Download Free Medical Hypertensive Disorders In Pregnancy PowerPoint Presentation

Hypertensive Disorders In Pregnancy PowerPoint Presentation

DOWNLOAD MEDICAL POWERPOINT PRESENTATION

About This Presentation

Description : Check out this medical PowerPoint presentation titled "Hypertensive Disorders in Pregnancy” by Francis Kamwendo.

This medical PowerPoint presentation is about hypertensive disorders in pregnancy, a group of conditions characterized by high blood pressure during pregnancy. These disorders can range in severity and can lead to complications for both the mother and the developing fetus.

There are several types of hypertensive disorders in pregnancy, including:

Gestational hypertension: This is high blood pressure that develops after 20 weeks of pregnancy and usually resolves after delivery.
Chronic hypertension: This is high blood pressure that is present before pregnancy or is diagnosed before 20 weeks of pregnancy.
Preeclampsia: This is a serious condition that can develop after 20 weeks of pregnancy and is characterized by high blood pressure and signs of damage to other organ systems, such as the liver and kidneys.
Eclampsia: This is a rare but serious complication of preeclampsia that involves seizures.
HELLP syndrome: This is a rare but serious complication of preeclampsia that involves hemolysis (destruction of red blood cells), elevated liver enzymes, and low platelet count.

Risk factors for developing hypertensive disorders in pregnancy include obesity, pre-existing hypertension, diabetes, multiple gestations (twins, triplets), and a history of preeclampsia. Treatment for these disorders may include blood pressure monitoring, medication, and delivery of the baby. It is important for pregnant women to receive regular prenatal care to monitor for and manage any potential hypertensive disorders.

Tags : Hypertensive Disorders in Pregnancy, Gestational hypertension, Chronic hypertension, Preeclampsia, Eclampsia, HELLP syndrome, Obstetrics and Gynecology, Obstetrics and Gynecology PowerPoint presentation

Published on : Jun 20, 2023 | Views : 1688 | Downloads : 1

Shareable Url :

Embed Code :

Comment

Transcript

Slide 1-

Hypertensive Disorders in Pregnancy By Francis Kamwendo @ Nkhota-kota Adapted from Obstetrics Simplified by Diaa M. EI-Mowafi
Slide 2-

Classification PRE-EXISTING (CHRONIC) HYPERTENSION PRE-ECLAMPSIA Differential Diagnosis Complications Treatment 4. ECLAMPSIA
Slide 3-

Pre-existing (chronic) hypertension: Hypertension is present before pregnancy, detected in early pregnancy (before 20 weeks in absence of vesicular mole) and postpartum. Examples: essential hypertension, secondary to chronic renal disorders e.g. pyelonephritis and renal artery stenosis, coarctation of the aorta, systemic lupus erythematosus and pheochromocytoma.
Slide 4-

PRE-EXISTING (CHRONIC) HYPERTENSION Causes Essential hypertension: of unknown aetiology. Secondary to chronic renal disorder: e.g. Glomerulonephritis. Hydronephrosis. Pyelonephritis. Renal artery stenosis. Secondary to cardiovascular disease: e.g. Coarctation of the aorta. Polyartheritis nodosa. Systemic lupus erythematosus.
Slide 5-

PRE-EXISTING (CHRONIC) HYPERTENSION Causes Secondary to endocrine disorders: e.g. Primary aldosteronism. Phaeochromocytoma. Adrenocortical tumours. Diabetes mellitus.
Slide 6-

Effect of Pregnancy on Chronic Hypertension Blood pressure falls by the second trimester in most of cases, but rises during the third trimester to a level some what above that in early pregnancy. Deterioration of the underlying disease.
Slide 7-

Effect of Chronic Hypertension on Pregnancy Maternal: superimposed pre-eclampsia/ eclampsia in 15-20% of cases Foetal: Intrauterine growth retardation. Intrauterine foetal death.
Slide 8-

Treatment General and medical treatment As pre-eclampsia regarding the following: Rest Antihypertensives Observation
Slide 9-

Pregnancy-induced hypertension (PIH): Transient hypertension: Late onset hypertension, without proteinuria or pathologic oedema Pre-eclampsia: Hypertension with proteinuria and / or oedema after 20 weeks of pregnancy, but may be earlier in vesicular mole. Eclampsia: Pre-eclampsia + convulsions.
Slide 10-

Superimposed pre-eclampsia or eclampsia: Development of pre-eclampsia or eclampsia in pre-existing hypertension detected by a further increase of 30 mmHg or more in systolic blood pressure or 15 mmHg or more in diastolic blood pressure.
Slide 11-

PRE-ECLAMPSIA Incidence: 5-10%. Aetiology: Although eclampsia had been described since 200 years, no definite aetiology is found for PIH and it is still a disease of theories.
Slide 12-

Predisposing factors Primigravidae more than multigravidae. Pre-existing hypertension. Previous pre-eclampsia. Family history of pre-eclampsia. Hyperplacentosis i.e. excessive chorionic tissue as in hydatidiform mole, multiple pregnancy, uncontrolled diabetes mellitus and foetal haemolytic diseases. Obesity.
Slide 13-

Theories The uteroplacental bed Immunological factor Genetic factor Renin- angiotensin system Atrial natriuretic peptide (ANP) Prostaglandins Neutrophils
Slide 14-

Pathological Changes Vasospasm Coagulation status Sodium and water retention
Slide 15-

Diagnosis Signs Symptoms
Slide 16-

Signs Hypertension: Proteinuria (albuminuria): Oedema:
Slide 17-

Hypertension Blood pressure of 140/90 mmHg or more or an increase of 30 mmHg in systolic and/or 15 mmHg in diastolic blood pressure over the pre- or early pregnancy level.
Slide 18-

How to measure the blood pressure in pregnancy 1 The patient should rest for at least 30 min. after arriving to the clinic. Remove any tight clothing from the right arm. The patient lies comfortably on the left side that her back makes an angle of about 30o with the bed. The right arm is supported to be with the sphygmomanometer at the same level with the patient’s sternum i.e. her heart. Each cm above or below the level of the heart induces a difference of 0.7mmHg in blood pressure reading. She should lie undisturbed in this position for 2-3 min. before blood pressure is measured.
Slide 19-

How to measure the blood pressure in pregnancy 2 The cuff should be applied to the right upper arm with the connecting tubes pointing downwards, the centre of the rubber bag in the cuff is directly over the brachial artery leaving ante-cubital fossa free. Apply cuff firmly but not tightly around the arm. Feel the brachial artery and apply the stethoscope directly over it without undue pressure. Pump up cuff rapidly to 20-30 mmHg above the point at which the pulse sound disappears, and take blood pressure reading without delay.
Slide 20-

How to measure the blood pressure in pregnancy 3 Let air out slowly so that mercury falls steadily by 2-3 mm/sec. Blood pressure measurement phases (Korotkoff): Korotkoff I¾ Appearance of the sound¾ systolic reading. Korotkoff II¾ Accentuation of the sound. Korotkoff III ¾ Sound becomes harsh. Korotkoff IV¾ Sound becomes muffled¾ diastolic reading. Korotkoff V¾ Disappearance of the sound. Korotkoff I and IV is the reading for systolic and diastolic blood pressure respectively. If you wait the disappearance of the sound to take the diastolic reading (as in non-pregnant state) you may reach down to zero because of the hyperdynamic circulation during pregnancy.
Slide 21-

How to measure the blood pressure in pregnancy 4 Use the right arm for measuring because it is more convenient to the physician, but if the reading is 10 mmHg or more higher in the left arm use it in the future readings. The blood pressure should be measured in two occasions at least 6 hours apart.
Slide 22-

Proteinuria (albuminuria) It is urinary protein greater than 0.3gm/L in 24 hours collection or greater than 1gm/L in two random samples obtained at least 6 hours apart. It indicates glomerular damage and almost always occurs after hypertension. Proteinuria is usually in the range of 1-3 gm daily, of which 50-60% is albumin but in severe cases it may exceed 15gm.
Slide 23-

Oedema It is weight gain of more than 1 kg in any one week or 2.25 kg in any one month. Clinical oedema is present in about two-thirds of patients with PIH. However, two-thirds of pregnant women with clinical oedema do not develop hypertension.
Slide 24-

Symptoms These are usually manifestations of severe pre-eclampsia. Headache: usually frontal but may be occipital. It is due to cerebral oedema and hypertension. Visual disturbances: blurring of vision, flashes of light or blindness. Epigastric or right upper quadrant pain: due to enlargement and subcapsular hemorrhage of the liver. Nausea and vomiting: due to congestion of gastric mucosa and/ or cerebral oedema. Oliguria or anuria: due to kidney pathology.
Slide 25-

Investigations Complete urine examination: for proteinuria, pus cells, RBCs, casts, specific gravity, culture and sensitivity. Kidney function tests: serum uric acid > 6 mg % is abnormal during pregnancy. It is more specific for pre-eclampsia than creatinine. Coagulation status: Platelet count, fibrinogen and FDP as DIC may develop. Eye fundus examination. Tests for foetal well being: as ultrasound, daily foetal movement count, non-stress test, oxytocin challenge test (if needed).
Slide 26-

N.B. Imminent eclampsia: It is a state in which the patient is about to develop eclampsia. Usually there are: blood pressure much higher than 160 /110 mmHg, heavy proteinuria (+++or ++++), hyperreflexia, severe continuous headache, blurring of vision, epigastric pain. Fulminating pre-eclampsia: a rapidly deteriorating pre-eclampsia to be imminent eclampsia
Slide 27-

ppt slide no 27 content not found
Slide 28-

ppt slide no 28 content not found
Slide 29-

Differential Diagnosis Other causes of hypertension Other Causes of proteinuria Other causes of oedema
Slide 30-

Other Causes of proteinuria Contamination of urine by vaginal discharge this is excluded by examination of a midstream sample after cleansing the introitus with sterile water or saline or by using a catheter. Urinary infection: excluded by microscopic examination and culture of urine. Congestive heart failure and severe anaemia due to hypoxia of the kidney. Orthostatic proteinuria: Proteinuria is detected at the end of the day while it is absent in the morning. This is due to pressure of the lumbar spines on the left renal vein during standing
Slide 31-

Other causes of oedema General causes: cardiac, hepatic, renal or nutritional oedema. Local causes: as inflammatory or deep vein thrombosis (usually unilateral). Pressure of the gravid uterus on the pelvic veins may produce ankle oedema.
Slide 32-

Complications Maternal: Convulsions and coma (eclampsia). Cerebral haemorrhage. Renal failure. Heart failure. Liver failure. Disseminated intravascular coagulation. Abruptio placentae. Residual chronic hypertension in about 1/3 of cases. Recurrent pre-eclampsia in next pregnancies. Foetal: Intrauterine growth retardation (IUGR). Intrauterine foetal death. Prematurity and its complications.
Slide 33-

Treatment Prophylactic Curative
Slide 34-

Prophylactic Proper antenatal care: To detect the high risk patients who may develop PIH through the screening tests. Early detection of cases who have already developed PIH and examine them more frequently. Low dose aspirin: It inhibits thromboxane production from the platelets and the AII binding sites on platelets. A low dose (60 mg daily) selectively inhibits thromboxane due to higher concentration of such a low dose in the portal circulation than systemic affecting the platelets when they pass through the portal circulation. The Prostacyclin production from the systemic vessels will not be affected.
Slide 35-

Curative Delivery of the foetus and placenta is the only real treatment of pre-eclampsia. As the conditions are not always suitable for this, the treatment aims to prevent or minimize the maternal and foetal complications (see before) till reasonable maturation of the foetus.
Slide 36-

General measures:Observation: Maternal: blood pressure twice daily. urine volume and proteinuria daily, oedema daily, body weight twice weekly, fundus oculi once weekly, blood picture including platelet count, liver and renal functions particularly serum uric acid on admission. Foetal: daily foetal movement count, serial sonography, non-stress and stress test if needed.
Slide 37-

Medical treatment Antihypertensives: decrease the maternal cerebral and cardiovascular complications but do not affect the foetal outcome. Alpha-methyl-dopa (Aldomet): It reduces the central sympathetic drive. Dose: 250-500 mg every 6-8 hours up to a maximum dose of 4 gm/day. Its effect appears after 48 hours. A loading single dose of 2 gm may act within 1-2 hours. Side effects: headache, athenia and nightmares. Hydralazine (Apresoline): It is a vasodilator, increases renal and uteroplacental blood flow. Dose: 20 mg slowly IV initially followed by 5mg every 20 min. until diastolic blood pressure is 100-110 mmHg. This regimen is used for severe and acute hypertension. Oral hydralazine can be used in the chronic situation as a second line treatment in a dose of 25-75 mg/ 6 hours. Side effects: tachycardia, headache, flushing, nausea and vomiting. Calcium channel blockers (Nifedipine): It is a vasodilator acting by blocking the Ca influx into smooth muscle cells. It can be given sublingually (acts within 10 minutes) or orally (acts within 30 minutes) in a dose of 10-20 mg 2-3 times daily. The higher the starting blood pressure the greater is the hypotensive effect. Side effects: headache and flushing.
Slide 38-

Obstetric measures Timing of delivery Method of delivery Intrapartum care Postpartum care
Slide 39-

Timing of delivery: Severe pre-eclampsia is usually treated conservatively till the end of the 36th week to ensure reasonable maturation of the foetus. Indications of termination before 36th week include: Foetal: deteriorating placental function as judged by: intrauterine growth retardation, oligohydramnios, reduced foetal movements, abnormal foetal heart patterns, or failing biochemical results. Maternal: deteriorating maternal condition as judged by: blood pressure is sustained or exceeds 180/110 mmHg, urine proteinuria > 5 gm/24 hours, oliguria, evidence of DIC, or imminent or already developed eclampsia.
Slide 40-

Method of delivery: Vaginal delivery may be commenced in vertex presentation by: amniotomy + oxytocin if the cervix is favourable. prostaglandin vaginal tablet (PGE2) if the cervix is not favourable. Caesarean section is indicated in: Foetal distress. Late deceleration occurs with oxytocin challenge test. Failure of induction of labour. Other indications as contracted pelvis, and malpresentations.
Slide 41-

Intrapartum care: Close monitoring of the foetus is indicated. Proper analgesia to the mother. Anti-Hypertensives may be given if needed. 2nd stage of labour may be shortened by forceps.
Slide 42-

Postpartum care: Methergin (Ergometrine) is better avoided as it may increase the blood pressure. Continue observation of the mother for 48 hours. Anti- hypertensive drugs are continued in a decreasing dose for 48 hours.
Slide 43-

Thank you