#Background
This section aims to cover medical conditions and diabetes in pregnancy. At present only medical conditions in pregnancy is included.
Recommendations, practice points and resources and tools have been developed for diabetes in pregnancy, however publication of these is pending the official release of the new Te Whatu Ora ‘Testing for, diagnosing and managing gestational diabetes (diabetes of pregnancy) Te whakamātau, te tautohu me te whakahaere i te mate huka hapūtanga’ Clinical Practice Guideline’. Publication is expected later in 2025.
Wāhine/people with medical conditions prior to pregnancy have a higher chance of complications during their pregnancies including spontaneous preterm birth and/or provider initiated preterm birth. Provider initiated preterm birth may be recommended due to exacerbations of a medical condition or the impact it may have on pregnancy-related conditions for māmā/person and/or pēpi, such as early-onset preeclampsia or fetal growth restriction (FGR).
There are a wide variety, and degrees of severity, of medical conditions that may impact on pregnancy and the chance of preterm birth. Due to the diverse nature of medical conditions in pregnancy, Taonga Tuku Iho recommendations focus on the general principles for care. Recommendations for two of the most common conditions are made separately with diabetes in pregnancy considered in more detail below and hypertension covered in preeclampsia and other hypertensive disorders in pregnancy section of Taonga Tuku Iho.
Diabetes in pregnancy includes pre-existing diabetes (type 1, type 2 and rarer forms of diabetes) and gestational diabetes (when the diagnosis of diabetes is made during pregnancy). In Aotearoa, the rates of diabetes in pregnancy are not recorded at a national level and vary according to the data sources used.1 There has been a large increase in rates of diabetes in pregnancy over the last few decades, reflecting change in the demographic and medical background of pregnant wāhine/people in Aotearoa, as well as screening and diagnostic thresholds. In an Auckland-wide cohort in 2009-2010, the rate of gestational diabetes was identified to be 6.2%.1 Data from Te Toka Tumai Auckland in 2023, reports rates of all diabetes in pregnancy to be over 20%, with 17.3% having gestational diabetes and 2.5% entering pregnancy with type 2 diabetes.2
Wāhine/people with diabetes in pregnancy, especially with pre-existing disease and/or when poorly controlled, have a higher chance of preterm birth.3-6 Rates of preterm birth have been reported to be as high as 40% for wāhine/people with type 1 diabetes and 22% for those with type 2 diabetes.4 This includes both spontaneous preterm birth (preterm labour and preterm prelabour rupture of membranes), as well as provider initiated preterm birth due to preeclampsia, FGR, antepartum haemorrhage and rarely for worsening organ damage (nephropathy, retinopathy, peripheral neuropathy and cardiovascular disease) for those with pre-existing diabetes. These adverse pregnancy outcomes, including the chance of preterm birth, have been shown to correlate with glycaemic control in wāhine/people with pre-existing diabetes.4 Hence there is a clear rationale to support appropriate screening, diagnosis and treatment of diabetes in pregnancy including to limit the impact of preterm birth on pregnancy outcomes. Provider initiated preterm birth should rarely be required or considered without additional clinical indications.
Taonga Tuku Iho focuses on aspects of diabetes in pregnancy care pertinent to preterm birth and limiting the impact of this for māmā/person and pēpi. It considers pre-existing diabetes and gestational diabetes separately. Preparation for preterm birth and the impact of corticosteroid treatment on glycaemic control and diabetes treatment is relevant to all with diabetes in pregnancy.
#Recommendations and Practice
Guideline Recommendations (pink boxes) and Good Practice (yellow boxes) are provided as recommendations of practice. Comprehensive clinical oversight of māmā/person and pēpi wellbeing is required, and this may influence how these recommendations of practice are used.
Each recommendation of practice should be considered in consultation with wāhine/people and whanāu, including clear explanations to allow informed decision-making. Wāhine/people have the right to decline a recommendation of practice. In these circumstances, healthcare providers should follow their professional responsibilities for ongoing care. 33,54-56
Medical conditions in pregnancy
Guideline Recommendations
Preconception care for wāhine/people with medical conditions that may impact on pregnancy
- The Rheumatic Disease and Pregnancy chapter of the Aotearoa New Zealand Guidelines for the Prevention, Diagnosis, and Management of Acute Rheumatic Fever and Rheumatic Heart Disease 2024 Update34 should be used to inform preconception assessment and counselling for wāhine/people with rheumatic heart disease.
Good Practice
Preconception care for wāhine/people with medical conditions that may impact on pregnancy
- Primary care providers should consider the medical conditions of wāhine/people of reproductive age and where appropriate offer referral to an obstetrician, discipline specific physician and/or specialist centre once pregnancy is being planned.
- A specialist centre team for preconception care should ideally be multidisciplinary and may include a maternal fetal medicine specialist, obstetrician, obstetric physician, discipline specific physician, dietician, educator, nurse specialist/midwife, and mental health support.
- In rural areas where distance may be a barrier to access preconception specialist centre review, telehealth options should be considered.
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Preconception review should broadly consider the impact of:
- the medical condition on pregnancy (including risks for māmā/person and pēpi and chance of obstetric complications such as FGR and preeclampsia)
- pregnancy on the medical condition
- the effect of medications on pregnancy (teratogenicity, contraindications)
- pregnancy on medications (pharmacokinetics and dose adjustments).
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The medical condition should be optimised where possible including baseline investigations and referral for any further investigations and/or treatment.
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Specifically, when considering preterm birth, both spontaneous and provider initiated preterm birth should be discussed. This should include the impact on pēpi outcomes by gestational age at birth including when there is significant chance of birth close to the limits of survival.
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General pregnancy and contraceptive advice should also be given.
- Wāhine/people and whānau should be provided with verbal and written information to support preconception care recommendations. These tools should allow for different levels of health literacy, ethnic and cultural backgrounds, and a variety of preferred first languages.
- Interpreter services and cultural support should be available and offered to all wāhine/people and whānau to support the provision of information.
Guideline Recommendations
Antenatal care for wāhine/people with medical conditions in pregnancy
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Lead maternity carers and primary care providers are guided by the Te Whatu Ora ‘Guidelines for Consultation with Obstetric and Related Medical Services (Referral Guidelines): Aratohu Aratohu Kimi Āwhina ki Te Ratonga Whakawhānau Pēpi, Ratonga Rata (Ngā Aratohu Tuku Atu)’33 and secondary and tertiary care providers are responsible for appropriate responses to referrals to support consistency in referral for initial review, consultation and/or transfer of care for wāhine/people with medical conditions in pregnancy (Consultation referral codes supplied):
- Automimmune/rheumatology: systemic lupus erythematosus and connective tissue disorders (1003/1004), thrombophilia including antiphospholipid syndrome (1005/1006).
- Cardiac disorders - cardiac valve disease (1008/1009), cardiac valve replacement (1011), cardiomyopathy (1012), congenital cardiac disease (1013), hypertension (1014), ischaemic heart disease (1016), pulmonary hypertension (1017).
- Endocrine: diabetes (1019, 1020, 1021), hypopituitarism (1023), Addison’s disease and Cushing’s disease (1076), prolactinoma (1024), thyroid disease (1022, 1082).
- Gastroenterology: bariatric surgery (1077), cholestasis of pregnancy/obstetric cholestasis (1026), hepatitis (1029, 1030, 1081), inflammatory bowel disease (1027, 1028), oesophageal varices (1031), previous fatty liver of pregnancy (1072).
- Genetic: any significant genetic condition (1032), Marfan syndrome (1033).
- Haematological: anaemia (Hb <90g/dL) (1034), bleeding disorders (1036), haemolytic anaemia (1035), sickle cell disease (1039), thalassaemia (1037), thrombocytopenia (1038), thromboembolism including previous (1040), thrombophilia (1041).
- Infectious diseases: CMV and toxoplasmosis (1042), HIV (1044), listeriosis (1045), rubella (1046), syphilis (1047), tuberculosis including contact (1048, 1073), varicella (1049).
- Mental health: current alcohol or drug misuse/dependence (1058), depression and anxiety disorders, (1078) other mental health conditions (1059, 1079, 1074)
- Neurological: arteriovenous malformation, cerebrovascular accident, transient ischaemic attacks (1050), epilepsy (1051. 1052, 1075), multiple sclerosis (1053), muscular dystrophy and myotonic dystrophy (1056), myasthenia gravis (1054), spinal cord lesion (1055).
- Renal: glomerulonephritis (1061), proteinuria (1062), pyelonephritis (1063), renal abnormality or vesicoureteric reflux, renal failure (1064), recurrent urinary tract infection (4032), polycystic kidneys (4039).
- Respiratory: acute respiratory condition (1069), asthma (1067, 1068) chronic obstructive pulmonary disease (1071) cystic fibrosis (1070).
- Transplant: any organ transplant (1080)
- Obesity: class II, III and IV (4017, 4034, 4035).
- Malignancy in current pregnancy (4015).
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For wāhine/people who decline a referral, consultation or transfer of care for obstetric and medical-related care, the lead maternity carer or primary provider should follow direction provided by the Te Whatu Ora Referral Guidelines (page 30).33
- All wāhine/people, regardless of the complexity of their medical condition, should have continuity of care through a single point of contact.33
- All wāhine/people, regardless of the complexity of their medical condition, should have care that considers and supports their holistic wellbeing including their ethnic and cultural backgrounds.33
- Wāhine/people with medical conditions that are major risk factors for preeclampsia (antiphospholipid syndrome, systemic lupus erythematosus, renal disease, chronic/pre-existing hypertension, pre-existing diabetes)57 and risk factors for early-onset FGR (chronic hypertension, renal impairment, antiphospholipid syndrome, diabetes with vascular disease)58 should be recommended aspirin prescribed as a daily 100 mg oral dose taken at night/evening from 12+0 weeks (and commencing up to 20+0 weeks) until 36+0 weeks for the prevention of preeclampsia and FGR.
- Wāhine/people with medical conditions that are major risk factors for preeclampsia should be recommended calcium prescribed as 1.5-2.0 g daily oral dose of elemental calcium from booking until birth for the prevention of preeclampsia.
- Wāhine/people with medical conditions that are major risk factors for preeclampsia should have uterine artery Doppler performed at 20 weeks gestation.
- Wāhine/people with medical conditions that are risk factors for early onset and/or major risk factors for FGR or major risk factors for FGR should have additional surveillance following the Preterm FGR risk assessment and antenatal surveillance Algorithm adapted from Te Whatu Ora SGA and FGR In Aotearoa New Zealand.58
- The Rheumatic Disease and Pregnancy chapter of the Aotearoa New Zealand Guidelines for the Prevention, Diagnosis, and Management of Acute Rheumatic Fever and Rheumatic Heart Disease 2024 Update34 should be used to inform antenatal care for wāhine/people with rheumatic heart disease.
Good Practice
Antenatal care for wāhine/people with medical conditions in pregnancy
- Depending on the type and severity of the medical condition, wāhine/people should be referred to a primary care provider, obstetrician, discipline specific physician and/or specialist centre.
- For more complex medical conditions, a specialist centre team should be multidisciplinary and may include a maternal fetal medicine specialist, obstetrician, obstetric physician, discipline specific physician, dietician, educator, nurse specialist/midwife, and mental health support.
- In rural areas where distance may be a barrier to access specialist centre review, telehealth options should be considered.
-
The first specialist review should broadly consider the impact of:
- the medical condition on pregnancy (including risks for māmā/person and pēpi and chance of obstetric complications such as fetal growth restriction and preeclampsia)
- pregnancy on the medical condition
- the effect of medications on pregnancy (teratogenicity, contraindications)
- pregnancy on medications (pharmacokinetics and dose adjustments).
-
The medical condition should be optimised where possible including baseline investigations, referral for any further investigations and/or treatment and adjustments to medication regimes as required.
-
Specifically, when considering preterm birth, both spontaneous and provider initiated preterm birth should be discussed. This should include the impact on pēpi outcomes by gestational age at birth including when there is significant chance of birth close to the limits of survival.
-
General pregnancy advice should also be given.
-
Clear communication including written/documented plan should be supplied to the referrer and lead maternity carer following specialist review.
- Schedules for frequency of antenatal visits and additional investigations should be individualised depending on each specific medical condition, its severity and additional co-morbidities.
- Where possible care should be provided as close to home and whānau support as possible.
- Wāhine/people and whānau should be provided with verbal and written information to support pregnancy care recommendations. These tools should allow for different levels of health literacy, ethnic and cultural backgrounds, and a variety of preferred first languages.
- Interpreter services and cultural support should be available and offered to all wāhine/people and whānau to support the provision of information.
Guideline Recommendations
Timing of and preparation for preterm birth for wāhine/people with medical conditions in pregnancy
- Some medical conditions in pregnancy may increase the chance of spontaneous preterm birth and so wāhine/people should be provided with clear information on the signs and symptoms of concern and need to report these to their lead maternity carer and/or hospital service early.
- Some medical conditions in pregnancy may increase the chance of provider initiated preterm birth but, in general, birth before 37+0 weeks should not be planned due to a medical condition alone.
- Planned birth at 35-36 weeks should be considered and discussed with wāhine/people with severe obstetric cholestasis (peak bile acids ≥100 µmol/L) due to the elevated chance of stillbirth.32
- When birth is considered before 37+0 weeks this should include multidisciplinary review (obstetrician, maternal fetal medicine, obstetric or discipline specific physician, specialist midwife/lead maternity carer and neonatal/paediatric teams) with consideration of gestational age, severity of medical condition and co-morbidities.
- When birth is considered before 37+0 weeks the balance of risks and benefits should be explained and discussed with the wahine/person and whānau.
- When preterm birth is anticipated or planned for wāhine/people with medical conditions in pregnancy the same interventions that may be applied in the antenatal period, during labour, and at the time of birth to improve outcomes for pēpi after preterm birth for wāhine/people without medical conditions should be considered.
- Magnesium sulphate for fetal neuroprotection at <30 weeks gestation should be avoided for wāhine/people with myasthenia gravis and other rare neuromuscular disorders involving the acetylcholine receptor.
Good Practice
Timing of and preparation for preterm birth for wāhine/people with medical conditions in pregnancy
- When using magnesium sulphate for fetal neuroprotection at <30 weeks gestation, for wāhine/people with renal impairment (serum creatinine >90 mmol/L), serum magnesium concentrations are recommended. Dose adjustment may be required, and should be undertaken in consultation with an obstetric physician if available.
- Wāhine/people should be provided with verbal and written information on place of preterm birth and hospital transfer, antenatal corticosteroids, antenatal magnesium sulphate, mode of preterm birth and care in preterm labour. These tools should allow for different levels of health literacy, ethnic and cultural backgrounds, and a variety of preferred first languages.
- Interpreter services and cultural support should be available and offered to all wāhine/people and whānau to support the provision of information.
Pre-existing and gestational diabetes
Recommendations, practice points and resources and tools have been developed for diabetes in pregnancy, however publication of these is pending the official release of the new Te Whatu Ora ‘Testing for, diagnosing and managing gestational diabetes (diabetes of pregnancy) Te whakamātau, te tautohu me te whakahaere i te mate huka hapūtanga’ Clinical Practice Guideline’. Publication is expected later in 2025.
#Auditable Standards
To be developed.