Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial

Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyo...
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Autor*in:	van den Bosch, A. A. S. [verfasserIn] Goossens, M. [verfasserIn] Bonouvrié, K. [verfasserIn] Winkens, B. [verfasserIn] Nijhuis, J. G. [verfasserIn] Roumen, F. J. M. E. [verfasserIn] Wassen, M. M. L. H. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2018

Schlagwörter:	Analgesia Childbirth Epidural Labor Quality of life Randomized trial

Übergeordnetes Werk:	Enthalten in: Quality of life research - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1992, 27(2018), 8 vom: 30. März, Seite 2027-2033
Übergeordnetes Werk:	volume:27 ; year:2018 ; number:8 ; day:30 ; month:03 ; pages:2027-2033

Links:	Volltext

DOI / URN:	10.1007/s11136-018-1838-z

Katalog-ID:	SPR017004268

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100	1		\|a van den Bosch, A. A. S. \|e verfasserin \|4 aut
245	1	0	\|a Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
264		1	\|c 2018
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520			\|a Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum.
650		4	\|a Analgesia \|7 (dpeaa)DE-He213
650		4	\|a Childbirth \|7 (dpeaa)DE-He213
650		4	\|a Epidural \|7 (dpeaa)DE-He213
650		4	\|a Labor \|7 (dpeaa)DE-He213
650		4	\|a Quality of life \|7 (dpeaa)DE-He213
650		4	\|a Randomized trial \|7 (dpeaa)DE-He213
700	1		\|a Goossens, M. \|e verfasserin \|4 aut
700	1		\|a Bonouvrié, K. \|e verfasserin \|4 aut
700	1		\|a Winkens, B. \|e verfasserin \|4 aut
700	1		\|a Nijhuis, J. G. \|e verfasserin \|4 aut
700	1		\|a Roumen, F. J. M. E. \|e verfasserin \|4 aut
700	1		\|a Wassen, M. M. L. H. \|e verfasserin \|4 aut
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773	1	8	\|g volume:27 \|g year:2018 \|g number:8 \|g day:30 \|g month:03 \|g pages:2027-2033
856	4	0	\|u https://dx.doi.org/10.1007/s11136-018-1838-z \|z kostenfrei \|3 Volltext
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912			\|a GBV_ILN_370
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951			\|a AR
952			\|d 27 \|j 2018 \|e 8 \|b 30 \|c 03 \|h 2027-2033

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allfields	10.1007/s11136-018-1838-z doi (DE-627)SPR017004268 (SPR)s11136-018-1838-z-e DE-627 ger DE-627 rakwb eng 100 ASE 44.52 bkl van den Bosch, A. A. S. verfasserin aut Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum. Analgesia (dpeaa)DE-He213 Childbirth (dpeaa)DE-He213 Epidural (dpeaa)DE-He213 Labor (dpeaa)DE-He213 Quality of life (dpeaa)DE-He213 Randomized trial (dpeaa)DE-He213 Goossens, M. verfasserin aut Bonouvrié, K. verfasserin aut Winkens, B. verfasserin aut Nijhuis, J. G. verfasserin aut Roumen, F. J. M. E. verfasserin aut Wassen, M. M. L. H. verfasserin aut Enthalten in Quality of life research Dordrecht [u.a.] : Springer Science + Business Media B.V, 1992 27(2018), 8 vom: 30. März, Seite 2027-2033 (DE-627)320474399 (DE-600)2008960-0 1573-2649 nnns volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033 https://dx.doi.org/10.1007/s11136-018-1838-z kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2938 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 44.52 ASE AR 27 2018 8 30 03 2027-2033
spelling	10.1007/s11136-018-1838-z doi (DE-627)SPR017004268 (SPR)s11136-018-1838-z-e DE-627 ger DE-627 rakwb eng 100 ASE 44.52 bkl van den Bosch, A. A. S. verfasserin aut Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum. Analgesia (dpeaa)DE-He213 Childbirth (dpeaa)DE-He213 Epidural (dpeaa)DE-He213 Labor (dpeaa)DE-He213 Quality of life (dpeaa)DE-He213 Randomized trial (dpeaa)DE-He213 Goossens, M. verfasserin aut Bonouvrié, K. verfasserin aut Winkens, B. verfasserin aut Nijhuis, J. G. verfasserin aut Roumen, F. J. M. E. verfasserin aut Wassen, M. M. L. H. verfasserin aut Enthalten in Quality of life research Dordrecht [u.a.] : Springer Science + Business Media B.V, 1992 27(2018), 8 vom: 30. März, Seite 2027-2033 (DE-627)320474399 (DE-600)2008960-0 1573-2649 nnns volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033 https://dx.doi.org/10.1007/s11136-018-1838-z kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2938 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 44.52 ASE AR 27 2018 8 30 03 2027-2033
allfields_unstemmed	10.1007/s11136-018-1838-z doi (DE-627)SPR017004268 (SPR)s11136-018-1838-z-e DE-627 ger DE-627 rakwb eng 100 ASE 44.52 bkl van den Bosch, A. A. S. verfasserin aut Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum. Analgesia (dpeaa)DE-He213 Childbirth (dpeaa)DE-He213 Epidural (dpeaa)DE-He213 Labor (dpeaa)DE-He213 Quality of life (dpeaa)DE-He213 Randomized trial (dpeaa)DE-He213 Goossens, M. verfasserin aut Bonouvrié, K. verfasserin aut Winkens, B. verfasserin aut Nijhuis, J. G. verfasserin aut Roumen, F. J. M. E. verfasserin aut Wassen, M. M. L. H. verfasserin aut Enthalten in Quality of life research Dordrecht [u.a.] : Springer Science + Business Media B.V, 1992 27(2018), 8 vom: 30. März, Seite 2027-2033 (DE-627)320474399 (DE-600)2008960-0 1573-2649 nnns volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033 https://dx.doi.org/10.1007/s11136-018-1838-z kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2938 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 44.52 ASE AR 27 2018 8 30 03 2027-2033
allfieldsGer	10.1007/s11136-018-1838-z doi (DE-627)SPR017004268 (SPR)s11136-018-1838-z-e DE-627 ger DE-627 rakwb eng 100 ASE 44.52 bkl van den Bosch, A. A. S. verfasserin aut Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum. Analgesia (dpeaa)DE-He213 Childbirth (dpeaa)DE-He213 Epidural (dpeaa)DE-He213 Labor (dpeaa)DE-He213 Quality of life (dpeaa)DE-He213 Randomized trial (dpeaa)DE-He213 Goossens, M. verfasserin aut Bonouvrié, K. verfasserin aut Winkens, B. verfasserin aut Nijhuis, J. G. verfasserin aut Roumen, F. J. M. E. verfasserin aut Wassen, M. M. L. H. verfasserin aut Enthalten in Quality of life research Dordrecht [u.a.] : Springer Science + Business Media B.V, 1992 27(2018), 8 vom: 30. März, Seite 2027-2033 (DE-627)320474399 (DE-600)2008960-0 1573-2649 nnns volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033 https://dx.doi.org/10.1007/s11136-018-1838-z kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2938 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 44.52 ASE AR 27 2018 8 30 03 2027-2033
allfieldsSound	10.1007/s11136-018-1838-z doi (DE-627)SPR017004268 (SPR)s11136-018-1838-z-e DE-627 ger DE-627 rakwb eng 100 ASE 44.52 bkl van den Bosch, A. A. S. verfasserin aut Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum. Analgesia (dpeaa)DE-He213 Childbirth (dpeaa)DE-He213 Epidural (dpeaa)DE-He213 Labor (dpeaa)DE-He213 Quality of life (dpeaa)DE-He213 Randomized trial (dpeaa)DE-He213 Goossens, M. verfasserin aut Bonouvrié, K. verfasserin aut Winkens, B. verfasserin aut Nijhuis, J. G. verfasserin aut Roumen, F. J. M. E. verfasserin aut Wassen, M. M. L. H. verfasserin aut Enthalten in Quality of life research Dordrecht [u.a.] : Springer Science + Business Media B.V, 1992 27(2018), 8 vom: 30. März, Seite 2027-2033 (DE-627)320474399 (DE-600)2008960-0 1573-2649 nnns volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033 https://dx.doi.org/10.1007/s11136-018-1838-z kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2938 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 44.52 ASE AR 27 2018 8 30 03 2027-2033
language	English
source	Enthalten in Quality of life research 27(2018), 8 vom: 30. März, Seite 2027-2033 volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033
sourceStr	Enthalten in Quality of life research 27(2018), 8 vom: 30. März, Seite 2027-2033 volume:27 year:2018 number:8 day:30 month:03 pages:2027-2033
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Analgesia Childbirth Epidural Labor Quality of life Randomized trial
dewey-raw	100
isfreeaccess_bool	true
container_title	Quality of life research
authorswithroles_txt_mv	van den Bosch, A. A. S. @@aut@@ Goossens, M. @@aut@@ Bonouvrié, K. @@aut@@ Winkens, B. @@aut@@ Nijhuis, J. G. @@aut@@ Roumen, F. J. M. E. @@aut@@ Wassen, M. M. L. H. @@aut@@
publishDateDaySort_date	2018-03-30T00:00:00Z
hierarchy_top_id	320474399
dewey-sort	3100
id	SPR017004268
language_de	englisch
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A. S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2018</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. 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author	van den Bosch, A. A. S.
spellingShingle	van den Bosch, A. A. S. ddc 100 bkl 44.52 misc Analgesia misc Childbirth misc Epidural misc Labor misc Quality of life misc Randomized trial Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
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topic_title	100 ASE 44.52 bkl Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial Analgesia (dpeaa)DE-He213 Childbirth (dpeaa)DE-He213 Epidural (dpeaa)DE-He213 Labor (dpeaa)DE-He213 Quality of life (dpeaa)DE-He213 Randomized trial (dpeaa)DE-He213
topic	ddc 100 bkl 44.52 misc Analgesia misc Childbirth misc Epidural misc Labor misc Quality of life misc Randomized trial
topic_unstemmed	ddc 100 bkl 44.52 misc Analgesia misc Childbirth misc Epidural misc Labor misc Quality of life misc Randomized trial
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title	Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
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title_full	Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
author_sort	van den Bosch, A. A. S.
journal	Quality of life research
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author_browse	van den Bosch, A. A. S. Goossens, M. Bonouvrié, K. Winkens, B. Nijhuis, J. G. Roumen, F. J. M. E. Wassen, M. M. L. H.
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author-letter	van den Bosch, A. A. S.
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title_sort	maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
title_auth	Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
abstract	Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum.
abstractGer	Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum.
abstract_unstemmed	Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. Differences in request for pain relief were comparable with other studies. Conclusion Routine administration of EA during labor and pain relief on maternal request only are associated with comparable changes of women’s QOL antepartum to 6 weeks postpartum.
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container_issue	8
title_short	Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial
url	https://dx.doi.org/10.1007/s11136-018-1838-z
remote_bool	true
author2	Goossens, M. Bonouvrié, K. Winkens, B. Nijhuis, J. G. Roumen, F. J. M. E. Wassen, M. M. L. H.
author2Str	Goossens, M. Bonouvrié, K. Winkens, B. Nijhuis, J. G. Roumen, F. J. M. E. Wassen, M. M. L. H.
ppnlink	320474399
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hochschulschrift_bool	false
doi_str	10.1007/s11136-018-1838-z
up_date	2024-07-04T01:50:13.761Z
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A. S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2018</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Introduction The purpose of this study was to evaluate the changes in maternal quality of life (QOL) from pregnancy to 6 weeks after delivery between routine labor epidural analgesia (EA) and pain relief on maternal request only. Methods \Women delivering of a singleton in cephalic presentation beyond 36 + 0 weeks’ gestation were randomly allocated to EA as a routine during labor (routine EA group), or to any kind of analgesia on request only (control group). The Short Form health survey (SF-36) was used to assess women’s QOL before randomization, and 6 weeks postpartum. Data were analyzed according to the intention to treat principle. Results A total of 488 women were included, and antepartum as well as postpartum SF-36 questionnaires were filled in by 356 (73.0%) women, 176 (49.4%) in the routine EA group, and 180 (50.6%) in the control group. Changes from the QOL antepartum to the QOL 6 weeks postpartum were comparable between both groups, also in the subgroup of women in the control group who gave birth without any pain medication (n = 41, 22.8%). Maternal age and the incidence of adverse events related to EA, which were both higher in the routine EA group, had no influence on the changes in QOL. 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Maternal quality of life in routine labor epidural analgesia versus labor analgesia on request: results of a randomized trial

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