt) | 2008-01-15 |
WO2005120604A1 (de) | 2005-12-22 |
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