Congenital Heart Disease
-
Upload
emira-ezuna -
Category
Documents
-
view
16 -
download
0
description
Transcript of Congenital Heart Disease
![Page 1: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/1.jpg)
CONGENITAL AND ACQUIRED
HEART DISEASES
FikrialiHidayahHafizah
Emira
![Page 2: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/2.jpg)
Changes in the circulation from fetus to newborn
![Page 3: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/3.jpg)
Congenital Heart Disease
• Heart defects are among the most common birth defects and are the leading cause of birth defect-related deaths• Approximately 8 people in 1000 are born with a congenital heart
defect• Many defects do not need treatment, but some complex congenital
heart defects require medication or surgery
![Page 4: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/4.jpg)
Causes
• Unknown (90%)• Genetic• Trisomies 13, 18, 21 & turner’s syndrome
• Environmental • Maternal infection (rubella), • Drugs (alcohol, warfarin)• Maternal illness (DM, phenylketonuria, and SLE)
![Page 5: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/5.jpg)
Classification
Acyanotic Cyanotic•Asymptomatic at birth•Cyanosis is late feature•Left to right shunt
•Bluish colour due to lack of oxygen in the body• Peripheral• Central
•Right to left shunt
•Atrial septal defects (ASD) – 7%•Ventricular septal defects(VSD) – 30%•Patent ductus arteriosus(PDA) – 12%
•Tetralogy of Fallot – 5%•Transposition of great arteries – 5%•Atrioventricular septal defect
![Page 6: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/6.jpg)
Atrial Septal Defect (ASD)
• Secundum (80%)• Defect in the center of the atrial septum involving foramen ovale
• Partial AVSD (20%)• Inter-atrial communication between the bottom end of the atrial septum
and the atrioventricular valves• Abnormal AV valves, with left AV valve which has three leaflets and tend
to leak (regurgitation valve)
![Page 7: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/7.jpg)
Clinical features
• Symptoms• Asymptomatic (commonly)• Recurrent chest infections / wheeze• arrhythmias
• Physical signs• Ejection systolic murmur (upper left sternal edge)• Fixed and widely split 2nd heart sound• Partial AVSD, pansystolic murmur from AV regurgitation
![Page 8: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/8.jpg)
Investigation • Chest radiograph• Cardiomegaly• Enlarged pulmonary arteries• Increased pulmonary vascular markings
• ECG• Secundum
• Partial right bundle branch block, right axis deviation• Due to R ventricular enlargement
• Partial • Superior axis (negative deflection)• Due to defect of the heart where the AV node is.• Displace the conduction to the ventricle superiorly.
• Echocardiography
![Page 9: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/9.jpg)
![Page 10: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/10.jpg)
Management
• Secundum• Cardiac catheterization with insertion of an occlusion device
• Partial • Surgical correction at 3-5 years old to prevent right heart failure
and arrhythmias in later life
![Page 11: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/11.jpg)
Complication
• Congestive heart failure• Arrhythmias• Pulmonary hypertension• Cyanosis dt Eisenmenger syndrome• Stroke
![Page 12: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/12.jpg)
VSD (30%)
• Defect anywhere in the ventricular septum, perimembranous (adjacent to the tricuspid valve) or muscular• Classification: i) Small VSD ii) Large VSD
![Page 13: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/13.jpg)
Small VSD
• Smaller than aortic valve (3mm)• Asymptomatic (common)• Physical signs: i) Loud pansystolic murmur at lower left sternal edge ii) Quiet pulmonary 2nd sound• Investigations: i) Chest radiography- Normal
ii) ECG – Normaliii) Echocardiography - Demonstrates the precise anatomy of defect
![Page 14: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/14.jpg)
Management of small VSD
• Mostly close spontaneously. No murmur with normal ECG on follow-up
• Prevention of bacterial endocarditis by maintaining good dental hygiene
![Page 15: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/15.jpg)
Large VSD
• > diameter of aortic valve• Clinical features– Symptoms• Heart failure with breathlessness and failure to thrive after 1 week• Recurrent chest infections
– Physical signs• Tachypnea, tachycardia and enlarged liver from heart failure• Soft pansystolic murmur / no murmur• Apical mid-diastolic murmur• Loud pulmonary 2nd sound
![Page 16: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/16.jpg)
![Page 17: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/17.jpg)
Management of large VSD
• Drug therapy with diuretics combined with captopril• Surgery was performed at 3- 6 months old in order to :– Manage heart failure and failure to thrive– Prevent permanent lung damage from pulmonary hypertension and
high blood pressure
![Page 18: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/18.jpg)
PERSISTENT DUCTUS ARTERIOSUS (PDA)
• Ductus arteriosus connects the pulmonary artery to the descending aorta.
• In term infants, it normally closes shortly after birth.• In PDA, it has failed to close by 1 month after the expected
date of delivery due to a defect in the constrictor mechanism of the duct.
• In the preterm infant, the presence of PDA is not from CHD but due to prematurity.
![Page 19: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/19.jpg)
![Page 20: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/20.jpg)
CLINICAL FEATURES
Continuous murmur beneath the left clavicle. Continuous because the pulmonary artery pressure < aorta throughout the
cardiac cycle.
Increased pulse pressure causing a collapsing or bounding pulse
When the duct is large there will be increased pulmonary blood flow with heart failure & pulmonary hypertension
![Page 21: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/21.jpg)
INVESTIGATIONS
Chest Radiograph- Normal or enlarged heart with increased pulmonary vasculature.
ECG- Usually normal
Echocardiograph- Diagnostic investigation.
![Page 22: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/22.jpg)
Management of PDA
Closure with coil or occlusion device introduced via a catheter at 1 year old.
![Page 23: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/23.jpg)
CYANOTIC HEART DISEASES
![Page 24: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/24.jpg)
TETRALOGY OF FALLOT
![Page 25: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/25.jpg)
TETRALOGY OF FALLOT (TOF)
• Most common cyanotic CHD
• Consist of 4 cardinal anatomical features A large VSD Overriding of the aorta Subpulmonary stenosis causing right ventricular tract obstruction Right ventricular hypertrophy
![Page 26: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/26.jpg)
![Page 27: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/27.jpg)
CLINICAL FEATURES
SYM
PTO
MS
Presence of murmur in the first 2 month of life
Severe cyanosis Depends on the severity of the subpulmonary stenosis
Hypercyanotic spells
Rapid increase in cyanosis, irritability / inconsolable crying, breathlessness
and pallor
May lead to myocardial infarction, cerebrovascular accident or death if
not treated earlier
Squatting on exercise
![Page 28: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/28.jpg)
![Page 29: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/29.jpg)
CLINICAL FEATURES
SIG
NSClubbing of the fingers and toes will develop in
older children
A loud harsh ejection systolic murmur at the left sternal edge from
day 1 of life
With increasing right ventricular outflow tract
obstruction, the murmur will shorten and cyanosis will
increase
![Page 30: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/30.jpg)
INVESTIGATIONS
Chest Radiograph- Boot-shaped heart, pulmonary artery bay and decreased pulmonary vascular markings.
ECG - Normal at birth. Right ventricular hypertrophy when older.
Echocardiograph- Demonstrate the cardinal features.
![Page 31: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/31.jpg)
![Page 32: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/32.jpg)
MANAGEMENT
• Initial management : medical palliation with IV PGE infusion.• Corrective surgery at 6 months or single stage repair at 1 -2
years closing VSD & artificial patch to relieve RV outflow obstruction.
• Modified Blalock Taussig shunt• After surgical repair : Need life-long follow up for late
ventricular dysfunction.
![Page 33: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/33.jpg)
![Page 34: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/34.jpg)
MANAGEMENT (HYPERCYANOTIC SPELL)
• Knee-chest/squatting position.• Administer 100% oxygen.• IV morphine• IV propranolol• IV crystalloid or colloid• IV sodium bicarbonate• Heavy sedation, intubation & mechanical ventilation• IV phenylephrine• Emergency Blalock Taussig shunt
![Page 35: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/35.jpg)
![Page 36: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/36.jpg)
![Page 37: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/37.jpg)
TRANSPOSITION OF THE GREAT ARTERIS
![Page 38: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/38.jpg)
TRANSPOSITION OF THE GREAT ARTERIES (TGA)
• The aorta is connected to the right ventricle and the pulmonary artery is connected to the left ventricle.
• The deoxygenated blood returning to the right side of the heart is being pumped out to the body while the well-oxygenated blood returning from the lungs enters the left side of the heart and is pumped back to the lungs.
• Incompatible with life unless there are VSD, ASD & PDA present.
![Page 39: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/39.jpg)
![Page 40: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/40.jpg)
![Page 41: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/41.jpg)
CLINICAL FEATURES
SYMPTOM
Neonatal cyanosis- Usually on day 2 of life when ductal closure leads to a marked reduction in mixing desaturated & saturated blood.- Cyanosis will be less severe if there is more mixing of blood from associated abnormalities.
![Page 42: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/42.jpg)
CLINICAL FEATURES
SIGNS
Cyanosis
No murmur but systolic murmur from increased flow or stenosis
within the left ventricular (pulmonary) outflow tract
Second heart sound is often loud & single
![Page 43: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/43.jpg)
INVESTIGATIONS
Chest Radiograph- Narrow upper mediastinum with an ‘egg on side’ appearance.
ECG - Rarely help, usually normal.
Echocardiograph- Demonstrate abnormal arterial connection.
![Page 44: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/44.jpg)
![Page 45: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/45.jpg)
MANAGEMENTSimple TGA (intact ventricular septum)
- IV PGE infusion promotes intercirculatory mixing at PDA.- Early balloon atrial septostomy (BAS) if restrictive interatrial communication.
- Surgical repair of choice : Arterial swicth operation 2 – 4 weeks age.
TGA with VSD- Does not usually require intervention during early neonatal period.
- Elective one-stage arterial switch operation + VSD closure < 3 months age.
TGA with VSD and PS- Blalock Taussig shunt during infancy followed by Rastelli repair at 4 – 6 years of
age.
![Page 46: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/46.jpg)
![Page 47: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/47.jpg)
![Page 48: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/48.jpg)
![Page 49: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/49.jpg)
RHEUMATIC FEVER(RF) & RHEUMATIC HEART DISEASE(RHD)
![Page 50: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/50.jpg)
RHEUMATIC FEVER(RF)
RHEUMATIC HEART DISEASE(RHD)
Is an acute, immunologically-mediated, multi-system inflammatory that follows an episode of GAS after interval of few weeks (<1 month)
Is the most serious complication of acute RF & end result of carditis, which affects 30-45% of patients with acute RF.
![Page 51: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/51.jpg)
RHEUMATIC FEVER
![Page 52: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/52.jpg)
PATHOGENESISBody produce antibody against GAS that cause pharyngitis
These antibody cross react with human tissues because of antigenic similarity between strep components & human CT (MOLECULAR MIMICRY)
Immunological mediated inflammation & damage to human tissues (heart, joint, brain & CT)
After latent period 1-3 weeks, damage to heart valves, joints, subcutaneous tissue & basal ganglia of brain.
Most patient with RF has elevated 1/ more ASOT
![Page 53: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/53.jpg)
WHY NOT ALL PATIENTS THAT HAVE GAS THROAT INFECTION WILL HAVE
RF?
1) MICROORGANISM VARIABLE• Only certain strain produce
immunologically active antigen
2) HOST VARIABLE• Some of us produce large
amount of antibody after infection
![Page 54: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/54.jpg)
CLINICAL FEATURES• Latent period : 1-3 weeks between the onset & previous
pharyngeal infection.• Symptoms are grouping together as no single laboratory/
symptoms can suggest ARF.• Modified Jones Criteria:
![Page 55: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/55.jpg)
MODIFIED JONES CRITERIA:• Initial episodes of ARF:-2 major-1 major + 2 minor-plus evidence of previous GAS infection
• Recurrent attack of ARF:-2 major-1 major + 2 minor-3 minor-plus evidence of previous GAS infection
MAJOR MINOR
SPACE
S-SUBCUTANEOUS NODULEP-PANCARDITISA-ARTHRITISC-CHOREA (sydeham chorea)E-ERYTHEMA MARGINATUM
LEAF
L-LEUCOCYTOSISE-ESR (elevated)A-ArthralgiaF-Fever
*raised CRP & ASOT*pallor, anorexia, LOW
![Page 56: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/56.jpg)
![Page 57: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/57.jpg)
![Page 58: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/58.jpg)
INVESTIGATIONS
1. Throat swab = for throat culture group A beta hemolytic2. ASOT = elevated > 200 Todd units3. FBC = anemia & leukocytosis4. ESR & CRP = elevated5. CXR & ECG = carditis features6. Echocardiogram = delineate valve involvement
![Page 59: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/59.jpg)
MANAGEMENT
1) Bed rest2) Anti-strep therapy:• IV/oral penicillin• Oral erythromycin if allergic to penicillin3) Anti-inflammatory therapy• Mild/no carditis = oral aspirin for 2-4 weeks, tapering over 4 weeks• Pericarditis/ moderate to severe carditis = oral prednisolone for 2-4 weeks, taper with
addition of aspirin as above.4) Anti failure medications • Diuretics, ACE inhibitors, digoxin
AIM TO SUPPRESS INFLAMMATORY RESPONSE to minimize cardiac damage, provide symptomatic relieve & eradicate pharyngeal strep infection
![Page 60: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/60.jpg)
SECONDARY PROPHYLAXIS
-As secondary prevention of ARF & development of CRF1) IM Bencathine Penicillin (3-4 weeks)2) Oral penicillin3) Oral erythromycin (if allergies to penicillin)
-Until age 21/ 5 years after last ARF attack which was longer-Lifelong for patient with carditis & vulvular involvement.
![Page 61: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/61.jpg)
COMPLICATION
CHRONIC RHEUMATIC HEART DISEASE
![Page 62: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/62.jpg)
RHEUMATIC HEART DISEASE
![Page 63: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/63.jpg)
Irreversible deformity of 1/more cardiac valves
Left sided of heart > right sided
Could be due to stenosis / regurgitation
Lead to cardiac failure
Predispose to infective endocarditis
Valve commonly involve=• Mitral valve (65-70%)• Aortic valve (25%)• Tricuspid valve (10%)• Pulmonary valve
![Page 64: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/64.jpg)
COMPLICATIONS
• ARRHYTHMIAS• HEART FAILURE
• INFECTIVE ENDOCARDITIS
![Page 65: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/65.jpg)
FEATURE RHEUMATIC FEVER RHEUMATIC HEART DISEASE
ONSET Acute Chronic
AGE Children Adults
PATHOLOGY SPACE Valvular disease(mitral stenosis/mitral
regurgitation)ASCHOFF BODIES Pathognomonic Not seen
DIAGNOSIS John’s criteria Not applicable
![Page 66: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/66.jpg)
![Page 67: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/67.jpg)
INFECTIVE ENDOCARDITIS(IE)
![Page 68: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/68.jpg)
DEFINITION
• Infection due to cardiac valves/mural surface of endocardium, resulting in mass
formation of thrombotic debris & organism name vegetations.
![Page 69: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/69.jpg)
• All children of any age group with congenital heart disease at risk of IE.
• The risk is highest when there is-turbulent jet of blood as with VSD, COA & PDA.-prosthetic material has inserted at surgery.• It subdivided into 2 clinical forms:-Acute bacterial endocarditis-Subacute bacterial endocarditis
![Page 70: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/70.jpg)
FEATURES ABE SABE
MOST COMMON ORGANISM
STAPH AUREUS STAPH VIRIDANS
VIRULENCE OF ORGANISMS
HIGHLY VIRULENT LESS VIRULENT
DURATION < 6 WEEKS > 6 WEEKS
PREVIOUS CONDITIONS OF VALVES
NORMAL, HEALTHY VALVE USUALLY PREVIOUSLY DAMAGE
LESION ON VALVES INVASIVE, DESTRUCTIVE,SUPPURATIVE
USUALLY NOT INVASIVE & SUPPURATIVE
CLINICAL FEATURES FEATURE OF ACUTE SYSTEMINC INFECTION
SPLENOMEGALY, CLUBBING, PETECHIAE
TREATMENT DIFFICULT TO CURE WITH ANTIBIOTIC & USUALLY REQUIRED SURGERY
CURES OFTEN WITH ANTIBIOTIC
![Page 71: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/71.jpg)
PREDISPOSING FACTOR
2) UNDERLYING HEART DISEASE• RHD
• Congenital heart disease
3) IMPAIRED HOST DEFENSE• Lymphoma• leukaemia
1) BACTERIMIA, SEPTICEMIA & PYAEMIA
• Periodontal infection• Infection of GIT
• IVDU
![Page 72: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/72.jpg)
PATHOGENESIS• Valve has no dedicate blood supply.• Defense mechanism (WBC) can’t reach valve via bloodstream.• If organism attach to valve surface & form vegetation, host
immune response blunted.• Lack of blood supply implication of treatment as drug don’t
reach valve.• Normally blood flows smoothly through these valves.• If they damaged (RHD), increase risk of bacteria attachment.
![Page 73: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/73.jpg)
BACTERIAL IMPLANTS ON VALVES:
CIRCULATING BACTERIA LODGED ON PREVIOUSLY DAMAGED VALVES
ALTERED B.FLOWHEMODYNAMIC STRESS ON VALVESDAMAGE TO ENDOTHELIUM FORMATION OF PLATELET THROMBIGET INFECTED FROM CIRCULATING BACTERIA
NON-BACTERIAL THROMBOTIC ENDOCARDITIS-dt endothelial abnormalities & hypercoagulability states followed by bacterial contamination
MICROORGANISM ESTABLISH THEMSELVES ON THE SURFACE OF VEGETATION, PLATELET AGGREGATION & FIBRIN DEPOSITION ACCELERATE AT THE SITE
BACTERIAL MULTIPLYCOVERED BY EVER-THICKENING LAYERS OF PLATELETS & THROMBIN, WHICH PROTECT THEM FROM NEUTROPHILS & OTHER HOST DEFENSE
![Page 74: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/74.jpg)
CLINICAL FEATURES
1) SEPTIC SIGNS = fever, rigors, night sweats, malaise, LOW, anemia, splenomegaly,clubbing
2) CARDIAC LESION = new murmur/change of murmur, abscess at aortic root causes prolong PR interval & complete AV block, HF
3) EMBOLIC PHENOMENON = causes abscess to relevant organ4) IMMUNE COMPLEX DEPOSITION = • Hematuria in GN & ARF• Roth spot & conjunctival hemorrhage• Splinter hemorrhage : Osler’s nodes, Janeway lesion• Skin : petechiae
![Page 75: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/75.jpg)
![Page 76: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/76.jpg)
MODIFIED DUKE CRITERIA
MAJOR CRITERIA MINOR CRITERIA
• Blood culture positive-typically from 2 seperated blood cultures:o Viridans strepo Strep boviso HACEK groupo Staph aureuso Community acquired enterococci• Evidence of endocardial involvement on
echocardiogram
• Predisposing heart condition :-prior surgery, indweling catheter• Fever >38C• Vascular phenomena-major arterial emboli-septic pulm infarcts-mycotic aneurysm-intracranial hemorrhage-conjunctival hemorrhage-Janeway’s lesion• Immunologic phenomena-glomerulonephritis-Osler’s nodes-Roth’s spots-+ve RF
![Page 77: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/77.jpg)
MAKING THE DIAGNOSIS
• DEFINITE : 2 major/ 1 major + 3 minor / 5 minor• POSSIBLE : 1 major + 1 minor / 3 minor• REJECTED-firm alternative diagnosis-resolution of IE after 4 or few days of antimicrobial therapy-no pathological evidence of IE at surgery or autopsy-not meet criteria possible IE
![Page 78: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/78.jpg)
INVESTIGATION
1) Blood culture2) ESR/CRP = inflammation3) FBC =leukocytosis4) Echocardiography5) UFEME = hematuria secondary to GN6) CXR = multiple cavitation in septic emboli or increase cardiothoracic
ratio
![Page 79: Congenital Heart Disease](https://reader036.fdocuments.net/reader036/viewer/2022062301/55cf917f550346f57b8df01c/html5/thumbnails/79.jpg)
MANAGEMENT
1) Bed rest2) Antibiotic therapy• EMPERICAL = IV penicillin (4 weeks)
+ IV/IM gentamycin ( 2 weeks)• VIRIDANS = vancomycin + gentamycin3) Surgery for removal of infected prosthetics material4) Prophylaxis = dental treatment & surgery aw bacteremia