Warning

Introduction

Syphilis is a bacterial infection, caused by the spirochete Treponema pallidum subspecies pallidum. It is transmitted through sexual contact, or from mother to fetus during pregnancy or at birth. Whilst overall the number of cases of syphilis amongst women is low, in recent years there has been a significant increase in the number of cases, usually in localised outbreaks.

Syphilis is classified according to stage as either early or late. Early syphilis includes both primary and secondary disease.

Primary syphilis – occurs 10-90 days after exposure, characterised by regional lymphadenopathy and (usually) single, painless, indurated ulcer (chancre). This will usually heal within 6 weeks.

Secondary syphilis – occurs 3-6 weeks following the initial chancre. Symptoms can include a generalised maculopapular rash, mucocutaneous lesions and generalised lymphadenopathy.

The risk of vertical transmission depends primarily on the stage of maternal syphilis and on the stage of the pregnancy at infection. Transmission is highest (60-90%) in untreated maternal primary or secondary syphilis. Transmission is also higher in the 3rd trimester or with coexisting HIV infection.

In untreated early syphilis, between 60-90% of infants will be infected, and stillbirth can occur in up to one-third of cases. Other risks include premature birth, low birth weight, polyhydramnios, and hydrops. Congenital syphilis is the result of transplacental transmission of spirochetes, and can occur at any stage of pregnancy. It can result in developmental delay, anaemia, and hepatosplenomegaly. Infants born to infected mothers who have received adequate penicillin treatment during pregnancy are at minimal risk for congenital syphilis.

Aim

This guideline is for midwifery and obstetric staff caring for women with a confirmed positive syphilis result in pregnancy, or who have a history of previously treated syphilis. Management of pregnant women with syphilis requires close liaison between Obstetric, Midwifery, Paediatric and Genitourinary medicine (GUM) colleagues.

Guidelines

1. General considerations


In general, GUM will manage the assessment, treatment and follow-up of women diagnosed with syphilis. Women with a history of previously treated syphilis should also be referred to GUM for monitoring, although further treatment may not be necessary.

Advice can always be sought from the on-call GUM doctor at Chalmers, available through switchboard.


2. Screening


All women should be offered a screening blood test for syphilis at booking, as per the UK national screening recommendations. The aim of screening is early maternal diagnosis in order to offer prompt treatment and minimise transmission risk. Women at high risk should be retested at 24 and 36 weeks.


• A 5ml clotted sample (brown tube) should be sent to microbiology for screening IgG at the booking appointment.


3. Diagnosis


When a presumptive positive result is received a second sample is required urgently to confirm the diagnosis.

• A 5ml brown tube should be sent as soon as possible either by the community midwife team or the antenatal clinic, and clearly documented on TRAK.

Full syphilis serology will be undertaken by the lab, but assessment of the result should only be undertaken by a GUM senior. Further interpretation of syphilis serology is complex and outwith the remit of this guideline.

For all patients, including those booked at St John’s:


• The laboratory will inform Dr Sarah Cooper/Sarah Stock and the specialist midwife of the result
• A joint appointment with GUM Consultant and Dr Sarah Cooper will be arranged asap at the Wednesday afternoon high risk antenatal clinic at RIE.
• Referral to Dr Laura Jones, Consultant Paediatrician at RHSC will be made antenatally to plan neonatal care. Older siblings may need to be screened for congenital syphilis.
• Discuss with fetal medicine team to evaluate fetal involvement. USS assessment for hydrops or hepatosplenomegaly may be required. Fetal monitoring may be needed if treatment is given after 26 weeks, due to the risk of Jarisch-Herxheimer reaction (see below).

Patients should be told of the need for further assessment with GUM to evaluate disease, offer partner notification, and further STI testing. They should be made aware of the significance of syphilis on their own health and on the pregnancy.

  • Following this, an entry should be made in Obstetric and Neonatal special features on TRAK.


4. Treatment and follow-up


• A treatment plan will be decided by GUM depending on disease stage following assessment. Treatment should be started as soon as possible following diagnosis. The result of the confirmatory test is not required if there is clinical suspicion.


• Treatment is a single dose of benzathine penicillin 2.4 megaunits IM single dose (if non penicillin allergic). Alternative regimes or penicillin desensitization may be considered in those with penicillin allergy, under the management of GUM. Consideration should be given to treatment at initial review, only on the advice of GUM, if there is a high risk the patient may default further review.


• Further treatment may be necessary, for those in whom the efficacy of treatment is uncertain, depending on the results of monitoring. If treatment is given in the 3rd trimester, a second dose is usually required one week later.


• Women should be offered further STI testing, including HIV, chlamydia and gonorrhoea.


• Follow-up will also be by GUM to ensure adequate treatment. Full syphilis serology will be checked at 1,2,3,6 months post treatment. Some of these tests may be performed at routine antenatal visits by agreement with GUM. Monitoring is essential to ensure adequate treatment and detect potential re-infection.

Jarisch-Herxheimer reaction
Approximately 40% of patients will experience an acute febrile reaction following penicillin treatment. This is characterised by headache, myalagia, chills and rigors which will resolve after 24 hours. In pregnancy this reaction may also cause transient uterine activity and fetal distress. There is a theoretical risk of iatrogenic or spontaneous pre-term labour.

Patients should be counselled about this potential reaction and advised to contact obstetric triage for advice and review.
If these symptoms occur:
• Patient should be admitted for observation and fetal monitoring.


• Treatment should be symptomatic with paracetamol for pyrexia.


• There is no evidence to support the use of high dose prednisolone to reduce uterine contractions.

5. Neonatal Management


Advice can be sought either from on-call GUM or from Dr Jones when available.


• Paediatric registrar should perform an examination at delivery for signs of congenital syphilis.


• If the mother has been adequately treated in pregnancy, syphilis titres are not required from the baby


• If there has been inadequate treatment, or reinfection, the baby needs to be evaluated for congenital infection. This includes taking venous bloods and CSF, and if required long bone xrays. Syphilis titres should be taken from baby at birth (venous sample, not cord blood).


• Swabs for syphilis PCR (red top swab) should be taken if the baby has suspicious lesions/discharge.

Treatment should be given to the baby in the following circumstances:


• Babies with suspected congenital syphilis


• Babies born to untreated (or inadequately treated) mothers, non-penicillin treated or those treated within 4 weeks of birth.


• Treatment: benzylpenicillin sodium (50,000 iu)30mg/kg 12-hourly IV for 7 days then 8-hourly for a further 3 days.

Follow-up should be arranged for six weeks of age.


• Dr Laura Jones (Paediatric Consultant) should be informed of the delivery. Subsequent follow-up should be at 6 weeks, 3, 6 and 12 months with clinical evaluation and syphilis serology.

6. Postnatal
• Breastfeeding can be safely initiated and should be supported.


• Advise GUM team of delivery. Postnatal follow-up testing will be arranged by GUM.

 

Contact details

On call GUM:                                                                                Via switchboard


GUM at Chalmers:                                                                         0131 536 1070


Dr Sarah Cooper - Consultant Obstetrician                                       22524

(Secretary – Lynne Glasgow)


Dr Laura Jones – Consultant Paediatrician via switchboard                 0131 536 0000

(Secretary – Betty Offerman)                                                          0131 536 0971

Associated documents

Appendix 1: Proforma for management of a screen-positive syphilis result

References

BASHH. UK National Guidelines on the Management of Syphilis 2008
http://www.bashh.org/documents/1879.pdf


BASHH. Update on management of syphilis in pregnancy 2011
http://www.bashh.org/documents/3693.pdf


UK National Screening Committee. Screening for syphilis in pregnancy 2013
www.screening.nhs.uk/policydb_download.php?doc=281

 

Appendix 1 - proforma for management of a screen positive antenatal screening result for syphilis

Proforma for management of a screen positive antenatal screening result for Syphilis - pdf

 

Antenatal  
Take maternal blood for confirmation testing, 1x brown top bottle, and send to microbiology URGENTLY requesting confirmation of Syphilis positive screening result.  
Urgent ANC appointment arranged at RIE to discuss screen positive result  
Make urgent referral to Genitourinary Medicine (GUM) consultant  
Complete ‘Special Features’ on TRAK  
Refer to Dr Laura Jones RHSC antenatally  
Referral made to FMU (Yes/No)  
Intrapartum / Immediate post delivery  
Paediatric registrar to perform neonatal examination and commence treatment if necessary as per protocol.  
Dr Jones (Paediatric Consultant) to be informed of delivery and arrange follow-up  
GUM to be informed of delivery to arrange maternal follow-up  

Editorial Information

Last reviewed: 02/05/2015

Next review date: 02/05/2025

Author(s): Lesley Curry, Sarah Cooper, Laura Jones.