Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy
We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxyge...
Ausführliche Beschreibung
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| Autor*in: |
GRONERT, B.J. [verfasserIn] DAVIS, P.J. [verfasserIn] COOK, D.R. [verfasserIn] |
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E-Artikel |
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| Erschienen: |
Oxford, UK: Blackwell Publishing Ltd ; 1992 |
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| Schlagwörter: |
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| Umfang: |
Online-Ressource |
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| Reproduktion: |
2007 ; Blackwell Publishing Journal Backfiles 1879-2005 |
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| Übergeordnetes Werk: |
In: Pediatric anesthesia - Oxford [u.a.] : Wiley-Blackwell, 1991, 2(1992), 2, Seite 0 |
| Übergeordnetes Werk: |
volume:2 ; year:1992 ; number:2 ; pages:0 |
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| DOI / URN: |
10.1111/j.1460-9592.1992.tb00184.x |
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| 520 | |a We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. | ||
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10.1111/j.1460-9592.1992.tb00184.x doi (DE-627)NLEJ241199514 DE-627 ger DE-627 rakwb GRONERT, B.J. verfasserin aut Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy Oxford, UK Blackwell Publishing Ltd 1992 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| anaesthetic techniques: intravenous DAVIS, P.J. verfasserin aut COOK, D.R. verfasserin aut In Pediatric anesthesia Oxford [u.a.] : Wiley-Blackwell, 1991 2(1992), 2, Seite 0 Online-Ressource (DE-627)NLEJ243926200 (DE-600)2008564-3 1460-9592 nnns volume:2 year:1992 number:2 pages:0 http://dx.doi.org/10.1111/j.1460-9592.1992.tb00184.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1992 2 0 |
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10.1111/j.1460-9592.1992.tb00184.x doi (DE-627)NLEJ241199514 DE-627 ger DE-627 rakwb GRONERT, B.J. verfasserin aut Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy Oxford, UK Blackwell Publishing Ltd 1992 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| anaesthetic techniques: intravenous DAVIS, P.J. verfasserin aut COOK, D.R. verfasserin aut In Pediatric anesthesia Oxford [u.a.] : Wiley-Blackwell, 1991 2(1992), 2, Seite 0 Online-Ressource (DE-627)NLEJ243926200 (DE-600)2008564-3 1460-9592 nnns volume:2 year:1992 number:2 pages:0 http://dx.doi.org/10.1111/j.1460-9592.1992.tb00184.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1992 2 0 |
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10.1111/j.1460-9592.1992.tb00184.x doi (DE-627)NLEJ241199514 DE-627 ger DE-627 rakwb GRONERT, B.J. verfasserin aut Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy Oxford, UK Blackwell Publishing Ltd 1992 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| anaesthetic techniques: intravenous DAVIS, P.J. verfasserin aut COOK, D.R. verfasserin aut In Pediatric anesthesia Oxford [u.a.] : Wiley-Blackwell, 1991 2(1992), 2, Seite 0 Online-Ressource (DE-627)NLEJ243926200 (DE-600)2008564-3 1460-9592 nnns volume:2 year:1992 number:2 pages:0 http://dx.doi.org/10.1111/j.1460-9592.1992.tb00184.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1992 2 0 |
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10.1111/j.1460-9592.1992.tb00184.x doi (DE-627)NLEJ241199514 DE-627 ger DE-627 rakwb GRONERT, B.J. verfasserin aut Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy Oxford, UK Blackwell Publishing Ltd 1992 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| anaesthetic techniques: intravenous DAVIS, P.J. verfasserin aut COOK, D.R. verfasserin aut In Pediatric anesthesia Oxford [u.a.] : Wiley-Blackwell, 1991 2(1992), 2, Seite 0 Online-Ressource (DE-627)NLEJ243926200 (DE-600)2008564-3 1460-9592 nnns volume:2 year:1992 number:2 pages:0 http://dx.doi.org/10.1111/j.1460-9592.1992.tb00184.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1992 2 0 |
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10.1111/j.1460-9592.1992.tb00184.x doi (DE-627)NLEJ241199514 DE-627 ger DE-627 rakwb GRONERT, B.J. verfasserin aut Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy Oxford, UK Blackwell Publishing Ltd 1992 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| anaesthetic techniques: intravenous DAVIS, P.J. verfasserin aut COOK, D.R. verfasserin aut In Pediatric anesthesia Oxford [u.a.] : Wiley-Blackwell, 1991 2(1992), 2, Seite 0 Online-Ressource (DE-627)NLEJ243926200 (DE-600)2008564-3 1460-9592 nnns volume:2 year:1992 number:2 pages:0 http://dx.doi.org/10.1111/j.1460-9592.1992.tb00184.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1992 2 0 |
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Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy |
| abstract |
We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. |
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We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. |
| abstract_unstemmed |
We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. The infants were randomly assigned to one of two groups. In all patients anaesthesia was induced with halothane, nitrous oxide and oxygen by mask, then atropine and atracurium were administered intravenously. In the alfentanil group, anaesthesia was maintained with nitrous oxide, oxygen and alfentanil (100 μg·kg-1) followed by a 2.0 μg·kg-1·min-1 continuous infusion whereas in the control group anaesthesia was maintained with nitrous oxide, oxygen, and halothane (1.5%). There were no differences between the groups with respect to intra-operative values of blood pressure and heart rate, post-operative values of oxygen saturation as measured by pulse oximetry and respiratory rate, or post-operative incidence of vomiting and use of pain medication. Sedation lasted longer post-operatively in the alfentanil group, delaying oral intake but not prolonging hospitalization time. This study affirms that intravenous anaesthesia with alfentanil is safe and effective in infants. |
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DAVIS, P.J. COOK, D.R. |
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NLEJ243926200 |
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10.1111/j.1460-9592.1992.tb00184.x |
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2024-07-05T22:13:53.983Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ241199514</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707130509.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">120426s1992 xx |||||o 00| ||und c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1111/j.1460-9592.1992.tb00184.x</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ241199514</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">GRONERT, B.J.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Continuous infusion of alfentanil in infants undergoing inguinal herniorraphy</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Oxford, UK</subfield><subfield code="b">Blackwell Publishing Ltd</subfield><subfield code="c">1992</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">We evaluated the safety and efficacy of continuous alfentanil infusions in 37 full-term infants aged 4 to 52 weeks undergoing inguinal herniorraphy as outpatients. 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7.3999977 |