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    • 7. 发明公开
    • Medical overflow protective device
    • MedizinischeÜberlaufschutzvorrichtung
    • EP1557184A1
    • 2005-07-27
    • EP05250230.9
    • 2005-01-18
    • Datex-Ohmeda, Inc.
    • Hodge, Colin G.Severns, Matthew L.
    • A61M1/00F16K31/00F16K31/56F16K37/00F16K21/18
    • A61M1/0049A61M1/005F16K21/18F16K31/003F16K31/56F16K37/0058
    • A protective device (18) that is used in a medical suction system withdrawing liquids from a patient. The device is located upstream of a vacuum regulator (10) and protects that regulator and other downstream components from contacting the liquid being withdrawn from the patient. The protective device has an inlet (24) and an outlet (22) and an actuator mechanism (26) that can move between a contracted position (Fig. 4) where a gas can communicate through the protective device between the inlet and the outlet and an expanded position (Figure 5) where the actuator mechanism occludes both the inlet and the outlet to shut off the vacuum supply to the patient. An electrical circuit having a pair of sensing electrodes (54,55) provides an electrical discharge to trigger a shape-metal alloy wire (58) to move the actuator mechanism from the contracted position to the expanded position when the sensing electrodes detect the presence of a liquid therebetween.
    • 一种用于从患者抽出液体的医用抽吸系统中使用的保护装置(18)。 该装置位于真空调节器(10)的上游,并且保护该调节器和其它下游部件免受从患者抽出的液体的接触。 保护装置具有可以在收缩位置(图4)之间移动的入口(24)和出口(22)和致动器机构(26),其中气体可以在入口和出口之间通过保护装置连通, 扩张位置(图5),其中致动器机构封闭入口和出口,以切断对患者的真空供应。 具有一对感测电极(54,55)的电路提供放电以触发形状金属合金线(58),以便当感测电极检测到所述致动器机构的存在时,将致动器机构从收缩位置移动到扩展位置 它们之间的液体。
    • 8. 发明公开
    • Integrated procedure light for infant care apparatus
    • Integriertes Untersuchungslichtfüreinen Inkubator
    • EP1525868A2
    • 2005-04-27
    • EP04256323.9
    • 2004-10-14
    • Datex-Ohmeda, Inc.
    • Mackin, Michael H.Dykes, Christopher A.
    • A61G11/00F21S8/00
    • A61G11/00A61N5/0621
    • An infant warming apparatus for supporting an infant upon an infant platform. The apparatus has a procedure light (38) that is recessed into the normal horizontal overhead housing (36) of the apparatus and thus integrated into the infant apparatus. The procedure light is conveniently located above and centrally positioned with respect to the infant so as to direct the light toward the infant. The mounting provides omnidirectional movement of the procedure light and the movement can be easily controlled by means of a control handle (40) that extends downwardly with a distal end readily accessible to the caregiver. At or proximate to the distal end there is an electrical controller (66) to enable the caregiver to change the intensity of the light beam. The light beam can also be easily focused so as to allow the caregiver to direct the desired beam of light onto the area of interest (70) of the infant.
    • 一种用于在婴儿平台上支撑婴儿的婴儿升温装置。 该装置具有凹入到装置的正常水平架空壳体(36)中并由此整合到婴儿装置中的步骤灯38。 手术灯方便地位于相对于婴儿的上方和中心定位,以便将光引向婴儿。 安装件提供了过程光的全方向运动,并且可以通过一个控制手柄(40)容易地控制运动,控制手柄(40)向下延伸,护理者容易接触到远端。 在远端处或附近,存在电控制器(66),以使护理人员能够改变光束的强度。 光束也可以容易地聚焦,以便护理者将期望的光束引导到婴儿的感兴趣区域(70)上。
    • 10. 发明公开
    • COMPENSATION OF HUMAN VARIABILITY IN PULSE OXIMETRY
    • 补偿在脉搏血氧饱和度HUMAN变异的
    • EP1474036A1
    • 2004-11-10
    • EP03701555.9
    • 2003-02-04
    • Datex-Ohmeda, Inc.
    • HUIKU, Matti
    • A61B5/00
    • A61B5/14551A61B5/1495
    • The invention relates to the calibration of a pulse oximeter intended for non-invasively determining the amount of at least two light-absorbing substances in the blood of a subject. In order to bring about a solution by means of which the effects caused by the tissue of the subject can be taken into account in connection with the calibration of a pulse oximeter, initial characterization measurements are carried out for a pulse oximeter calibrated under nominal conditions. Based on the characterization measurements, nominal characteristics are established describing the conditions under which nominal calibration has been defined, and reference data indicating the nominal characteristics are stored. In-vivo measurements are then performed on living tissue and based on the in-vivo measurements and the reference data stored, tissue-induced changes in the nominal characteristics are determined. Subject-specific variation in the in-vivo measurements is compensated for by correcting the nominal calibration on the basis of the tissue-induced changes.