Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
C Jane Morrell a Medical Care Research Unit, School of Health and
Related Research (ScHARR), University of Sheffield, Sheffield S1 4DA, b Obstetrics
and Gynaecology Management, Northern General Hospital, Sheffield S5 7AU, c Sheffield Health Economics Group, ScHARR,
University of Sheffield
Correspondence to: C J Morrell
J.Morrell1{at}Sheffield.ac.uk
| |
Abstract |
|---|
|
|
|---|
Objectives:
To establish the relative cost
effectiveness of postnatal support in the community in addition to the
usual care provided by community midwives.
The extent of enduring physical and psychological morbidity after
childbirth and the potential consequences for infants may be
unrecognised by health professionals.1-3 Although the
effectiveness of elements of traditional postnatal care has been
questioned,4 the importance of emotional support for women
after childbirth has been emphasised.5 While the total
annual cost of maternity care in England and Wales is around £1.1
billion, there is little evidence of the appropriateness, clinical
effectiveness, or efficiency of the care provided.6
There is increasing evidence of the beneficial effect of social support
on health during pregnancy and labour and in encouraging successful
breast feeding.7-9 It may also help in the treatment of
postnatal depression.10 In the Netherlands, a maternity
aide provides care in the woman's home postnatally,11 but
in the United Kingdom there is no model offering similar postnatal support.
We undertook a randomised controlled trial to assess whether additional
postnatal support provided by trained community postnatal support
workers could have a positive effect on women's general health and
cost savings to the NHS.
Study population Intervention Outcomes and follow up Statistical analysis Assignment Economic analysis Recruitment
Table 1.
Design:
Randomised controlled trial with six month follow up.
Setting:
Recruitment in a university teaching hospital and care provided in women's homes.
Participants:
623 postnatal women allocated at random
to intervention (311) or control (312) group.
Intervention:
Up to 10 home visits in the first
postnatal month of up to three hours duration by a community postnatal
support worker.
Main outcome measure:
General health status as
measured by the SF-36 and risk of postnatal depression. Breast feeding
rates, satisfaction with care, use of services, and personal costs.
Results:
At six weeks there was no significant
improvement in health status among the women in the intervention group.
At six weeks the mean total NHS costs were £635 for the intervention group and £456 for the control group (P=0.001). At six months figures
were £815 and £639 (P=0.001). There were no differences between the
groups in use of social services or personal costs. The women in the
intervention group were very satisfied with the support worker visits.
Conclusions:
There was no health benefit of additional home visits by community postnatal support workers compared with traditional community midwifery visiting as measured by the SF-36. There were no savings to the NHS over six months after the introduction of the community postnatal support worker service.
![]()
Introduction
Top
Abstract
Introduction
Methods
Results
Discussion
References
![]()
Methods
Top
Abstract
Introduction
Methods
Results
Discussion
References
The trial was approved by the local
research ethics committee, and women were recruited on postnatal wards from October 1996 to November 1997. The planned trial population was
women aged 17 years or over who delivered a live baby and lived in the
area served by community midwives at the recruiting hospital.
Information on the trial was given to women from the 32nd week of
pregnancy. Women who could not give informed consent or communicate in
English or who had a baby in the special care baby unit for more than
48 hours were excluded.
The planned postnatal intervention aimed to
help women rest and recover after childbirth. Midwives were involved in
formulating the intervention and defining the support workers' role
and their eight week training programme. This aimed to enable the
support workers to provide effective practical and emotional support,
including helping the mother gain confidence in caring for her baby and
reinforcing midwifery advice on infant feeding. The support workers
achieved their national vocational qualification (level 2) postnatal
care award and completed endorsement units accredited to the
domiciliary care award and competence in the care of young children.
All women in the trial were offered postnatal care at home by community
midwives. The intervention group were also offered 10 visits from a
support worker for up to three hours per day in the first 28 postnatal days.
Postal follow up questionnaires were
issued at six weeks and six months postnatally. The primary outcome measure was the short form-36 (SF-36) general health perception domain
measured at six weeks.12 Secondary outcomes were the other
SF-36 domains, the Edinburgh postnatal depression
scale,13 the Duke functional social
support scale,14 and breast feeding rates. To have an 85%
chance of detecting as significant (at the two sided 5% level) a five
point difference between the two groups in the mean SF-36 general
health perception scores, with an assumed standard deviation of
20.0015 and a loss to follow up of 20%, 360 women (720 in
total) in each group were required.
All analyses were completed on an
intention to treat basis. Demographic and clinical data were compared between the two groups. The health status scores (SF-36, Edinburgh postnatal depression scale, Duke functional social support scale) were
assumed to be continuous measurements and were compared with t test or Mann-Whitney U test. For categorical data we used
2 test or
Fisher's exact test. We estimated non-parametric bootstrap
centile confidence intervals for the difference in mean scores between the groups.16
Individual women were randomly allocated to
intervention or control group with sequentially numbered, sealed opaque envelopes. The allocation schedule was prepared in advance by using
random digit tables. The process achieved a balanced randomisation and
concealed the group of allocation from all parties until after recruitment.
The aim of the economic evaluation was to
compare costs and outcomes at six weeks and at six months after delivery. All costs were identified, measured, and valued from an NHS
perspective. Secondary analysis compared use of social services and
personal expenditure. The support workers and midwives recorded the
number of their visits to each woman. Visit costs were estimated by
multiplying the duration of the visit in minutes by salary per minute.
Women reported contacts with general practitioners, health visitors,
hospitals, and mental health services and use of social services and
personal expenditure. We used data on local costs to value all
resources except contact with general practitioners, health visitors,
and social services, which were valued using national
estimates.17
![]()
Results
Top
Abstract
Introduction
Methods
Results
Discussion
References
We recruited 623 women: 311 intervention,
312 control (figure). There were no significant differences between groups in 26 birth details or 88 socioeconomic details, except for
incidence of twins, use of transcutaneous electrical nerve stimulation
(TENS) machines during labour, and adults living with the mother (table
1). There was a one year mean difference in age between the recruited
women and those who declined to take part (95% confidence interval 0.5 to 1.6), though this difference was not clinically important. The women
who consented to take part were more likely to be white (P=0.001) and
to have had an elective caesarean section (P=0.02), suggesting some
self selection among women who perceived the need for additional
support. The most commonly reported reason for not taking part was the
availability of other help at
home.

View larger version (33K):
[in a new window]
Diagrammatic representation of sample size
Intervention
Most women received six visits from a support
worker, and 48 (15%) received 10 visits. Thirty eight women (12%) declined all visits but were included in the follow up and analysis. The length of visits ranged from 10 to 375 minutes, with most time
spent on housework (38%), talking with the mother (23%), dealing with
the baby (9%), dealing with other siblings (8%), bottle feeding
(7%), talking about the baby (6%), and discussing breast feeding
(3%).
Outcome at six weeks
Health status
At six weeks 551 (88.4%) women returned their questionnaire, with a 93% minimum completion for all
the main outcomes. There was no evidence of a difference between the
two groups in the primary outcome (table 2). There was evidence of a
difference in physical functioning, social functioning, and scores for
physical role limitation, indicating better self perceived health in
the control group. There was some evidence of a difference in mean
scores on the Edinburgh postnatal depression scale in favour of the
control group (P=0.05). There was no evidence of a difference in scores
on the Duke functional social support scale or rates of breast feeding
between the two groups.
|
There was a high level of
satisfaction with the support worker service, which fulfilled a range of needs, but no difference between groups in satisfaction with their
midwife, health visitor, and general practitioner. More women in the
intervention group reported that their partner was supportive (P=0.04).
NHS resource use and costs
There were no significant
differences between the two groups in resource use or costs for any NHS service for which data were collected, except for the support worker
service. The difference in mean total NHS costs per woman of £179.58
(table 3) was mainly because of the additional costs of providing the
support worker service to the intervention group. This cost difference
was significant (P=0.001).
|
Outcome at six months
Health status measures
At six months 493 (79.1%) women returned their questionnaire. There was no evidence of
differences in health status scores (SF-36, Edinburgh postnatal
depression scale, and Duke functional social support scale) and rates
of breast feeding between the two groups (table
4).
|
On average women
received six visits from support workers, who spent 143 minutes per
visit (median 150 minutes) and 24 minutes on travel and administration. Visit costs comprised staff time (84%), travel expenses (8%), education and training (5%), and equipment (3%). The mean (SD) cost
per support worker visit was £27.70 (£6.20). The mean (SD) cost per
woman who received the visits was £179.30 (£83.30). The total cost of
the support worker service provided was £48 960.
NHS resource use and costs
At six months there were no
significant differences between the groups in NHS resource use except for the support worker service. The mean (SD) total NHS cost for the
intervention group was £815.20 (£564.70) and for the control group
was £638.9 (£500.40). The mean difference in total NHS costs between
the groups was £178.61 (95% confidence interval £79.60 to £272.40)
(table 5).
|
| |
Discussion |
|---|
|
|
|---|
The trial was established to assess whether there were any positive outcomes for the women in the intervention group. The data indicate no improvements in health status for these women for any measures used. There was even an indication that some domains of health status in the intervention group may have worsened in relation to the control group.
As is typical of trials, the participants were self selected, but the only significant difference between the women who were recruited and those who declined to take part was a one year difference in mean age, which seems of little importance to health outcomes. There were very good rates of response and completion in those recruited. Although by chance more women with twins were recruited to the intervention group, the outcomes for these few women were no poorer than for all the other women.
Outcome measures
The generic SF-36 may have been too insensitive to detect change
or distinguish differences in outcomes between the groups.
Nevertheless, the trial had over 80% power to detect a 5 point
difference in general health perception scores, which is the smallest
change in score considered "clinically and socially relevant."12 When we planned the trial we could not find
any measures for evaluating women's experiences of motherhood.
Further research is needed to establish the outcomes that mothers
themselves value.
|
What is already known on this topic
Previous work has indicated that additional postnatal support could improve wellbeing, reduce the risk of postnatal depression, and improve rates of breast feeding What this study addsWomen valued and were highly satisfied with the additional postnatal support from the support worker service There was no difference in health status between groups for the primary outcome and no improvement in self perceived health status in the intervention group with the SF-36, Edinburgh postnatal depression scale, or Duke functional support scale or in rates of breast feeding There was little difference between groups in use of NHS services and costs, but there was an additional cost for the support worker service |
Satisfaction with support worker service
More than 75% of women in the intervention group thought the
support worker service was better than expected, and some indicated
that women could be charged for the service. A subsequent study on
willingness to pay could place a financial value on the intangible
benefits of the service.19 Some women would have preferred
the intervention to have lasted longer, perhaps six weeks, which may
have provided more enduring benefits.
Economic evaluation
There was no evidence that women receiving the support worker
service used fewer NHS services than those receiving standard care at
either six weeks or six months. The incremental cost of introducing a
support worker service would therefore comprise mainly the costs of
setting up and running the service. The main issue of uncertainty
surrounds the cost of the developing service, which could be expected
to evolve over time. We therefore used the sensitivity analysis to
explore the cost implications of an increased throughput for the
service. By limiting each visit to 120 minutes, with each support
worker making a minimum of three visits a day, total costs per woman could be reduced from £179 to £151. By imposing these restrictions, however, the support workers would be unlikely to achieve their objectives because of lack of time.
| |
Acknowledgments |
|---|
We are grateful to all the women who participated in the trial, and we thank the support workers and are grateful for their contribution. We acknowledge the important contribution of the trial research midwife, Sue Crowther.
Contributors: CJM was the principal investigator, was responsible for the design and execution of the study, coordinated the formulation of the research hypothesis and the protocol design, participated in recruitment of women to the trial, and participated in the collection, management, analysis, and interpretation of the data and writing of the paper. HS initiated the research, discussed core ideas, contributed to the development of the primary study hypothesis, participated in the protocol design and recruitment of women to the trial, and participated in data collection, analysis, and interpretation of the data and writing of the paper. PS initiated the research, discussed core ideas, contributed to the development of the primary study hypothesis, and participated in the protocol design, interpretation of the data, and writing of the paper. SW prepared the calculation of sample size and the random allocation schedule, performed the recruitment monitoring, and participated in the analysis and interpretation of the data and writing of the paper. AM participated in the analysis and interpretation of the data and writing of the paper. CJM is the guarantor.
| |
Footnotes |
|---|
Funding: This trial was prioritised, commissioned, and funded by the NHS Research and Development, Health Technology Assessment programme. The views expressed are those of the authors and not necessarily those of the commissioning board of the programme.
Competing interests: None declared.
| |
References |
|---|
|
|
|---|
| 1. | Bick D, MacArthur C. The extent, severity and effect of health problems after childbirth. Br J Midwifery 1995; 3: 27-31. |
| 2. | Murray L. The impact of postnatal depression on infant development. J Child Psychol Psychiatry 1992; 33: 543-561[Medline]. |
| 3. | Glazener CMA, MacArthur C, Garcia J. Postnatal care: time for change. Contemp Rev Obstet 1993; 5: 130-136. |
| 4. | Montgomery E, Alexander J. Assessing postnatal uterine involution: a review and a challenge. Midwifery 1994; 5: 9-12. |
| 5. | Kumar R, Marks M, Jackson K. Prevention and treatment of postnatal psychiatric disorders. Br J Midwifery 1995; 3: 314-317. |
| 6. | Audit Commission. First class delivery: improving maternity services in England and Wales. London: Audit Commission, 1997. |
| 7. | Cohen S, Syme SL. Social support and health. Orlando: Harcourt Brace Jovanovich, 1985. |
| 8. | Elbourne D, Oakley A, Chalmers I. Social and psychological support during pregnancy. In: Chalmers I, Enkin M, Keirse MJNC, eds. Effective care in pregnancy and childbirth. Oxford: Oxford University Press, 1989:221-236. |
| 9. | Matich JR, Sims LS. A comparison of social support variables between women who intend to breast or bottle feed. Soc Sci Med 1992; 34: 919-927. |
| 10. | Ray KL, Hodnett ED. Caregiver support for postpartum depression. In: Cochrane Collaboration,ed. Cochrane Library. Issue 1. Oxford: Update Software, 2000. |
| 11. | Spiby H, Crowther S. Dutch maternity aides: a transferable model? RCM Midwives J 1999; 2: 20-21. |
| 12. | Ware J, Sherbourne C. The MOS 36 item short-form health survey (SF-36). Med Care 1992; 30: 473-483[Medline]. |
| 13. |
Cox JL, Holden J, Sagovsky R.
Detection of postnatal depression: development of the 10-item Edinburgh postnatal depression scale (EPDS).
Br J Psychiatry
1987;
150:
782-786 |
| 14. | Broadhead WE, Gehlbach SH, De Gruy FV, Kaplan BH. The Duke-UNC functional social support questionnaire measurement of social support in family medicine patients. Med Care 1988; 26: 709-723[Medline]. |
| 15. | Brazier JE, Harper R, Jones NMB, O'Cathain A, Thomas KJ, Usherwood T, et al. Validating the SF-36 health survey questionnaire: new outcome measures for primary care. BMJ 1992; 306: 1407-1440. |
| 16. | Efron B, Tibishirani RJ. An introduction to the bootstrap. New York: Chapman and Hall, 1993. |
| 17. | Netten A, Dennett J. Unit costs of health and social care. Canterbury: University of Kent, Personal Social Services Research Unit, 1997. |
| 18. |
Dennis M, O'Rourke S, Slattery J, Staniforth T, Warlow C.
Evaluation of a stroke family care worker: results of a randomised controlled trial.
BMJ
1997;
314:
1071-1076 |
| 19. | Drummond M, O'Brien B, Stoddart G. Torrence GW. In: Methods for the economic evaluation of health care programmes. Oxford: Oxford University Press, 1997. |
| 20. | Oakley A, Rajan L, Grant A. Social support and pregnancy outcome. Br J Obstet Gynaecol 1990; 97: 155-162[Medline]. |
| 21. | Oakley A, Hickey D, Rajan L. Social support in pregnancy: does it have long-term effects? J Reprod Infant Psychol 1996; 14: 7-22. |
| 22. | Olds DL, Eckenrode J, Henderson CR, Kitzman H, Powers J, Cole R, et al. Long-term effects of home visitation on maternal life course and child abuse and neglect. JAMA 1997; 278: 637-643[Abstract]. |
| 23. | Kitzman H, Olds DL, Henderson CR, Hanks C, Cole R, Tatelbaum R, et al. L Effect of prenatal and infancy home visitation by nurses on pregnancy outcomes, childhood injuries, and repeated childbearing. JAMA 1997; 278: 644-652[Abstract]. |
| 24. | Houston MJ, Howie PW, Cook A. Do breast feeding mothers get the home support they need? Health Bull 1981; 39: 166-172. |
(Accepted 18 May 2000)
Read all Rapid Responses
Israeli students are refusing to perform intimate examinations on anaesthetised women without their informed consent.