PRE-TERM LABOUR Guideline Pre-term birth occurs in 7-12% of all births and accounts for over 85% of all perinatal morbidity and mortality. Significant underlying pathology triggering pre-term labour should be identified and appropriately managed. Consultation with the Obstetrician on call for the day is recommended for labour onset prior to 37 weeks. Prior to 35 weeks (+0 days) gestation, ‘transfer of care’ to secondary care is indicated and prior to 32 weeks (+ 0 days) ‘transfer of care’ to tertiary services (CCDHB) is indicated. Neonatal morbidity and mortality will be minimised by thorough clinical assessment, management of infectious risk, appropriately directed tocolysis and additional cares during progressive labour and delivery. Liaison with paediatric and SCBU staff is fundamentally important. Scope All medical and midwifery staff employed by Hutt Valley DHB. All Hutt Valley DHB Maternity access holders. All Special Care Baby Unit staff Definitions Pre-term labour: Painful regular contractions with associated cervical changes prior to 37 weeks (+0 days) gestation. CTG EFM CBC HVDHB MSU SCBU CCDHB Cardiotocograph Electronic fetal monitoring Full blood count Hutt Valley District Health Board Midstream urine Special Care Baby Unit Capital and Coast District Health Board Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 1 of 7 Procedures Principles of care for threatened pre-term labour include: Accessing specialist obstetric and neonatal services Establishing a diagnosis, including underlying pathology. Steroids administration if the pregnancy is less than 37 weeks (+0 days) gestation. Prophylaxis for Group B Streptococcus and treating intrapartum fever. Planning management in accordance with degree of prematurity. Tocolysis when appropriate Expedite delivery for chorioamnionitis, perceived fetal compromise or major antepartum haemorrhage Avoiding perinatal asphyxia and trauma during labour and birth. Consultation with Obstetrician on call / Transfer of care Obstetric Consultation All women with threatened or active pre-term labour should be admitted to Hutt Valley DHB. Consultation with the Obstetrician on call is recommended for gestations prior to 37 weeks (+0 days). For gestation < 35 weeks, the LMC must recommend that responsibility for care be transferred to secondary care (MOH, 2007). The obstetrician on call / registrar must liaise with SCBU and paediatrician re availability of bed in SCBU. If none available, consider transfer to CCDHB (refer transfer to CCDHB policy). For gestations < 32 weeks, transfer of care to CCDHB (refer transfer to CCDHB policy). The Obstetrician on call or registrar must consult with Obstetrician and Neonatal consultant at CCDHB regarding transfer. The midwife liaises with CCDHB midwife. If the clinical situation is sufficiently stable, then antenatal maternal transfer is to be arranged. If the threatened pre-term labour completely settles, the woman will be transferred back to the care of the referring practitioner or LMC on discharge from hospital. The LMC will be contacted by a core midwife upon hospital discharge. Acute assessment in Delivery Suite LMCs are expected to give antenatal advice about the symptoms and signs of labour, and the woman’s care plan should indicate who they are to contact if these develop prematurely. Prior to 37 weeks gestation, it is recommended that a consultation occurs and there will be an assessment on delivery suite . Assessment to include: Confirm gestational age: o Reviewing clinical data regarding LMP and scan results o When possible, a copy of an early scan report should be obtained and reviewed. Consider underlying pathology: eg. Chorioamnionitis, antepartum haemorrhage. Clinical examination should include: o Maternal temperature and pulse o Contraction pattern o Fetal size, lie and presentation, liquor volume Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 2 of 7 o Sterile speculum assessing for leakage of liquor o Low vaginal / rectal (not anogenital) swab for Group B Streptococcus o Cervical changes: avoid unnecessary vaginal examination especially if membranes ruptured o Continuous CTG while contracting o MSU and CBC Ultrasound: a formal scan at HVDHB scanning department is recommended when clinical situation permits. Antibiotics (Refer Appendix I) Tocolysis (Refer Nifedipine Protocol) Steroids (Refer Appendix II) IV access Delivery will be expedited when: Significant placental abruption Chorioamnionitis Fetal compromise Gestational Age Based Management Pre-term labour less than 32 weeks: If pre-term labour is not settling after steroids and nifedipine then the Obstetrician / registrar on call is to arrange for transfer to CCDHB after first consulting with the Obstetrician and Neonatal consultant at CCDHB (refer Transfer to Wellington Women’s Hospital policy). Management of progressive pre-term labour 32-34 weeks (+ 6 days). Clinical assessment as above Liaison with SCBU and paediatrician re availability of bed on SCBU. Transfer to secondary care as per referral guidelines (MOH, 2007). Midwifery care negotiated Continuous EFM throughout labour Paediatric attendance at birth Obstetric Registrar or Consultant to attend birth whenever feasible If an assisted vaginal delivery is indicated, forceps are preferable < 34 weeks gestation Elective episiotomy if perineum resistant Pethidine should be used sparingly 35 weeks (+ 0 days) – 36 weeks (+6 days) gestation Under care of LMC unless other obstetric indications Consultation with Obstetrician on call advised –transfer of care only if other clinical complications Clinical assessment (as above) Continuous EFM in labour with gestations 35+0 –35+6 weeks. For gestation 36+0 – 37 +0 weeks, continuous EFM only if indicated by other risk factors. Tocolysis not indicated Steroids (refer Appendix II) Antibiotics (refer Appendix I) Paediatric attendance at birth recommended. Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 3 of 7 References Bramberger, P. & Lawrence, J., Braun, D. & Saunders, B., Contreras, R. & Petitti, D. (2000). The influence of intrapartum antibiotics on the clinical spectrum of early onset Group B Streptococcal infection in term infants. Pediatrics, (106) 244-250. Capital and Coast District Health Board. (2010). Pre-term Labour. Capital and Coast District Health Board, Women’s and Children’s Health Directorate – Policies, Procedures Protocols, Guidelines. Policy No. OB IP-16 Carlan, S. J., O’Brien, W. F., Parsons, M. T., Lense, J. J. (1993). Preterm premature rupture of membranes; a randomised study of home versus hospital management. Obstetric Gynaecology, 81 (1) 61-64. Flenady, V. & Jenkins-Manning, S. (2007). For the Queensland Clinical Practice Guidelines Working Party on the prevention of early onset Group B Streptococcal Disease, Centre for Clinical Studies, Mater Health Services: Brisbane Grant, A. & Glazener, C. M. Elective caesarean section versus expectant management for delivery of the small baby. [update of Cochrane Database Syst Rev. 2001; (1): CD000078; 11279676]. Grimwood, K., Darlow, B., Gosling, I., Green, R., Lennon, D., Martin, D. & Stone, P. (2001). Early onset neonatal group B Streptococcal management strategy survey of New Zealand Centres: Research Summary. Wellington Guinn, D. A., Atkinson, M. W.(2001). Single vs weekly courses of antenatal corticosteroids for women at risk of preterm delivery: A randomised controlled trial. JAMA, 286 (13) 1581-1587. Kenyon, S. L., Taylor, D. J., Tarnow-Mordi, W. for the ORACLE II Collaborative Group. (2001). Broad spectrum antibiotics for spontaneous preterm labour: The Oracle II randomised trial. Lancet, 357; 989994 Ministry of Health (2007). Guidelines for Consultation with Obstetric and Related Specialist Medical Services (Referral Guidelines). Wellington: Ministry of Health Norwitz, E. R. & Robinson, J. N. (2001). A systematic approach to the management of preterm labour. [Review] [86 refs] [Journal Article. Review, Tutorial] Seminars in Perinatology. 25 (4): 223-235 Stutchfield, P., Whitaker, R., Russell, I. (2005). Antenatal betamethasone and incidence of neonatal respiratory distress after elective caesarean section; Pragmatic randomised trial. http://www.bmj.com/cgi/content/full/331/7518/662 Appendices Appendix 1: Maternity Unit Antibiotic Guidelines (laminated and issued to HVDHB Quick Reference folders) Appendix 2: Steroid administration for anticipated pre-term birth (laminated and issued to HVDHB Quick Reference Folders) Appendix 3: Pre-term labour management algorithm (laminated and issued to HVDHB Quick Reference Folders) Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 4 of 7 Appendix I Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 5 of 7 Appendix II Steroid Administration for Anticipated Pre-term Delivery Steroid Administration Steroids are indicated when delivery is anticipated at 24-34 weeks (+ 6 days) gestation. Betamethasone 11.4mg (Celestone chronodose, 2 x 5.7mg ampoules) IM stat Repeat one dose after 12 hours. In a non-acute setting 24 hours. Delivery is ideally delayed until 24 hours after the first dose. Steroids given even 30 minutes prior to delivery may be valuable. Give 1st dose even if labour advanced. Not contraindicated in presence of SRM or sepsis. Maternity Unit Antibiotic Guidelines for Surgical Procedures Caesarean Section Manual removal of placenta Repair of extensive vaginal tears Emergency cervical cerclage Cefuroxime 1.5g IV stat Or if high risk anaphylaxis: clindamycin 900mg IV stat Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 6 of 7 Appendix III Policy Number: MATY056 Approved by Maternity Quality Committee Facilitated by: Karen Wakelin Next due date: October 2015 Page 7 of 7