Saturday, June 29, 2019

NICE 133: Hypertension in Pregnancy— Part 1

NICE 2019 hypertension in pregnancy mrcog part 2 exam

Post # 1
This blogpost is Part #1 of summary of latest NICE guideline “NG 133: Hypertension in pregnancy: diagnosis and management released in June 2019. As this is a long guideline, so I will be covering the topic in 2 posts.
This post covers diagnosis / management of hypertension, gestational hypertension, pre-eclampsia (PET) during pregnancy. This guideline has significant changes in recommendations. I have tried my best to extract all the important points.
You must go through the original guideline, which can be downloaded here: NG133
Let me know in comments if I need to add more to the post. 
Thanks

You can access the Part #2 here: NICE: 133 Hypertension in Pregnancy— Part 2

Hypertension in pregnancy: diagnosis and management
Some important numbers (from old guideline)
  • Eclampsia rate fallen in UK 
  • HTN remains one of leading cause of Maternal Death
  • Severe maternal morbidity 1/3 due to HTN
  • ICU admitted with PET/eclampsia: 1 in 20 (5%)
  • Stillbirth without anomaly (with PET): 1 in 20 (5%)
  • 8-10% ALL preterm births due to HTN disorders
  • Primigravida 1 in 250 (0.4%) will deliver before 34wks
  • In PET Less than 10th centile of birth weight for gestation
  •     20-25% preterm births
  •     14-19% term birth
Reducing the risk of hypertensive disorders in pregnancy
Symptoms of Pre-eclampsia
  • Seek immediate advice if:
    • Severe headache
    • Vision problem (blurring/flashing)
    • Severe pain below ribs
    • Vomiting
    • Sudden swelling of face, hands or feet
Antiplatelet agents
  • Advised to take 75-150 mg aspirin daily from 12 wks until birth of baby
    • One high risk factor
    • > One moderate risk factor
High Risk
Moderate Risk
H/o HTN in previous pregnancy
First pregnancy
Chronic kidney disease
Age ≥40 yrs
Autoimmune disease (SLE, APS)
Pregnancy interval >10 yrs
Type 1/2 DM
BMI ≥35 kg/m 2 at 1st visit
Chronic HTN
Family history of PET

Multi-fetal Pregnancy
  • DONOT use following with the aim of prevention of hypertensive disorders in pregnancy 
    • Nitric oxide donors, progesterone, diuretics, LMWH
  • Do not recommend 
    • Mg, Folic acid, antioxidants (Vit C & E), fish oils or algal oils, garlic
  • No restriction of dietary salt
  • Same advice for rest, exercise and work 
Assessment of proteinuria in hypertensive disorders of pregnancy
  • Interpret proteinuria measurements in context of full clinical review (symptoms, signs & other tests)
  • Use automated reagent-strip reading device for dipstick screening (in secondary care settings)
  • Dipstick screening positive (≥1+) use albumin:creatinine ratio or protein:creatinine ratio to quantify proteinuria
  • To quantify proteinuria
    • Do not use first morning urine void
    • Do not routinely use 24-hour urine collection
  • If using protein:creatinine ratio (PCR)
    • Threshold for significant proteinuria 30 mg/mmol 
    • If ≥30 mg/mmol + uncertainty about diagnosis Consider re-testing on new sample alongside clinical review
  • If using albumin:creatinine ratio (ACR)
    • Diagnostic threshold 8 mg/mmol
    • If ≥8mg/mmol + uncertainty about diagnosis Consider re-testing on new sample alongside clinical review
  • ** both PCR and ACR haven high sensitivity and specificity at thresholds of 30mg/mmol & 8 mg/mmol respectively. Either of these can be used depending on local availability
Management of chronic hypertension in pregnancy
Pre-pregnancy advice
  • Offer referral to specialist in hypertensive disorders of pregnancy
  • Advice women taking ACE or ARBS or thiazide/thiazide-like diuretics 
    • risk of congenital abnormalities if taken during pregnancy 
    • Discuss alternative drugs if planning pregnancy, or if these drugs taken for conditions like renal disease
    • If get pregnant stop ACE/ ARB (preferably within 2 days of pregnancy notification) & offer alternatives
  • Other than ACE/ARB/Thiazide diuretics limited evidence for risks for congenital malformations 
Treatment of Chronic HTN
  • Offer advice on weight management, exercise, healthy eating, lower salt in diet
  • Continue anti-hypertensive treatment if safe or switch to an alternative, unless
    • sustained systolic BP is less than <110 mmHg or 
    • sustained diastolic BP <70 mmHg or 
    • woman has symptomatic hypotension
  • Chronic HTN + no t/m offer antihypertensive t/m if:
    • sustained systolic BP ≥140 mmHg or 
    • sustained diastolic BP ≥90 mmHg
  • Aim for target BP 135/85 mmHg 
  • Consider
    • Labetolol for chronic HTN in pregnancy
    • Nefidipine if labetolol not suitable 
    • Methyldopa if both labetalol/ nefidipine not suitable
  • Offer aspirin 75-150 mg once daily from 12 wks
  • Offer placental growth factor (PIGF)-based testing to rule out PET b/w 20wks and up to 35 wks (if suspected to develop PET)
Antenatal appointments
  • Additional appointments depending on individual needs
    • If poorly controlled HTN weekly
    • If well controlled HTN every 2 - 4 wks
Timing of birth
Chronic HTN + BP <160/110 mmHg with/ without treatment
  • Before 37 wks do not offer planned early birth before 37wks (unless other medical indications)
  • After 37 wks timing of birth to be agreed b/w mother & senior obstetrician
  • If early birth needed offer steroids and magnesium sulfate (if indicated)
Postnatal investigation, monitoring and treatment
Chronic HTN + delivered measure BP after birth
    • Daily x first 2 days
    • At least once b/w day 3 & 5 
    • As clinically indicated (if anti-htn t/m changed)
  • Aim keep BP < 140/90 mmHg
  • Continue anti-htn t/m if required
  • Review anti-htn t/m 2 wks after birth
  • If used methyldopa stop within 2 days & change to alternative
  • Offer Medical Review 6-8 wks postnatal with GP/specialist 
Management of gestational hypertension
Assessment and treatment
  • Full assessment in secondary care settings
  • Take account of gestation at presentation
  • Additional assessment and follow up needed in
    • Nulliparaous Age ≥40 Pregnancy interval >10 yrs
    • Family h/o PET
    • Multi-fetal pregnancy BMI≥35
    • H/o Gestational HTN/PET Pre-existing vascular disease
    • Pre-existing kidney disease

Management of pregnancy with gestational hypertension (Ref: NICE)

Hypertension
BP 140/90 — 159/109 mmHg
Severe Hypertension
BP ≥160/110 mmHg
Admission to hospital
Not routinely
Admit
If BP falls below 160/110 manage as for HTN
Antihypertensive Drug t/m
Offer if BP remain >140/90
Offer to ALL
Target BP once on t/m
≤135/85 mmHg
≤135/85 mmHg
BP measurement
Once or twice per week until ≤135/85 mmHg
Every 15-30 min untill <160/110 mmHg
Dipstick proteinuria
Once or twice a week
Daily while admitted
Blood tests
FBC, LFT, RFT at presentation & then weekly
FBC, LFT, RFT at presentation & then weekly
PlGF-based testing
ONCE if PET suspicion
ONCE if PET suspicion
Fetal assessment
Offer FHR auscultation each visit
USG at diagnosis & if normal repeat every 2-4 wks (if clinically indicated)
CTG only if clinically indicated
Offer FHR auscultation each visit
USG at diagnosis & if normal repeat every 2-4 wks (if clinically indicated)
CTG only if clinically indicated

  • Offer PIGF-based testing to help rule out PET in women presenting with suspected PET b/w 20 wks and up to 35 wks
  • Consider
    • Labetolol to treat gestational hypertension
    • Nefidipine if labetaolol not suitable
    • Methyldopa if both labetolol & nefidipine not suitable
    • Choose according to side-effects, risks & woman preference
  • Do not offer bed rest as t/m of gestational HTN
Timing of Birth
Gestational HTN BP <160/110 mmHg
  • Before 37 wks do not offer planned early birth before 37wks (unless other medical indications)
  • After 37 wks timing of birth to be agreed b/w mother & senior obstetrician
  • If needed early birth offer steroids/ magnesium sulfate (if indicated)
Postnatal investigation, monitoring and treatment
  • Gestational HTN + given birth measure BP after birth
    • Daily x first 2 days
    • At least once b/w day 3 & 5
    • As clinically indicated (if anti-htn t/m changed)
  • Gestational HTN + given birth
    • Continue anti-htn t/m if required
    • Advice that duration of t/m will be similar to antenatal t/m (may be longer)
    • Reduce anti-htn t/m if BP falls <130/80 mmHg
  • If taken methyldopa stop within 2 days & change to other drug (if needed)
  • Gestational HTN + not taken t/m + given birth start anti-htn t/m if BP ≥150/100 mmHg
  • Write care plan for women being transferred to community & include
    • Who will follow up 
    • BP check frequency
    • Threshold for reducing or stopping t/m
    • Indications for referral to primary care for BP review
  • Gestational HTN + remain on anti-htn t/m Offer medical review (GP/ specialist) 2 wks after transfer to community care
  • ALL women with gestational HTN Offer medical review (GP/Specialist) 6-8 wks after birth
Management of pre-eclampsia
Assessing pre-eclampsia
  • Assessment to be performed by trained person
  • Full clinical assessment at each antenatal appointment 
  • Offer admission if ANY of the concerns 
    • Sustained systolic BP ≥160 mmHg
    • New or persistent
      • creatinine ≥90 ÎĽmol/l or ≥1mg/100ml
      • ALT ( >70 IU/l or twice upper limit of N)
      • in platelet count (<150000/ÎĽliter)
    • Signs of impending eclampsia/ PE
    • Suspected fetal compromise
    • Any other clinical signs that cause concern (2019)
Risk prediction models
  • Consider using fullPIERS or PREP-S for most appropriate place of care/ threshold for interventions
    • fullPIERS used any time in pregnancy
    • PREP-S used only up to 34 wks
    • Both models do not predict outcomes for babies
  • Offer
    • Labetalol to treat hypertension with PET
    • Nefidipine if labetalol not suitable
    • Methyldopa if both labetolol & nefidipine not suitable
    • Choose according to pre-existing treatment side-effects, risks & woman preference
Treatment of pre-eclampsia

Management of pregnancy with pre-eclampsia

Hypertension:
BP 140/90 — 159/109 mmHg
Severe Hypertension
BP ≥160/110 mmHg
Admission to hospital
Admit if any clinical concerns for mother/baby
High risk of adverse events (fullPIERS or PREP-S predicted)
Admit
If BP <160/110 mmHg manage as for HTN
Antihypertensive pharmacological treatment
Offer if BP >140/90 mmHg
Offer to ALL
Target BP once on t/m
≤135/85 mmHg
≤135/85 mmHg
BP measurement
At least every 48 hrs
More frequently if admitted
Every 15-30 min until BP <160/110 mmHg , then
At least 4 times per day (while inpatient)
Dipstick proteinuria
Only repeat if clinically indicated
Only repeat if clinically indicated
Blood tests
FBC, LFT, RFT twice a week
FBC, LFT, RFT 3 times a week
Fetal assessment
Offer FHR auscultation at each visit
USG at diagnosis & if normal repeat every 2 wks
CTG at diagnosis & then only if clinically indicated
Offer FHR auscultation at each visit
USG at diagnosis & if normal repeat every 2 wks
CTG at diagnosis & then only if clinically indicated
Timing of Birth
  • Record maternal and fetal threshold for planned early birth before 37 wks
  • Thresholds could include but not limited to
    • Uncontrolled BP in spite of ≥3 classes of drugs
    • Maternal pulse O2 <90%
    • Progressive deterioration of LFT, RFT, Platelets or hemolysis
    • Ongoing neurological feature like serve headache, eclampsia
    • Placental abruption
    • Reversed end-diastolic flow in umbilical artery doppler/ non-reassuring CTG or stillbirth
    • Other features (not listed) may also be considered for early delivery
  • Any decision for delivery Involve senior obstetrician
  • Birth planned discuss with anaesthetic team / neonatal team (if complications to neonate anticipated)
  • If planned early delivery corticosteroids + Mg Sulphate (if indicated)
Timing of birth in pre-eclampsia women (NICE)
Weeks of pregnancy
Timing of Birth
Before 34 wks
Continue surveillance unless indications for planned early delivery
Offer I/V magnesium sulfate and corticosteroids 
From 34 - 36+6 wks
Continue surveillance unless indications for planned early delivery
When considering early birth take into account fetomaternal wellbeing, risk factors and neonatal unit bed availability
Consider I/V magnesium sulfate and corticosteroids 
37wks onwards
Initiate birth within 24 hrs

Postnatal investigation, monitoring and treatment (including after discharge from critical care)
Blood pressure
PET + given birth + did not take anti-htn t/m
  • Check BP
    • Inpatient : at least 4 times per day
    • At least once b/w day 3 & 5
    • If abnormal on days 3-5 on alternate days until normal BP
  • If BP ≥150/100 mmHg start anti-htn t/m
  • PET + given birth ask about severe headache & epigastric pain each time when BP checked
PET+given Birth + took anti-htn t/m Continue t/m after birth
    • BP <140/90 Consider reducing t/m
    • BP <130/80 Reduce t/m
  • If taken methyldopa stop within 2 days of delivery & change to another if necessary
  • Offer transfer to community if ALL criteria met
    • No pre-eclampsia symptoms
    • BP with or without t/m : ≤150/100 mmHg
    • Blood tests stable or improving
  • Write care plan for women being transferred to community & include ALL
    • Who will  provide follow up (medical review if needed)
    • BP check frequency
    • Threshold for reducing or stopping t/m
    • Indications for referral to primary care for BP review
    • Self-monitoring for symptoms 
  • PET + remain on anti-htn t/m offer medical review (GP/ specialist) 2 wks after transfer to community care
  • ALL women with PET offer medical review (GP/Specialist) 6-8 wks after birth
  • Haematological and biochemicaL monitoring. 
Women with PET with mild or moderate HTN or after step-down from critical care

  • Check platelet, transaminases and S.creatinine 72 hrs after birth or step-down
    • If results are normal Do not repeat
    • If results not normal repeat as clinically indicated till results return to normal
  • PET + given birth do urinary reagent-strip test 6-8 wks after birth
  • PET + still proteinuria ≥1+ at 6-8 wks Offer further review at 3 months to assess kidney function (GP/Specialist) 
  • If abnormal kidney function consider referral for specialist kidney assessment

5 comments:

  1. Dear dr Rubaab really it’s very precise summery done in a professional way.i appreciate ur effort.its very easy to digest.stay blessed

    ReplyDelete
  2. drrubab v well summarised and good effort .may allah bless you with immense happiness .ameen

    ReplyDelete
  3. Informative Post. If you are looking for best gynecologist in Bhubaneswar then Dr SN Mohanty is the leading & best gynecologist in Bhubaneswar.

    ReplyDelete
  4. under severe ghtn, ctg should also be done at diagnosis i guess mam.

    ReplyDelete
  5. God bless you mam 🙏 always thnks for nice effort

    ReplyDelete