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PREEKLAMSIA

dr. FRIANTON TS,Sp.OG (K)

DINAS KESEHATAN KABUPATEN CILACAP


TAHUN 2019
TERMINOLOGI
HIPERTENSI DALAM KEHAMILAN (HDK)

HIPERTE
HIPERTE
NSI NSI
GESTASI
KRONIS
ONAL
HDK
SUPERIMP SINDRO Cunningham et.al, 2018. Williams
OSED MA
PREEKLA PREEKLA Obstetrics, 25 ed and ACOG, 2013
MSIA MSIA MedScape, Kee-Hak Lim, MD; Ronald M Ramus, MD 
Preeclampsia Updated: Feb 16, 2018
8/3/22 2
HIPERTENSI
DALAM
KEHAMILAN (HDK)
(HYPERTENSIVE DISORDERS)
TERMINOLOGI DAN DIAGNOSIS .
(ISSHP, 2000; 2014)
HT HT
KLASIFIKASI DASAR HDK : White- KRONI
1. HIPERTENSI KRONIK, coats S
HT
2. HIPERTENSI KEHAMILA
N
GESTASIONAL,
3. DE NOVO - PREEKLAMSIA
atau SUPERIMPOSED
PREEKLAMSIA,
4. HIPERTENSI WHITE-COAT. PE
de novo/
HT
GESTASION
AL
superimpo
sed

James D, et.al., 2017. High-Risk Pregnancy, management option, 5th ed.


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KLASIFIKASI HDK
I. GESTASIONAL HIPERTENSI,
II. GESTASIONAL PROTEINURIA,
III. PE (HT ± PROTEINURIA),
IV. KRONIK HIPERTENSI,
V. SUPERIMPOSED PE,
VI. SUPERIMPOSED PEB.

Foley MR, et., 2018. Obstetric


Intensive Care Manual.
DIAGNOSIS HDK
HIPERTENS
I 1. HT + P(-) + UK ≥ 20 
HIPERTENSI GESTASIONAL
≥ 140/90
1 2. HT + P(-) + UK < 20 
HIPERTENSI KRONIK

3. HT + P (+/-) + UK ≥ 20 
PROTEIN PROTEIN SINDROMA PREEKLAMSIA
URIA URIA
POSITIF NEGATIF 4. HT + P (-)  P (+/-) UK ≥ 20
2 3  PREEKLAMSIA
SUPERIMPOSSED

Cunningham et.al, 2018. Williams MedScape, Kee-Hak Lim, MD; Ronald M Ramus,
Obstetrics, 25 ed and ACOG, 2013 MD  Preeclampsia Updated: Feb 16, 2018
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PREEKLAMSIA
H
HT (HIPERTENSI) : T
 TEKANAN DARAH ≥
140/90.
 TEKANAN SISTOLIK NAIK
P
E
30, DIATOLIK NAIK 15.
 DELTA HIPERTENSI 
KENAIKAN MAP PADA
TRIMESTER III
 HIPERTENSI White Coats,
adalah DIPERIKSA (Dr/Per/
Bidan) ≥ 140/90, monitor 24 P
R
O

jam < 140/90


T

James D, et.al., 2017. High-Risk


+/
-

Pregnancy, management option, 5th ed.


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Sindroma PREEKLAMSIA
 Diskripsi yang paling baik, adalah sindroma spesifik kehamilan yang
pada hakekatnya dapat mempengaruhi setiap sistem organ.

 Dasar diagnosis- paling sederhana- adalah TEKANAN DARAH ≥ 140/90


mmHg ( 2 X pemeriksaan, ≥ 4 jam- 1 mgg) + POSITIF PROTEINURIA
( gambaran kerusakan endothelial-karakteristik sindroma Preeklamsia)

 Abnormal ekskresi PROTEIN, adalah 300 mg/ 24 jam, atau rasio protein :
kreatinin urine ≥ 0,3, atau persisten 30 mg/dL (1+ dipstik).
Foley MR, et., 2018. Obstetric Intensive Care
Manual.
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PREEKLAMSIA BERAT
(Gabbe, et.al, 2017; Cunningham, et.al 2018; Lim KH, 2018)

Ditandai (salah satu): HIPERTENSI (baru) tanpa


proteinuria, didiagnosis PE, jika
 Tek sistolik >/= 160 mmHg, atau didapatkan salah satu :
tekanan diastolik >/= 110 mmHg.
 Kegagalan fungsi hati,  Trombositopenia,
 Insufisiensi ginjal progresif,  Serum kreatinin > 1,1 mg/dl, atau
2 kali lipat Normal,
 Gangguan serebral atau pandangan
(baru muncul),  SGOT dan SGPT 2 kali Normal,
 Edema pulmonum,  Edema pulmonum,
 trombositopenia  Gangguan serebral dan
pandangan.

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Superimposed preeclampsia
One or more of the following
criteria:
1. New onset of proteinuria (≥300 mg in 24
hours without prior proteinuria) after 20
weeks in a woman with chronic HTN or
sudden increase in proteinuria in a
woman with known proteinuria before or
early in pregnancy

2. A sudden increase in
hypertension previously well
controlled or escalation of antihypertensive
medication to control BP

Berghella V, 2017. Maternal-Fetal Evidence Based Guidelines, 3rd ed


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Superimposed preeclampsia with severe
features
Superimposed preeclampsia and one or more of the following
criteria:
1. Severe range of BP (≥160/110 mmHg) despite escalation of
antihypertensive medication
2. Platelet count <100,000/mm3
3. Increased hepatic transaminases (AST and/or ALT) two times the upper
limit of normal concentration at a particular laboratory
4. New onset or worsening renal insufficiency (creatinine ≥1.1
mg/dL or a doubling of the serum creatinine)
5. Pulmonary edema
6. Persistent neurological symptoms (e.g., headache, visual changes)

Berghella V, 2017. Maternal-Fetal Evidence Based Guidelines, 3rd ed


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Eclampsia
Seizures (grand mal) in the presence of
preeclampsia and/or HELLP
syndrome.
Berghella V, 2017. Maternal-Fetal Evidence Based Guidelines, 3rd ed

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HELLP syndrome
Tennessee Classification (most commonly used)

• Hemolysis as evidenced by an abnormal peripheral smear in


addition to either serum LDH >600 IU/L or total bilirubin ≥1.2
mg/dL (≥20.52 μmol/L)
• Elevated liver enzymes as evidenced by an AST or ALT two
times the upper limit of normal concentration at a particular
laboratory
• Platelets <100,000 cells/mm3.
• If all the criteria are met, the syndrome is defined “complete”; if only
one or two criteria are present, the term “partial HELLP” is preferred.

Berghella V, 2017. Maternal-Fetal Evidence Based Guidelines, 3rd ed

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ATYPICAL PREECLAMPSIA
The criteria for atypical
preeclampsia include gestasional
proteinuria or FGR plus one or more of
the following symptoms of preeclampsia :
hemolysis, thrombocytopenia, elevated
liver enzymes, early signs and symptoms
of preeclampsia-eclampsia earlier than 20
weeks, and late postpartum preeclampsia-
eclampsia ( > 48 hours postpartum).
Gabbe et.al, 2017

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Risk factors- preeclampsia
Risk factors for preeclampsia and their odds
ratios are as follows [2] :

1. Nulliparity (3:1)
2. Age older than 40 years (3:1)
3. Black race (1.5:1)
4. Family history (5:1)
5. Chronic renal disease (20:1)
6. Chronic hypertension (10:1)
7. Antiphospholipid syndrome (10:1)
8. Diabetes mellitus (2:1)
9. Twin gestation (but unaffected by zygosity) (4:1) MedScape, Kee-Hak Lim, MD; Ronald M
10. High body mass index (3:1) Ramus, MD  Preeclampsia Updated: Feb 16,
11. Homozygosity for angiotensinogen gene T235 (20:1) 2018
12. Heterozygosity for angiotensinogen gene T235 (4:1)

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Penanganan
 Hanya persalinan obat  Pasien dengan PEB
preeklamsia. induksi persalinan
 Pasien dengan PE tidak berat seharusnya dilakukan
perlu induksi setelah umur setelah umur
kehamilan 37 mgg. kehamilan 34 mgg.
 Sebelumnya pasien biasanya diawasi  Dalam kasus ini, memberatnya
dengan ketat atau dirawat untuk penyakit dipertimbangkan
perkembangan, perburukan atau dengan risiko prematuritas
komplikasi PE, dan imaturitas janin
janin.
ditangani ekspektatif dengan
pemberian kortikosteroid guna  Dalam kondisi darurat kontrol
memacu pematangan paru janin untuk TD dan kejang harus
persiapan persalinan prematur. diprioritaskan.

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MgSO4 MgSO4 ADALAH OBAT
PILIHAN UNTUK PENCEGAHAN
EKLAMSIA, MENURUNKAN 59%
 DOSIS AWAL 4 gram iv RISIKO EKLAMSIA, 36%
BOLUS, DILANJUTKAN SOLUSIO PLASENTA, 46%
DENGAN DRIPS 8 gram (STATISTIK TIDAK SIGNIFIKAN)

20 tpm. KEMATIAN MATERNAL.


 SYARAT PEMBERIAN MgSO4 ADALAH
 PEMBERIAN ULANG iv 2 gr REFLEKS PATELLA +, URINE OUTPUT >30
(BB≤ 70 kg), ATAU 4 gr (BB> CC/JAM, DAN REPIRASI > 16 KALI/MENIT,
70 kg), MINIMAL 3-5/ 5-10 SERTA TERSEDIA ANTIDOTUMNYA YAITU
Ca Gluconas.
MENIT KEMUDIAN
(JARANG),  TOKSISITAS MgSO4 BERUPA
 JIKA PERLU DAPAT DIBERIKAN HILANGNYA REFLEKS PATELLA,
Na-AMOBARBITAL 250 mg IV DEPRESI RESPIRASI, PERUBAHAN
MINIMAL 3-5 MENIT KONDISI JANTUNG, CARDIAC
ARREST.

8/3/22 Preeklamsia, Daliman.DM 18 16


REKOMENDASI PNPK-Preeklamsia
1. Pemberian MgSO4 pada PEB berguna
untuk mencegah terjadinya kejang
eklamsia atau kejang berulang.
2. Rute administrasi MgSO4 yang
dianjurkan adalah IV untuk mengurangi
nyeri pada lokasi suntikan.
3. MgSO4 merupakan pilihan utama pada
pasien PEB dibandingkan diazepam atau
fenitoin, untuk mencegah terjadinya
kejang/ eklamsia atau kejang berulang.
Level evidence Ia, Rekomendasi A

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ALTERNATIF OBAT ANTIHIPERTENSI, ADALAH :
OBAT
ANTIHIPERTENSI 1. Labetalol 20 mg iv bolus,
dilanjutkan 40 mg, 80 mg, 80 mg jika
diperlukan, setiap 10 menit dengan
DIBERIKAN APABILA
dosis maksimal total 220 mg.
TEKANAN SISTOLIK
≥160 DAN ATAU TEKANAN 2.Nifedipin 10-20 mg po, diulang
DIASTOLIK ≥110 tiap 30 menit (bisa sampai 8 x per 24 jam)
(NHBPEP-WG,2000; RCOG,2006: dalam Cunningham 2014).

3. Hydralazine 5-10 mg iv/ im, tiap 20


menit, dosis maksimal 30 mg.
4. Sodium nitroprusside dimulai 0,25
ug/kg/min sampai dosis maksimal 5
ug/kg/min (second line).(Cunningham,2018)

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Sample Order Set for Severe Intrapartum or Postpartum Hypertension
Initial First-line Management With Immediate-Release Oral Nifedipine*

Notify physician if systolic blood pressure (BP) is greater than or equal to 160 mm Hg or if diastolic
BP is greater than or equal to 110 mm Hg.

 Institute fetal surveillance if undelivered and fetus is viable.


1. If severe BP elevations persist for 15 minutes or more, administer nifedipine (10 mg
orally).
2. Repeat BP measurement in 20 minutes and record results. If either BP threshold is still
exceeded, administer nifedipine capsules (20 mg orally).
3. If BP is below thresh-old, continue to monitor BP closely. Repeat BP measurement in 20
minutes and record results. If either BP threshold is still exceeded, administer nifedipine
capsule (20 mg orally).
4. If BP is below thresh-old, continue to monitor BP closely. Repeat BP measurement in 20
minutes and record results. If either BP threshold is still exceeded, administer labetalol
(40 mg intravenously over 2 minutes) and obtain Give additional antihypertensive
medication per specific order.
 Once the aforementioned BP thresholds are achieved, repeat BP measurement every 10 minutes for 1 hour,
then every 15 minutes for 1 hour, then every 30 minutes for 1 hour, and then every hour for 4 hours.
Institute additional BP timing per specific order.
ACOG, 2017. COMMITTEE OPINION

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TERAPI HIPERTENSI KRONIK
1. PERUBAHAN GAYA HIDUP BERUPA DIET KAYA PROTEIN, BUAH, SAYUR,
RENDAH LEMAK, MENGURANGI SATURASI DAN TOTAL LEMAK, (MENGURANGI
MASUKAN GARAM SAMPAI < 2,4 gram/ HARI  TIDAK DIANJURKAN LAGI).
2. BEDREST DI RS DIHUBUNGKAN PENGURANGAN 42% HIPERTENSI BERAT, 47%
PERSALINAN PRETERM.

3. OBAT ANTIHIPERTENSI – METHYLDOPA, LABETALOL,


BETABLOKER, NIFEDIPIN, DIURETIK.
4. ACE-INHIBITOR KONTRAINDIKASI DIBERIKAN PADA TRIMESTER PERTAMA,
DIHUBUNGKAN DENGAN PENINGKATAN 2 KALI TERJADINYA MALFORMASI, DAN
JANGKA PANJANG IUGR, OLIGOHIDRAMNION, GAGAL GINJAL DAN KEMATIAN
NEONATUS.

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MANAJEMEN CAIRAN pada
PEB
1. Hindari pemberian • TOTAL CAIRAN secara
diuretik. umum seharusnya dibatasi
2. Resusitasi volume TIDAK LEBIH dari
cairan yang agresif
penyebab utama 1. 80 mL/jam, atau
untuk EDEMA 2. 1 mL/kg/jam, atau
PULMONUM. 3. (60-125 ml/jam)
3. Sedapat mungkin pasien harus
RESTRIKSI CAIRAN, minimal (Cunningham, 2018)
sampai periode DIURESIS
POSTPARTUM.

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Postpartum management
 Many patients will have a brief (up  If a patient is discharged with BP
to 6 hours) period of oliguria medication, reassessment and a BP
check should be performed, at the
following delivery
latest, 1 week after discharge
 Magnesium sulfate seizure
 Unless a woman has undiagnosed
prophylaxis is continued for 24
chronic hypertension, in most cases
hours postpartum of preeclampsia, the BP returns to
 Liver function tests and platelet baseline by 12 weeks’ postpartum
counts must document decreasing  Patients should be carefully
values prior to hospital discharge monitored for recurrent
 Elevated BP may be controlled with preeclampsia, which may develop up
nifedipine or labetalol to 4 weeks postpartum, and for
postpartum eclampsia that has occurred up to 6
weeks after delivery

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Offer women with pre-eclampsia who have
given birth transfer to community care if all of
the following criteria have been met:

 there are no symptoms of pre-eclampsia


 blood pressure, with or without
treatment, is 149/99 mmHg or lower
 blood test results are stable or improving.

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KOMPLIKASI PRE-EKLAMSIA
 IBU, BERUPA HELLP SYNDROME (20%), DIC (10%), EDEMA
PULMONUM (2-5%), SOLUSIO PLASENTA (1-4%), GAGAL GINJAL (1-
2%), KEJANG EKLAMSIA (<1%), PERDARAHAN SEREBRAL (<1%),
PERDARAHAN HEPAR (<1%) DAN KEMATIAN (JARANG).

 BAYI, BERUPA PERSALINAN PRETERM (15-60%), IUGR


(10-25%), KEMATIAN PERINATAL (1-2%), TRAUMA
HIPOKSEMIA-NEROLOGIK (<1%), MORBIDITAS
KARDIOVASKULER JANGKA PANJANG (TIDAK
DIKETAHUI)

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KOMPLIKASI EKLAMSIA
 KEMATIAN MATERNAL 1-2% DI NEGARA
MAJU, LEBIH DARI 10% DI NEGARA BERKEMBANG.
 KEMATIAN PERINATAL 6-12% DI NEGARA MAJU,
LEBIH DARI 25% DI NEGARA BERKEMBANG.
 SOLUSIO PLASENTA 7-10%, DIC 7-11%, HELLP 10-15%,
EDEMA PULMONUM 3-5%, GAGAL GINJAL 5-9%,
PNEUMONIA ASPIRASI 2-3%, CARDIOPULMONARY ARREST
2-5%, PERSALINAN PRETERM 50%.

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MORBIDITAS DAN MORTALITAS
JANGKA PANJANG PENDERITA
PREEKLAMSIA, TERNYATA
MENINGKAT SECARA BERMAKNA
DIBANDINGKAN BUKAN
PENDERITA PREEKLAMSIA,
TERHADAP KEJADIAN
HIPERTENSI, IHD,
STROKE, DAN
PENYEBAB LAIN
KEMATIAN.
Long-term cardiovascular consequences of preeclampsia. All
differences p ≤.001 except p = 0.03 for all-cause mortality.
(Data from Bellamy and colleagues, 2007.)

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Acute Treatment of Severe Hypertension in
Pregnancy

In the setting of  The goal of hypertension


severe hypertension treatment is to lower BP
to prevent
(SBP >160 mm Hg; cerebrovascular and
DBP >110 mm Hg), cardiac complications
antihypertensive while maintaining
treatment is uteroplacental blood flow
recommended. (ie, maintain BP around
140/90 mm Hg).

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Prophylactic treatment with
magnesium sulfate
 Prophylactic treatment with magnesium sulfate is indicated for
all patients with severe preeclampsia. However, no
consensus exists as to whether patients with mild preeclampsia
need magnesium seizure prophylaxis.

magnesium sulfate
 Although ACOG recommends

in severe preeclampsia, it has not recommended


this therapy in all cases of mild preeclampsia.
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Some Indications for Delivery
with Early-Onset Severe Preeclampsia (Cunningham, 2018):

Maternal ONE OR MORE


≤ 72 JAM
1. Persistent severe headache or visual changes; eclampsia
2. Shortness of breath; chest tightness with rales and/or SaO2 < 94 percent
breathing room air; pulmonary edema
3. Uncontrolled severe hypertension despite treatment
4. Oliguria < 500 mL/24 hr or serum creatinine 1.5 mg/dL
5. Persistent platelet counts < 100,000/L,
6. AST or ALT > 2 x upper limit of normal with RUQ or epigastric pain,
7. Suspected abruption, progressive labor, and/or ruptured
membranes,
Foley MR, et., 2018. Obstetric AFI = amnionic fluid index; EGA = estimated gestational age;
Intensive Care Manual. SaO2 = oxygen saturation.
From Sibai and Barton (2007).
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Fetal ONE OR MORE
≤ 72 JAM
1. Severe growth restriction—< 5th percentile for
EGA
2. Persistent severe oligohydramnios—AFI < 5 cm/
DVP < 2 cm.
3. Biophysical profile 4 done 4-6 hr apart
4. Reversed end-diastolic umbilical artery flow
5. Repetitive late or severe variable heart rate
deceleration,
6. Fetal death Foley MR, et., 2018. Obstetric Intensive
Care Manual.

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ABSTRACT: Patient care
emergencies may occur at any
Preparing for Clinical Emergencies
time in any setting, particularly in Obstetrics and Gynecology
the inpatient setting. It is
important that obstetrician–
gynecologists prepare themselves
Managing
Examples of Tools for
by assessing potential
emergencies, establishing
Clinical Emergencies
early warning systems, 1. Availability of appropriate emergency
designating specialized first supplies in a resuscitation cart (crash cart) or
responders, conducting kit
emergency drills, and 2. Development of a rapid response team
debriefing staff after actual 3. Development of protocols that include
events to identify strengths
and opportunities for clinical triggers
improvement. Having such 4. Use of standardized communication tools for
systems in place may reduce or huddles and briefs (eg, SBAR)
prevent the severity of medical
5. Implementation of emergency drills and
emergencies.
simulations
ACOG COMMITTEE OPINION Number
590, March 2014 (Replaces Committee Abbreviation: SBAR, Situation–Background–
Opinion Number 487, April 2011) Assessment–Recommendation.
(Reaffirmed 2018)

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Wassalamu’alaikum
warahmatullahi wabarakaatuh

Terima Kasih
Atas
perhatiannya

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