JP2021164646A - 多数の薬剤の誤送出を防止するための注入システム - Google Patents
多数の薬剤の誤送出を防止するための注入システム Download PDFInfo
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Abstract
【解決手段】多薬剤注入システム(10)は、注入ポンプ(12)と、薬剤タンク(16A,16B)と、多チャンネルルーメン(18)と、注入セット(20)とを含むことができる。これら薬剤タンクは、該薬剤タンクが固有の構成でのみ注入ポンプに挿入できるように寸法決め及び形成してもよい。多チャンネルルーメンは、注入ポンプに設けられた対応するコネクタと注入セットとに固有の構成でのみ嵌合するコネクタを含むことができる。この多注入システムの様々な部品は固有の構成のみで接続できるため、予期した薬剤が適切に投与され、正しい注入部位に送出される。
【選択図】図1
Description
本発明は、アメリカ国立衛生研究所により与えられた契約番号DK085633号に基づく政府支援を受けてなされた。米国政府は、本発明に一定の権利を有する。
本出願は、次の米国特許出願、すなわち2013年10月24日付けで提出され「異なるバイアルから薬剤を誤送出なしで移送するためのマニホルド」と題された米国特許出願第61/895,270号と、2013年10月24日付けで提出され「2つの薬剤の多チャンネル注入システムにおける注入部位を用いた注入源を繋ぐための装置」と題された米国特許出願第61/895,279号と、2013年10月24日付けで提出され「多数のカテーテル又はカニューレの配列を介して2つ以上の薬剤を注入するための注入セット又は投与セット」と題された米国特許出願第61/895,288号と、2014年1月29日付けで提出され「薬剤を誤送出なしで届けるためのバイアルの固有な投入を可能とする多注入装置」と題する米国特許出願第61/932,835号と、2014年6月12日付けで提出され「多数の薬剤の誤送出を防止するための注入システム」と題された米国特許出願62/011,306号との優先権を主張する。上記出願の内容は、本明細書に引用して援用する。
本発明は、薬剤を糖尿病患者に投与するためのシステム及び方法に関する。より詳細には、本発明は、誤った薬剤を糖尿病患者に不注意で投与するのを避けるために薬剤の誤送出を防止するためのシステム及び方法に関する。
よって、溝56が形成されたタンク16Bは、マニホルド14Bの対応するリブ54に収容され嵌め合うよう適合されている。現在の例では、リブ54及び溝56の位置がリブ48及び溝50の位置とは異なる。従って、タンク16Bのマニホルド14A内への取り付けは防止されており、タンク16Aのマニホルド14B内への取り付けも防止される。この構成は、薬剤タンクが正しくないマニホルドに不注意に装填されるのを防止し、よって正しくない薬剤の患者への不注意の投与を防止する。
Claims (30)
- 多チャンネルルーメンアッセンブリであって:
注入ポンプの第1出口ポート及び第1薬剤バイアルに同時に結合するよう構成された第1タンクコネクタと;
入口ポート及び出口ポートを含む第1チューブであって、前記入口ポートは、前記第1タンクコネクタから流体を受け取るよう構成され、前記出口ポートは、注入セットの第1入口に係合するよう構成された特徴要素を備えた第1チューブと;
前記注入ポンプの第2出口ポート及び第2薬剤バイアルに同時に結合するよう構成された第2タンクコネクタと;
入口ポート及び出口ポートを含む第2チューブであって、前記入口ポートは、前記第2タンクコネクタから流体を受け取るよう構成され、前記出口ポートは、前記注入セットの第2入口に係合するよう構成された特徴要素を備えた第2チューブとを含み;
前記多チャンネルルーメンアッセンブリの前記第1出口ポートの前記特徴要素は、前記多チャンネルルーメンアッセンブリの前記第2出口ポートの前記特徴要素とは異なり、前記多チャンネルルーメンアッセンブリの前記第1出口ポートの前記特徴要素は、前記注入セットの前記第2入口との係合を防止するよう構成されている、多チャンネルルーメンアッセンブリ。 - 前記第1チューブ及び前記第2チューブは互いに接続されている、請求項1に記載の多チャンネルルーメンアッセンブリ。
- 前記各第1及び第2タンクコネクタには、前記第1及び第2タンクをそれぞれ穿孔するための穿孔要素が形成されている、請求項1又は2に記載の多チャンネルルーメンアッセンブリ。
- 前記穿孔要素は接触防止である、請求項3に記載の注入システム。
- 前記多チャンネルルーメンアッセンブリの前記第1チューブ及び前記第2チューブが、前記アッセンブリの長さの少なくとも一部に沿って互いに結合されている、請求項1-4の何れかに記載の多チャンネルルーメンアッセンブリ。
- 前記第1チューブは、表面特徴が関連付けられた外側表面を含み、前記第2チューブは、表面特徴が関連付けられた外側表面を含み、前記第1及び第2チューブの前記表面特徴は形状が補完的であり、互いに係合して前記第1及び第2チューブを互いに結合させるよう構成されている、請求項1-5の何れかに記載の多チャンネルルーメンアッセンブリ。
- 前記注入セットをさらに含み、前記注入セットは、前記第1及び第2薬剤を患者に送出するよう構成されている、請求項1-6の何れかに多チャンネルルーメンアッセンブリ。
- 前記注入セットは、ベース部を備えかつそれに結合された第1及び第2穿孔要素を備える、請求項7に記載の多チャンネルルーメンアッセンブリ。
- 前記穿孔要素が金属、非金属、又はそれらの組合せから作製されている、請求項8に記載の多チャンネルルーメンアッセンブリ。
- 前記第1タンクコネクタは、前記注入ポンプの前記第1入口ポートと嵌合するよう構成された特徴要素を含み、前記第2タンクコネクタは、前記第2入口ポートと嵌合するよう構成された特徴要素を含み、前記第1タンクコネクタの前記特徴要素は、前記第2タンクコネクタの前記特徴要素とは異なる、請求項1-9の何れかに多チャンネルルーメンアッセンブリ。
- 前記第1タンクコネクタの前記特徴要素は、前記第1タンクコネクタが前記第2入口ポートに係合するのを防止するよう構成されており、前記第2タンクコネクタの前記特徴要素は、前記第2タンクコネクタが前記第1入口ポートに係合するのを防止するよう構成されている、請求項10に記載の多チャンネルルーメンアッセンブリ。
- 前記第1タンクコネクタの前記特徴要素は、前記第1入口ポート一致すると共に前記第1入口ポートのスロットを介して前記第1入口ポートに係合するよう構成された移動止めである、請求項10又は11に記載の多チャンネルルーメンアッセンブリ。
- 前記第2タンクコネクタの前記特徴要素は、前記第2入口ポート一致すると共に前記第2入口ポートのスロットを介して前記第2入口ポートに係合するよう構成された移動止めである、請求項10又は12に記載の多チャンネルルーメンアッセンブリ。
- 前記第1タンクコネクタは、前記第2薬剤バイアルには係合しないよう構成されており、前記第2コネクタは、前記第1薬剤バイアルには係合しないよう構成されている、請求項1-13の何れかに記載の多チャンネルルーメンアッセンブリ。
- 前記第1薬剤バイアルは調整剤を保持するよう構成されており、前記第2薬剤バイアルは対抗制御的薬剤を保持するよう構成されている、請求項1-14の何れかに記載の多チャンネルルーメンアッセンブリ。
- 前記調整剤はインシュリンであり、前記対抗制御的薬剤はグルカゴンである、請求項15に記載の多チャンネルルーメンアッセンブリ。
- 患者に多数の流体を送出するためのコネクタセットであって:
第1タンクコネクタであって:
第1薬剤タンクに係合するよう構成された第1特徴要素と;
注入ポンプの第1入口ポートの対応する第1特徴要素に係合するよう構成された第2特徴要素とを含む第1タンクコネクタと;
第2タンクコネクタであって:
第2薬剤タンクに係合するよう構成された第1特徴要素と;
前記注入ポンプの第2入口ポートの対応する第2特徴要素に係合するよう構成された第2特徴要素とを含む第2タンクコネクタとを含み;
前記第1タンクコネクタの前記第1特徴要素は、前記第2タンクコネクタの前記第1特徴要素とは異なり;
前記第1タンクコネクタの前記第2特徴要素は、前記第2タンクコネクタの前記第2特徴要素とは異なる、コネクタセット。 - 前記第1タンクコネクタは、前記注入ポンプの前記第2入口ポートに係合しないよう構成されている、請求項17に記載のコネクタセット。
- 前記第2タンクコネクタは、前記注入ポンプの前記第1入口ポートに係合しないよう構成されている、請求項18に記載のコネクタセット。
- 前記第1タンクコネクタの前記第2特徴要素は、前記第1タンクコネクタの前記移動止めに対応するスロットを介して前記第1入口ポートに係合するよう構成された移動止めである、請求項17に記載のコネクタセット。
- 前記第1タンクコネクタの前記移動止めは、前記第1タンクコネクタの前記第2入口ポートへの係合を防止する、請求項20に記載のコネクタセット。
- 前記第2タンクコネクタの前記第2特徴要素は、前記第2タンクコネクタの前記移動止めに対応するスロットを介して前記第2入口ポートに係合するよう構成された移動止めであり、前記第2タンクコネクタの前記移動止めは、前記第2タンクコネクタの前記第1入口ポートへの係合を防止する、請求項21に記載のコネクタセット。
- 前記第1タンクコネクタに結合されると共に前記第1タンクコネクタに流体連通した第1チューブと、前記第2タンクコネクタに結合されると共に前記第2タンクコネクタに流体連通した第2チューブと、を備えた多チャンネルルーメンアッセンブリをさらに含む、請求項17に記載のコネクタセット。
- 前記第1チューブは、表面特徴が関連付けられた第1端部を含み、前記第2チューブは、表面特徴が関連付けられた第2端部を含み;
前記第1端部の前記特徴要素は、注入セットのベース部の第1入口ポートに係合するよう構成されており;
前記第2端部の前記特徴要素は、前記注入セットの前記ベース部の第2入口ポートに係合するよう構成された、請求項23に記載のコネクタセット。 - 前記第1端部は、前記注入セットの前記第1入口ポートに結合し、前記第2入口ポートには係合しないよう構成されている、請求項24に記載のコネクタセット。
- 前記第2端部は、前記注入セットの前記第2入口ポートに結合し、前記第1入口ポートには係合しないよう構成されている、請求項25に記載のコネクタセット。
- 各前記第1及び第2タンクコネクタには、前記第1薬剤タンク及び前記第2薬剤タンクをそれぞれ穿孔するための穿孔要素が形成されている、請求項17に記載のコネクタセット。
- 前記穿孔要素は、ユーザによる接触を防止するよう構成されている、請求項27に記載のコネクタセット。
- 多数の流体を前記患者に送出するための注入システムであって、請求項1-28の何れかの多チャンネルルーメンアッセンブリと前記注入ポンプとを含む注入システム。
- 前記注入システムは、前記第1薬剤タンク及び前記第2薬剤タンクを含む、請求項29に記載の注入システム。
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