A pilot study to compare the Episure™ Autodetexct™ syringe with the glass syringe for, identification of the epidural space in parturients
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Habib, Ashraf S.
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Duke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USA
Habib, Ashraf S.
[1
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George, Ronald B.
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Duke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USA
George, Ronald B.
[1
]
Allen, Terrence K.
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Duke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USA
Allen, Terrence K.
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]
Olufolabi, Acleyemi J.
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Duke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USA
Olufolabi, Acleyemi J.
[1
]
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[1] Duke Univ, Med Ctr, Dept Anesthesiol, Div Womens Anesthesia, Durham, NC 27710 USA
The Episure (TM) AutoDetect (TM) syringe, a spring-loaded syringe, is a new loss-of-resistance syringe with an internal compression spring that applies constant pressure on the plunger. In this pilot study, we compared the spring-loaded syringe with the standard glass syringe for identification of the epidural space during initiation of epidural analgesia in parturients. The primary outcome was the incidence of failed epidural analgesia. Three-hundred and twenty-five women were enrolled. Eight residents performed 291 procedures (90%) and two attendings performed 34 procedures (10%). Epidural analgesia failed in five subjects in the glass syringe group and in no subject in the spring-loaded syringe group (P = 0.025).