Health resource utilization of labor induction versus expectant management
Copyright © 2020 Elsevier Inc. All rights reserved..
BACKGROUND: Although induction of labor of low-risk nulliparous women at 39 weeks reduces the risk of cesarean delivery compared with expectant management, concern regarding more frequent use of labor induction remains, given that this intervention historically has been thought to incur greater resource utilization.
OBJECTIVE: The objective of the study was to determine whether planned elective labor induction at 39 weeks among low-risk nulliparous women, compared with expectant management, was associated with differences in health care resource utilization from the time of randomization through 8 weeks postpartum.
STUDY DESIGN: This is a planned secondary analysis of a multicenter randomized trial in which low-risk nulliparous women were assigned to induction of labor at 39 weeks or expectant management. We assessed resource utilization after randomization in 3 time periods: antepartum, delivery admission, and discharge through 8 weeks postpartum.
RESULTS: Of 6096 women with data available, those in the induction of labor group (n = 3059) were significantly less likely in the antepartum period after randomization to have at least 1 ambulatory visit for routine prenatal care (32.4% vs 68.4%), unanticipated care (0.5% vs 2.6%), or urgent care (16.2% vs 44.3%), or at least 1 antepartum hospitalization (0.8% vs 2.2%, P < .001 for all). They also had fewer tests (eg, sonograms, blood tests) and treatments (eg, antibiotics, intravenous hydration) prior to delivery. During the delivery admission, women in the induction of labor group spent a longer time in labor and delivery (median, 0.83 vs 0.57 days), but both women (P = .002) and their neonates (P < .001) had shorter postpartum stays. Women and neonates in both groups had similar frequencies of postpartum urgent care and hospital readmissions (P > .05 for all).
CONCLUSION: Women randomized to induction of labor had longer durations in labor and delivery but significantly fewer antepartum visits, tests, and treatments and shorter maternal and neonatal hospital durations after delivery. These results demonstrate that the health outcome advantages associated with induction of labor are gained without incurring uniformly greater health care resource use.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2020 |
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Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:222 |
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Enthalten in: |
American journal of obstetrics and gynecology - 222(2020), 4 vom: 01. Apr., Seite 369.e1-369.e11 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Grobman, William A [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 12.05.2020 Date Revised 19.09.2021 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.ajog.2020.01.002 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM305296264 |
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100 | 1 | |a Grobman, William A |e verfasserin |4 aut | |
245 | 1 | 0 | |a Health resource utilization of labor induction versus expectant management |
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500 | |a Date Revised 19.09.2021 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2020 Elsevier Inc. All rights reserved. | ||
520 | |a BACKGROUND: Although induction of labor of low-risk nulliparous women at 39 weeks reduces the risk of cesarean delivery compared with expectant management, concern regarding more frequent use of labor induction remains, given that this intervention historically has been thought to incur greater resource utilization | ||
520 | |a OBJECTIVE: The objective of the study was to determine whether planned elective labor induction at 39 weeks among low-risk nulliparous women, compared with expectant management, was associated with differences in health care resource utilization from the time of randomization through 8 weeks postpartum | ||
520 | |a STUDY DESIGN: This is a planned secondary analysis of a multicenter randomized trial in which low-risk nulliparous women were assigned to induction of labor at 39 weeks or expectant management. We assessed resource utilization after randomization in 3 time periods: antepartum, delivery admission, and discharge through 8 weeks postpartum | ||
520 | |a RESULTS: Of 6096 women with data available, those in the induction of labor group (n = 3059) were significantly less likely in the antepartum period after randomization to have at least 1 ambulatory visit for routine prenatal care (32.4% vs 68.4%), unanticipated care (0.5% vs 2.6%), or urgent care (16.2% vs 44.3%), or at least 1 antepartum hospitalization (0.8% vs 2.2%, P < .001 for all). They also had fewer tests (eg, sonograms, blood tests) and treatments (eg, antibiotics, intravenous hydration) prior to delivery. During the delivery admission, women in the induction of labor group spent a longer time in labor and delivery (median, 0.83 vs 0.57 days), but both women (P = .002) and their neonates (P < .001) had shorter postpartum stays. Women and neonates in both groups had similar frequencies of postpartum urgent care and hospital readmissions (P > .05 for all) | ||
520 | |a CONCLUSION: Women randomized to induction of labor had longer durations in labor and delivery but significantly fewer antepartum visits, tests, and treatments and shorter maternal and neonatal hospital durations after delivery. These results demonstrate that the health outcome advantages associated with induction of labor are gained without incurring uniformly greater health care resource use | ||
650 | 4 | |a Comparative Study | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Multicenter Study | |
650 | 4 | |a Randomized Controlled Trial | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a cesarean delivery | |
650 | 4 | |a costs | |
650 | 4 | |a expectant management | |
650 | 4 | |a induction of labor | |
650 | 4 | |a resources | |
650 | 7 | |a Anti-Bacterial Agents |2 NLM | |
700 | 1 | |a Sandoval, Grecio |e verfasserin |4 aut | |
700 | 1 | |a Reddy, Uma M |e verfasserin |4 aut | |
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700 | 1 | |a Silver, Robert M |e verfasserin |4 aut | |
700 | 1 | |a Mallett, Gail |e verfasserin |4 aut | |
700 | 1 | |a Hill, Kim |e verfasserin |4 aut | |
700 | 1 | |a Rice, Madeline Murguia |e verfasserin |4 aut | |
700 | 1 | |a El-Sayed, Yasser Y |e verfasserin |4 aut | |
700 | 1 | |a Wapner, Ronald J |e verfasserin |4 aut | |
700 | 1 | |a Rouse, Dwight J |e verfasserin |4 aut | |
700 | 1 | |a Saade, George R |e verfasserin |4 aut | |
700 | 1 | |a Thorp, John M |c Jr |e verfasserin |4 aut | |
700 | 1 | |a Chauhan, Suneet P |e verfasserin |4 aut | |
700 | 1 | |a Iams, Jay D |e verfasserin |4 aut | |
700 | 1 | |a Chien, Edward K |e verfasserin |4 aut | |
700 | 1 | |a Casey, Brian M |e verfasserin |4 aut | |
700 | 1 | |a Gibbs, Ronald S |e verfasserin |4 aut | |
700 | 1 | |a Srinivas, Sindhu K |e verfasserin |4 aut | |
700 | 1 | |a Swamy, Geeta K |e verfasserin |4 aut | |
700 | 1 | |a Simhan, Hyagriv N |e verfasserin |4 aut | |
700 | 1 | |a Macones, George A |e verfasserin |4 aut | |
700 | 0 | |a Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal-Fetal Medicine Units (MFMU) Network |e verfasserin |4 aut | |
700 | 1 | |a Peaceman, A |e investigator |4 oth | |
700 | 1 | |a Plunkett, B |e investigator |4 oth | |
700 | 1 | |a Paycheck, K |e investigator |4 oth | |
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700 | 1 | |a Meadows, C |e investigator |4 oth | |
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