CN102548476A - 医疗装置插入物以及插入和使用医疗装置的方法 - Google Patents
医疗装置插入物以及插入和使用医疗装置的方法 Download PDFInfo
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Abstract
提供了一种将医疗装置插入对象皮肤中的设备、以及插入医疗装置的方法。
Description
相关申请
本申请要求以下美国临时申请的权益:2010年3月24日提交的第61/317,243号美国临时申请;2010年5月17日提交的第61/361,374号美国临时申请;2010年6月29日提交的第61/359,774号美国临时申请;2010年7月2日提交的第61/411,262;以及2010年11月8日提交的第61/411,774号美国临时申请,这些文献的公开内容为了所有目的而以引证方式结合于此。
通过引证结合
为了所有目的而将这里描述的专利、申请和/或公开(包括以下专利、申请和/或公开)通过引证结合于此:美国专利号4,545,382;4,711,245;5,262,035;5,262,305;5,264,104;5,320,715;5,356,786;5,509,410;5,543,326;5,593,852;5,601,435;5,628,890;5,820,551;5,822,715;5,899,855;5,918,603;6,071,391;6,103,033;6,120,676;6,121,009;6,134,461;6,143,164;6,144,837;6,161,095;6,175,752;6,270,455;6,284,478;6,299,757;6,338,790;6,377,894;6,461,496;6,503,381;6,514,460;6,514,718;6,540,891;6,560,471;6,579,690;6,591,125;6,592,745;6,600,997;6,605,200;6,605,201;6,616,819;6,618,934;6,650,471;6,654,625;6,676,816;6,730,200;6,736,957;6,746,582;6,749,740;6,764,581;6,773,671;6,881,551;6,893,545;6,932,892;6,932,894;6,942,518;7,041,468;7,167,818;以及7,299,082;7,381,184;7,740,581;7,811,231;美国公开申请号2005/0182306;2006/0091006;2007/0056858;2007/0068807;2007/0095661;2007/0108048;2007/0149873;2007/0149875;2007/0199818;2007/0227911;2007/0233013;2008/0058625;2008/0064937;2008/0066305;2008/0071157;2008/0071158;2008/0081977;2008/0102441;2008/0148873;2008/0161666;2008/0179187;2008/0267823;2008/0319295;2008/0319296;2009/0018425;2009/0247857;2009/0257911;2009/0281406;2009/0294277;2009/0054748;2009/0054749;2010/0030052;2010/0065441;2010/0081905;2010/0081909;2010/0213057;2010/0325868;2010/0326842;2010/0326843;2010/0331643;2011/0046466;美国专利申请序列号12/624,767;12/625,185;12/625,208;12/625,524;12/625,525;12/625,528;12/628,177;12/628,198;12/628,201;12/628,203;12/628,210;12/698,124;12/698,129;12/699,653;12/699,844;12/714,439;12/730,193;12/794,721;12/807,278;12/842,013;12/870,818;12/871,901;12/873,301;12/873,302;13/011,897;以及美国临时申请号61/238,646;61/246,825;61/247,516;61/249,535;61/317,243;61/325,155;61/345,562和61/359,265。
背景技术
检测和/或监测某些个体的葡萄糖水平或其它分析物,比如乳酸、氧、AIC等对其健康是至关重要的。例如,监测葡萄糖对糖尿病患者来说尤其重要。糖尿病患者通常通过监测葡萄糖水平来确定葡萄糖水平是否维持在临床安全范围内,同样还利用该信息来确定是否需要胰岛素来降低体内的葡萄糖水平和/或确定什么时候需要胰岛素来降低体内的葡萄糖水平或者什么时候需要额外的葡萄糖来提高体内的葡萄糖水平。
增加的临床数据表明葡萄糖监测和葡萄糖控制的频率之间有很大的关联。尽管存在上述关联,但由于便利性、测试判定、葡萄糖检测造成的疼痛及成本等一系列因素,许多经诊断患有糖尿情况的患者仍然不能经常监测葡萄糖水平。
已开发了装置用于自动监测分析物,比如血液或间质液(“ISF”)等体液中或其他生物体液中的葡萄糖。一些分析物测量装置构造成使得将至少一部分装置放置在使用者皮肤表面的下面,例如使用者的血管或皮下组织中,以便在体内完成监测。
随着分析物监测装置和系统的不断开发,需要低成本、方便且能减少疼痛、提供谨慎监测以支持频繁地监测分析物以提高葡萄糖控制水平的分析物监测装置、系统及方法、以及制作该分析物监测装置和系统的工艺。
发明内容
提供了一种用于将医疗装置插入对象的皮肤中的设备,其包括:在其中限定纵向腔体和延伸进入腔体中的干扰件的壳体;偏压件;与偏压件接合以从近端位置移动至远端位置,并进一步被配置为在未对准结构和对准结构之间移动的驱动件,在未对准结构中,驱动件的远端移动被干扰件阻止,在对准结构中,驱动件的远端移动不被干扰件阻止;以及具有对准表面的用于使驱动件从未对准结构移动至对准结构的致动器。
在一些实施方式中,致动器可从近端位置移动至远端位置。在一些实施方式中,致动器的远端移动压缩第一偏压件。在一些实施方式中,驱动件的第一位置在相对于纵向腔体成斜角处。在一些实施方式中,驱动件的第二位置包括与纵向腔体基本上对准的结构。
提供了一种用于将医疗装置插入通过对象的皮肤中的设备,其包括:限定悬臂件的壳体;可在壳体内从收回位置移动至部分暴露位置的尖端;以及可释放地与尖端接合以与尖端一起移动然后插入对象皮肤的电化学传感器;其中,悬臂件弹性地接触尖端和传感器中的至少一个。
在一些实施方式中,壳体包括用于释放电化学传感器的远端开口。在一些实施方式中,壳体限定用于容纳插入物的驱动件的纵向凹口。在一些实施方式中,壳体包含干燥剂。在一些实施方式中,壳体限定一个或多个用于对准尖端和传感器中的一个的纵向脊部。
对于本领域的技术人员来说,在阅读如下更充分地描述的详细说明的基础上,所公开的主题的这些和其他特征、目的和优点将变得显而易见。
附图说明
参考以下简要描述的附图,提供了这里描述的主题的各种方面、特征和实施方式的详细描述。这些附图是示意性的而并不必成比例地画出,为了清楚起见,放大了部分部件和特征。附图示出了本主题的各种方面和特征,并可能整体或部分地示出本主题的一个或更多个实施方式或实例。
图1示出了一些实施方式中的用于实时测量分析物(例如葡萄糖)、数据采集和/或处理的分析物监测系统;
图2至图3是根据所公开的主题的另一实施方式的电化学传感器的视图;
图4至图5是根据所公开的主题的一个实施方式的针插座(needlehub)的示意图;
图6是根据所公开的主题的一个实施方式的尖端的远端视图;
图7是根据所公开的主题的一个实施方式的尖端的侧视图;
图8是根据所公开的主题的一个实施方式的尖端的侧视图;
图9是根据所公开的主题的一个实施方式的插入物的透视图;
图10是用于形成将在根据所公开的主题的一个实施方式的插入物中使用的尖端的替代实施方式的示意图;
图11是根据所公开的主题的一个实施方式的插入物的透视图;
图12是根据所公开的主题的一个实施方式的插入物的分开部分的透视图;
图13是根据所公开的主题的一个实施方式的插入物的分开部分的放大截面图;
图14是根据所公开的主题的另一插入物的侧视图;
图15至图17是根据所公开的主题的另一实施方式的图14的插入物的截面透视图;
图18是根据所公开的主题的另一插入物的透视图;
图19至图21是根据所公开的主题的另一实施方式的图18的插入物的透明侧视图;
图22是根据所公开的主题的另一插入物的透视图;
图23至图25是根据所公开的主题的另一实施方式的图22的插入物的截面透视图;
图26是根据所公开的主题的插入物的另一实施方式的截面的截面图;
图27是根据所公开的主题的图26的插入物的透视图;
图28至图31是根据所公开的主题的图26的插入物的部件的透视图;
图32示出了根据所公开的主题的图26的插入物的分解图;
图33是根据所公开的主题的图26的插入物的侧视图;
图34至图36是根据所公开的主题的图26的插入物的透明侧视图;
图37是根据所公开的主题的另一实施方式的插入物;
图38是根据所公开的主题的图37的插入物的截面的透视图;
图39是根据所公开的主题的图37的插入物的横截面图;
图40是根据所公开的主题的图37的插入物的侧视图;
图41至图44是根据所公开的主题的图37的插入物的部件的透视图;
图45是根据所公开的主题的图37的插入物的分解图;
图46是根据所公开的主题的图37的插入物的透明侧视图;
图47至图51是根据所公开的主题的另一插入物的透视图;
图52是所公开的主题的另一实施方式的分解透视图;
图53是根据所公开的主题的插入物的截面图;
图54至图55是从图53的插入物的下方看的透视图;
图56是根据所公开的主题的另一插入物的透视图;
图57至图60是图56的插入物的各种部件的透视图;
图61至图62是图56的插入物的各种部件的透视图;
图63至图65示出了图56的插入物的部件的不同子组件;
图66至图67是图56的插入物的部件的子组件的横截面图;
图68至图70示出了用来启动图56的插入物的步骤;
图71是根据所公开的主题的插入物组件的透视图;
图72是根据所公开的主题的图71的插入物组件的部件的透视图;
图73是根据所公开的主题的分析物测量系统的部件的透视图;
图74是根据所公开的主题的图71的插入物组件的分开部分的透视图;
图75是根据所公开的主题的图71的插入物组件的横截面图;
图76是根据所公开的主题的插入物组件的一部分的侧视图;
图77是根据所公开的主题的分析物传感器的视图;
图78至图79是根据所公开的主题的插入物组件的一部分的透视图;
图80至图90是根据所公开的主题的分析物传感器的视图;
图91至图92是根据所公开的主题的插入物组件的横截面图;
图93至图94是根据所公开的主题的另一插入物组件的横截面图;
图95至图96是根据所公开的主题的另一插入物组件的横截面图;
图97至图98是根据所公开的主题的插入物组件的一部分的视图;
图99是根据所公开的主题的插入物组件的一部分的横截面图;
图100至图101是根据所公开的主题的插入物组件的一部分的透视图;
图102至图105是根据所公开的主题的各种插入物组件的侧视图;
图106至图112是根据所公开的主题的尖端和尖端载体的视图;
图113是根据所公开的主题的插入物组件的一部分的透视图;
图114至图117是示出了根据所公开的主题的插入物组件的操作的透视图;
图118是根据所公开的主题的插入物组件的侧视图;
图119至图121是根据所公开的主题的插入物组件的横截面图;
图122是根据所公开的主题的尖端/传感器盒的一个实施方式的分开部分的透视图;
图123是根据所公开的主题的第一配置阶段中图122的盒子的透视图;
图124是根据所公开的主题的中性(neutral)状态中图122的盒子的横截面图;
图125是根据所公开的主题的中性状态中图122的盒子的透视图;
图126是根据所公开的主题的第一配置阶段中图122的盒子的横截面图;
图127是根据所公开的主题的第二配置阶段中图122的盒子的透视图;
图128是根据所公开的主题的第二配置阶段中图122的盒子的横截面图;
图129是根据所公开的主题的第三配置阶段中图122的盒子的透视图;
图130是根据所公开的主题的第三配置阶段中图122的盒子的横截面图;
图131是根据所公开的主题的插入物的部件的另一实施方式的分开部分的透视图;
图132是根据所公开的主题的中性状态中图131的盒子的透视图;
图133是根据所公开的主题的中性状态中图131的盒子的横截面图;
图134是根据所公开的主题的第二配置阶段中图131的盒子的透视图;
图135是根据所公开的主题的第二配置阶段中图131的盒子的横截面图;
图136是根据所公开的主题的第三配置阶段中图131的盒子的透视图;
图137是根据所公开的主题的第三配置阶段中图131的盒子的横截面图。
具体实施方式
这里提供了本公开的详细描述。应理解,结合以下描述,该主题并非限于所描述的特定实施方式,因为该主题的特定实施方式当然可以改变。还将理解,这里使用的术语仅是为了描述特定实施方式的目的,并非意在是限制性的,因为所公开的主题的范围将仅由所附权利要求限制。
在提供一定范围的值的地方,可理解,该范围的上限和下限之间的插入值、以及该所述范围中的任何其他所述的或插入的值均包含在所公开的主题内。每个所述范围还意在特别地公开所述范围的每个“子范围”。也就是说,还将每个比由对一个范围(其上限和下限在从外部下限到外部上限的范围内(除非上下文清楚地表明不是这样))给定的外部上限和外部下限的值指定的外部范围小的范围理解成包含在所公开的主题内,服从任何特定排除的范围或所述范围内的限制。在通过指定上限和下限中的一者或两者来规定范围的情况下,排除那些所述极限中的任一者或两者的或包括极限中的一者或两者的范围也包含在所公开的主题内,不管在描述范围时是否使用诸如“从”、“到”、“通过”或“包括”的词语。
除非另有规定,本文使用的所有科技词汇具有本发明所属领域的普通技术人员通常所了解的相同含义。尽管任何类似于或等同于本文所述的方法及材料也可用于对本公开的主题进行实践或测试,但现在只对优选方法及材料进行阐述。
除非另外说明,否则为了所有目的通过引证结合于此的在本公开中提到的所有公开物包括但不限于公开和描述这些公开物所提到的方法和/或材料。
仅为了其在本申请的申请日之前的公开而提供这里讨论的公开物。不应将这里的任何公开物理解成不允许在这种公开物之前由于在先发明而授权本公开的主题。此外,所提供的公开日可能与实际的公开日不同,此实际的公开日可能需要单独确认。
如这里使用的和在所附权利要求中使用的,单数形式“一”、“该”、“所述”包括复数对象,除非上下文明确表示不是这样。
不应将摘要或发明内容中包含的任何部分理解成限制公开范围。为了著录和方便的目的而提供摘要和发明内容,由于其格式和目的的原因,不应将其认为是全面的。
如本领域的技术人员将在阅读此公开内容的基础上理解的,这里描述并示出的各个实施方式中的每一个均具有不连续的部件和特征,在不背离本公开的主题的范围或实质的前提下,可容易将其与任何其他几个实施方式的特征分离或组合。可以所述事件的顺序、或以逻辑上可能的任何其他顺序执行任何所述方法。
对单个物品的参考包括存在多个相同物品的可能性。当用替代性的“或”提到两个或更多个物品(例如,部件或方法)时,这表示,任一个可分开地存在,或者其任何组合可一起存在,除了必须排除另外一个或更多个存在的情况。
通常,本公开的实施方式涉及用于将医疗装置至少部分地插入患者的皮肤中的设备。一些实施方式涉及检测体液中的至少一种分析物(例如葡萄糖)的体内方法和装置。因此,实施方式包括体内分析物传感器,其被构造为使得将传感器的至少一部分定位在用户体内(例如ISF内),以获得关于身体的至少一种分析物的信息,例如经皮定位在用户的身体中。在某些实施方式中,将体内分析物传感器与保持在用户身体上的电子装置单元接合,以处理从传感器获得的信息。
在某些实施方式中,将分析物信息从第一装置(例如体上电子装置单元)传递至第二装置(其可能包括用户界面特征,包括显示器等)。当可获得分析物信息时,可将信息从第一装置自动地和/或连续地传递至第二装置,或者可以不自动地和/或连续地传递,而是储存或记录在第一装置的存储器中。因此,在系统的许多实施方式中,仅当用户询问时,以用户可用的或看得见的形式获得由传感器/体上电子装置(例如体上电子装置)得到的分析物信息,从而使得用户选择数据通信的定时。在一些实施方式中,在没有数据通信的定时时,用户选择显示信息。
这样,在一些实施方式中,仅当用户需要时,向用户提供分析物信息,该信息对用户来说是明显的(设置在用户界面装置上),即使体内分析物传感器自动和/或连续监测体内分析物水平,即传感器在其使用寿命期间按照预定时间间隔自动监测分析物(如血糖)。例如,在指定的检测时间段内(如约14天)将分析物传感器进行体内定位并耦连至体上电子装置。在某些实施例中,将传感器产生的分析物信息自动从传感器电子组件传输至远程监测装置或显示装置,以便根据体上电子装置设定的时间表(例如约每1分钟、约每5分钟或约每10分钟等)在14天内输出至用户。在某些实施例中,传感器产生的分析物信息在用户规定的时间(例如当用户决定检查分析物信息的任何时间)只从传感器电子组件传输至远程监测装置或显示装置。此时,激活通信系统,并然后将传感器产生的信息从体上电子装置发送至远程装置或显示装置。
在其他实施例中,当分析物信息可用时,可将信息自动和/或连续地从第一装置传输至第二装置,并且第二装置存储或记录接收的信息而不向用户呈现或输出该信息。在此类实施例中,当信息可用时(例如,当传感器根据时间表检测分析物水平时),通过第二装置从第一装置接收该信息。然而,接收的信息最初存储在第二装置中,并且在检测到对第二装置上的信息的请求时,只输出给第二装置的用户界面或输出装置(如显示器)。
相应地,在某些实施例中,一旦本文所述的插入物用来将传感器电子组件件放置到身体上,使得体内传感器的至少一部分与体液(如ISF)接触。一旦传感器与电子部件电耦连时,可以通过给显示装置通电(或连续供电)并执行存储在并取自显示装置的存储器的软件算法将传感器产生的分析物信息从体上电子装置传输至所需显示装置,生成一个或更多个请求命令,控制信号或数据包发送至体上电子装置。显示装置的微处理器或专用集成电路(ASIC)的控制下执行的软件算法包括检测体上电子装置相对于显示装置的位置的程序,以促使传输生成的请求命令、控制信号和/或数据包。
显示装置可还包括存储在存储器中由一个或更多个微处理器和/或ASIC执行的程序,以响应于用户激活显示装置上的输入机构(如按下显示装置上的按钮、触发数据通信功能相关的软按钮等),生成一个或更多个请求命令、控制信号或数据包,并传输以发送至体上电子装置。将输入机构可替换地或额外地设置在构造成用于用户激活的体上电子装置上或之中。在某些实施例中,语音命令或音频信号可用于促使或指示微处理器或ASIC执行存储在存储器中的软件程序,以生成一个或更多个请求命令、控制信号或数据包并传输至体内装置。在语音激活或响应于语音命令或音频信号的实施例中,体上电子装置和/或显示装置包括麦克风、扬声器及存储在体上电子装置和/或显示装置的各个存储器中用来处理语音命令或音频信号的处理程序。在某些实施例中,将体内装置和显示装置相对于彼此定位于预定距离(例如接近距离)内启动了一个或更多个存储在显示装置的存储器中的软件程序,以生成并传输请求命令、控制信号或数据包。
可发送不同类型和/或形式和/或数量的信息以满足每个所需阅读,阅读需求包括但不限于以下的一个或更多个:当前分析物水平信息(即时间上与启动阅读的时间相对应的实时或最近获得的分析物水平信息)、预定时间段内的分析物的变化率、分析物变化率的速率(变化率加速度)、与在指定阅读之前获得并存储在组件的存储器中的分析物信息相对应的历史分析物信息。可以将实时、历史、变化率、变化率速率(如加速度或减速度)信息中的一些或全部发送至显示装置,供指定阅读。在某些实施例中,发送至显示装置的信息的类型和/或形式和/或数量可以是被预编程和/或不可更改的(如在制造过程中预设),或可以不是被预编程和/或不可更改的,以便在本领域可选择和/或可更改一次或多次(如通过激活系统的开关等)。相应地,在某些实施例中,针对每个所需阅读,显示装置将输出当前(实时)传感器产生的分析物数值(如以数字格式)、当前分析物变化率(如以分析物速率指示物的形式,比如指向指示当前速率的方向的箭头)、以及基于由体上电子装置的存储器获取并存储于其中的传感器读数的分析物走势历史数据(如,以图形轨迹形式)。另外,将与每个所需阅读相关的皮肤上或传感器上的温度读数或测量值从体上电子装置传输至显示装置。但是,温度读数或测量值可能不输出或显示在显示装置上,而可以结合由显示装置执行的软件程序使用以便纠正或补偿在显示装置上向用户输出的分析物测量值。
如上所述,实施例包括体内分析物传感器和体上电子装置,体内分析物传感器和体上电子装置一起提供躯体可佩戴式传感器电子组件。在某些实施例中,体内分析物传感器与体上电子装置完全接合为一体(制造期间固定连接),然而在其他实施例中,体内分析物传感器与体上电子装置在制造后是独立但可连接的(例如,在传感器插入身体之前、插入过程中或插入之后)。体上电子装置可包括容纳(除了用于体内定位的传感器部分之外)在包括粘附垫或可附接至粘附垫的防水外壳中的体内葡萄糖传感器、电子装置、电池及天线。在某些实施例中,该外壳能承受浸在水下一米处高达至少30分钟。在某些实施例中,该外壳能承受连续水下接触例如超过约30分钟,并根据其预期使用继续正常运转,而例如在外壳适用于水浸没的情况下不会对外壳电子装置造成水损坏。
实施例包括传感器插入装置,其还可被称为传感器传送单元等。插入装置可将体上电子装置组件完全保持在内隔室中,即,插入装置在制造过程期间可预装有体上电子装置组件(例如,可将体上电子装置封装在插入装置的无菌内隔室中)。在此类实施例中,插入装置可形成用于预先使用的传感器组件封装件(包括无菌封装件)或新的体上电子装置组件、和构造为将体上电子装置组件应用于患者身体的插入装置。
实施例包括便携式手持显示装置,便携式手持显示装置作为与体上电子装置组件间隔开的独立装置,从组件收集信息并为用户提供传感器产生的分析物读数。这种装置还可被称为计量器、读取器、监测器、接收器、人机接口装置、成对部件等。某些实施例可包括一体的体外分析物计量器。在某些实施例中,显示装置包括一个或更多个有线或无线通信端口,如USB、串行端口、并行端口等,构造为建立显示装置与另一单元(如体上电子装置、给电池再充电的供电单元、PC等)之间的通信。例如,显示装置的通信端口可以能够利用各自的充电电缆对显示装置电池充电和/或在显示装置与其兼容信息软件之间进行数据交换。
某些实施例中的兼容信息软件包括但不限于例如在显示装置、个人计算机、服务器终端上存在或在其上运行的独立或网络连接使能的(enabled)数据管理软件程序,例如以便进行数据分析、制作图表、数据存储、数据存档和数据通信以及数据同步化。某些实施例中的信息软件还可包括这样的软件,该软件用于执行可现场升级功能对显示装置和/或体上电子部件的硬件进行升级以便对显示装置和/或体上电子部件上存在的软件进行升级,而例如包括其他部件和/或包括软件缺陷或误差的硬件版本是固定的等等。实施例可包括触觉反馈部件(如振动马达等),其构造使得可以触觉反馈的形式传递相应的通知(例如,显示装置接收的成功所需读数)。
实施例包括嵌入计算机可读介质上的程序,即基于计算机的应用软件(本文中还可被称为信息软件或程序等),其具有从系统获得的分析物信息和/或用户自报数据。通过显示装置或体上电子部件将应用软件安装到主机,例如手机、PC、诸如网络电话的互联网使能的人机接口装置、个人数字助理等。信息程序可以转换在显示装置上或体内单元上获得的并存储的数据,以供用户使用。
仅为了方便起见,主要针对葡萄糖监测装置和系统、及葡萄糖监测方法描述了本公开的实施例,并且该描述并不用来限制本发明的范围。应理解,分析物监测系统可构造为在相同时间或不同时间监测各种分析物。
详细描述如下,实施例包括在预定监测时间段监测一个或更多个生理参数的装置、系统、试剂盒和/或方法,参数诸如为但不限于分析物水平、温度水平、心率、用户活动水平。还提供了制造方法。预定监测时间段可以小于约1小时,或者可包括约1小时以上,例如约几小时以上、例如约几天以上、例如约3天以上、例如约5天以上、例如约7天以上、例如约10天以上、例如约14天以上、例如约几个星期、例如约1个月以上。在某些实施例中,预定监测时间段到期后,系统的一个或更多个部件可自动在体上电子装置组件和/或显示装置中停用或禁用。
例如,预定监测时间段可始于将传感器定位于体内并与体液(诸如ISF)接触,和/或始于体上电子装置的启动(或通电为完全运作模式)。体上电子装置的初始化可通过由以下之一生成并传输的命令来实现:通过显示装置响应于开关的激活、和/或通过将显示装置放置到距体上电子装置在预定距离(如接近距离)内、或通过用户手动激活体上电子单元上的开关(例如按下按钮),或者这些激活可以由插入装置产生,例如正如2010年2月1日提交的第12/698,129号美国专利申请、及第61/238,646、61/246,825、61/247,516、61/249,535、61/317,243、61/345,562及61/361,374号美国临时申请所述,这些文献中的每一个的公开内容均通过引证结合于本文用于所有目的。
当响应于接收的来自显示装置的命令进行初始化时,体上电子装置从其存储器获取并执行软件程序以便充分对体上电子装置的部件进行通电,响应于从显示装置接收激活命令而有效地将体上电子装置置于完全运作模式。例如,在接收到来自显示装置的命令之前,通过内部电源(诸如电池)对体上电子装置中的一部分部件供电,而体上电子装置中的另一部分部件处于掉电或低功率(包括无功率)停用模式,或者所有部件都处于停用模式、掉电模式。当接收命令时,将体上电子装置部件的剩余部分或所有部分切换为主动全运行模式。
体上电子装置的实施例可包括具有包括在ASIC、微处理器、存储器等中执行的控制逻辑的电子装置的一个或更多个印刷电路板、以及形成单一组件的经皮定位的分析物传感器。当在一个预定的接近一时间段(例如约2分钟、例如小于约1分钟、例如小于约30秒、例如小于约10秒、例如小于约5秒、例如小于约2秒)内检测分析物监测系统的显示装置时、和/或直到在显示装置上输出确认(诸如声音和/或视频和/或触觉(振动))通知以指示成功从体上电子装置获取分析物相关信号时,体上电子装置可构造为提供与监测到的分析物水平相关的一个或更多个信号或数据包。在某些实施例中,对于失败的采集,还可以输出不同的通知。
在某些实施例中,监测到的分析物水平可以与血液或其他液体(如ISF)中的葡萄糖水平相关联和/或转换为葡萄糖水平。可利用体上电子装置来完成这种转换,但在许多实施例中,这种转换通过显示装置电子装置来完成。在某些实施例中,葡萄糖水平来源于ISF中监测的分析物水平。
分析物传感器可以是可插入于静脉、动脉或身体的包含分析物的其他部分。在某些实施例中,分析物传感器可定位成与ISF接触以检测分析物水平,其中检测到的分析物水平可用于推断用户血液或间质组织中的葡萄糖水平。
实施例包括经皮传感器以及可整体植入式传感器和可整体植入式组件,其中将包括分析物传感器的单一组件和电子装置设置在密封外壳(例如,密封的生物相容性外壳)中,以便植入用户体内用于监测一个或更多个生理参数。
实施方式包括设置于小的、重量轻的、电池供电的和用电控制的系统中的分析物监测器。可将这种系统构造为,用电化学传感器检测对象的物理参数(例如表示体内分析物水平的信号),并通过或不通过处理来收集这种信号。可用任何适当的测量技术从传感器获得信号,例如,可检测电流,可使用电位法等。这些技术可包括,但不限于电流分析法、电量分析法和伏安法。在一些实施方式中,传感系统可以是光学的、比色的,等等。在一些实施方式中,可将执行此初始处理的系统的部分构造为对另一单元提供原数据或至少初始处理的数据,以进一步收集和/或处理。例如,可通过有线连接(例如电连接),或用无线连接(例如IR或RF连接)来提供这种数据。
在某些系统中,分析物传感器与体上电子装置通信。体上单元可包括体上电子装置和传感器的至少一部分容纳于其中的壳体。
某些实施方式是模块化的。可将体上单元单独提供为在物理上与监测器单元不同的组件,例如,其对用户显示或以其他方式表示分析物水平。可将体上单元构造为,在通信链路上对监测器单元提供由传感器检测的分析物水平和/或其他信息(例如温度、传感器使用寿命等)。在一些实施方式中,监测器单元可包括例如移动电话装置、体内葡萄糖测量计、个人数字助理,或其他消费者电子装置(例如MP3装置、照相机、收音机、个人电脑等),或其他使得能够通信的数据处理装置。
显示器单元可执行各种功能,例如但不限于对所接收的分析物数据的数据存储和/或处理和/或分析和/或通信等,以产生与所监测的分析物水平相关的信息和/或处理其他信息。监测器单元可包含显示屏(其例如可用来显示所测量的分析物水平)、和/或以用声音对用户提供信息的音频部件(例如扬声器)、和/或对用户提供触觉反馈的振动装置。对于分析物监测系统的用户来说,能够看到趋势指示(包括任何正在进行的趋势的大小和方向,例如分析物的变化率或其他参数、以及对象高于和/或低于阈值(例如低葡萄糖和/高葡萄糖阈值)的时间量等)也是有用的;可用数字和/或用可视指示器显示这种数据,例如可改变可视属性的箭头,例如大小、形状、颜色、行为或方向。监测器单元可进一步适于从体内分析物测试条或者在体内分析物测试条附近接收信息,所述测试条可手动地或自动地进入监测器单元。在一些实施方式中,监测器单元可包含体内分析物测试条端口和相关的电子装置,以能够用体内测试条进行不连续的(例如血糖)测量(例如见6,175,752,其公开内容为了所有目的而通过引证结合于此)。
在可将一个或更多个部件可构造为单次使用和可将一个或更多个部件可构造为可重复使用的情况下,这些系统的模块性可改变。在一些实施方式中,将传感器设计为能够与体上电子装置附接和从体上电子装置拆离(并且体上单元可以是可重复使用的),例如,使得部件中的一个或更多个可重复使用一次或多次,而在其他实施方式中,可将传感器和体上电子装置提供为一体的、不可拆离的封装,可将其设计为在使用后是抛弃的,即是不可重复使用的。
体内监测系统的实施方式
为了说明而不是限制的目的,这里描述的插入物可与图1所述的示例性分析物监测系统一起使用。应理解,这里描述的插入物可自己地或与系统接合地与任何医疗装置一起使用。图1示出了根据本公开实施方式的示例性的基于体内的分析物监测系统100。如所示出的,在某些实施方式中,分析物监测系统100包括与体内分析物传感器14电接合的体上电子装置1100(其近端部分在图1中示出,并附接至粘附层218以用于附接在用户身体上的皮肤表面上)。体上电子装置1100包括限定内部隔室的体上壳体122。
图1中还示出了插入装置200(或这里描述的插入装置300、400、2400、2500、2700、3700),当操作时,入装置将分析物传感器14的一部分穿过皮肤表面经皮定位并与ISF流体接触,并将体上电子装置1100和粘附层218定位在皮肤表面上,如将在这里更详细地描述的。在某些实施方式中,在使用前将体上电子装置1100、分析物传感器14和粘附层218密封在插入装置200的壳体内,并且,在某些实施方式中,也将粘附层218密封在壳体内,或者粘附层能够提供密封以保持设备的无菌状态。例如,在美国专利申请号12/698,129和美国临时申请号61/238,646、61/246,825、61/247,516、61/249,535和61/345,562中讨论了与插入装置相关的其他细节,每篇申请的公开内容为了所有目的通过引证而结合于此。
返回参照上图1,分析物监测系统100包括:显示装置1200,该显示装置包括向用户输出信息的显示器1220;输入部件1210,诸如按钮、致动器,触敏开关、电容式开关、压敏开关、缓动盘(jog wheel)等,以向显示装置1200输入数据或命令或者控制显示装置1200的操作。值得注意的是,某些实施例可包括不含显示器的装置或没有用户界面部件的装置。这些装置可作为数据记录装置来用于存储数据和/或提供一根管道将数据从体上电子装置和/或不含显示器的装置传输至另一装置和/或位置。本文将阐述用作示例性目的的显示装置的实施例,其并不限制本发明的实施例。显而易见的是同样可以在某些实施例中使用不含显示器的装置。
在某些实施例中,体上电子装置1100构造为在监测时间段内将一些或所有接收自分析物传感器14的监测分析物相关数据存储在存储器中,并保持在存储器中直至使用期结束。在此类实施例中,在监测时间段结束时,例如,在通过从皮肤表面拆下在监测时间段内定位的体上电子装置1100而将分析物传感器14从用户身上拆下来之后,从体上电子装置1100获取存储的数据。在此类数据记录构造中,实时监测到的分析物水平在监测时间段内不传输至显示装置1200,或者以其它方式从体上电子装置1100传输而来,而是在监测时间段之后从体上电子装置1100获取。
在某些实施例中,显示装置1200的输入部件1210可包括麦克风,并且显示装置1200可包括构造为分析接收自麦克风的音频输入的软件,因此显示装置1200的功能和操作可由语音命令控制。在某些实施例中,显示装置1200的输出部件包括用于输出作为音频信号的信息的扬声器。为体上电子装置1100设置类似的语音响应部件,诸如扬声器、麦克风、及用于生成、处理和存储语音驱动信号的软件程序。
在某些实施例中,显示器1220和输入部件1210可集成到单一部件中,例如能够检测在显示器(如触摸屏用户界面)上的身体接触触摸的存在和位置的显示器。在此类实施例中,用户可通过使用一组预编程移动命令来控制显示装置1200的操作,包括但不限于单击或双击显示器、在显示器上拖动手指或仪器、朝彼此移动多个手指或仪器、将远离彼此移动多个手指或仪器等。在某些实施例中,显示器包括具有像素区的触摸屏,像素区具有用作LCD部件和触摸传感器的单一功能或双功能电容部件。
显示装置1200还包括与诸如远程终端(个人计算机)1700等外部装置进行有线数据通信的数据通信端口1230。数据通信端口1230的实例包括构造为连接至可兼容数据电缆的USB端口、迷你USB端口、RS-232端口、以太网端口、火线端口或其类似数据通信端口。显示装置1200还可包括整体式体外葡萄糖仪,葡萄糖仪包括接收用于体外葡萄糖测量的体外葡萄糖试纸的体外试纸端口1240。
仍然参照图1,某些实施例中的显示器1220被构造为显示多种信息,即,部分或全部信息可在同一时间或不同时间显示在显示器1220上。在某些实施例中,显示的信息是用户可选择的,以便用户能够自定义显示在指定显示屏上的信息。显示器1220可包括但不限于例如在监测时间段内提供葡萄糖值图形输出的图形显示器1380(其可显示诸如饮食、移动、睡眠、心率、血压等重要指标)、例如提供监测的葡萄糖值(该葡萄糖值是响应于信息请求获取或接收的)的数字显示器1320、以及例如通过移动显示器1220上的位置来指示分析物变化率和/或分析物变化率速率的走势或方向箭头显示器1310。
图1还示出,显示器1220还可包括例如为用户提供日期信息的日期显示器1350、为用户提供当日时间信息的当日时间信息显示器1390、以图形方式显示显示装置1200的电池状况(充电式或抛弃式)的电池电量指示显示器1330、例如在需要定期、常规或预定数量的用户校准事件的监测系统中通知用户有必要进行分析物传感器校准的传感器校准状态图标显示器1340、用于显示音频/振动输出或报警状态的音频/振动设置图标显示器1360、以及提供与诸如体上电子装置、数据处理模块1600和/或远程终端1700的其他装置进行无线通信连接指示的无线连接状态图标显示器1370。如图1另外示出的,显示器1220可进一步包括用于访问菜单、改变显示图形输出构造或用于控制显示装置1200操作的模拟触摸屏按钮1250、1260。
返回参照图1,在某些实施例中,显示装置1200的显示器1220(其附加于视觉显示器、或者替代视觉显示器)可构造为输出诸如报警和/或警报通知、葡萄糖值等的警告通知,警告通知可以是听得见的、可感触的或即听得见又可感触的。在一方面,显示装置1200可包括其他输出部件(如扬声器、振动输出部件等),以便除显示器1220上提供的可视输出指示外还为用户提供可听见的和/或振动的输出指示。在例如美国专利申请号12/871,901、美国临时申请号61/238,672,61/247,541,61/297,625中可获取进一步详情及其他显示器实施例,这些文献中的每一个的公开内容通过引用结合于本文用于所有目的。
在将体上电子装置1100定位于皮肤表面上并将分析物传感器14定位于体内与ISF(或其他合适体液)建立流体接触后,某些实施例中的体上电子装置1100构造为当体上电子装置1100从显示装置1200接收命令或请求信号时无线传输分析物相关数据(诸发,例如与监测到的分析物水平相对应的数据和/或监测到的温度数据、和/或存储的历史分析物相关数据)。在某些实施例中,体上电子装置1100可构造为至少定期传播与监测到的分析物水平相关的实时数据,当显示装置1200在体上电子装置1100传播的数据的通信范围内时,该数据由显示装置1200接收,即不需要来自显示装置的命令或请求来发送信息。
例如,显示装置1200可构造为向体上电子装置1100发送一个或更多个命令以启动数据传输,并且作为响应,体上电子装置1100可构造为将在监测时间段内收集的存储分析物相关数据无线发送至显示装置1200。显示装置1200进而可连接至远程终端1700(诸如个人计算机),并用作数据管道以将存储分析物水平信息从体上电子装置1100传输至远程终端1700。在某些实施例中,从体上电子装置1100接收的数据可存储在显示装置1200的一个或更多个存储器中(永久或暂时地)。在某些其他实施例中,显示装置1200被构造为数据管道,以将接收自体上电子装置1100的数据传递至与显示装置1200连接的远程终端1700。
仍然参照图1,还示出了分析物监测系统1000中具有数据处理模块1600和远程终端1700。远程终端1700可包括个人计算机、服务器终端、笔记本电脑或其它合适的包括用于数据管理和分析并与分析物监测系统1000中的部件进行通信的软件的数据处理装置。例如,远程终端1700可与局域网(LAN)、广域网(WAN)、或其它数据网络连接,以便于在远程终端1700和显示装置1200和/或数据处理模块1600之间进行单向或双向数据通信。
某些实施例中的远程终端1700可包括医生办公室或医院的一个或更多个计算机终端。例如,远程终端1700可位于除显示装置1200位置以外的位置。远程终端1700和显示装置1200可位于不同房间或不同建筑物内。远程终端1700和显示装置1200可至少间隔约一英里,例如至少间隔约100英里、例如至少间隔约1000英里。例如,远程终端1700可与显示装置1200在同一个城市中,远程终端1700可与显示装置1200在不同城市中,远程终端1700可与显示装置1200在同一个州(省)中,远程终端1700可与显示装置1200在不同州(省)中,远程终端1700可与显示装置1200在同一个国家中,或者例如远程终端1700可与显示装置1200在不同国家中。
在某些实施例中,诸如数据处理模块1600的独立可选数据传输/处理装置可设置在分析物监测系统1000中。数据处理模块1600可包括利用一个或更多个无线通信协议进行通信的部件,无线通信协议例如但不限于红外线(IR)协议、蓝牙协议、Zigbee协议及802.11无线LAN协议。包括基于蓝牙协议和/或Zigbee协议描述的通信协议的附加描述可在美国专利申请公开号2006/0193375中找到,该申请通过引用结合于本文用于所有目的。数据处理模块1600可进一步包括通信端口、驱动器或连接器,以与显示装置1200、体上电子装置1100、或远程终端1700中的一者或多者建立有线通信连接,所述通信端口、驱动器或连接器包括但不限于USB连接器和/或USB端口、以太网连接器和/或端口、火线连接器和/或端口、或RS-232端口和/或连接器。
在某些实施例中,数据处理模块1600被编程为按预定时间间隔(如每分钟一次、每五分钟一次等)将轮询或查询信号发送至体上电子装置1100,并作出回应从体上电子装置1100接收监测到的分析物水平信息。数据处理模块1600将接收到的分析物水平信息存储在其存储器中,和/或将接收到的信息传送或转发至另一个装置(如显示装置1200)。更具体地说,在某些实施例中,数据处理模块1600可构造为数据传送装置,以将接收到的分析物水平数据从体上电子装置1100转发或传递至显示装置1200或远程终端(例如通过数据网络,诸如蜂窝或WiFi数据网络)或转发或传递至显示装置1200和远程终端两者。
在某些实施例中,体上电子装置1100和数据处理模块1600可在彼此的预定距离(例如,约1-12英寸、或约1-10英寸、或约1-7英寸、或约1-5英寸)内定位于用户的皮肤表面上,从而维持体上电子装置1100与数据处理模块1600之间的定期通信连接。可替换地,数据处理模块1600可佩戴在用户的皮带或衣物上,从而维持体上电子装置1100与数据处理模块1600之间进行通信的所需距离,以便进行数据通信。在另一方面,数据处理模块1600的外壳可构造为与体上电子装置1100耦连或接合,从而使得两个装置组合或整合为单一组件并设置皮肤表面上。在其他实施例中,数据处理模块1600可拆卸地接合或连接至提供附加模块化的体上电子装置1100,使得数据处理模块1600根据需要可选地拆除或重新附接。
再次参照图1,在某些实施例中,数据处理模块1600被编程为按预定时间间隔(诸如每分钟一次、或每5分钟一次或每30分钟一次)或任何其他合适的或期望的可编程时间间隔向体上电子装置1100发送命令或信号,以向体上电子装置1100请求分析物相关数据。在收到请求的分析物相关数据时,数据处理模块1600保存所接收到的数据。这样,分析物监测系统1000可构造为按编程或可编程时间间隔接收连续监测到的分析物相关信息,该信息被存储和/或向用户显示。随后,可向显示装置1200、远程终端1700等提供或发送数据处理模块1600中存储的数据,以便于随后进行数据分析(诸如识别在监测时间段内葡萄糖水平偏移期间的频率、或者监测时间段内警告事件发生的频率),例如以便改善与治疗相关的决策。利用该信息,医生、医护人员或用户可对饮食、日常生活习惯和日常例行事务(如移动)等进行调整或进行修改。
在另一实施例中,数据处理模块1600向体上电子装置1100发送命令或信号,以便响应于用户激活设置于数据处理模块1600上的开关或响应于接收自显示装置1200的用户发起命令而接收分析物相关数据。在其他实施例中,数据处理模块1600构造为仅在预定时间间隔过去之后响应于接收用户发起命令而向体上电子装置1100发送命令或信号。例如,在某些实施例中,如果用户在编程时间段(如从上次通信约5小时(或从上次通信10小时、或从上次通信24小时))内不发起通信,则数据处理模块1600可被编程为自动向体上电子装置1100发送请求命令或信号。可替换地,数据处理模块1600可被编程为发起警告,以通知用户自上次数据处理模块1600与体上电子装置1100之间的通信以来预定时间时间段已结束。这样,用户或医护人员可对数据处理模块1600进行编程或构造以便提供对分析物监测方案的一定程度的服从,从而由用户维持或进行分析物水平的频率测定。
在某些实施例中,当检测编程或可编程警告条件时(例如,由分析物传感器14监测到的不在预定可接受的范围内的检测葡萄糖水平,其表示医疗或分析需要注意或干预的生理状态(例如低葡萄糖条件、高葡萄糖条件、即将发生的低葡萄糖条件、或即将发生的高葡萄糖条件)),一个或更多个输出指示可由体上电子装置1100的控制逻辑或处理器生成并在体上电子装置1100的用户界面上输出给用户,从而可及时采取纠正措施。另外地或可替换地,如果显示装置1200在通信范围内,则将输出指示或警告数据传输至显示装置1200,在检测到收到警告数据时,显示装置的处理器控制显示器1220输出一个或更多个通知。
在某些实施例中,体上电子装置1100的控制逻辑或微处理器包括基于从分析物传感器14获取的信息(例如当前分析物水平、分析物水平变化率、分析物水平变化加速度、和/或基于存储的监测到的分析物数据确定的且用于在监测时间段内根据时间提供分析物水平波动的历史走势或方向的分析物走势信息)来确定未来或预期分析物水平的软件程序。预测警告参数可以在显示装置1200中、或在体上电子装置1100中或在两者中被编程或可编程,并在预见用户的分析物水平达到未来水平前向用户输出。为用户提供了及时采取纠正措施的机会。
信息(比如在提供分析物走势信息的监测时间段内根据时间发生的监测分析物水平的变化或波动)可由显示装置1200、数据处理模块1600、和/或远程终端1700、和/或体上电子装置1100中的一个或更多个控制逻辑或微处理器确定。这种信息可以作为例如图表(诸如线条图)显示,以向用户指示由分析物监测系统1000测量的和预测的当前和/或历史和/或预测将来的分析物水平。这种信息还可显示为方向箭头(例如,见走势或方向箭头显示器1310)或其他图标,例如其在屏幕上相对于指示分析物水平是否增加或降低以及分析物水平增加或降低的加速度或减速度的参考点的位置。用户可利用该信息确定任何必要的纠正措施,以确保分析物水平保持在可接受的和/或临床安全范围内。其他视觉指示器(包括颜色、闪光、褪色等)、以及音频指示器(包括音高变化、音量变化、或音频输出和/或振动音调变化)或其他触觉指示器可结合于走势数据的显示器中,以便通知用户监测到的分析物水平的当前水平和/或方向和/或变化率。例如,基于确定的葡萄糖变化率、编程的临床意义的葡萄糖阈值水平(例如,高葡萄糖水平和/或低葡萄糖水平)、以及由体内分析物传感器产生的当前分析物水平,系统1000可包括存储在计算机可读介质上的算法,以用来确定达到临床意义水平所花费的时间和在读取临床意义水平之前(例如在预见临床意义水平之前30分钟、和/或20分钟、和/或10分钟、和/或5分钟、和/或3分钟、和/或1分钟等)输出通知的时间,且输出的强度等增加。
再次参照上图1,在某些实施例中,由数据处理模块1600执行的软件算法存储在外部存储器装置中,外部存储器装置诸如SD卡、微SD卡、紧凑闪存卡、XD卡、Memory Stick卡、Memory Stick Duo卡、或USB记忆棒/装置,这些装置包括存储在此类装置中的可执行程序,以便在连接至体上电子装置1100、远程终端1700或显示装置1200中的相应一个或更多个时执行。在另一方面,可为通信装置(诸如手机,例如包括WiFi或互联网使能的智能手机或个人数字助理(PDA))提供由数据处理模块1600执行的软件算法,作为用于由下载通信装置执行的可下载应用程序。
智能手机的实例包括基于AndroidTM、操作系统、WebOSTM、操作系统、或操作系统的手机,其具有数据网络连接功能以便通过因特网连接和/或局域网(LAN)进行数据通信。如上所述,PDA包括例如便携式电子装置,其包括一个或更多个微处理器及与用户界面(例如显示/输出单元和/或输入单元)进行数据通信的能力,并被构造为用于执行数据处理,例如,在互联网上传/下载数据。在此类实施例中,当建立远程终端1700与上述通信装置中的一个或更多个装置之间的通信时,远程终端1700可构造为向所述装置提供可执行应用软件。
在又一实施例中,可执行软件程序可设置于无线(OTA)作为OTA下载,从而无需与远程终端1700的有线连接。例如,可执行程序可作为软件下载自动下载到通信装置,并根据通信装置的构造安装在装置上供自动使用,或基于用户确认或认可而安装在通信装置上以执行应用程序的安装。软件的OTA下载和安装可包括更新或升级到数据处理模块1600和/或显示装置1200的现有功能或特征的软件应用和/或程序。
返回参照图1的远程终端1700,在某些实施例中,当建立远程终端1700和显示装置1200和/或数据处理模块1600之间的通信时,为显示装置1200和/或体上电子装置1100和/或数据处理模块1600的新软件和/或软件升级(诸如软件补丁或修复、固件升级或软件驱动程序升级等)可由远程终端1700提供。例如,对体上电子装置1100的软件升级、可执行程序变更或修改可由显示装置1200或数据处理模块1600中的一个或更多个从远程终端1700接收,然后提供到体上电子装置1100以对其软件或可编程功能进行升级。例如,在某些实施例中,体上电子装置1100中接收和安装的软件可包括软件缺陷修复程序、对先前停滞软件参数的修改(对分析物相关数据存储时间间隔的修改、重置或调整体上电子装置1100的时间基准或信息、对传输数据类型、数据传输序列、或数据存储时间段的修改等)。美国申请号12/698,124、12/794,721、12/699,653及12/699,844、以及美国临时申请号61,359,265及61/325,155中提供了描述便携式电子装置的软件的领域可升级性及数据处理的其他详细情况,这些文献的公开内容通过引用结合于本文用于所有目的。
传感器
分析物测量系统100的分析物传感器14可用来监测多种分析物的水平。可被监测的分析物包括例如乙酰胆碱、淀粉酶、胆红素、胆固醇、绒毛膜促性腺素、肌酸激酶(例如CK-MB)、肌酸、DNA、果糖胺、葡萄糖、谷氨酰胺、生长激素、激素、酮、乳酸、氧、过氧化物、前列腺特异性抗原、凝血酶原、RNA、促甲状腺激素、及肌钙蛋白。还可监测药物(诸如例如抗生素(如庆大霉素、万古霉素等)、洋地黄毒苷、地高辛)的浓度、滥用药物、茶碱及华法林。可用给定的传感器监测一种或多种分析物。在这些监测一种以上分析物的实施例中,可以在相同时间或不同时间通过单个传感器或通过使用(例如,同时地使用)相同体上电子装置的多个传感器或通过不同体上电子装置监测分析物。
在本公开的一个实施方式中,将传感器14物理地定位在监测其分析物水平的用户的身体之中或之上。可将传感器14构造为连续地采样用户的分析物水平并将所采样的分析物水平(例如葡萄糖浓度)转换成相应的数据信号(例如电流或电压),以输入于体上电子装置中。可替换地,可将传感器14构造为根据需要采样分析物水平。体上电子装置可放大、过滤、平均和/或以其他方式处理由传感器所提供的信号。
在图2中示出了传感器14的一个实施方式。应理解,这里描述的插入物可与其他医疗装置一起使用。这里描述的形状仅是说明性的。考虑其他传感器形状。在一些实施方式中,传感器14包括介电的基板,例如聚合物或塑料材料,诸如聚酯或聚酰胺。在此实施方式中,将传感器构造为使得一部分定位在皮肤下方并且一部分定位在皮肤上方。因此,传感器14包括插入部或内部部分30和外部或电接触部分32。在一些实施方式中,接触部分32包括多个用于与其他电子装置连接的导电触点36、38和40(这里示出了三个触点),例如位于体上电子装置1100处(见图1)。在此实施方式中提供的触点用于工作电极、参考电极和对电极。在一些实施方式中,提供两个或更多个工作电极。这些电极的操作部分(即工作电极、参考电极和对电极(未单独示出))设置于插入部分处,例如位于插入部分30的远端处,例如位于部分34处。在一些实施方式中,一个或更多个电极可在身体之外,例如外部的对电极。通过在基板表面上延伸的电路道(circuit trace)42、44和46将触点和电极的操作部分连接。在一些实施方式中,电路道设置于通道中,或可埋入基板内,或可横过基板的不同侧面。用导电材料制造导电触点、导电道和电极,例如铂、钯、金、碳等。不止一种材料可用于给定传感器。例如,在美国专利号6,175,572和6,103,033中描述了传感器的其他细节,这些专利为了所有目的通过引证而结合于此。
传感器14可包括近端保持部分48。将插入部分30和近端保持部分48的尺寸和结构构造为,用尖端定位以安装在对象的皮肤中,如这里描述的。在使用中,可将传感器14构造为弯曲(例如沿着线B),并由此定位在两个基本上垂直的相交平面中。这种弯曲可出现在与体上电子装置的接合之前或接合过程中,如下面描述的(见图17)。
部分48和52在传感器的近端和远端部分之间提供电连接路径,例如导电道。传感器14进一步设置有凹口或切口54。这种结构利于弯曲传感器14(例如沿着由线B表示的线)使得保持部分48保持直立并由此定位在两个基本上垂直的相交平面中,如图3所示。如将在下面描述的,可将传感器拉片(tab)50装在体上壳体122中,以帮助固定并定位传感器14。近端保持部分48保持其与插入部分30的纵向对准,用于定位在插入尖端内。
这里已经描述了分析物传感器的实施方式,以便通过应用有化学感测层的电极的布置来电化学地操作,通过产生与分析物的氧化还原反应的体积(以及分析物浓度的指示)成比例的电流,由特定分析物氧化酶催化。存在这样的实施方式:被提供为产生并检测这些反应的水平的电极数量是两个、三个或更多个。然而,如这里描述的,可使用其他类型的传感器。
传感器14的一部分可位于皮肤表面的上方,其中远端部分30穿透皮肤并进入与用户生物流体(例如ISF)接触的皮下空间。在美国专利号5,264,104;5,356,786;5,262,035;5,320,725和6,990,366中提供了与传感器14的电化学相关的进一步细节,每篇专利为了所有目的通过引证而结合于此。
在一些实施方式中,可在使用期内(例如一分钟或更长时间、至少一天或更长时间、大约1至大约30天或甚至更长、大约3至大约14天、大约3至大约7天,或在一些实施方式中,高达几周的更长的时间段)将传感器植入对象体内,以接触并监测存在于生物流体中的分析物。在这点上,可将传感器设置在对象体内的各种位置(例如腹部、上臂、大腿等),包括设置在肌肉中,经皮设置、设置在血管内,或设置在体腔中。
在一些实施方式中,在一段使用期中通过插入和/或植入用户体内来使用传感器14。在这种实施方式中,可用相对柔性的材料制造基板。
虽然图2至图3所示的实施方式具有三个电极,但是其他实施方式可包括更少或更多数量的电极。例如,可利用双电极传感器。传感器14可以是外部供电的并允许电流通过,所述电流与存在的分析物的量成比例。可替换地,传感器14本身在一些实施方式中可用作电流源。在一些双电极实施方式中,传感器可以是自偏压的,可能不需要参考电极。在2009年2月26日提交的名称为“自供电分析物传感器”的美国专利申请序列号12/393,921中描述了一种示例性的自供电双电极传感器,该专利为了所有目的通过引证而结合于此。在某些实施方式中,自供电传感器所提供的电流的水平可能较低,例如在毫微安的等级。
插入组件
提供了用来将医疗装置安装至对象的插入组件。在一些实施方式中,插入组件包括插入物和医疗装置本身。可将插入物构造为将各种医疗装置插入对象体内,例如分析物传感器、输液装置或套管。在一些实施方式中,可将插入物构造为在相同或不同的时间或位置安装这种装置的组合,例如组合式传感器/输液装置,等等。例如,在某些实施方式中,可将给定插入物构造为在不同的时间安装第一装置和第二装置。在这点上,插入物可以是可重复使用的。例如,插入物可以是可更改的,以与不止一种医疗装置一起使用,以包括不止一种类型的医疗装置,例如通过附接适配器和/或移除拆卸插入物的一部分。插入物可将医疗装置安装在对象皮肤中、其下方或穿过其中,或将医疗装置放在皮肤表面上。医疗装置可包括诸如倒刺(barb)、拉片(tab)、粘附剂等的特征或结构,以在插入之后将装置相对于皮肤保持就位。插入物装置还可用作小刀,例如,以不插入或安装医疗装置而刺穿皮肤。
在一些实施方式中,插入组件包括插入物、医疗装置(例如分析物传感器)和用于将医疗装置至少部分地支撑在对象皮肤之中或之上的底座。在一些实施方式中,底座是支撑结构、板和/或附接、粘附或以其他方式固定至对象皮肤的构件。可用插入物将底座与医疗装置同时插入。在其他实施方式中,在安装医疗装置之后或之前安装底座。底座可由插入物施加或分开施加。底座可包括在插入传感器和/或将其相对于传感器控制单元保持在相对位置之后相对于皮肤将传感器保持就位的特征或结构(例如粘合剂、引导件、倒刺、拉片等)。在一些实施方式中,用粘附垫或粘附条固定医疗装置,例如传感器和/或传感器控制单元,并且不使用底座。
在一些实施方式中,插入组件包括插入物、分析物传感器、底座和电源。可通过插入物将底座和电源与分析物传感器同时插入。在其他实施方式中,在安装分析物传感器之后或之前安装底座和电池。在这种情况中,底座和/或电源可由插入物施加或分开施加。可用电源对传感器提供电流或电压和/或提供向监测器单元传递一个或多个信号所需的功率。
在一些实施方式中,插入组件包括插入物、医疗装置(例如分析物传感器)、底座和传感器控制单元。可用插入物将底座和传感器控制单元与分析物传感器同时布置和/或安装。在其他实施方式中,在安装分析物传感器之后或之前安装底座和传感器控制单元。例如,可通过插入物安装底座和分析物传感器,并且可安装传感器控制单元。在其他实施方式中,安装底座,然后用插入物插入分析物传感器,再然后安装传感器控制单元。在其他实施方式中,首先安装底座和传感器控制单元,并然后安装分析物传感器。
在一些实施方式中,传感器控制单元的电子装置对分析物传感器提供电压或电流。在一些实施方式中,电子装置处理由分析物传感器提供的信号。在其他实施方式中,电子装置可包括用于对其他部件(诸如,例如监测器单元、计算机或其他部件)提供与分析物传感器提供的信号相关的信号的通信功能。在一些实施方式中,提供通信电路,例如RFID天线或其他通信电路。可用电源对这些功能中的部分或者所有提供功率。在一些实施方式中,从监测器单元提供功率,例如经由电感耦合。
插入物可包括多个不同的部件。例如,插入物可包括一个或多个用于使尖端朝着对象皮肤前进的部件。可用支撑结构(例如支架)支撑传感器和传感器控制单元和/或底座结构。可提供用于使尖端和/或分析物传感器/支撑结构前进的驱动器。在一些实施方式中,将致动器与尖端和/或支撑结构直接或间接地接合,使得将由对象施加给致动器的人力和速度传递至尖端和/或支撑结构。在一些实施方式中,所施加的力在收回位置和前进位置之间驱动尖端和/或支撑结构。在一些实施方式中,在通过接触从护套向内延伸的伸出部来安装之前,将传感器与传感器控制单元和/或底座结构保持在收回位置。根据此实施方式,将传感器与传感器控制单元和/或底座结构暂时操作地保持在支撑结构和设置于护套内壁上的伸出部之间。
插入物还可包括一个或更多个用于在允许分析物传感器和可选的体上电子装置保持在对象上的同时收回尖端的部件。用于收回尖端的该部件可包括牵引器(收回装置,retractor)。应理解,牵引器和致动器可具有相同的结构或包括一些公共部件。在一些实施方式中,牵引器与尖端直接或间接地接合,使得将由用户施加的人力从牵引器传递至尖端,以从皮肤收回尖端。在其他实施方式中,可提供驱动组件以收回尖端。例如,驱动组件可包括弹簧、马达、液压活塞等,以远离对象的皮肤地收回尖端。驱动组件还可包括线性驱动部件。
在一些实施方式中,牵引器在用户启动后收回尖端。在这种情况中,当用户希望收回尖端时其启动牵引器。例如,牵引器可包括释放开关。在激活释放开关后,驱动组件(例如弹簧或其他驱动器)从皮肤收回尖端。在其他实施方式中,牵引器和致动器包括公共部件。在激活致动器以使尖端和分析物传感器前进之后,用户释放致动器,这允许驱动组件从皮肤收回尖端。
在一些实施方式中,牵引器在插入启动之后不需要与用户进一步的交互便可收回尖端。例如,插入物可包括在尖端和支撑结构前进预定量后自动地收回尖端的特征或部件。在插入之后不需要用户进一步的动作即可启动尖端收回的插入物装置在这里被称为具有尖端的“自动”回收。
插入物装置
在图4至图5中示出了用于插入物的针插座的一个实施方式。针插座136支撑尖端124,其具有变尖的远端部分160。在一些实施方式中,如这里讨论的,在尖端124的壁部的至少一部分中设置纵向壁部开口或间隙162。将间隙162的长度N选择成,与插入部分30至传感器的近端保持部分48的长度相当,并且,在某些实施方式中,可以是大约3mm至大约50mm,例如大约5mm,或大约10mm,或大约15mm,或大约20mm。尖端124的长度L可以是大约3mm至大约50mm,例如5mm或更长,或大约10mm,或大约20mm,或大约30mm,或大约50mm,并在传感器的插入部分30的长度和传感器14的插入部分30的所需深度的基础上选择长度L。在一些实施方式中,间隙的两个边缘之间的距离或间隔是大约0.2mm至大约0.5mm,例如大约0.22mm,大约0.25mm,等等。
在图6至图8中更详细地示出了尖端124的远端部分160。如图6所示,在此实施方式中,尖端124具有基本上“C”形或“U”形的轮廓,但是可具有其他结构,例如基本上“V”形。在尖端124的壁部中设置纵向间隙162。图7示出了设置有有角度的末端的远端部分160。在一些实施方式中,有角度的末端可设置有第一有角度的末端部分164和第二较陡角度末端部分166。包括多个边缘和面的示例性结构提供锋利的点,以对对象减小穿透力、外伤和流血。传感器本体的远端部分具有尺寸为装配在插入尖端124的凹口162内的宽度,插入尖端124具有小于大约20至大约26口径的直径,例如为21口径至大约25口径,其中,在某些实施方式中,尖端是21口径或23口径或25口径。这种尖端可与具有宽度或直径为大约0.20mm至大约0.80mm(例如大约0.25mm至大约0.60mm)的至少由尖端承载的部分的传感器一起使用,其中,在一些实施方式中,传感器的至少一部分的宽度或直径是0.27mm或0.33mm或0.58mm。在一些实施方式中,尖端124由片状金属制成,并在横截面中折叠成基本上“V”形或“U”形或“C”形的结构。可用多种技术制造折叠的金属片以形成尖端124。例如,可用蚀刻片状金属技术来形成尖端124。以此方式,可形成具有非常尖的边缘的尖端,使得在插入过程中穿透皮肤不太疼痛。在其他实施方式中,可用顺序冲模技术来形成具有尖端边缘的复杂的片状金属形状,如图9所示。在一些实施方式中,可用塑料帽模制尖端124,使得可在插入物装配过程中处理尖端。此外,可用塑料模制冲切尖端,以加固“V”形、“U”形或“C”形的片状金属结构。在其他实施方式中,可形成激光切割的尖端。以此方式,可用激光形成壁部开口或间隙162以及第一角度末端部分164和第二较陡角度末端部分166。
在另一实施方式中,可用利用图10所述的方法的标准皮下注射针形成尖端124。首先,将皮下注射针(具有圆形横截面)切割成尖端124所需的长度。接下来,压缩皮下注射针,使得其横截面从圆形永久地变形成椭圆形。然后,将皮下注射针的末端被研磨成一定的斜角以产生锋利的点,从而减小所需的穿透力,如之前讨论的。最后,用适当的技术移除针的顶部(例如研磨、电抛光等)。产生的尖端124具有“U”形结构并对传感器14的插入提供充足的空间。在一些实施方式中,可以相反的顺序执行末端研磨步骤和压缩步骤。
由于压缩步骤,用户初始时可通过更大直径的皮下注射针开始,使得完成的尖端124将具有与之前描述的尖端相似的尺寸。
图11至图12示出了体上壳体122相对于针插座136和尖端124的位置。可将体上壳体122构造为保持传感器14的至少一部分和传感器控制单元12。如图11所示,尖端124延伸穿过体上壳体122中的孔168。因此,在一些实施方式中,将尖端124与体上壳体122分离。通过尖端124定位传感器14的远端部分。如在图12中进一步示出的,将传感器控制单元12的电子装置80(例如包含体上单元16的电子部件的印刷电路板),并且传感器插座123定位在体上壳体122内。传感器14可包括定位结构或缝隙127,定位结构或缝隙容纳定位件(例如传感器插座123的拉片129)。提供电源82,例如电池,例如单次使用可抛弃型电池,或可充电的电池。在一些实施方式中,电源82用来对传感器提供电压或电流。在使用无源通信协议(例如无源RIFD)的实施方式中,不对通信提供电源。用监测器单元18提供这种电源(功率)。在一些实施方式中(其中,用传感器控制单元发送一个或多个信号),可用一个或多个电源对这种通信电路提供功率。在一些实施方式中,电池的有效使用寿命可超过传感器14的有效使用寿命。
图13示出了体上壳体122相对于插入物(例如图13至图17所示的插入物1500)的尖端124的方向的横截面图。如这里讨论的,在一些实施方式中,将传感器14设置在基本上弯曲的结构中,使得传感器的一部分(例如插入部分30和近端保持部分48)是基本上竖直的(即,基本上与插入物的纵向轴线对准并基本上垂直于皮肤表面),并且,将接触部分32(以轮廓示出)定向在基本上水平的结构中,并与数据处理单元电子装置(例如电路80)电接触。传感器拉片50可被包围在体上壳体122(“二次模制(overmolded)”)的塑料中并固定就位。凹口56对传感器14提供进一步的稳定性,例如,通过允许用体上壳体122的材料包围传感器拉片50,并进一步提供用于在安装过程中竖直地定向传感器14的装置,例如通过允许相对于体上壳体122的竖直标志竖直地定位凹口56。
可将安装有体上壳体122的传感器14设置在支架130的凹槽内,例如支架130中的凹入凹槽。可替换地,可将安装有体上壳体122的传感器14设置在支撑结构与从护套的壁部延伸的一个或多个伸出部之间。在又一替代方式中,可用与尖端124接合的可释放摩擦配合将安装有体上壳体122的传感器14保持就位。以此方式,支架不需要具有将安装有体上壳体的传感器设置于其内的凹槽。在插入物的初始结构中,尖端124延伸穿过形成于支架130中的纵向孔168。在一些实施方式中,使孔168具有适当的大小,使得尖端124或针插座136都不会接触支架130。因此,一方面针插座136(和尖端124)以及另一方面支架130(图13)和体上壳体122同时但是彼此独立地移动。在其他实施方式中,可在孔和尖端之间提供摩擦配合。
将传感器14的插入部分30和近端保持部分48设置在尖端124内的纵向孔162内(例如见图6)。将近端保持部分48设置在尖端124的纵向孔内,并对传感器14在尖端124内的安装提供额外的稳定性。将尖端124的纵向壁部间隙或开口162与传感器14对准,使得拉片50和接触部分32从尖端124横向地向外延伸。
在图14至图17中示出了插入物的一个实施方式。插入物900包括手柄902,并可包括用于对容纳于其中的医疗装置和尖端保持无菌环境的可去除的远端帽或密封件(未示出)。如图14所示,从手柄902去除远端帽或密封件。插入物900包括限定用于放在对象皮肤上的远端表面912的底座942。可用插入物900使医疗装置进入对象的皮肤。在一些实施方式中,使手柄902相对于底座942前进,以使传感器进入患者的皮肤。
如图15所示,插入物900包括这样的初始结构:手柄902相对于底座942设置在近端位置中。在这种结构中,尖端924设置在与粘附层918的孔920隔开的位置中。在远端从手柄902的上表面延伸的是终止于肩部975中的侧壁974。
针载体934可在箭头N的方向上在手柄902和底座942内轴向地滑动。针载体934支撑针插座936,尖端924从针插座936在插入物900内纵向地延伸。在一些实施方式中,相对于皮肤表面以斜角(例如大约0°和90°之间)支撑尖端。初始时,通过针载体934的指部986与内轨道的肩部987的相互接合将针载体934与内轨道928接合。
插入物900包括前进弹簧947。内轨道928包括用于前进弹簧947的弹簧保持部分984。手柄902的内表面用作用于前进弹簧947的上接合面。在一些实施方式中,将弹簧保持部分984制造为具有多个延伸穿过底座942的壁部中的孔982的伸出部。弹簧保持部分984是可弹性移动的。当对手柄902施加向下的力时,手柄902的凸缘937接触弹簧保持部分984,向内驱动这些伸出部。这种向内移动释放内轨道928,并允许前进弹簧947使内轨道928在远端前进,从而使尖端924进入对象的皮肤,如图16所示。
将收回弹簧946设置在底座942的弹簧保持部分948和针载体934的肩部949之间。初始时,收回弹簧946处于压缩状态中。当支架930到达远端位置时,体上壳体122的远端表面与粘附垫918的上表面接合,从而粘附至对象的皮肤表面S。同时,底座942的凸缘970与设置于针载体934上的指部986接合。通过凸缘970使指部986向外枢转。指部974的这种枢转导致指部986与内轨道928的肩部984分离。从而将往复装置(shuttle)934与内轨道928分离。
如图17所示,往复装置934与内轨道928的分离允许弹簧946扩展,从而使针载体934前进至近端位置,从而从对象的皮肤S收回尖端934,同时将传感器14留在皮肤中。
在图18至图21中示出了插入物的另一实施方式,并表示为插入物1000。插入物1000与这里描述的插入物900基本上相同,这里指出了并在附图中表示了主要差异。
插入物1000包括壳体1002,并可包括用于对容纳于其中的医疗装置和尖端保持无菌环境的可去除的远端帽或密封件(未示出)。如图18所示,从手柄1002去除远端帽或密封件。插入物1000包括限定放在对象的皮肤上的远端表面1012的底座1042。可用插入物1000使医疗装置进入对象的皮肤。在一些实施方式中,相对于底座1042按下侧按钮1084,以使传感器进入患者的皮肤。
如图19所示,插入物1000包括这样的初始结构:将尖端1024设置在与底座1042的远端部分1012隔开的结构中。应理解,插入物1000可包含定位在底座1042的远端部分1012上的粘附层(未示出)。
体上单元插入物1028包括用于支撑体上壳体122的支架1030。体上单元插入物1028还包括通常位于肩部1086上的凸缘1029(如图19至图21所示)。当向内按下侧按钮1084时,将凸缘1029上的插锁部分偏转,与肩部1086分离。如图20所示,将前进弹簧1047从压缩状态释放,从而使体上单元插入物1028前进至别的地方,与针载体1034一起进入对象的皮肤。
将收回弹簧1046设置在针载体1034与壳体1002之间。初始时,收回弹簧1046处于压缩状态。当支架1028到达远端位置时,将体上单元插入物1028与针载体1034分离。体上壳体122的远端表面与皮肤或粘附垫(未示出)的上表面接合,从而粘附至对象的皮肤表面S。针载体1034上的插锁将其附接至体上单元插入物1028。在通过按下拉片1084来触发插入物后,用弹簧1047朝着皮肤表面推动体上单元插入物1028,连同携带针载体1034并加载拉伸弹簧1046。当体上单元插入物1028到达远端位置时(朝着对象的皮肤),壳体1002上的伸出部与针载体1034上的插锁分离,将其与体上单元插入物1028连接。拉伸弹簧1046现在将针载体1034拉回近端位置中。
如图21所示,针载体1034与内轨道1028的分离允许弹簧1046通过偏压而收缩,从而使针载体1034前进至近端位置并从对象的皮肤S收回尖端1024,同时将传感器14留在皮肤中。
在图22至图25中示出了插入物的另一实施方式。插入物1100与这里描述的插入物900和1000基本上相同,这里指出了并在附图中表示了主要差异。
插入物1000包括壳体1102,并可包括用于对容纳于其中的医疗装置和尖端保持无菌环境的可去除的远端帽或密封件(未示出)。如图22所示,从壳体1102去除远端帽或密封件。插入物1100包括限定用于放在对象的皮肤上的远端表面1112的底座1142。可用插入物1100使医疗装置进入对象的皮肤。在一些实施方式中,相对于底座1142按下手动致动杆1114,以使医疗装置进入患者的皮肤。应理解,插入物1100可包含定位在底座1142的远端部分1112上的粘附层(未示出)。
如图23所示,插入物1100包括这样的初始结构:尖端1124设置在与底座1142的远端部分1112隔开的结构中。可通过致动杆1114的远端前进执行致动器的手动前进。
体上单元插入物1128包括用于支撑体上壳体122的支架1130。将收回弹簧1146设置在针载体1134和底座1102之间。初始时,收回弹簧1146处于压缩状态。当致动杆1114在远端移动时,支架1128在远端移动并到达远端位置,使得底座1142的凸缘1188与设置于往复装置1134上的指部1186接合。通过凸缘1188使指部1186向外枢转。指部1186的这种枢转导致指部1186与内轨道1128的肩部1187分离。从而将往复装置1134与内轨道1128分离。体上壳体122的远端表面与皮肤或粘附垫(未示出)的上表面接合,从而粘附至对象的皮肤表面(图24)。
如图25所示,往复装置1136与内轨道1028的分离允许弹簧1146通过偏压而扩展,从而使针载体1136前进至近端位置并从对象的皮肤S收回尖端1124,同时将传感器14留在皮肤中。一旦已从对象收回尖端1124,便不再能接触到插入物1100的远端部分,并且不能与对象的皮肤意外地接触。
在图26至图36中示出了插入物的另一实施方式。插入物1200与这里描述的插入物900,1000和1100基本上相同,这里指出了并在附图中表示了主要差异。
插入物1200包括壳体1202、体上单元插入物1228、针牵引器1234和具有扭簧(未示出)的转子1208,所有这些在图28至图31中分别示出。如图28至图31所示,壳体1202包括槽1254;体上单元插入物1228包括槽1252、拉片1253和开口1262;针牵引器1234包括拉片1250和开口1260;并且转子1208包括转子从动件1264。
图32示出了插入物1200的分解图。如所示出的,在一些实施方式中,插入物1200包括壳体1202、体上单元插入物1228、针牵引器1234和转子1208。可将拉片1250设置在针牵引器1234上,并将其配置为当如图33所示地装配时与设置于体上单元插入物1228上的槽1252接合。可将拉片1253设置在体上单元插入物1228上,并将其配置为与设置于壳体1202上的槽1254接合。针牵引器1234和体上单元插入物1228中的每个可分别包含在已将转子1208插入壳体1202后容纳设置于转子1208上的转子从动件1264的开口1260,1262。另外,体上单元插入物1228可对体上壳体122(未示出)提供支撑,以安装至对象的皮肤。
如图34所示,在一些实施方式中,手动地按下体上单元插入物1228可导致,当转子1208旋转时扭簧拧紧,由凸轮路径引导。如图35所示,体上单元插入物1228的继续远端前进导致转子从动件1264在凸轮1264内“超过中心”。在这个点处,允许松开扭簧(未示出)(图93)。参考图36,扭簧的进一步松开将针牵引器1234从插入位置拉起,同时使体上单元插入物就位。
在图37至图46中示出了插入物的另一实施方式。插入物1300与这里描述的插入物900,1000,1100和1200基本上相同,这里指出了并在附图中表示了主要差异。
插入物1300包括壳体1302、体上单元插入物1334、针牵引器1328和具有扭簧1367的转子1308。如图37、图38、图39、图45和图46所示,将体上单元插入物1334和针牵引器1328设置在壳体1302内。转子1308包括与设置于针牵引器1328中的槽1362和体上单元插入物1334中的槽1360接合的转子从动件1364。体上单元插入物1334提供用于支撑体上壳体1302(未示出)的支撑部分。
在操作中,对扭簧1365加载。按下释放按钮(未示出)以释放扭簧1365。转子1308同时向下驱动体上单元插入物1334和针牵引器1328。压缩弹簧1367抑制体上单元插入物1334。当转子1308继续旋转时,槽1360允许体上单元插入物1334向下延伸然后对体上单元插入物进行抑制,同时槽1362允许针牵引器1328向下延伸然后返回,以从插入位置提升针。
在图47至图51中示出了插入物的另一实施方式。插入物1400与这里描述的插入物900,1000,1100,1200和1300基本上相同,这里指出了并在附图中表示了主要差异。
插入物1400可用于医疗装置(例如体上壳体122)与盒子或载体1406一起的安装。在一些实施方式中,插入物1400包括本体1402和致动器1404。载体1406可包括针插座1436,其包括尖端(未示出)和体上壳体122。在使用中,通过使用粘附垫1418将本体1402放在附接至对象的底座1408上。如图47所示,如所示出地将载体1406横向地加载在插入物1400中。
参考图48,插入物1400的第一一次性部分包括粘附垫1418和底座1408。插入物1400的第二一次性部分包括可去除地包含针插座1436和传感器插座1437(未示出)的载体1406,其与这里描述的体上壳体122基本上相同。插入物1400进一步包括本体1402、致动器1404和复位弹簧1409(未示出)。将底座1408可去除地附接至本体1402。载体1406可在本体1402上滑动,以将针插座1436和载体1406移动至插入物1400。如图48所示,然后可从插入物1400去除载体1406。针插座1436和传感器插座1437留在插入物1400中。然后将粘附垫1418粘着地应用于对象的皮肤。可替换地,可在连接本体1402和底座1408之前对对象的皮肤应用粘附垫1418。
在图49中,按下致动器1404,执行针插座1436和传感器插座1437的手动插入,位于针插座1436中的针和远端传感器部分刺入对象的皮肤。当从致动器1404释放压力时,复位弹簧1409(未示出)从对象的皮肤收回针并使其离开传感器插座1437。如图50所示,可从底座1408去除本体1402,将传感器插座1437留在安装底座1408中。在图51中,在一些示例性实施方式中,载体1406在壳体1402上滑动,将针1436移动至载体1406。然后,可从壳体1402去除并适当地处理载体1406和针1436,插入物1400准备好再次使用。然后将通信电子装置(未示出)附接至安装底座1408,使得与传感器插座1437电接触。
在图52中示出了插入物的另一实施方式。插入物1500与这里描述的插入物900,1000,1100,1200,1300和1400基本上相同,这里指出了并在附图中表示了主要差异。
插入物1500包括可由模制塑料管制造并可进一步包括活动铰接设备1504的壳体1502。在一些实施方式中,活动铰链是将两个匹配部分连接的薄柔性塑料接头。铰链保持零件连接并可不会失效地完全折叠,以允许两个零件完全匹配。
帽部1504可进一步设置有切口部分,以提供对食指的接触并沿着所需轴线限制插入移动。在提供波纹管按钮组件(这里描述的)之后,通过化学或超声结合将帽部1504封闭并结合至壳体。
插入物进一步包括波纹管1506,其在一些实施方式中用具有整体压缩弹簧的模制薄壁塑料制成,压缩弹簧在插入作用的过程中折叠并在插入之后提供力以收回尖端1524。波纹管1506还防止尖端1524暴露。将波纹管1506的顶部1520固定至按钮1514,并将底部1521固定至壳体1502。
按钮1514对用户提供将体上壳体122插入对象皮肤的能力。按钮1514可由塑料制成并可进一步包括防旋转特征,例如沿着纵向脊部1517滑动的凹槽1515,将移动限制于所期望的纵向轴线。将针插座1536粘附或直接模制在按钮1514上。将尖端1524牢固地保持在体上壳体122上,如这里描述的(例如见图11至图13)。
粘性贴片1518将体上壳体122固定至对象的皮肤。在一些实施方式中,粘性贴片1518包括与皮肤接触的高粘性(即高强度粘性)区域。提供在插入之前去除的保护性衬垫。在面向粘性贴片的插入物1500的一侧上,在贴片的外围上设置低粘性区域1530,以允许在完成插入之后轻松地去除壳体1502。在贴片的中心部分中设置高粘性区域1532,以将体上壳体122固定就位。
参考图53至图55,将插入物盒1600示出为插入物2310和粘性底座2312可去除地附接至其底部。在美国专利号7,381,184中进一步描述了插入物1600,该专利为了所有目的结合于此以供参考。
在皮肤上准备插入位置(一般是在腹部区域)之后,用户从粘性底座2312去除衬垫(未示出),以暴露位于底座2312下方的胶带2320的底面和一部分顶面。然后,将插入物2310所附接的底座2312在插入位置应用于对象的皮肤。按下致动器按钮2324,导致触发插入物2310,从而用预定的速度和力将传感器2314插入对象的皮肤。一旦已将传感器2314插入皮肤,通过按下插入物2310的相对侧上的拉片(未示出)并将插入物2310从底座2312拉开,患者从底座2312去除插入物2310。
一旦从底座2312去除插入物2310,通信电子装置(未示出)便可滑动就位。在通信电子装置完全位于底座2312上时,通信电子装置的电路与传感器2314上的接触垫电接触。一旦完成初始化和同步过程,便可将来自传感器2314的电化学测量结果从通信电子装置无线地发送至接收器单元。
在一些实施方式中,用以下部件装配插入物工具包1600:壳体2334、致动器按钮2324、驱动弹簧2336、往复装置2338、引导尖端2340、传感器2314、收回弹簧2342、插入物底座2344、上衬垫(未示出)、粘性底座2312、胶带2320和下衬垫(未示出)。
用弓形引导件2360将往复装置2338滑动地和非旋转地限制在底座2344上。往复装置2338通常由用两个桥部2366连接的外环2362和内杯形柱2364形成。桥部2366在两个形成于引导件2360之间的槽(未示出)之间滑动,并允许往复装置2338沿着引导件2360在不旋转的情况下移动。用引导件2360限制收回弹簧2342的外圆周、用底座2344的底面2370限制其底部、用桥部2366限制其顶部,并用往复柱(shuttle post)2364的外表面限制其内圆周。用往复柱2364的内表面限制驱动弹簧2336的底部和外圆周,用致动器按钮2324内的平顶2372限制其顶部,并用从平顶2372悬垂的杆部2374限制其内圆周。当在致动器按钮2324和往复装置2338之间压缩驱动弹簧2336时,其朝着底座2344推动往复装置2338。当在往复装置2338和底座2344之间压缩收回弹簧2342时,其朝着按钮324推动往复装置338。
在触发之后收回弹簧2342将使往复装置2338返回至所示中性位置,但是没有保持插在对象皮肤中的传感器2314。优选地,将驱动弹簧2336设计为比收回弹簧2342硬,使得快速减弱往复装置2338的振动,因此引导尖端2340不会返回至传感器2314或患者而导致伤害。由于传感器2314插在对象的皮肤中,所以可从底座2312去除插入物2310,然后将插入物2310提起使其从底座2312离开。在处理插入物2310的过程中,引导尖端2340保持被保护在壳体2334内。通信电子装置现在可在底座2312滑动就位,如之前描述的。
在一些实施方式中,放大杆部2374的近端部分,以与弹簧2336的盘卷干涉配合。例如,对杆部2374增加一个或多个横向延伸的肋部2610。一般在弹簧2336的近端(顶部)盘卷处设置肋部2610和弹簧2336之间的干涉配合。
弹簧2336的盘卷的直径当压缩时稍微增加,当延伸时稍微减小。当弹簧2336延伸时,杆部2374上的肋部2610提供最大的干涉。在插入过程中,干涉配合提供往复装置2338的增加的稳定性。在一些实施方式中,干涉配合防止或减小弹簧2336的远端移动,该移动可能导致弹簧2336在往复装置2338上的冲击以及这些部件的远端移动的结束。
参考图56至图70,在另一示例性实施方式中,插入物2600通常包括:致动器按钮2602(图57)、往复装置2604(图58)、具有皮肤刺穿边缘2612的插入物尖端2610(图58)、收回弹簧2608(图59)、传感器2614(图60)、壳体2616(图61)和底座2618(图62)。应理解,插入物2600可包括比这里描述的更多或更少的部件。插入物2600与这里描述的插入物1600基本上相同,这里指出了并在附图中表示了主要差异。在图63至图65中描述了插入物2600的不同部件的装配。如图63所示,致动器按钮适于滑动地插入往复装置2604中的开口,其在那里锁定就位。此外,如图64所示,收回弹簧2608适于插入往复装置2604的相对侧上的第二开口。另外,在此视图中,传感器2614已附接至插入物尖端2610。如图60所示,传感器2614包含使传感器2614正向地位于插入物尖端2610中的偏压臂2615。这允许插入物尖端2610和传感器插入部分30更小,减小了对对象的损伤和疼痛。可利用多种和插入物2600一起的上述传感器连接方法。例如,插入物尖端2610可设置有轨道和凹痕,如之前描述的,以固定传感器2614,尖端2610具有大约20至大约26口径的直径,例如21口径至大约25口径,其中,在某些实施方式中,尖端是21口径或23口径或25口径。这种尖端可与具有大约0.20mm至大约0.80mm,例如大约0.25mm至大约0.60mm的宽度或直径的传感器(至少由尖端承载的部分具有这种宽度或直径)一起使用,其中,在一些实施方式中,传感器的至少一部分的宽度或直径是0.27mm或0.33mm或0.58mm。
图66示出了已经完全装配插入物2600(将壳体2616与底座2618连接)之后的图65的装配的横截面图。如所示出的,当装配插入物2600时,收回弹簧2608由其侧面上的引导件2622并由往复装置2604和底座2618包围。另外,往复装置2604适于在底座2618内的轨道(未示出)上滑动地移动,从而允许当按下致动器按钮2602时其在直线方向上移动。图66示出了用两个棘爪凹槽2607中的第一个锁定在往复装置2604上的致动器按钮2602。在此结构中,往复装置2604和致动器按钮2602相对于壳体2616和底座2618处于锁定状态中,防止在运输和处理过程中意外地布置往复装置。此结构还允许明显更小的封装,实现更低的运输成本和改进的批量处理效率,例如消毒。图67示出了用两个棘爪凹槽2607中的第二个锁定在往复装置2604上的致动器按钮2602。在此结构中,往复装置准备好被布置。通过用户轴向地拉动致动器按钮2602和壳体2616,将致动器按钮2602移动至第二棘爪凹槽2607。
图68至图70示出了用插入物2600布置传感器2614的步骤。图68示出了第一结构中的插入物2600。收回弹簧2608施加在往复装置2604上(以及由此施加在致动器按钮2602上)的向上的力将插入物2600保持在第一结构中的其竖立位置中。当用户克服收回弹簧2608的偏压按下致动器按钮2602时,其在往复装置2604和收回弹簧2608上施加向下的力。从而向下驱动传感器2614安装于其上的引导尖端2610,并使其进入对象的皮肤(例如成为第二结构)。皮肤刺穿边缘2612刺穿对象的皮肤并允许适当地插入传感器2614,如图69所示。
当从致动器按钮2602去除力时,收回弹簧2608在往复装置2604上施加向上的力,从而导致引导尖端2610在近端返回至其在壳体2616内的初始位置(例如成为第一结构)。传感器2614保持植入在患者的皮肤中,如图70所示。在此位置中,用户将活塞弯曲大约90度,这防止进一步使用装置,提供使用装置并将除去的明显的视觉和触觉指示。
在所公开的主题的另一方面中,如图71所示,提供对将医疗装置(例如分析物传感器)安装在对象的皮肤中来说有用的插入物组件。插入物组件4300可包括插入物、医疗装置(例如分析物传感器)和用于将医疗装置至少部分地定位在对象的皮肤之中或之上的底座。在一些实施方式中,底座是支撑结构、板和/或附接、粘附或以其他方式固定至对象皮肤的构件。可用插入物将底座与医疗装置同时应用于对象的皮肤。在其他实施方式中,在安装医疗装置之后或之前安装底座。底座可由插入物施加或分开施加。底座可包括在插入传感器和/或将其相对于传感器控制单元保持在相对位置之后相对于皮肤将传感器保持就位的特征或结构(例如粘合剂、引导件、倒刺、拉片等)。
插入物组件4300对于分析物测量系统来说是有用的,例如包括可装配在对象皮肤上的体上单元的葡萄糖测量系统。例如,体上单元可包括传感器和传感器控制单元。一般将传感器安装在患者体内。然后,安装传感器控制单元并将其与传感器接合。在其他实施方式中,首先将传感器控制单元安装在患者处,然后安装传感器,然后传感器与传感器控制单元接合。在其他实施方式中,将传感器和传感器控制单元同时安装和接合。可选的底座可能用来或可能不用来定位传感器和/或传感器控制单元。
通常,插入物组件4300对于将传感器安装在对象的皮肤中是有用的。可在安装之前将传感器(未示出)预加载在插入物4310内。在对象的皮肤上准备好插入位置之后,用户从底座4312去除上衬垫4316和下衬垫4318,以暴露位于底座4312的底面上的胶带的底面和一部分顶面。然后,将插入物4310所附接的底座4312在插入位置处应用于对象的皮肤。在一些实施方式中,首先连接底座4312,然后将插入物接合或定位在底座4312内和/或其附近。插入物包括将按下以导致触发插入物4310的致动器按钮4324,从而将传感器插入用户的皮肤。如将在这里描述的,某些实施方式在启动后用预定的速度和力安装传感器。在所公开的主题的一些实施方式中,插入物包括阻止启动插入物的安全件,如下所述。
在一些实施方式中,用一种或多种定位技术保持传感器4314定位在底座4312处。例如,如图72所示,传感器4314具有从主表面4346正交地延伸的表面4356。表面4356可包括接触对象皮肤4328或底座4312的粘附部分。在一些实施方式中,底座4312的凸起端部挡块4444设置有凸起珠缘或凸块,其容纳在传感器4314的孔中。在将传感器4314插入皮肤后,用户可从底座4312去除插入物4310,例如通过按下插入物4310的相对侧上的释放拉片4326并提起插入物4310使其离开底座4312。在一些实施方式中,用其他技术固定插入物4310,例如与底座4312的摩擦配合或搭扣配合。
一旦从底座4312去除插入物4310,便可将传感器控制单元4330相对于底座4312就位。在传感器控制单元4330位于底座4312上之后,传感器控制单元4330的电路与传感器4314上的触点电接触。例如,如图72所示,密封件具有用于包围传感器4314(未在图72中示出)上的电触点的外壁和用于将电触点彼此隔离的内壁。在一些实施方式中,传感器控制单元4330上的轨道可在底座4312上的相应轨道或凹槽4434内滑动。
在一些实施方式中,完成初始化和同步过程,然后可将来自传感器4314的电化学测量结果从传感器控制单元4330提供给监测器单元,例如便携监测器单元4332,如图73所示。传感器控制单元4330和监测器单元4332经由连接20(在此实施方式中,无线射频(RF)连接)通信。例如,可经由RF通信、红外通信、蓝牙通信、Zigbee通信、802.1x通信或WiFi通信等而出现通信。在一些实施方式中,通信可包括433MHz、13.56MHz等的无线电频率。在一些实施方式中,传感器控制单元4330和监测器单元4332之间的通信可包括射频识别(RFID)技术,并可以是有源RFID或无源RFID的,其中,在一些实施方式中,无源RFID技术和相应的系统部件包括对其来说必须的部件。例如,在一个实施方式中,监测器单元可包括反向散射RFID读出器,其被构造为发射RF范围,使得当传感器控制单元在所发射的RF范围内时,转动天线,然后对监测器单元提供反射或响应信号(例如反向散射信号)。反射或响应信号可包括从分析物传感器采样的分析物水平数据。例如,可在2010年2月1日提交的美国专利申请序列号12/698,124中发现各种实施方式的附加示例性细节,该申请为了所有目的而结合于此以供参考。
传感器4314、底座4312和传感器控制单元4330可在预定的最大时间段内(可包括几小时、几天、几周或一个月或更长时间)保持在对象上的适当位置。然后去除这些部件,使得在一些实施方式中可适当地丢弃传感器4314和底座4312。然后可用新的插入物4310、传感器4314和底座4312重复以上整个过程,重新使用传感器控制单元330和监测器单元332。在其他实施方式中,可重新使用插入物4310。
参考图74,可如从以下部件中示出的装配根据一个实施方式的插入物组件4300:壳体4334、致动器按钮4324、驱动弹簧4336、往复装置4338、引导尖端4340、传感器4314、收回弹簧4342、插入物底座4344、上衬垫4316、粘性底座4312、胶带4320和下衬垫4318。
在一些实施方式中,传感器主表面4346可滑动地安装在引导尖端4340的U形轨道4348之间。除了设置于引导件上的支持件以外,如上所述,在某些实施方式中提供在储存插入物4300的过程中和/或在将传感器4314插入对象的皮肤的过程中将传感器4314固定在尖端4340上的适当位置的固定技术。例如,提供接合引导件凹痕(未示出)的传感器凹痕(也未示出)。可将引导尖端4340安装至往复装置4338的面部4354,例如用粘合剂、热熔或超声波焊接。
在一些实施方式中,用弓形引导件4360将往复装置4338滑动地和非旋转地限制在底座4344上。往复装置通常由用两个桥部4366连接的外环4362和内杯形柱4364形成。桥部4366可被配置为在两个形成于引导件4360之间的槽4368之间滑动,并允许往复装置4338沿着引导件4360不旋转地移动。在一些实施方式中,提供收回弹簧4342,可用引导件4360限制其外圆周,用底座4344的底面4370限制其底部,用桥部4366限制其顶部,并用往复柱4364的外表面限制其内圆周。在一些实施方式中,提供用于使传感器4314和尖端4340进入对象皮肤的驱动弹簧。例如,用往复柱4364的内表面限制驱动弹簧4336的底部和外圆周,用致动器按钮4324内的平顶4372限制其顶部,并用从平顶4372悬垂的杆部4374限制其内圆周。在一些实施方式中,从插入物组件省略驱动弹簧。在这种情况中,例如,由用户施加的手动力使传感器4314和尖端4340在远端前进。
当在致动器按钮4324和往复装置4338之间压缩驱动弹簧4336时,其可朝着底座4344推动往复装置4338。当在往复装置4338和底座4344之间压缩收回弹簧4342时,其朝着致动器按钮4324推动往复装置4338。
当如图74至图75所示并如上所述地在底座4344和壳体4334之间装配传感器4314、引导件4340、往复装置4338、收回弹簧4342、驱动弹簧4336和致动器按钮4324时,将壳体4334扣入底座4344上的适当位置中。用接合壳体4334中的上开口4392的上底座倒刺4390和接合壳体4334中的下开口4396的下底座倒刺4394将底座4344保持在壳体4334上。在美国专利号7,381,184中提供了与插入物4300的结构和操作相关的其他细节。该专利为了所有目的而整体结合于此以供参考。
在一些实施方式中,提供了在储存和插入过程中帮助相对于尖端4340支撑传感器4314的固定技术和/或结构。如图76至图90所示,提供了位于传感器和/或尖端上的固定机构。
图76至图77示出了设置有一个或两个横向延伸的拉片4560的传感器4514。拉片4560接合尖端4540的轨道4548以进行固定。在一些实施方式中,耳部上的辐射式边缘允许其在两次冲压操作中形成,例如孔冲压和笔直切割。在触发过程中,左手挡块4549和传感器4514的顶部之间的间隙产生将传感器顶端偏压至尖端通道中的力矩。在布置过程中,传感器偏转以与尖端分离。
图78至图79示出了具有根据主题公开内容的另一实施方式的传感器固定机构的插入物。尖端4640设置有夹具4660,其与传感器4614顶部处的固定窗4662接合,提供传感器4614在尖端4640中的固定并提供垂直对准。载体4654上的两个驱动块4659和4661穿过尖端4640,以与传感器4614的顶边缘接合。在左驱动块4659和传感器4614的顶边缘之间存在间隙。右驱动块4661与传感器4614的顶边缘接触。在插入过程中,皮肤上的传感器4614的向上的驱动力在传感器4614上产生顺时针的旋转力矩,其将尖端4614偏压至尖端通道中。
可将夹具特征4660和窗口4662移动至左侧,以在运输过程中将传感器4614的顶端偏压至通道中。在布置过程中,传感器4614和夹具4662偏转,以将传感器4614移动至底座4312。
图80示出了传感器固定技术的另一实施方式。特别地,传感器4714设置有从传感器4714的接触部分4732延伸的固定件4760。如所示出地,将固定件4760弹性地偏压就位中。当将传感器4714插入尖端(未示出)内时,固定件与尖端的轨道(未示出)的内部接合,并对传感器4714提供固定力。
图81示出了传感器固定技术的另一实施方式,传感器4814设置有用热形成的凹痕4860。如图82所示,尖端4840上的凸起凸块4864与用热形成的凹痕4860摩擦地接触,以对传感器4814提供固定力。在一些实施方式中,用热量形成凸起凸块。在另一实施方式中,在传感器上形成凸起凸块,在尖端上形成凹痕。
图83至图84示出了形成于传感器4914的接触部分中的孔4960。在尖端4940上设置凸起凸块或拉片4962。拉片4962在传感器4914的孔4960内的相互作用帮助将传感器4914固定在插入物内。
图85至图86示出了传感器5014的固定技术,其与图81至图84所示的技术相似。例如,在与传感器5014的接触部分5032接合的尖端5040上设置凸起凸块5062。在这种结构中,凸起凸块5062产生与接触部分5032相反的偏压力。这种力用作帮助将传感器5014固定在尖端5040内的摩擦力。
图87和图88示出了具有与尖端上的凸起柱或按钮接合的固定件的传感器。图87示出,传感器5114的接触部分5132包括一对“钳状指部”5160,其具有包围并接合设置于尖端上的柱5162的基本上弓形的结构。类似地,图88示出了具有一对与尖端上的柱5262接合的在近端延伸的臂部5260的传感器5214。
图89示出了具有横向延伸的臂部5360的传感器5314,臂部5360在臂部5360和传感器5314的接触部分5332之间限定通道5364。如图所示可将柱5360定位在通道5364内,并提供摩擦阻力,以将传感器5314保持在尖端内。
图90示出了具有在近端延伸的臂部5460的传感器5414,臂部5460在臂部5460和传感器5414的接触部分5432之间限定通道5362。如图所示,在臂部5460上设置拉片5364,并将其容纳在设置于尖端的轨道中的间隙内。拉片5364与间隙的此相互作用提供摩擦阻力,以将传感器5414保持在尖端内。
图91至图92涉及包括提供基本上垂直于(垂直于)传感器的表面的摩擦力的固定件的传感器固定技术。图91和图92示出了设置于插入物5510的壳体5534内的固定件。例如,固定件5560可从壳体5534在远端延伸并包括横向延伸的拉片5562,拉片5562接触传感器5563并提供摩擦力,以帮助将传感器固定在尖端5540内。
图93和图94示出了设置有插入物5610的底座5644的固定件。例如,固定件可包括从插入物5610的底座5644在近端延伸的悬臂5660。悬臂5660可包括横向延伸的构件5662,其接触传感器5661并提供摩擦力,以帮助将传感器固定在尖端5640内。当载体5666向下到达底部时,悬臂5660中止接触,并出现传感器的释放。
图95和图96示出了设置于插入物5710的壳体5734内的弹性或弹性体构件。例如,弹性体构件5760由TPE制成并压在传感器上,产生的摩擦将传感器保持就位。TPE材料相对于传感器产生更高的摩擦,从而需要更少的压力来产生传感器支持力。当启动插入物5710时,向上引导摩擦力,将传感器保持在尖端内。当载体向下到达底部时,与摩擦肋的接触中止,并且传感器释放至底座。在一些实施方式中,用第二波喷射模制方法或压力配合将弹性体构件5760或肋部制造在壳体5734中。
图97和图98涉及在基本上共面的方向上对传感器的表面提供摩擦力的固定件。图97示出了偏压在传感器5814的接触部分5832的侧边缘上的固定件或悬臂5860。在一些实施方式中,将悬臂5860设置在载体或尖端(未示出)上。图98示出了包括如图97所示偏压在传感器上的固定件或悬臂5960的传感器固定技术。悬臂5960包括至少部分地容纳在传感器5914中的任选提供的凹口5964中的横向延伸的部分。另外,提供被偏压以与传感器的前面接合的第二固定件或固定弹簧5990。在一些实施方式中,将固定弹簧5990部分地容纳在切口5994(或槽)中,以捕获传感器。
在一些实施方式中,提供包括可重复使用的插入物设备的插入物组件。插入物的重复使用包括可去除且可互换传感器和尖端的使用,其在传感器的布置过程中可与插入物接合,并且在布置之后去除并丢弃尖端。
图99至图101示出了包含多个传感器/尖端组合6006的尖端/传感器包装6002的系统。如图99和图101所示,提供包括多个对包含传感器/尖端结构6006有用的托盘6004和包含在腔室6008中的干燥剂6010的支撑部。在托盘6004的一侧上设置适应安装在患者体内的传感器尖端的容器6012。对支撑部的顶部应用盖子(例如薄盖6014),以保持传感器/尖端组合的无菌状态,直到安装在对象体内为止。图100是示出了包装6002的示例性结构的透视图。用于每个托盘6004的薄盖6014可包括利于从托盘6004去除盖子的拉片6016(图100,图101)。
图102至图105示出了多个与这里描述的尖端/传感器包装6002一起有用的可重复使用的插入物。图102示出了插入物6030,其包括本体部分6032、加载或竖立结构6036,以及用于将传感器布置在对象的皮肤中的致动器按钮6040。插入物6030的前进结构可包括竖立结构,例如通过从壳体6932收回竖立结构6036而将其拉至臂部;例如通过将竖立结构6036按入壳体6032而将其推至臂部;或例如通过以平行于插入物6030的纵向轴线或垂直于插入物6030的纵向轴线的旋转移动旋转竖立结构6036而旋转其。插入物6030的驱动机构与在美国专利公开2008/0082166,美国专利号6,197,040或美国专利号4,976,724中公开的驱动机构基本上相似,这些专利为了所有目的而整体结合于此以供参考。
为了将尖端/传感器组合插入插入物6030,从尖端/传感器包装6002去除薄盖。将插入物6030的远端部分6034定位在托盘6002的壁部6004内,如在箭头E的方向上指示的。远端部分6034位于干燥剂腔室6008的上表面上,使得插入尖端保持暴露。
图103示出了与这里描述的插入物6030基本上相同的插入物6130。与尖端/传感器托盘6102一起使用插入物6130。托盘6102包括位于托盘6102的中心部分中的干燥剂腔室6108。因此,通道6112包围干燥剂腔室6108的外围。当将插入物6130应用于尖端/传感器托盘6102时,可将远端部分6134定位在通道6112内。如图103所示,此结构允许将传感器和尖端完全容纳在插入物6130内。
图104示出了与这里描述的插入物6030和6130基本上相同的插入物6230,这里指出了并在附图中表示了差异。可与尖端/传感器托盘6204一起使用插入物6230。将托盘6204和插入物6230的尺寸和结构构造为,使得能够将托盘6204完全定位在插入物6230的远端部分6234内。在远端部分6234附近设置一个或多个支撑柱6220,以使插入物相对于任何为了插入步骤而将插入物6230和托盘6204置于其上的表面稳定。在插入过程中,支撑柱6220还可将插入物6230固定至粘性底座(未示出)。
图105示出了与这里描述的插入物6030,6130和6230基本上相同的插入物6330,这里指出了并在附图中表示了差异。可与尖端/传感器托盘6304一起使用插入物6330。在一些实施方式中,托盘6304包括在远端伸出的手柄部分6340,其可由用户抓住以利于将尖端/传感器插入插入物。
图106至图107示出了用于与这里描述的插入物6030,6130,6230和6330一起使用的示例性尖端/传感器组合。尖端6440包括用于将传感器滑动地容纳于其中的侧轨道6448。锁定拉片6450也设置于尖端的近端部分上,并包括用于与插入物6030(或6130,6230或6330)的载体互锁的切口部分6452。如图108至图112所示,载体6466包括用于匹配地容纳尖端6440的容纳结构。例如,载体6466可包括一对提供通道6480的壁部6478,可将所述尖端6440定位在通道6480中。壁部6478设置有用于容纳锁定拉片6450中的底切部分6452的切口部分6482。将一对固定件6484可移动地安装在载体6466上。例如,经由弹簧6486朝着载体6466的中心部分偏压构件6484。如图111所示,固定件6484可克服弹簧的偏压向外移动,以允许将锁定拉片6450插入载体的切口部分6482。然后释放固定件6484并使其返回至与底切部分6452接合的位置,以防止将尖端和传感器意外地从插入物去除(图112)。应理解,可用替代技术(例如摩擦配合、搭扣配合、插座安装、磁耦合等)提供尖端和载体的接合。
图113至图117示出了可重复使用并可与这里讨论的尖端/传感器包装一起使用的主题公开内容的另一实施方式。图113示出了与这里描述的传感器包装6200相似的传感器包装6504。尖端/传感器包装6504还包括一个或多个当将传感器插入插入物时防止包装6504的意外变形的加固肋6574。
如图114所示,提供与这里描述的插入物6030,6130,6230和6330基本上相似的插入物6530,这里指出了并在附图中表示了差异。插入物6530包括用于与尖端/传感器组合结合的载体(未示出)。如图所示,将插入物6530降低至尖端/传感器包装6504上,以将尖端6506与载体接合。如图115所示,将现在包含尖端/传感器6506的插入物6530定位在底座6512的上方。底座6512可包含用于固定至对象的皮肤的粘合剂。插入物6530包括允许将插入物6530与底座6512暂时接合的锁定结构6526。
如图116所示,通过按下插入物6530上的启动按钮6532来布置传感器,以通过使用内部驱动机构(例如弹簧)使传感器进入皮肤。应理解,或者可通过使用允许用户提供手动远端力以布置传感器的插入物来执行上述过程。
在安装传感器后,例如通过按下插入物6530上的锁定按钮6526,将插入物6530与底座分离。一旦将插入物6530与底座分离,用户便可去除并丢弃尖端。在一些实施方式中,插入物6530包括允许去除尖端的滑动杆6540。应理解,可以几种方式中的一种执行尖端与载体的分离,例如滑动开关允许固定件(这里讨论的)向外滑动并允许固定件6484的接触部分6483与锁定拉片6450的底切部分6452的分离。
图118示出了插入物6630和用于安装在底座6612上的接合结构。插入物6630包括被配置为使尖端/传感器盒沿着纵向轴线LON进入对象的皮肤S的本体部分6640。纵向轴线LON可基本上垂直于皮肤表面。在一些实施方式中,轴线LON与皮肤表面形成锐角。底座6612和插入物6630分别设置有互补的底座6612上的锁定结构6662和插入物上的6664。使插入物在底座6612上横向地(方向LAT)前进。可通过使锁定结构6632围绕支点6626枢转而将插入物6630锁定就位。在这种枢转动作之后,将锁定结构6632的接合部分6666容纳在底座6612中的凹槽6668中。通过在插入物6630和底座6612之间插入尖端/传感器盒6650,来进一步提供插入物对底座的固定。例如,盒子6650包括可在设置于插入物6630和底座6612上的互补凹槽6652内滑动的凸起拉片6654。在与插入物附接至底座的方向垂直的方向上(例如,垂直于页面的方向)执行盒子的插入。
图119至图121示出了根据所公开的主题的插入物的另一实施方式。插入物6730对于使医疗装置(例如分析物传感器)进入对象的皮肤来说是有用的。插入物6730包括累积前进能量以提供更快速且更有力的前进行程的锤子构件6760。如图119所示,初始时将锤子构件6760定位为相对于装置的纵向轴线是稍微歪斜的。当使对准触发器6734在远端前进时,对准套筒6736将锤子构件6760逐渐枢转至纵向结构中。当将锤子构件6760枢转至适当的位置中时,前进弹簧继续压缩。参考图120,将锤子构件6760枢转至与插入物6730的中心孔对准,例如沿着由箭头代表的纵向轴线。因此,立即释放前进弹簧6742的张力,这允许锤子构件6760的快速远端移动。锤子构件6760接触载体6744,然后载体6744接触尖端/传感器组合6712,以提供远端移动。
如图121所示,凸缘或横向构件6726设置有插入物的内孔。当锤子构件6760在远端前进时,锤子构件的远端表面接触凸缘6726。锤子构件6760与凸缘6726的相互接合阻止锤子构件6760的进一步远端移动。
图122示出了简化单元或保持某些部件的无菌状态然后与对象相互作用的盒子6800的一个示例性实施方式。在一些实施方式中,部件包括尖端6840、壳体6860和传感器6814。可将盒子6800与这里描述的任何插入物6030,6130,6230,6330,6530和/或6730一起使用。在一些实施方式中,盒子包括将尖端和传感器包含于其中的壳体和盖子。在一些实施方式中,用弹性件或其他悬臂结构保持尖端和传感器在盒子内的对准。盒子与插入物的相互作用使传感器和尖端前进,使得将传感器安装在对象处。
如图123至图124所示,尖端6840和传感器6814可位于一次性盒子6800的凹入部分中。壳体盖上的弹簧指部或悬臂6876保持尖端6840和传感器6814上的负载,以保持其陷入腔体中。在上图中未示出盖子与盒子壳体6860的底座的连接,但是可用诸如按扣、热熔或超声波焊接的方法连接组件中的两个壳体。将传感器6814包含在尖端6840内,横向地由尖端的两个圆形端6848固定,在正交的横向方向上(相对于以上示出的视图)由尖端6840上的两个弯曲拉片6849和盒子壳体底座腔体固定。不仅用腔体将尖端保持在其横向位置,而且用在壳体底座6870上示出的凸起金字塔形特征6878保持。在上图中,定位棱锥位于从尖端中的弯曲拉片产生的开口6882中。在上图中未示出将盒子定位/附接/接合装置的插入物部分的接合特征,但是可包括这种如以上图106至图112所示的特征。
如图125和图126所示,当将盒子6800装载在装置的可重复使用的插入物部分上时,用构造在插入物(未示出)上的固定部件将尖端从其腔体拉起。插入物的可重复使用的部分的特征进入两个图122所示的更短的槽6864。在插入物装置的传感器传送动作中,这些特征将保持固定。
在更长的中间槽6866中,插入物的阶梯特征与尖端上的开口匹配(在上图中示出为两个孔6864)。特征的阶梯部分在尖端的后部上提供力,以将其克服壳体上的松动悬臂6876的力拉起。插入物的此特征将相对于盒子移动,并通过传感器的插入和传送而对尖端提供驱动和收回移动。在一些实施方式中,通过驱动销传递力,驱动销是插入物装置的可移动部分的部分。驱动销通过孔6864伸出。在驱动销(未示出)的稍微不对准的情况中,盒子壳体盖上的肋部将限制尖端向上倾斜。
一旦从盒子的腔体部分升高尖端和传感器,其不再由壳体底座的凹入腔体部分和保持尖端位置的棱锥特征限制。用插入物的固定和阶梯驱动特征将尖端保持在其凸起位置,与盖子壳体上的悬臂指部的力平衡。通过挤压(pinch)壳体盖上的悬臂指部,将传感器保持就位。用插入物的匹配驱动特征将尖端限制在其收回位置。
当启动插入物时,当其通过上图所示的更长的槽时,匹配插入物驱动特征向下驱动尖端(见图127至图129)。所驱动的尖端沿着插入物的固定肋部、构造在盒子壳体中的有肋的特征,以及壳体盖悬臂指部滑动。悬臂的摩擦力保持传感器面临尖端片状金属中的“驱动块”弯曲,以确保尾部在插入过程中不会从尖端通道暴露。在一些实施方式中,“驱动块”特征是构造在尖端或载体中的纵向限制,其限制传感器相对于尖端的近端移动。在另一实施方式中,驱动块特征是载体上的伸出部或尖端上的弯曲部,当在远端推进尖端时,其推动传感器。
用构造在壳体盖中的固定肋部保持传感器在驱动块特征上弹出。当悬臂在传感器的顶边缘上滑动时,从传感器解除固定力,并可用相对小的力将其捕获在装置的底座部分上。可替换地,如果几何形状允许,并适当地定位指部,那么悬臂在尖端上的收缩可对尖端的返回移动提供足够的阻力,以将传感器保持在其插入位置,甚至不需要底座上的捕获装置。然后,插入物驱动特征收回尖端,将传感器留在装置的底座部分(其附接至皮肤)上的适当位置中。
可从插入物去除盒子。当去除盒子时,来自壳体盖悬臂的力将尖端压回盒子底座壳体上的凹槽中。去除并可丢弃底座壳体。
在图131至图137中示出了盒子的另一实施方式。如图131所示,在此实施方式中,尖端6940和传感器6914与肋部6972和6974邻接,并在尖端6940将被驱动且将由插入物收回到皮肤中的插入平面上。用构造在盒盖壳体6970上的中心悬臂特征6976将尖端和传感器保持就位。此悬臂6976具有这样的几何形状,使得将悬臂端部的垂直部分与尖端6940和传感器6914连接。
如图132和图133所示,将盒子6900装载在插入物中,其中,插入物(未示出)上的固定特征升高盒子悬臂,使得悬臂端部特征的斜面部分现在与尖端的插入平面成一直线。而且,插入物(未示出)的驱动部件安装在尖端上的槽开口中。在这里描述的实施方式中,在此设计的驱动部件上不需要阶梯。
当向下驱动尖端时(见图134至图135),向上推悬臂6976,将传感器保持在与尖端6940相反的位置。壳盖上的固定肋部确保尖端6940在插入过程中保持其插入平面,还确保悬臂的挤压力不会导致传感器跳过集成在尖端中的驱动块部件。在插入移动中,固定肋部保持传感器与尖端相平。
如图136至图137所示,将传感器6914捕获在其在底座上的移动的底部,如以上讨论的。插入物上的驱动部件将尖端6940收回至其起始位置。悬臂6976返回至其原始未偏压结构。从插入物去除并可丢弃盒子6900。
应理解,这里描述的主题不限于所述特定实施方式,当然同样是可变化的。还将理解,这里使用的术语仅是为了描述特定实施方式的目的,并非旨在是限制性的,因为本主题的范围只由所附权利要求限制。
Claims (10)
1.一种用于将医疗装置插入通过对象的皮肤中的设备,其包括:
壳体,限定位于所述壳体中的纵向腔体以及延伸进入所述腔体中的干扰件;
偏压件;
驱动件,与所述偏压件接合以用于从近端位置移动至远端位置,并且所述驱动件进一步被构造成在未对准结构与对准结构之间移动,在所述未对准结构中,所述驱动件的远端移动被所述干扰件阻止,在所述对准结构中,所述驱动件的远端移动不被所述干扰件阻止;以及
致动器,具有对准表面,用于使所述驱动件从所述未对准结构移动至所述对准结构。
2.根据权利要求1所述的设备,其中,所述致动器可从近端位置移动至远端位置。
3.根据权利要求1所述的设备,其中,所述致动器的远端移动压缩第一偏压件。
4.根据权利要求1所述的设备,其中,所述驱动件的第一位置位于相对于所述纵向腔体成斜角处。
5.根据权利要求1所述的设备,其中,所述驱动件的第二位置包括与所述纵向腔体基本上对准的结构。
6.一种用于将医疗装置插入通过对象的皮肤中的设备,其包括:
壳体,限定悬臂件;
尖端,能够在所述壳体内从收回位置移动至部分暴露位置;以及
电化学传感器,可释放地与所述尖端接合,用于与所述尖端一起移动并随后插入对象的皮肤中;
其中,所述悬臂件弹性地接触所述尖端和所述传感器中的至少一个。
7.根据权利要求6所述的设备,其中,所述壳体包括远端开口,用于从所述远端开口释放所述电化学传感器。
8.根据权利要求6所述的设备,其中,所述壳体限定用于容纳插入物的驱动件的纵向凹口。
9.根据权利要求6所述的设备,其中,所述壳体包含干燥剂。
10.根据权利要求6所述的设备,其中,所述壳体限定用于对准所述尖端和所述传感器中的一个的一个或多个纵向脊部。
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