CN104971390A - 用于控制体内压力的装置和方法 - Google Patents
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Abstract
本发明公开了用于控制体内压力的装置和方法。本发明提供一种差动压力调节装置来控制体内,特别是心脏内的压力。该装置可包括一分流器,其位于体内两个或多个内腔之间以使得液体能够在所述两个内腔之间流动;和一可调整的流量调节机构,其被设置为可选择性地覆盖所述分流器的开口以与所述体内腔之间压力差有关地调节流过所述分流器的液流。在一些实施例中,可提供一控制机构,其与可调整的流量调节机构相连接以遥控启动该可调整的流量调节机构。
Description
本申请是申请人为:V波有限公司,申请日为:2005年2月3日,申请号为:200580010735.1,名称为:用于控制体内压力的装置和方法的发明的分案申请。
技术领域
本发明涉及用于降低或调节血液循环系统内压力,特别是调节心脏血液压力的装置和方法。
背景技术
充血性心力衰竭(CHF)在西方社会被认为是导致住院治疗和大量死亡的最普遍的原因,其对生活质量有严重的影响。CHF是一种低系统灌注和心脏机能低下的病症。CHF的原因可包括由于肌肉萎缩而导致的心肌损伤、心肌症和其它病症。与CHF直接相关的病理生理的机理包括心脏输出量减少,心脏充盈压力增加,流量积累,这些可以导致例如,肺充血和呼吸困难。心脏收缩机能的损伤可能导致左心室收缩减弱和心输出量减少,这些可以产生的临床症状包括:不耐力症(effort intolerance),呼吸困难,寿命减少,浮肿(肺或体表)和疼痛。心脏收缩机能紊乱的病人通常有一个较大的左心室,这是由于为了保持足够心搏量出现了心脏重塑的现象。这种病理生理的机理是与心房压力和左心室充盈压力的增高有关。伴随心脏舒张机能异常,由于异常放松而导致在正常压力下心脏充盈不充分,左心室可能变得僵硬而且局部明显缺乏顺应性。在较高充盈压力下要保持适当的心脏充盈可能需要维持心输出量。这种为保持心脏充盈和输出量的强制性的充盈压升高会导致肺静脉高血压和肺气肿。
目前用于治疗CHF的方法通常分为三种:(1)药理学,例如利尿剂;(2)辅助系统,例如泵;以及(3)手术治疗。关于药物治疗,血管舒张药已被用于通过降低全身血管阻力来降低心脏的工作负荷,利用利尿剂来阻止液体积累和浮肿发生,同时降低心脏充盈压力。
用来治疗CHF的辅助设备可包括,例如,机械泵。机械泵通过全部或部分地完成正常情况下由心脏所作的泵功能而减少了心脏的负载。目前,机械泵被用于例如当病人可得到用于移植的捐献心脏的同时,对病人进行维持。还有许多起搏器也用来治疗CHF。再同步(Resysnchronization)起搏器也已经用来治疗CHF。最后,至少还有三种极端侵入性和复杂的外科手术方法用于治疗心力衰竭:(1)心脏移植;(2)动态心肌成形术;和(3)Batista左心室局部切除术。
在极端紧急状况时,临时性辅助仪器和大动脉内的气囊可以是有帮助的。心脏移植和长期性左心室辅助仪(LVAD)的植入通常可被用作最后的手段。然而,目前使用的所有辅助仪器目的都是增加心脏泵容量和增加心输出量来达到与正常的生活一致的状态,减少充盈压和/或防止形成浮肿。最终,心脏移植可以被用来治疗极端的心脏功能紊乱病症。然而这个手段有很高的侵害性,并且受到了捐助心脏可获得性的限制。机械装置可以允许推进大量的血液(公升/分),然而这个也是它们的主要局限。对电源的需要,相当大的泵以及溶血和传染的可能性所有这些都要考虑到。
发明内容
本发明可以提供调节体内压力的方法和器械。根据本发明的一些实施例,差动压力调节装置可包括位于体内两个或多个内腔之间的分流器,以使得液体能够在这些内腔之间流动,以及一个被设置为可选择性地盖住分流器开口的可调节流量调节机构,以调节穿过分流器的与体内腔之间压差有关的液流的。
根据一些实施例,压力调节装置可包括位于心脏两个或多个内腔之间的分流器,以使得液体能够在这些内腔之间流动,一被设置为可选择性地盖住分流器开口,以调节穿过分流器的液流的可调节流量调节机构,以及一与可调节流量调节机构相连的控制机构,以遥控启动该可调节流量调节机构。
在另一个装置中提供了一种控制体内压力的方法,该方法包括将一差动压力调节装置植入体内,该压力调节装置包括一位于体内两个或多个内腔的分流器,配置一个流量调节机构,以及根据这些内腔之间压差的变化来控制流量调节机构的设置。
在本发明的另一个实施例中提供了一种控制体内压力的方法,该方法包括采用已植入体内的控制机构来控制一流量调节机构的设置,该流量调节机构被放置在包括一分流器的差动压力调节装置,该分流器例如,放在两个或多个内腔之间,如心脏左心房和右心房之间。
附图说明
本发明的主题在说明书结论部分被特别指出并且清楚地提出了主张。然而,通过项目的详细描述并参考阅读附图,本发明的结构和操作方法两方面以及它们的特性和优点都可以得到最好的理解。附图其中:
图1A示意性说明了根据本发明典型实施例的一差动压力调节装置(DPRD);
图1B-1I示意性说明了根据本发明一些实施例的差动压力调节装置(DPRD)的其它实施例;
图1J是根据本发明典型实施例的描述压力曲线的一个实例的示意图,该示意图涉及两个内腔间压差的变化,流过流量控制机构的流量以及孔口面积之间的关系;
图2A和2B分别示意性说明了根据本发明一典型实施例可调节分流器、管或其它结构的横截面图和侧面图;
图3示意性说明了根据本发明另一典型实施例的分流管;
图4示意性说明了根据本发明一典型实施例的包含流量调节机构(FRM)的分流器;
图5示意性说明了根据本发明典型实施例的图4中的分流器,其结合有打开状态的FRM;
图6示意性说明了根据本发明另一典型实施例的FRM,其可用于与例如图1中的DPRD、图2A-2B中的分流器,或者图3中的分流器相结合;
图7示意性说明了根据本发明另一典型实施例的FRM,其可用于与例如图1中的DPRD、图2A-2B中的分流器,或者图3中的分流器相结合;
图8示意性说明了根据本发明另一典型实施例的FRM,其可用于与例如图1中的DPRD、图2A-2B中的分流器,或者图3中的分流器相结合;
图9示意性说明了根据本发明另一典型实施例的在心脏内部的FRM。
图10示意性说明了根据本发明另一典型实施例的FRM,其可用于与例如图1中的DPRD、图2A-2B中的分流器,或者图3中的分流器相结合。
图11示意性说明了根据本发明另一典型实施例的FRM,其可用于与例如图1中的DPRD、图2A-2B中的分流器,或者图3中的分流器相结合;
图12示意性说明了根据本发明另一典型实施例的FRM,其可用于与例如图1中的DPRD、图2A-2B中的分流器,或者图3中的分流器相结合;
图13A示意性说明了根据本发明的一些实施例用于遥控DPRD的装置;
图13B-E示意性说明了根据本发明的一些实施例用于遥控DPRD的机构;
图14示意性说明了根据本发明的一些实施例用于说明控制压力,例如心脏血压的方法的流程图。
应该理解的是为了简单和清楚地说明,图中所示的元件没有必要地按比例画。例如,为了清楚起见,一些元件的尺寸相对于其它元件被夸大了。进一步,在适当的地方,参考数字在这些附图中可以重复使用以表示相应的或类似的元件。
具体实施方式
为了完整地理解本发明,在下列的详述中,阐述了多个具体细节。然而,本领域普通技术人员将认识到没有这些具体细节也可实施本发明。在其它例子中,可能没有具体描述公知的方法、过程、部件及结构,以免与本发明混淆。
应该意识到,尽管为了示意的目的,此处部分讨论涉及到心脏、心内腔和/或心房,但是本发明实施方式并不限于这方面,其可以用于各种各样其它的血管、内腔室、器官或身体部位。例如本发明的实施例可包括在脑内腔之间、所选器官之间、血管等之间(例如,在大动脉和内腔静脉之间),和/或其它的合适的内腔之间,比如,在身体内的带、内腔、器官、导管、区域或地区之间调节液体转移。
本发明的一些实施例包括,例如,一种通过减少或别的方式控制两个或两个以上身体部位,例如心脏的两个内腔(如,左心房和右心房)之间的压力差来控制体内压力的方法和装置。例如,这样的压力控制可以用来帮助解决具有充血性心力衰竭和突出的心脏舒张性功能紊乱的病人心脏充盈压力增高的问题,从而帮助尽量减少或阻止肺部液体积聚、水肿形成和临床呼吸困难疾病。另一个例子是,压力控制可以用来减少左心室充盈压。本发明的一些实施例可以包括差动压力调节装置(DPRD),例如,包括分流器、管或其它具有孔口、管或开口的结构以液体地连接两个或更多内腔,如连接心脏的左右心房。根据本发明的一些实施例,该DPRD可包括一个调整装置或调节装置,其能够校正、改变或用其它方式调节例如孔口的横截面,例如与第一和第二内腔之间压力差变化有关的孔口的横截面,从而增加和/或减小这两个内腔之间的血液流速。
本发明的一些实施例可用来,例如消除充血性心力衰竭(CHF)病人左心室的额外充盈压,以及潜在地防止或减少肺气肿的发生。
本发明的一些装置包括,例如,在两个心内腔,例如左心房和右心房之间的壁内植入一个可调节的DPRD。这个压力调节装置可以,例如容许一选定的血液量从左心房流向右心房,这与左右心房之间的压差有关。该压力调节装置例如可进行调节,以选择性地改变开口的大小和形状、允许流过的血液量等等。
在一些实施例中,该压力调节装置可设计为保持两个或多个内腔之间,例如左右心房之间有一连续流量。又如,一分流器、管或其它结构可连接到一盖子,阀孔,阀杆,或其它可设置为连续半开的流量调节机构上,以使得所选的最小量液体能够在体内两个内腔,例如两个心内腔之间持续流动。随后可调节所述盖子,例如进一步打开或关闭盖子来控制内腔之间的液体量。流过DPRD的液体可以根据两个内腔之间的压力或压差的变化而增加或减少。例如,当左心房的压力相对于右心房的压力增大或减小时,盖子可以打开和/或关闭。在一些实施例中,DPRD可如此设计以使得孔口盖与分流器的开口不直接接触,以使对复原的帮助最小化或阻止组织在孔盖上或孔盖周围的生长。这样一个构造可使连续的液体流过DPRD,并且可以阻止或减少血液凝结、生物膜形成或其它不想要的生长的发生。在一些实施例中,DPRD可以被用来冲洗或清洁分流器和/或分流器盖等。
参见图1A,其示意性地说明根据本发明典型实施例植入心脏109中的DPRD101。DPRD101可以被植入两个或多个体内腔之间,例如,植入左心房102和右心房103之间。采用不同的心内腔排列方式,DPRD101可以植入其它心内腔,和/或被植入其它体内腔内或植在体内腔之间。一些实施例中,使用例如安装在导管远端的穿孔或切口仪器或其它合适的穿孔装置,可在两个体内腔之间的壁内,例如,左心房102和右心房103之间的隔膜105内,形成一开口、穿孔或其它结构。然后用导管或其它的输送装置将DPRD101放置于穿孔中。在一些实施例中,一个或多个组织固定元件,例如,支撑臂106可以将DPRD101支撑在生成孔或穿孔中所需要的位置。
DPRD101可以包括,例如一个可调节的分流器,管子或通道107,使得液体在两体内腔之间、器官之间、部位或区域等之间流动,比如在左心房102和右心房103之间流动。DPRD101可以包括一个在此所述的流量调节器(FRM)108,例如流体阀、盖子,阀孔,阀杆或帽,以对分流管107的参数进行所选择的改变,例如,通过改变分流器107开口的横截面或分流器形状等,从而调节从左心房102自右心房103的血流量。在一些实施例FRM108可设置为连续半开位置以使左右心房之间有一连续血流量。例如,FRM108可有目的地处于半开以使得一选择的血液量连续在心内腔之间流动。随后可通过选择地改变开孔的大小和形状,血液的容许流过量,来调节FRM108,使得分流器107开口和FRM108周围的区域能够受到限制和/或扩张,从而影响分流器107的有效流通,同时能够控制各内腔之间的血流量。DPRD101可以包括一个或多个控制设备110,例如,导线、弹簧、绳索等,使得FRM108能够被动地或主动地受到控制。在一个实施例中,例如,通过被预加载一选定的拉力,弹簧可以用来使得FRM108依照压差的变化而动作,以一个可控方式响应一个或多个压力阈值的变化。
FRM108可以设置为响应所选的压力分布,从而提供一个已知的压力释放分布。举例来说,FRM108可以预调、预校准和/或预配置,以根据左右心房之间压力差的变化而改变其设置,调整其配置或位置,和/或改变其孔口宽度或流量等。FRM108可以对于例如连续可变设置进行连续调节,例如响应于环境条件和/或外部控制。在至少这些方式中,DPRD101可以在两个或多个体内腔或区域之间提供一选择的、可预知的和/或有保证的液流。在一些实施例中,FRM108的静止或缺省设置,开口大小,流量水平或位置可以通过例如预先设置好的参数和/或遥控机构来改变。在一些实施例中持续打开或半开的FRM108可以帮助阻止分流器107的堵塞。
在一些实施例中,在低于某一压力或压差时,阀门或仪器可以完全关闭;然而在其它一些实施例中,在低于某一压力或压差时,阀门不能完全闭合或者处于微开的状态。例如,阀门可有一个最小打开尺度。
在一些实施例中,DPRD的一个或多个性能,例如,压力调节装置的横截面开口大小可能取决于左右心房之间的血压差。因此,在一些实施例中,左右心房之间的血流可能受到左右心房之间血压差变化的影响。
根据本发明一些实施例的DPRD可以通过减少心房压力而使得心室的压力减少。
在一些实施例中,DPRD可以用于心膜炎(ASD)病人,例如那些不能耐受完全不受控制的心房关闭过程的人,以有选择地关闭隔膜中的孔或间隙。
在一些实施例中,DPRD可以用于将液体从左心房移到右心房,例如救护肺动脉高血压病人。在这些例子中,DPRD可以与FRM108一起放置在左心房中。根据本发明的一些实施例,FRM108可以是单向的或双向的。
在一些装置中,可将多个DPRD植入一个壁或其它结构内,例如,帮助提供备份,以植入设置范围不同的仪器来获得更高水平的开口控制,和/或能够增加另外的仪器。当两个或多个更小直径的DPRD可被输送时,植入多个DPRD可减小输送导管的直径。
在其它的实施例中,FRM108可以包括盖子、帽或其它合适的具有多种形式的机构,以使FRM 108能够部分或完全关闭。现在参见图1B-1G。图1B中,FRM108可以包括两个或多个臂120,上述臂可设置为在分流器122的开口125处连续或恒定地保持微开。举例来说,FRM108可设置为至少局部地连续保持与分流器107分离,以容许左心房102和右心房103之间有一持续液流量。臂120可以响应心内腔间的压差的变化而进一步地打开和/或关闭。臂120可以由柔韧的聚合物或其它合适材料构成。在臂末端130臂处120可具有,例如圆形形状,以帮助防止血液停滞。
在图1C中,FRM108可包括分流器122,以及两个或多个柔性膜135,该膜可设置为在开口125处恒定地半开状态,以使血液能持续流过分流器122。例如,在这里讨论的多种实施例中,一设备可如此安置使得无论心内腔之间的压力或压差是多少,都可以设置最小的开口大小或可以产生流量。膜135可以包括至少一个弹簧机构,以响应心内腔间压差的变化,帮助膨胀或收缩所述膜135。
在图1D中,FRM 108可以包括分流器122,以及一个或多个柔韧的或弹簧为基础的帽、膜或叶状物150,其通过弹簧或其它合适的压力敏感机构155与分流器122可选择地相连。在一个实施例中,压力敏感机构155可利用一可控方式响应一个或多个压力阈值的变化被预加载。帽150可设置为在开口125处持续微开,来使得血液能够持续流过分流器122。FRM 108可包括一个或多个凸起区域160,例如,棘状物或其它合适形状的物体以帮助阻止盖子150与分流器122完全接触。
在图1E中,FRM108可以包括分流器122,以及一个或多个有角度的柔性膜或叶状物165,其设置为在开口125处持续微开以使血液能够持续流过分流器122。在一个实施例中,叶状物165可在选定张力下预加载以用可控方式响应一个或多个压力阈值的变化。叶状物165可以包括至少一个弹簧机构或其它合适的机构以响应心内腔之间的压差变化,帮助关闭和/或打开叶状物165。叶状物165可以包括至少一个磁铁或电磁铁170或其它合适的机构以远距离地帮助叶状物165关闭和/或打开。导线172或其它合适的机构可用于启动磁铁或电磁铁170。
在图1F中,FRM108可以包括分流管122、和罩、阀孔、阀杆或其它流量调节机构175,其设置为在开口125处一直保持半开以使血液能够持续流过分流器122。罩175可以和弹簧177或其它合适的压力敏感机构连接在一起。在一个实施例中,弹簧177可在选定张力下预加载以用一可控方式响应一个或多个压力阈值的变化。FRM 108可以包括一个或多个罩的活动限制器179。FRM 108可以包括一个固定的极化磁铁181以及带有一个或多个导体185的电磁线圈183。罩175可响应心内腔之间压差的变化,和/或通过遥控启动磁铁181和/或电磁线圈183而打开和/或关闭。例如,当磁铁181启动时,罩175可以进一步地打开,而当线圈183启动时,罩175可以进一步地关闭。
如图1G所示,FRM 108可以包括分流器122,以及罩175,其设置为在开口125处一直保持半开以使血液能够持续流过管道122。罩175可通过连接臂185与分流器相连接。罩175可包括切口,狭槽,凹槽或裂缝187等以使血能够连续流过分流器。狭槽187可具有不同的大小、深度、宽度或密度,这可帮助指示罩175的各种区域是较结实和柔韧性较差,还是较软弱和较柔韧,因此可以根据体内腔间压差的变化而做出不同地反应。举例来说,在具有更多或更深侵入的区域中,该区域可以是比较软弱和有柔韧性的,从而使罩175至少局部打开,允许压力相对低的血流流过分流器122。在具有较少或较浅侵入的区域,该区域可以相对结实且缺乏柔韧性,因此仅仅使罩175至少局部打开,允许压力相对高的血流流过分流器122。
在图1H和1I所示,FRM108可包括分流器122和罩175,其可以设置为在开口125处保持一直半开的状态以使得血液能够连续流过分流器122。罩175可以与弹簧190或其它适合的血压感应装置相连接。弹簧190和罩175可以与一活塞或泵机构192相连接。如图1I所示,罩175可以响应于心内腔之间压力差的变化,和/或通过活塞192激活弹簧190,延长和/或扩大罩175而被打开和或者关闭,从而改变了开口125的大小。
根据本发明的一些实施例,使用DPRD101能够生成一压力曲线,该曲线涉及两个内腔间压差的变化,流过流量控制装置的流量和孔口面积之间的关系。可采用任何所需或所选的设计参数。现在参照图1J,该图表示了这种压力曲线的一个例子。在图1J中可以看到,在12毫米汞柱压力差以下,开口或孔口的大小可以相对稳定,而流量主要受压差影响。当压差上升到大约12毫米汞柱以上20毫米汞柱以下时,流量可按一较高速度增长,这时它既受孔口面积增加的影响,也受压差增长的影响。当压差上升到大约20毫米汞柱以上时,由于孔口区域可能已经达到了其最大横截面,因此流速以较低速度增长,流量主要受压差的影响。压差可受孔口面积的线形和/或非线性变化的影响。可采用其它的压差,流量和/或孔口面积水平,各种关系,以及相互关系,作为其它参数,变量,最小和最大限制等。
参见图2A和2B,它们分别示意性说明了根据本发明的典型实施例可调节DPRD 201的横截面图和侧视图。DPRD 201可包括例如一个框架220,该框架与一个或多个支撑臂,例如,支撑臂211-216相连接。框架220可包括例如一个柔性固定架,环或管。框架220由柔性材料,例如柔性金属,超柔性合金,和/或形状记忆材料做成,形状记忆合金采用例如镍钛诺(Nitinol)或其它合适的材料。
尽管在这里为示意的目的,将DPRD201描述为有着六个臂或附肢211-216,但本发明的装置并不受到此限制,且可包括不同数量的臂,例如一个臂、两个臂、十个臂等等。
为了获得期望的功能,臂或附肢211-216可以是柔韧的和/或预先塑形的。例如,臂211-216在插入过程中,例如在插入一合适的输送管中时可以被折叠起来。在一些实施例中,臂211-216可以由超弹性材料,例如形状记忆合金(SMA)制成,该记忆合金如镍钛(NiTi)合金。其它合适的材料可以包括,例如,金属、不锈钢,和/或其它合适的材料。至少部分臂211-216或所选的其它DPRD201元件可以被涂敷和/或被赋予某种结构,以增加它们的生物相容性和/或增加这些元件可选择性地成为内皮细胞状的等级,如在某些移植条件中所要求的。
DPRD201可包括,例如,FRM 250,又如,包括一个盖子、阀口、阀杆,或其它的带有一个或多个预设位置的流量调整设备,以有选择性地覆盖由于DPRD201的展开而造成的开口。FRM将在下面详细描述。
如图2B所示,DPRD201可有两个侧面,这里分别指近侧251和远侧252。例如DPRD 201可被植入心脏109中,这样DPRD201的近侧251可面对着右心房103,而DPRD201的远侧252可面对着左心房102。可使用其它方向的侧面251和252,同样可使用其它数目的侧面。
在有些实施例中,DPRD201的远侧252可与远端的一组臂或附肢相连,例如,臂211-213,而DPRD201的近侧251可与近端的一组臂或附肢相连,例如,臂214-216。因此,当DPRD201植入心脏109时,远端的一组臂211-213可首先在例如左心房102内放开,进入图1中隔膜105的右侧,从病人的透视图看,将DPRD201支持在隔膜105的左侧。然后,随着DPRD201插入过程的完成,例如通过收回运载DPRD201的导管或输送管,近端的一组臂214-216在右心房103内放开,例如进入图1中隔膜105的左侧,从病人的透视图看,因此支持隔膜105的右侧。用这种方式,支撑臂211-216可以将DPRD201的框架220支撑在左心房102和右心房103之间所期望的位置。
现在参见图3,其示意性说明了根据本发明另一实施例DPRD301。DPRD301可包括,例如框架302,该框架连接到一个或多个臂或附肢,例如臂303和304。
框架302可包括,例如由柔性材料构成的柔性固定架,该柔性材料如柔性金属,该柔性金属例如为镍钛诺如或镍钛诺丝。框架302可具有如图3所示的通常螺旋形状,并可与框架302每个末端的弯臂303和304一体成型,如图3所示。其它合适的形状也可以被采用。臂303和304可以是柔性的并且能够预先塑形以实现想要的功能。举例来说,臂303和304在插入过程,可以被折叠在例如一合适的输送管内,以便随后放开将框架302定位到小孔中。根据本发明的一些实施例,DPRD301也包括FRM305,比如这里详细介绍的FRM。
同样参见图4,其示意性说明了根据本发明实施例包括DPRD405的DPRD401。DPRD405可以作为FRM250和FRM350的例子。尽管DPRD405可以用于结合DPRD301或其它合适的分流管或医疗器械,但为了示意的目的,这里仅仅展示了DPRD405与DPRD401相结合,其中DPRD401可与DPRD201相似。
DPRD405可包括例如一通过弹簧433连接到环431上的盘432。盘432可由生物相容性材料,比如,由热解碳(Pyrolitic carbon)或不锈钢形成。弹簧433可包括一个或多个旋转弹簧、螺旋弹簧或任何其它弹性元件,当DPRD401的两侧,比如图2B中DPRD201的近侧251与远侧252之间没有很大压差时,这些弹簧将盘432托在环431内部。
响应于DPRD401两侧之间的压差,盘432可以离开压力相对较高的心房,典型地如左心房,接着弯曲弹簧433,这会对盘432的移动施加一反作用力,从而打开和/或扩大血液会从中流过的内腔室。弹簧433所施加的反作用力取决于DPRD401两侧之间的压差,例如当一个心室内的压力迫使弹簧433压缩,这样通过DPRD401的压差越高,则允许通过从高压侧向低压侧流动的液体来释放这个压差的开口就越大。以这种方式,DPRD401的远端与近端之间的压差可根据一个或多个所选水平进行控制。在一些实施例中,这里描述的DPRD的各种各样的配置可容许随着压力差而不断改变的开口大小和流速。
要理解的是,当DPRD401两侧之间基本没有压差,或者当压差相当小时,盘432可能会完全闭合,或者另外不会完全阻塞通过DPRD450,比如通过盘432和环431之间区域的血流。举例来说,盘432可以选择在环431和盘432之间设置间隙,这样盘432可作为漏泄阀使得血液持续地流过穿孔。连续自由流过DPRD401的流体可以,例如阻止在盘432内部和/或周围形成血液凝结和/或血栓。
在一些实施例中,环432可以是不对称的,例如它可具有相对较宽的上部451和相对较窄的下部452。这样可以允许,例如当盘432在增加的压力下倾斜期间,血液以相对小的流速经过,直到盘432弯曲到超过环431上部位,从而提供一压力或压差阈值,在此阈值下阀门打开或开始打开,以增加通过血管的血流截面。压力阈值可以是一组连续(比如无限变化的)的压力点,在这些压力点,阀门打开或允许一根据该压力的压流。例如,在达到某一压力之前,阀门可保持闭合或者微微张开,然后在高于那个压力时不断地打开直到达到一更高压力,在该更高压力下阀门完全打开。要注意根据本发明的实施例,可使用不对称环432或其它不对称部件来得到与各种FRMs,DPRDs,分流管和/或仪器相类似的功能。
在一些实施例中,环431可以由合适的金属形成。在一些实施例中,环431可以结合在框架220内,或者环431与框架220可以采用整体的环-框部件来实现。环431和/或框架220可以由合适的线和管组成。环431和/或臂211-216可以由合适的线和管组成,例如,相同的线和管和/或相同的材料。
参见图5,其示意性说明了根据本发明实施例植入心脏109的DPRD401,其结合有打开状态的DPRD450。一压差可存在于左心房102和右心房103之间,例如左心房102的压力大于右心室103的压力。压差可以引起所述盘432朝着右心房103移动并使弹簧433弯曲,从而产生一个扩大的开口,通过这个开口更多的血液可从左心房102流向右心房103。随着血液流向右心房103,左心房102的压力会降低,同时右心房103的压力会升高,从而降低了左心房102和右心房103之间的压差,并且允许弹簧433朝着闭合或基本上闭合位置拉回盘432。也可以使用其它能够使盘432移动的设备。
图6示意性地说明了依照本发明另一个实施例的DPRD 650。DPRD650可以是FRM 108、FRM250或FRM350的一个例子。DPRD650可包括,例如环431和预先塑形的线634。线634可包括一柔性金属线,例如该金属线由镍钛诺或其它合适材料形成。在一种实施例中线634可以被弯曲成马蹄形、舌形或其它适合的形状。在一些实施例中,线634的末端可以与环431连接,或者线634和环431由相同的线、管或其它合适的材料形成。
线634可以通过或连接到一盖子或者板635的方式被覆盖,该盖子或板可包括,例如,一生物相容性材料的平板,该材料例如为与人工阀叶片一起使用的生物组织材料。板635可以采用例如一或多根缝合线636与线634相连。
DPRD 650包括在植入心脏内的DPRD 201或DPRD 301中。在左心房102和右心房间存在一压差,比如,左心房102的压力可大于右心室103。利用线634的弹性,该压差能够引起板635移动,从而形成一个内腔,血液可通过该内腔从左心房102流向右心房103。当血液以此方向流动时,左心房102的压力会降低,同时右心房103的压力会增加,从而降低了左心房102和右心房103之间的压差,并且允许板635朝向关闭或基本上关闭位置或朝向板635在边上打开的位置移动。
要注意的是,当左心房102和右心房103之间没有压差,或者压差相当小时,板635可能不完全阻塞穿过DPRD650,例如穿过板635周围,或板635和环431之间区域的血流。这可以,例如阻止在板635或DPRD之内和/或周围形成血液凝结和/或血栓。然而,如在此讨论的其它配置一样,在其它实施例中,开口或阀门可以在某一压差下完全关闭。
图7示意性说明了依照本发明另一个实施例的FRM750。FRM750可包括,例如采用一或多个弹簧738与锥体737相连接的环431。锥体737可以放在环431内,且可以例如由生物相容性材料制成,该生物相容性材料如,热解碳或不锈钢。锥体737可以有合适的形状,比如,矩形、方形、圆形、椭圆形、梯形、锥形或其它合适的形状。
FRM750可包括在植入心脏109中的分流管,例如,DPRD201或DPRD301中。弹簧738可包括一个或多个压缩弹簧,以及例如当左心房102和右心房103之间基本不存在压差时,将锥体737保持在环431内。
当左心房102和右心房103之间存在压差,比如,当左心房102的压力大于右心室103时,FRM750能允许血液从左心房102流向右房室103。该压差可以引起锥体737向弹簧738的反方向后退,从而打开或扩大了一个内腔,血液可穿过该内腔从左心房102流向右心房103。随着血液沿该方向流动,左心房102的压力会降低,同时右心房103的压力会增加,从而降低了左心房102和右心房103之间的压差,并且允许锥体737朝着关闭或基本上关闭位置退回。
要注意的是,当左心房102和右心房103之间没有压差,或者压差相当小时,锥体737可能不完全阻塞穿过FRM750,例如穿过FRM750周围,或FRM750和环431之间区域的血流。这样可以,例如阻止在锥体737或FRM750之内和/或周围形成血液凝结和/或血栓。
图8示意性说明了依照本发明另一个实施例的FRM850。FRM850可包括例如一与环431连接并放在其内的柔性阀门839。阀门839例如可由生物相容性材料制成,例如该生物相容性材料为聚亚胺酯或硅树脂。通过例如在环431内粘合或缝合阀门839的底部840,阀门839可与环431相连接。阀门839可包括一个或多个小叶片,例如,小叶片841与842能够移动并建立或扩大一个开口843。在一些实施例中,开口843的大小会与施加在小叶片841与842上的压力有关。
FRM850可包括在植入心脏109内的分流管、导管或管道例如,DPRD201或DPRD301中。当左心房102和右心房103之间存在压差,比如,当左心房102的压力大于右心室103时,FRM850能允许血液从左心房102流向右房室103。该压差可能延伸、展开或推动叶片841和/或842,从而增加它们之间的距离并且扩大了开口843,血液可通过该开口843从左心室102流向右心室103。随着血液沿该方向流动,左心房102的压力会降低,同时右心房103的压力会增加,并且允许叶片841和/或843朝着关闭或基本上关闭的位置退回。
要注意的是,当左心房102和右心房103之间没有压差,或者压差相当小时,阀门839、叶片841和843可能不完全阻塞穿过FRM850,例如穿过开口843的血流。这样可以,例如阻止在阀门839或FRM850之内和/或周围形成血液凝结和/或血栓。
图9示意性说明了根据本发明另一个实施例在心脏109内部的DPRD950。DPRD950可包括大量通过一个或多个管子内部相连的气囊或液囊,比如,一不柔软气囊943通过管子944与柔软气囊945相连接。不柔软气囊943可放在左心房102和/或刺孔内,而柔软气囊945可放在右心房103内。在一些实施例中,不柔软气囊943和/或柔软气囊945连接到一环(例如环431)。在一些实施例中,不柔软气囊943和/或柔软气囊945含有液体920。
液体920可以例如从气囊943流向气囊945或反之亦然,这与左心房102和右心房103之间的压差有关。举例而言,当左心室102的压力相对较大时,液体920可通过管子944从不柔软气囊943流向柔软气囊945,从而缩小了不柔软气囊943和膨胀了气囊945。要注意的是柔软气囊945比不柔软气囊943更柔软,从而允许柔软气囊945作为一弹簧装置来控制不柔软气囊943的缩小。
图10示意性说明了根据本发明另一个实施例的DPRD1050。DPRD1050可包括,例如环431和带有孔1047的柔性盘1046。在一些实施例中,孔1047可以是大体上圆形的并且位于例如大体上柔性盘1046中心的位置。柔性盘1046可例如由柔性聚合材料形成,例如硅橡胶或聚亚胺酯。
DPRD1050可以植入心脏109,孔1047可以随着左心房102和右心房103之间的压差而改变直径。例如,压差可以向后推或伸展柔性盘1046,从而扩大孔1047,同时允许血液可从左心房102穿过一较大区域流向右心房103。
要注意的是,当左心房102和右心房103之间没有压差,或者压差相当小时,孔1047仍可以打开并具有一相当小的直径,柔性盘1046不能完全阻止血液通过DPRD1050。这样可以,例如阻止在DPRD1050之内和/或周围形成血液凝结和/或血栓。
图11示意性说明了根据本发明另一个实施例的DPRD1150。DPRD1150可包括,例如一气囊或液囊1148,如象含有液体的不柔软气囊。气囊1148可放在或连接在环1131内,其可包括,例如类似于环431和/或框架的环。一管1149可将气囊1148连接到容器1155上,该容器可包括一或多个活塞1151,该活塞能够抵抗压缩弹簧1152而运动。弹簧1152例如可以由金属或合适的弹性材料构成。
DPRD1150可植入心脏109中,而气囊1148的体积可随着左心房102和右心房103之间的压差而改变。例如,该压差可以推动或缩小气囊1148,从而造成液体1120从气囊1148流向容器1155。这可以形成或扩大环1131内的开口,血液可以通过该开口从左心房102流到右心房103。
图12示意性说明了根据本发明另一个实施例的DPRD1250。DPRD1250可包括,例如气囊1148,如象含有液体的不柔软气囊。气囊1148可放在或连接在环1131内,其可包括,例如类似于环431和/或框架的环。一管1149可将气囊1148连接到容器1155上,该容器可包括一或多个能够运动的活塞1151。该活塞可以通过使用一发动机1153来运动,该发动机可包括一电动机,如步进电动机或其它合适的电动机。发动机1153可以移动、推或拉所述活塞1151,从而使液体1120从气囊1148流到容器1155,反之亦然。这可以改变气囊1148的体积,从而增大或减小环1131内的开口的尺度,通过该孔血液可以从左心房102流到右心房103。
根据本发明另一个实施例,可以例如通过病人或医疗服务提供者主动地控制DPRD1250。在一种实施例中DPRD可采用外部和/或人工提供的指令来进行操作。例如,发动机1153可根据外部和/或人工提供的指令运转。附带地或可替换地,发动机1153可根据左心房102和右心房103之间的压差来运转。例如可采用结合有一个或多个压力传感器1254的与压力有关的闭环1260。该压力传感器1254可测量一个或多个心内腔中,例如左心房102和右心房103的绝对压力,或者测量两心内腔之间,例如左心房102和右心房103之间的压力差。基于该压力信息,发动机1153可以运转并移动、推或拉所述活塞1151。
在另一个实施例中可以采用一个或多个电动机构、机械机构、无线机构、气动机构或其它合适的机构遥控操作DPRD。例如可将一金属线、线、弹簧、钉、电缆、钩、销、发动机或磁铁连接到DPRD以使得可由病人和/或医疗服务提供者遥控DPRD。如图13A所示,至少一根线或控制导线1320可以将DPRD1300连接到例如一控制盒的控制机构1310上。例如,控制导线1320可通过穿孔或孔1335从血管1330出来。控制机构1310可包括,例如一机械接口、电子接口、拉/推线,弹簧、磁铁或其它合适的元件或机构以使DPRD1300能被遥控。
控制机构1310可以是一个可放在外部或内部的微型机构,例如它可以放进病人皮下的组织中,以为医疗服务提供者提供一外通道,或者它可以内部地放在最接近于使医疗服务提供者用最小侵入技术就可进入的部位。
在一个实施例中,DPRD1300可以由以外部“发射”单元无线控制。例如控制信号可以在病人体外采用遥测,局部无线电频率(RF)发射,局部超声发射,外磁场,局部加热或其它合适的信号发生装置。在这种实施例中DPRD1300可包括一“接收”单元。该接收单元可包括一内部电源(如电池),或可以从控制信号或其它所发射信号接收激励动力。该接收单元例如可经由一植入插头连接到一外电源,或者可直接连接到临时基地的DPRD1300(例如在医生办公室),所植入的插头可转送指令信号和/或电源以启动DPRD 1300。
现在参见图13B,其表示被布置在皮肤表面1360下的控制机构1310的例子。在一个例子中,控制线1320可通过采用传统针或注射器1365,例如通过作一小切口进入病人来放入。可在外部或内部地控制一根或一些控制线1320以使得DPRD 1300能够被控制。在某些实施例中,一个(或一些)线1320可在管,例如在硅压管1370内操作。控制机构1310可包括例如一远程阀打开/关闭机构以使得能够监测心脏压力,监测DPRD功能等。在一种实施例中,控制机构1310可用于响应阀的位置来监测血流变化。控制机构1310可使得在临床需要的情况下,能够人工地减少心脏压力或某一内腔体或心脏中的血压。控制机构1310可以以选定间隔,通过例如增加内部血压或液体压力的方式冲洗或清洁DPRD1300。在另一个实施例中能够采用冲洗或清洁液,例如在选定压力下,食盐水可以进入控制导管1320而对所述孔口进行清洁或冲洗。这种清洁可以帮助减少与DPRD1300有关的不想要的生长、感染等。
控制机构1310可包覆一种或几种物质以防止血栓或其它病症。DPRD1300可包括尖、刺或其它结构以避免FRM与分流器完全接触或保证FRM与分流器之间只有最小接触。控制机构1310可使DPRD的多个部分能够远距离地被替换、清洁、维修或进行其它操作。控制机构1310可使预先配置或设计的漏洞能够根据临床需要而被远距离地打开、关闭或进行其它改变。控制机构1310能够阻塞DPRD的孔或内腔,例如通过远距离在孔内安放栓塞以终止DPRD的作用。上述的一种或多种性能可使得公共医疗卫生服务提供者能够远程控制DPRD1300的功能。
如图13C所示的实施例中,控制机构1310可包括可以用手指或其它合适器具控制的一或多个揿下旋钮1340或其它合适的控制器或机构。例如,多个揿下旋钮1340可单独、同时和/或以多种其它结合方式被揿下以在DPRD1300中达到所期望的效果。在一个实施例中控制机构1310可包括,例如一个或多个杆或导电体1350以帮助控制DPRD1300。在一个实施例中控制机构1310可包括,例如一个或多个安全机构1345,如锁定钮以帮助防止不需要的改变被加到DPRD1300的操作上。在另一个实施例中控制机构1310可包括,例如一个或多个与杆1350和DPRD1300连接的弹簧或其它合适的控制机构。
如图13D所示的实施例中,控制机构1310可用于控制DPRD1300,例如采用一个或多个杆或线1375等在管1370内可选择地操作。DPRD1300可包括一盖1377,例如柔性或非柔性盖,其例如可保持恒定微开,以形成一间隙1379。在一个实施例中,盖1377可由刚性材料构造并可以刚性方式被装配或连接到一锁定机构1380。一旦盖1377通过锁定机构1380一直固定在选定位置,那么它就保持稳定,例如不受血压变化的影响,直到盖1377重新定位。在这种情况下,盖1377只能用控制机构1310,如信号线,或其它合适的通讯线路通过有意识的和受控制的行动进行调整。
锁定机构1380可使盖1377遥控地被设置在一个或多个位置上。锁定机构1380可包括,例如一个或多个弹簧、插销、控制杆、凹口、槽、钩、滑轨或其它合适的锁定机构。例如位置#1可以是一较低位置,例如在此位置钩子1325固定在所示的抓钩机构1332上;位置#2可以是一中间位置,例如在此位置钩子1325固定在所示的抓钩机构1333上;位置#3可以是一较高位置,例如在此位置钩子1325固定在所示的抓钩机构1334上。也可采用其它的设置、开口大小、流动水平、位置和位置数目。控制机构1310可包括例如安全部件,以帮助防止未经授权人员启动DPRD1300(如特殊工具和磁铁,编码序列、密码等)。
如图13E所示的实施例中,控制机构1310可用于控制DPRD1300,例如采用辅助液力系统。控制机构1310例如可经由一个或多个管1390连接到该液力系统,上述管可帮助控制通过DPRD1390供给的液体的压力和/或流速。DPRD1390可在需要时连接到一液压系统,或者可永久地连接到一液压系统。在一个实施例中,管1390例如可增加DPRD1300的液体压力,以在分流器上或分流器内提供一显著的力。管1390可附加地或可替换地用于“维护”,例如通过迫使液体如经由分流器底部1392流过分流器,来冲洗、清洁和/或润滑分流器和/或FRM1396,和/或来释放EPRD的运动部件以便保持DPRD1300处于所需的运行条件或状态。在一个实施例中,一种物质(如盐溶液)可注射进所述管1390或从中进行抽取,以改变底部1392的压力并且从而使活塞膜1394活动起来。活塞膜1394可被伸展和/或扩大从而引起FRM1396动作起来,例如来打开和/或关闭FRM1396,以允许液体选择性地流过DPRD1300。管1390可被连接到管1320上(见图13A和13B)和/或与适合于穿刺进入病人皮肤与管1390连接的针头1366或其它器械相连。在一个实施例中,液压机构可以在DPRD1300放置到体内以后使用,例如来检验DPRD1300的可操作性。在另一个实施例中,液压机构可以在DPRD1300放置到体内后检查DPRD1300可操作性的时候使用。
要理解的是,本发明的某些实施例可采用例如一个或多个阈值、预定参数、条件和/或标准,以触发分流器、DPRD或FRM起作用或不起作用。
根据本发明的一实施例,可以采用各种植入一个装置的合适的技术。按照某些实施例,可采用最小侵入手术,例如采用经皮导入的方法将压力调节装置导入和植入病人体内。在这种实施例中,该装置可固定在一导管导入系统上并经由小切口插入身体。一旦该装置位于体内的正确部位,则它就可被操作者布置、扩大和锁定在合适位置。由导管传导的装置可以例如被收缩或折叠成小尺度,该装置在布置时可自张开。在另一个实施例中该压力调整装置可采用侵入性外科手术被导入,例如外科医生在体内作一较大开口以便实现与该装置植入部位更直接的接触。
在本发明的一实施例中,如2001年4月提交的,名称为“降低局部血液循环系统压力的方法和装置”的美国专利09/839643,特别是图3-5中所描述的,一组横膈膜针头可被推入右前房隔膜壁(Right atrial septum)。可以从股静脉制造一入口,同时该装置穿过下内腔静脉推进并进入右心房。一旦横膈膜穿刺已完成,则一引导线可交换针头部件,然后进入左心房。用横膈膜穿刺的方式将导管安装进入左心房的方法是本领域公知的。当横膈膜护套定位于左心房之后,如上所述,可以开始放置根据本发明的实施例所作的分流器。
扩张器和线可随后从该护套中抽回,该护套现在可以从病人腹股沟的股静脉入口点伸出来进入左心房、穿过股静脉、髂静脉、下内腔静脉、右心房和前房隔膜等。输送导管可以在荧光镜显影下穿过该护套。为了定位一些特殊的点可以在该导管以及护套上提供不透射线的标志物。输送导管可以小心地和缓慢地前进,因此左心房固定元件的最远部分从导管的远端开口被放出并进入左心房的内腔室。该固定元件可由类似弹簧的材料构成和/或可以是超弹性形状记忆合金,因此当它脱离该输送导管内部区域的限制时,它就变成预先设置的完全成形的形状。然后护套和输送导管的组件可缓慢地整体缩回以便朝着前房隔膜抽回固定元件。当通过荧光镜显影以及通过触觉反应很清楚该固定元件已靠着前房隔膜被固定时,医生可停止这种收回。在那个点,护套可单独被缩回,露出分流器并将其定位于前房隔膜内已形成的开口中。然后护套可进一步缩回,允许右前房的固定元件变成其完全成形的形状。整个分流器组件和DPRD可随后与输送导管系统分离。在输送导管内部该DPRD可通过长控制线进行控制,该控制线在导管区域内部有独立的移动控制。这种连接可通过任何传统方法来构成,如焊接或粘接,或者在规定张力水平下可机械地分离的类似方式进行连接,所述张力水平由医生在坚决收回该控制线的过程中被超过。DPRD和/或FRM的其它应用方法也可以采用。
现在参见图14,其示出了根据本发明的一些实施例,将DPRD和/或FRM输送到体内,例如左心房和右心房之间的心脏隔膜的方法。将一设备植入隔膜内可包括下列步骤中的一个或多个:a)识别用于植入的精确部位;b)将该设备对准所选定部位;和c)确保植入的精确性和完整性。理想的植入位置可以例如由专业医生通过使隔膜成像并分析隔膜的解剖结构(如用TEE)而进行选择。所述对准可包括采用“绘制”隔膜位置的已知工具识别该精确设备输送工具的位置。可将标记物加到该输送工具和设备(如金的标记物)。一旦已识别该位置并且已经配置该设备,专业医生可检查和测试该设备安装,可选择地在完全取回该输送系统之前进行。例如,专业医生可采用例如身体挑动(physically challenging)的直接接触或拉整个设备(如通过轻拉该设备以确保正确地锚定)。该锚定可通过非接触装置来测试(如采用电磁成像、回波、X-线,用造影材料的血管造影术等)。
在框140,可采用例如导管将DPRD植入体内两个或多个室、内腔、器官、区域、带等之间。在框141,FRM可配置在例如所选定部位或位置以使在两个或多个内腔之间能够有一连续的液流,并且可根据这些内腔之间压力差的变化而选择性地起作用或不起作用。在框142,FRM例如可响应于这些内腔之间压力差的变化而被控制(如被动地),FRM可响应压力的变化被进一步地打开和/或关闭。可选择地,在框143,DPRD和/或FRM可被遥控以帮助控制这些内腔之间的液流。在某些实施例中,DPRD和/或FRM的遥控能够清洁DPRD和/或FRM、使DPRD和/或FRM功能停止、改变DPRD和/或FRM的部件等。上述步骤中的任意组合可以被实现。进一步地,可以采用其它一些步骤或步骤系列。
为了说明和描述的目的,已经介绍了前面所述的本发明的这些实施例。这并不意味着是穷举或将本发明限制为所精确公开的方式。本领域技术人员应该认识到根据上述的教导有可能存在许多改进、变形、替代或变化以及等价物。因此要理解的是,所附的权利要求书意图包括所有在本发明真实精神内的这样的改进和变型。
Claims (11)
1.一种用于心脏的装置,包括:
一具有两个端的分流器,所述分流器适合于以这样的方式被定位于心脏的左心房和右心房之间的前房隔膜中,使得经由分流器从左心房到右心房能够进行液流,而每端各自面对相应的心房;和
一被动控制的流量调节机构,适合于通过相对于心脏的左心房和右心房之间压力差的变化调整通过所述分流器的液流横截面积,来调整通过所述分流器的液流,该被动控制的流量调节机构位于分流器的被构造成用于植入右心房的一端部,从而当植入该装置时,被动控制的流量调节机构完全处于右心房内并且与前房隔膜分隔开。
2.如权利要求1的装置,其中所述流量调节机构还适合于响应穿过所述流量调节机构的压力差而打开或关闭。
3.如权利要求1或2的装置,其中流量调节机构适合于相对于压力差的变化而选择性地改变液流横截面积的尺寸或形状或者改变允许流经其的血液量。
4.如权利要求1或2的装置,其中在达到一压力差阈值之前,所述流量调节机构适合于保持闭合或者微微张开,然后在高于该压力差阈值时不断地打开直到达到一更高压力差,在该更高压力下流量调节机构完全打开。
5.如权利要求4的装置,其中压力差阈值大致为12mmHg。
6.如权利要求1或2的装置,其中所述流量调节机构连续地允许通过所述分流器的液流。
7.如权利要求1或2的装置,其中所述流量调节机构包括一双向阀。
8.如权利要求1或2的装置,其中所述流量调节机构包括一个盘,所述盘适合于从分流器具有高压的一端移开,允许液流从高压端流向低压端。
9.如权利要求1或2的装置,其中所述分流器包括固定架、环或管。
10.如权利要求1的装置,其中流量调节机构被预配置,以根据心脏的左心房和右心房之间压力差的变化而调整其配置。
11.如权利要求1的装置,其中流量调节机构包括一个或多个有角度的柔性膜或叶状物。
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US60/541,267 | 2004-02-03 | ||
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- 2005-02-03 WO PCT/IL2005/000131 patent/WO2005074367A2/en active Application Filing
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EP1771132A2 (en) | 2007-04-11 |
EP1771132B1 (en) | 2019-03-27 |
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US20220183838A1 (en) | 2022-06-16 |
CA2554595A1 (en) | 2005-08-18 |
US20220338989A1 (en) | 2022-10-27 |
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US10912645B2 (en) | 2021-02-09 |
CA2554595C (en) | 2016-03-29 |
US11266501B2 (en) | 2022-03-08 |
WO2005074367A3 (en) | 2008-12-31 |
US20110218481A1 (en) | 2011-09-08 |
US20170325956A1 (en) | 2017-11-16 |
US20200060825A1 (en) | 2020-02-27 |
US11382747B2 (en) | 2022-07-12 |
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WO2005074367A2 (en) | 2005-08-18 |
US20050148925A1 (en) | 2005-07-07 |
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