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How do we make decisions? (In
medicine)
How do we make decisions? In
medicine
• Dogma:” Doctrine/Teaching”
• Tradition: “We’ve always done it that way”
• Convention: “Everyone does it this way”
• Evidence-Based: “Evidence supports this way”
Evidence Based Medicine(EBM)
• Conscientious, ^yDoh idÌshg wkql+,&
• Explicit, ^iqmeyeos,s&
• Judicious ^m%{djkA;&
• use of
• “current best evidence in making decisions
about the care of individual patients”
• First BSAC guidelines- in 2004- Mostly the
expert opinions
• Latest in 2012 –
– Majority of recommendations are evidence
based,
– Rest are consensus among the working party
members (Expert Opinion)
What is included in 2012 BSAC
• Mx of Native valve endocarditis(NVE) &
• Mx of Prosthetic valve endocarditis (PVE).
• PVE includes infections in
– Prosthetic valves of all types,
– Annuloplasty rings,
– Intracardiac patches and
– Shunts.
What is excluded from 2012
• Infective Endocarditis related to
– pacemakers,
– defibrillators or
– ventricular-assist devices
• These dealt in a separate BSAC review
The aim of these guidelines
• Standardize the initial investigation and
treatment of IE;
• Identify the patients who can develop adverse
drug reactions (Side Effects and Toxicity)
• identify pts fail to respond to initial antimicrobial
therapy and may require a change in therapy or
surgery.
Summary
2004 Vs 2012
• 2004 guidelines based on expert opinion
• 2012 – Mostly are evidence based: When
evidence is not available→ Consensus
– A-high-quality randomized controlled trials and
meta-analysis of randomized controlled trials;
– B -observational data and non-randomized trials;
and
– C - expert opinion or Working Party consensus.
Level of evidence gradation according
to strength of evidence
C<B<A
IE- The clinical presentation is highly
variable,
• Vary according to the causative microorganism,
• Vary according to presence or absence of pre-
existing cardiac disease,
• Presence of co-morbidities
• Risk factors for the development of IE.(IVDU,HD,
etc)
IE may present as
• An acute, rapidly progressive infection,
• as a subacute or chronic disease,
• low-grade fever and non-specific symptoms that may
cause confusion in initial assessment.
• Patients present to a variety of specialists/GPs who
may consider a range of alternative diagnoses,
– Any chronic infection,
– Rheumatological disorder
– and autoimmune disease or
– malignancy.
Presentation
• The majority (90%) of patients present with fever,
– with systemic symptoms of chills,
– poor appetite
– weight loss.
• Heart murmurs up to 85% (Pre existing heart murmur
should prompt heighten degree of suspicion for look for IE)
• New murmurs reported in 48%.
• New valvular regurgitation is more specific for a diagnosis of
IE
• Classic textbook signs( Rare)
• Peripheral stigmata of IE are increasingly
uncommon (patients generally present at an
early stage of the disease)
• Immunological phenomena, such as
– Splinter hemorrhages,
– Roth spots and
– glomerulonephritis, are now less common,
• Emboli to brain, lung or spleen occur in 30% of
patients(Often could be presenting symptom)
Six right sided endocarditis patients
were followed up….
Present/Yes Absent/No Total
Embolic
phenomena
3
Pneumonia
3 6
Isolate MRSA (3 out of 3 sets) 3
patients
3 6
Risk factor Present in 3 cases
1. CVP cannulation @
ICU 3/12 before for
MX of DHF
2. Recurrent Blood
transfusion for Thal
3. Criminal Abortion
4. Long Term HD
5. Long Term HD
Risk factors not present in
one case
6
Classical risk factors
such as IVDU
No Not present in all 6 case 6
Outcome with
surgery
3 responded for
vegetectomy
one died and 1 responded
for treatment, one
undergoing treatment
6
• Atypical presentations
– e.g. absence of fever is more common in the elderly,
after antibiotic pre-treatment,
– in the immunocompromised patients and
– in IE involving less virulent or atypical organisms.
• The diagnosis of IE should also be considered in
patients who present with
– a stroke or transient ischaemic attack and a fever.
BSAC Guidelines
Summary of ECHO Recommendation of IE
The Duke criteria has
clinical,
echocardiographic
and microbiological findings,
Were developed as a research tool- provide high specificity and moderate
sensitivity for the diagnosis of IE.
These criteria an objective tool for evaluating the strength of evidence to support a
diagnosis of IE, particularly in difficult cases.
IE is a condition where you get
continuous bacteremia
• Generally all three blood cultures will be
positive
• Single blood culture = No culturing
WE have stopped giving sensitivities on the isolates directly to the wards. AST should
be interpreted with the help of CLIN_MICRO TEAM
Why monitor only aminoglycosides
(and Vancomycin?)
• Low therapeutic index.
• Bactericidal efficacy ᾀ peak concentrations
• Toxicity is related to total drug exposure
• Nephrotoxicity (usually reversible) and ototoxicity
(often irreversible)
• The desired plasma concentration-time profile for
aminoglycosides differs to most other drugs.
Amino glycoside toxicity
• More with divided doses than single once
daily dose
• Body weight is measured according to ideal
body weight (not the actual body weight)
• Ideal body weight ± 20% is allowed
Monitoring For Aminoglycosides and
Vancomycin
levels- THK Protocol
• RECEIVE THIS FROM MICRO DEPARTMENT
Use of Ɓ-Lactams
• Can amphicillin/amoxycillin use fro treatment of IE
• Why only penicillin is used?
• What are the drugs given in pen allergy?
• How do you ascertain a history of pen allergy as a true
immediate type of HS?
• With a history of rash with Amp, can you give pen?
• In the backdrop of anaphylaxis, can you give CRO?
5.3 b-Lactams
• Amoxicillin and ampicillin → microbiologically equivalent and
either can be used.
• Amoxicillin can be used instead of benzylpenicillin for
susceptible isolates (greater risk of Clostridium difficile
infection)
• Need to be given more frequently (due to short t1/2)
• No comparison of continuous with intermittent penicillin
administration for streptococcal endocarditis.
• Dose modifications necessary for renal failure
A history of a rash with ampicillin or amoxicillin may not indicate true allergy.
Unless signs of immediate-type hypersensitivity (anaphylaxis, angio-oedema, bronchospasm
and urticaria) were reported, a trial with penicillin may be warranted,(A emergency trolley
need to be kept bear)
A rash occurs after 72 h- unlikely to be an immediate IgE-mediated
reaction (type I hypersensitivity).
In a recent study, 72% of patients with a delayed-type hypersensitivity reaction to
aminopenicillins had no cross-reactivity with penicillin.
The American Heart Association (AHA) advises ceftriaxone for the penicillin-allergic pts,
(for allergy other than immediate-type hypersensitivity, because of the risk of cross-
sensitivity with penicillin)
5.5 Other antibiotics
• linezolid and daptomycin
• Only after consultating Micro Team
Infective endocarditis
Infective endocarditis
Infective endocarditis
Infective endocarditis
Infective endocarditis
Infective endocarditis
Infective endocarditis

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Infective endocarditis

  • 1. How do we make decisions? (In medicine)
  • 2. How do we make decisions? In medicine • Dogma:” Doctrine/Teaching” • Tradition: “We’ve always done it that way” • Convention: “Everyone does it this way” • Evidence-Based: “Evidence supports this way”
  • 3. Evidence Based Medicine(EBM) • Conscientious, ^yDoh idÌshg wkql+,& • Explicit, ^iqmeyeos,s& • Judicious ^m%{djkA;& • use of • “current best evidence in making decisions about the care of individual patients”
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  • 9. • First BSAC guidelines- in 2004- Mostly the expert opinions • Latest in 2012 – – Majority of recommendations are evidence based, – Rest are consensus among the working party members (Expert Opinion)
  • 10. What is included in 2012 BSAC • Mx of Native valve endocarditis(NVE) & • Mx of Prosthetic valve endocarditis (PVE). • PVE includes infections in – Prosthetic valves of all types, – Annuloplasty rings, – Intracardiac patches and – Shunts.
  • 11. What is excluded from 2012 • Infective Endocarditis related to – pacemakers, – defibrillators or – ventricular-assist devices • These dealt in a separate BSAC review
  • 12. The aim of these guidelines • Standardize the initial investigation and treatment of IE; • Identify the patients who can develop adverse drug reactions (Side Effects and Toxicity) • identify pts fail to respond to initial antimicrobial therapy and may require a change in therapy or surgery.
  • 13. Summary 2004 Vs 2012 • 2004 guidelines based on expert opinion • 2012 – Mostly are evidence based: When evidence is not available→ Consensus – A-high-quality randomized controlled trials and meta-analysis of randomized controlled trials; – B -observational data and non-randomized trials; and – C - expert opinion or Working Party consensus.
  • 14. Level of evidence gradation according to strength of evidence C<B<A
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  • 16. IE- The clinical presentation is highly variable, • Vary according to the causative microorganism, • Vary according to presence or absence of pre- existing cardiac disease, • Presence of co-morbidities • Risk factors for the development of IE.(IVDU,HD, etc)
  • 17. IE may present as • An acute, rapidly progressive infection, • as a subacute or chronic disease, • low-grade fever and non-specific symptoms that may cause confusion in initial assessment. • Patients present to a variety of specialists/GPs who may consider a range of alternative diagnoses, – Any chronic infection, – Rheumatological disorder – and autoimmune disease or – malignancy.
  • 18. Presentation • The majority (90%) of patients present with fever, – with systemic symptoms of chills, – poor appetite – weight loss. • Heart murmurs up to 85% (Pre existing heart murmur should prompt heighten degree of suspicion for look for IE) • New murmurs reported in 48%. • New valvular regurgitation is more specific for a diagnosis of IE
  • 19. • Classic textbook signs( Rare) • Peripheral stigmata of IE are increasingly uncommon (patients generally present at an early stage of the disease) • Immunological phenomena, such as – Splinter hemorrhages, – Roth spots and – glomerulonephritis, are now less common, • Emboli to brain, lung or spleen occur in 30% of patients(Often could be presenting symptom)
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  • 22. Six right sided endocarditis patients were followed up…. Present/Yes Absent/No Total Embolic phenomena 3 Pneumonia 3 6 Isolate MRSA (3 out of 3 sets) 3 patients 3 6 Risk factor Present in 3 cases 1. CVP cannulation @ ICU 3/12 before for MX of DHF 2. Recurrent Blood transfusion for Thal 3. Criminal Abortion 4. Long Term HD 5. Long Term HD Risk factors not present in one case 6 Classical risk factors such as IVDU No Not present in all 6 case 6 Outcome with surgery 3 responded for vegetectomy one died and 1 responded for treatment, one undergoing treatment 6
  • 23. • Atypical presentations – e.g. absence of fever is more common in the elderly, after antibiotic pre-treatment, – in the immunocompromised patients and – in IE involving less virulent or atypical organisms. • The diagnosis of IE should also be considered in patients who present with – a stroke or transient ischaemic attack and a fever.
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  • 28. Summary of ECHO Recommendation of IE
  • 29. The Duke criteria has clinical, echocardiographic and microbiological findings, Were developed as a research tool- provide high specificity and moderate sensitivity for the diagnosis of IE. These criteria an objective tool for evaluating the strength of evidence to support a diagnosis of IE, particularly in difficult cases.
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  • 34. IE is a condition where you get continuous bacteremia • Generally all three blood cultures will be positive • Single blood culture = No culturing
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  • 39. WE have stopped giving sensitivities on the isolates directly to the wards. AST should be interpreted with the help of CLIN_MICRO TEAM
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  • 47. Why monitor only aminoglycosides (and Vancomycin?) • Low therapeutic index. • Bactericidal efficacy ᾀ peak concentrations • Toxicity is related to total drug exposure • Nephrotoxicity (usually reversible) and ototoxicity (often irreversible) • The desired plasma concentration-time profile for aminoglycosides differs to most other drugs.
  • 48. Amino glycoside toxicity • More with divided doses than single once daily dose • Body weight is measured according to ideal body weight (not the actual body weight) • Ideal body weight ± 20% is allowed
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  • 50. Monitoring For Aminoglycosides and Vancomycin levels- THK Protocol • RECEIVE THIS FROM MICRO DEPARTMENT
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  • 52. Use of Ɓ-Lactams • Can amphicillin/amoxycillin use fro treatment of IE • Why only penicillin is used? • What are the drugs given in pen allergy? • How do you ascertain a history of pen allergy as a true immediate type of HS? • With a history of rash with Amp, can you give pen? • In the backdrop of anaphylaxis, can you give CRO?
  • 53. 5.3 b-Lactams • Amoxicillin and ampicillin → microbiologically equivalent and either can be used. • Amoxicillin can be used instead of benzylpenicillin for susceptible isolates (greater risk of Clostridium difficile infection) • Need to be given more frequently (due to short t1/2) • No comparison of continuous with intermittent penicillin administration for streptococcal endocarditis. • Dose modifications necessary for renal failure
  • 54. A history of a rash with ampicillin or amoxicillin may not indicate true allergy. Unless signs of immediate-type hypersensitivity (anaphylaxis, angio-oedema, bronchospasm and urticaria) were reported, a trial with penicillin may be warranted,(A emergency trolley need to be kept bear) A rash occurs after 72 h- unlikely to be an immediate IgE-mediated reaction (type I hypersensitivity). In a recent study, 72% of patients with a delayed-type hypersensitivity reaction to aminopenicillins had no cross-reactivity with penicillin. The American Heart Association (AHA) advises ceftriaxone for the penicillin-allergic pts, (for allergy other than immediate-type hypersensitivity, because of the risk of cross- sensitivity with penicillin)
  • 55. 5.5 Other antibiotics • linezolid and daptomycin • Only after consultating Micro Team