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Treatment Guidelines for
Antimicrobial Use in Common
Syndromes
Based on ICMR Guidelines,
New Delhi, India(2017)
Dr SD Sanyal
Principles of Initial Empirical
Antimicrobial Therapy in Patients
with Severe Sepsis and Septic
Shock in The Intensive Care Units
Definitions
• SIRS:
- Two or more of the following variables:
i. Fever > 38°C (100.4°F) or hypothermia <
36°C (96.8°F)
ii. Tachypnea (>20 breaths/min) or PaCO2 < 32
mmHg
iii. HR >90 beats/min
iv. WBC > 12,000/<4000 cells/mm3, 10%
immature band forms
Definitions
• Sepsis : Systemic inflammatory response
syndrome that occurs due to a “known or
suspected” pathogen (bacteria, viruses, fungi
or parasites)
Definitions
• Severe sepsis:
- Sepsis plus evidence of organ dysfunction or tissue hypoperfusion
as follows:
i. Altered mental status.
ii. Hypoxemia, with PaO2/FIO2 <250
iii.Thrombocytopenia < 100,000/cmm
iv. Bilirubin >2mg/dl
v. INR >1.5 or aPTT> 60 seconds.
vi. Urinary output of 0.5 ml/kg for at least 2 hours or Serum
creatinine >2mg/dl despite fluid resuscitation.
Definitions
vii. Tissue hypoperfusion as suspected by mottled skin,
capillary refilling time ≥ 2 seconds or lactate >4 mmol/l
viii. Hypotension : Systolic blood pressure (SBP) ≤90
mmHg or mean arterial pressure ≤70 mm Hg
• Sepsis induced hypotension: SBP<90mmHg or
MAP<70mmHg or SBP fall > 40 mm Hg
• Septic shock:
- Sepsis induced hypotension that persists despite
adequate fluid resuscitation, requiring vasopressors to
maintain the blood pressure.
Common Pathogens
• Gram negative:
-Pseudomonas aeruginosa
-E. coli
-Klebsiella pneumoniae
-Acinetobacter spp
Common Pathogens
• Gram Positive:
- Methicillin resistant Staphylococcus aureus
(MRSA)
- Entercoccus faecium
- Vancomycin resistant enterocccci
• Fungi:
- Candida spp
Susceptible Individuals
• Antimicrobial therapy in preceding 90 days
• Current hospitalization of 5 days or more
• High frequency of community or hospital
antibiotic resistance
• Immunosuppressive disease or therapy
Susceptible Individuals
• Presence of multiple risk factors for Health Care
Associated Infections:
- Hospitalization for ≥2 days in preceeding 90
days
- Residence in nursing home or long term care
facility
-Home infusion therapy
-Chronic dialysis within 90 days
-Family member with MDR pathogen
Patterns of Antimicrobial
Resistance
S.aureus and Enterococci
Enterobacteriacae
P. aeruginosa & A.baumanii
Candida species
Principles of Emperical Therapy
• Form probable diagnosis
• Obtain cultures
• Source control
• Broad spectrum cover
• Antibiotics within the first hour
• Early Antifungal cover
• Antivirals
Choice of AMA
• The suspected site of infection
• The clinical syndrome
• The setting in which the infection developed
(i.e., home, nursing home, or hospital)
• Medical history
• Epidemiology, susceptibility patterns of bacteria
in the hospital and ICU, local microbial-
susceptibility patterns, resistance potential
Choice of AMA
• Prior antibiotic therapy(previous 3 months)
• Immunological competence of patient
• Severity of underlying illness
• Microbes that previously have been documented to
colonize or infect the patient
• Pharmacokinetics of the chosen antimicrobial agent
• Drug allergies / toxicities
• Cost
De-escalation
• As soon as the causative organism is identified
on culture
• Choose an agent which is CHEAP and COST
EFFECTIVE
• Daily reassessment to perform de-escalation
and prevent resistance, reduce costs and avoid
super-infections
• Use of LOW PROCALCITONIN levels
Recomendations
Clinical
condition
Common
pathogens
Emperical AMA Alternate AMA Comments
Urosepsis E. coli,
Pseudomonas
spp,
Enterococcus
spp.,
Klebsiella spp.,
Proteus spp.,
Anaerobes
Candidia spp
BL-BLI or
Meropenem or
Imipenem-
cilastatin.
Fluconazole if
Candida
Colistin with
Meropenam
In
pyelonephritis
with sepsis,
Echiocandins
may be
considered if
Candida
species
are likely to be
resistant to
Fluconazole
Recommendations
Clinical
condition
Common
pathogens
Emperical AMA Alternate AMA Comments
Intra-
abdominal
Sepsis
E. coli,
Pseudomonas
spp,
Enterococcus
spp.,
Klebsiella spp.,
Acinetobacter
spp,
Proteus spp.,
Candidia spp
BL-BLI or
Meropenem or
Imipenem-
cilastatin.
Colistin with
Meropenam
Source control
vital
Vancomycin or
Teicoplanin if
Enterococcus
spp isolated
Fluconazole or
Echinocandins
if Candida spp
isolated
Echinocandins
if prior h/o
Azole exposure
or Fluconazole
resistance is
suspected
Recommendations
Clinical
condition
Common
pathogens
Emperical AMA Alternate AMA Comments
Catheter
related
blood
stream
infections
Gram –
negative
pathogens
Ecoli Klebsiella
spp
Enterobacter
spp
P aeruginosa
Gram-positive
pathogens
CONS
S aureus,
MRSA
Fungi
Candida spp
Carbapenem,
or BL-BLI,
with or without
an
aminoglycoside
Vancomycin in
settings of high
MRSA
prevalence;
Echinocandin
or fluconazole
if fungal
infection
suspected
Add colistin for
Gram-negative
cover where
carbapenem
resistance rates
are high
Where MRSA
isolates have
vancomycin
MI 2 mg/mL,
daptomycin,
should be used
Cause Undetermined
Surgical Site Infections
Classification of Surgical Wounds
• Class I/Clean:
-Uninfected, operative wound with no inflammmation
and Resp/GI/Genital/Urinary tract is not entered
• Class II/Clean contaminated:
- Resp/GI/Genital/Urinary tract is entered under
controlled conditions without unusual contamination
• Class III/Contaminated:
- Open fresh accidental wounds. Operations with major
break in sterile technique with gross spillage from GIT
• Class IV/ Dirty-infected:
- Old traumatic wounds with retained devitalized tissue
and those that involve existing clinical infections and
perforated viscera
Superficial Incisional SSI
- Within 30 days of surgery and infection involves only
skin or SC tissue of the incision+ 1 of the following:
1. Purulent drainage, with or without laboratory
confirmation, from the superficial incision
2. Organisms isolated from an aseptically obtained
culture of fluid or tissue from the superficial incision
3. At least one of the following signs or symptoms of
infection:
- pain or tenderness
- localized swelling, redness, heat
- superficial incision is deliberately opened by surgeon,
unless incision is culture-negative
4. Diagnosis of superficial incisional SSI by the surgeon
or attending physician
Superficial Incisional SSI
• Following conditions not to be reported as SSI:
- Stitch abscess
- Infection of an episiotomy or newborn
circumcision site
- Infected burn wound
- Incisional SSI that extends into the fascial
and muscle layers (see deep incisional SSI)
Deep Incisional SSI
- Within 30 days without implant or within 1 year with implant
- Infection is likely due to surgery and involves fascial and muscle
layers) + 1 of the following:
1. Purulent drainage from the deep incision but not from the
organ/space component of the surgical site
2. Spontaneous dehiscence/deliberate opening by a surgeon when
the patient has at least 1 of the following :
- Fever (>38ºC)
- Localized pain or tenderness, unless site is culture-negative
- An abscess or infection of the deep incision is found on direct
examination, during reoperation, or by histopathologic or radiologic
examination.
- Diagnosis of a deep incisional SSI by a surgeon or attending
physician.
Deep Incisional SSI
• Notes:
i. Report infection that involves both
superficial and deep incision sites as deep
incisional SSI
ii. Report an organ/space SSI that drains
through the incision as a deep incisional SSI
Organ space SSI
• Within 30 days after the operation if no implant is left in place
or within 1 year if implant is in place
• Appears to be related to the operation and infection involves
any part of the anatomy (e.g., organs or spaces), other than
the incision, which was opened or manipulated during an
operation and + 1 of the following:
-Purulent drainage from a drain
- Organisms isolated from an aseptically obtained culture of fluid or tissue
in the organ/space.
- An abscess or other evidence of infection involving the organ/space that
is found on direct examination, during reoperation, or by histopathologic
or radiologic examination.
-Diagnosis of an organ/space SSI by a surgeon or attending physician.
Operations and Likely Surgical Site Infection
(SSI) Pathogens
Operations and Likely Surgical Site Infection
(SSI) Pathogens
Resistance patterns of S.aureus
Resistance patterns of Enterobacteriacae
Resistance patterns of Pseudomonas
Peri-operative Prophylaxis
• Choice of AMA:
- Dictated by the most common pathogen
encountered
- Skin pathogens are usual targets: 1st
Generation Cephalosporins
- H/o allergy to penicillins:
Vancomycin/Clindamycin
• Timing of administration:
- Before skin incision
- All agents 30-60 mins prior
- Vancomycin and Flouroquinolones 120mins
prior
Peri-operative Prophylaxis
• Route of administration:
- Intravenous
• Dosage:
- Same as therapy
• Duration:
- No longer than 24hrs
- Single dose as effective as multiple doses
- Multiple doses assoc with a higher risk of Resistance
& Colitis
• Re-dosing:
- If duration of surgery exceeds 2 x half lives
- Blood loss > 1500ml or Haemodilution> 15ml/kg
Pathogen specific AMA therapy
AMA Guidelines for SSI’s
AMA Guidelines for Skin & Soft tissue infections
AMA Guidelines for Skin & Soft tissue infections
Dosages of AMA’s active against MDR organisms
Thank You

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Treatment Guidelines for Antimicrobial Use in Common Syndromes

  • 1. Treatment Guidelines for Antimicrobial Use in Common Syndromes Based on ICMR Guidelines, New Delhi, India(2017) Dr SD Sanyal
  • 2. Principles of Initial Empirical Antimicrobial Therapy in Patients with Severe Sepsis and Septic Shock in The Intensive Care Units
  • 3. Definitions • SIRS: - Two or more of the following variables: i. Fever > 38°C (100.4°F) or hypothermia < 36°C (96.8°F) ii. Tachypnea (>20 breaths/min) or PaCO2 < 32 mmHg iii. HR >90 beats/min iv. WBC > 12,000/<4000 cells/mm3, 10% immature band forms
  • 4. Definitions • Sepsis : Systemic inflammatory response syndrome that occurs due to a “known or suspected” pathogen (bacteria, viruses, fungi or parasites)
  • 5. Definitions • Severe sepsis: - Sepsis plus evidence of organ dysfunction or tissue hypoperfusion as follows: i. Altered mental status. ii. Hypoxemia, with PaO2/FIO2 <250 iii.Thrombocytopenia < 100,000/cmm iv. Bilirubin >2mg/dl v. INR >1.5 or aPTT> 60 seconds. vi. Urinary output of 0.5 ml/kg for at least 2 hours or Serum creatinine >2mg/dl despite fluid resuscitation.
  • 6. Definitions vii. Tissue hypoperfusion as suspected by mottled skin, capillary refilling time ≥ 2 seconds or lactate >4 mmol/l viii. Hypotension : Systolic blood pressure (SBP) ≤90 mmHg or mean arterial pressure ≤70 mm Hg • Sepsis induced hypotension: SBP<90mmHg or MAP<70mmHg or SBP fall > 40 mm Hg • Septic shock: - Sepsis induced hypotension that persists despite adequate fluid resuscitation, requiring vasopressors to maintain the blood pressure.
  • 7. Common Pathogens • Gram negative: -Pseudomonas aeruginosa -E. coli -Klebsiella pneumoniae -Acinetobacter spp
  • 8. Common Pathogens • Gram Positive: - Methicillin resistant Staphylococcus aureus (MRSA) - Entercoccus faecium - Vancomycin resistant enterocccci • Fungi: - Candida spp
  • 9. Susceptible Individuals • Antimicrobial therapy in preceding 90 days • Current hospitalization of 5 days or more • High frequency of community or hospital antibiotic resistance • Immunosuppressive disease or therapy
  • 10. Susceptible Individuals • Presence of multiple risk factors for Health Care Associated Infections: - Hospitalization for ≥2 days in preceeding 90 days - Residence in nursing home or long term care facility -Home infusion therapy -Chronic dialysis within 90 days -Family member with MDR pathogen
  • 14. P. aeruginosa & A.baumanii
  • 16. Principles of Emperical Therapy • Form probable diagnosis • Obtain cultures • Source control • Broad spectrum cover • Antibiotics within the first hour • Early Antifungal cover • Antivirals
  • 17. Choice of AMA • The suspected site of infection • The clinical syndrome • The setting in which the infection developed (i.e., home, nursing home, or hospital) • Medical history • Epidemiology, susceptibility patterns of bacteria in the hospital and ICU, local microbial- susceptibility patterns, resistance potential
  • 18. Choice of AMA • Prior antibiotic therapy(previous 3 months) • Immunological competence of patient • Severity of underlying illness • Microbes that previously have been documented to colonize or infect the patient • Pharmacokinetics of the chosen antimicrobial agent • Drug allergies / toxicities • Cost
  • 19. De-escalation • As soon as the causative organism is identified on culture • Choose an agent which is CHEAP and COST EFFECTIVE • Daily reassessment to perform de-escalation and prevent resistance, reduce costs and avoid super-infections • Use of LOW PROCALCITONIN levels
  • 20. Recomendations Clinical condition Common pathogens Emperical AMA Alternate AMA Comments Urosepsis E. coli, Pseudomonas spp, Enterococcus spp., Klebsiella spp., Proteus spp., Anaerobes Candidia spp BL-BLI or Meropenem or Imipenem- cilastatin. Fluconazole if Candida Colistin with Meropenam In pyelonephritis with sepsis, Echiocandins may be considered if Candida species are likely to be resistant to Fluconazole
  • 21. Recommendations Clinical condition Common pathogens Emperical AMA Alternate AMA Comments Intra- abdominal Sepsis E. coli, Pseudomonas spp, Enterococcus spp., Klebsiella spp., Acinetobacter spp, Proteus spp., Candidia spp BL-BLI or Meropenem or Imipenem- cilastatin. Colistin with Meropenam Source control vital Vancomycin or Teicoplanin if Enterococcus spp isolated Fluconazole or Echinocandins if Candida spp isolated Echinocandins if prior h/o Azole exposure or Fluconazole resistance is suspected
  • 22. Recommendations Clinical condition Common pathogens Emperical AMA Alternate AMA Comments Catheter related blood stream infections Gram – negative pathogens Ecoli Klebsiella spp Enterobacter spp P aeruginosa Gram-positive pathogens CONS S aureus, MRSA Fungi Candida spp Carbapenem, or BL-BLI, with or without an aminoglycoside Vancomycin in settings of high MRSA prevalence; Echinocandin or fluconazole if fungal infection suspected Add colistin for Gram-negative cover where carbapenem resistance rates are high Where MRSA isolates have vancomycin MI 2 mg/mL, daptomycin, should be used
  • 25. Classification of Surgical Wounds • Class I/Clean: -Uninfected, operative wound with no inflammmation and Resp/GI/Genital/Urinary tract is not entered • Class II/Clean contaminated: - Resp/GI/Genital/Urinary tract is entered under controlled conditions without unusual contamination • Class III/Contaminated: - Open fresh accidental wounds. Operations with major break in sterile technique with gross spillage from GIT • Class IV/ Dirty-infected: - Old traumatic wounds with retained devitalized tissue and those that involve existing clinical infections and perforated viscera
  • 26. Superficial Incisional SSI - Within 30 days of surgery and infection involves only skin or SC tissue of the incision+ 1 of the following: 1. Purulent drainage, with or without laboratory confirmation, from the superficial incision 2. Organisms isolated from an aseptically obtained culture of fluid or tissue from the superficial incision 3. At least one of the following signs or symptoms of infection: - pain or tenderness - localized swelling, redness, heat - superficial incision is deliberately opened by surgeon, unless incision is culture-negative 4. Diagnosis of superficial incisional SSI by the surgeon or attending physician
  • 27. Superficial Incisional SSI • Following conditions not to be reported as SSI: - Stitch abscess - Infection of an episiotomy or newborn circumcision site - Infected burn wound - Incisional SSI that extends into the fascial and muscle layers (see deep incisional SSI)
  • 28. Deep Incisional SSI - Within 30 days without implant or within 1 year with implant - Infection is likely due to surgery and involves fascial and muscle layers) + 1 of the following: 1. Purulent drainage from the deep incision but not from the organ/space component of the surgical site 2. Spontaneous dehiscence/deliberate opening by a surgeon when the patient has at least 1 of the following : - Fever (>38ºC) - Localized pain or tenderness, unless site is culture-negative - An abscess or infection of the deep incision is found on direct examination, during reoperation, or by histopathologic or radiologic examination. - Diagnosis of a deep incisional SSI by a surgeon or attending physician.
  • 29. Deep Incisional SSI • Notes: i. Report infection that involves both superficial and deep incision sites as deep incisional SSI ii. Report an organ/space SSI that drains through the incision as a deep incisional SSI
  • 30. Organ space SSI • Within 30 days after the operation if no implant is left in place or within 1 year if implant is in place • Appears to be related to the operation and infection involves any part of the anatomy (e.g., organs or spaces), other than the incision, which was opened or manipulated during an operation and + 1 of the following: -Purulent drainage from a drain - Organisms isolated from an aseptically obtained culture of fluid or tissue in the organ/space. - An abscess or other evidence of infection involving the organ/space that is found on direct examination, during reoperation, or by histopathologic or radiologic examination. -Diagnosis of an organ/space SSI by a surgeon or attending physician.
  • 31. Operations and Likely Surgical Site Infection (SSI) Pathogens
  • 32. Operations and Likely Surgical Site Infection (SSI) Pathogens
  • 34. Resistance patterns of Enterobacteriacae
  • 35. Resistance patterns of Pseudomonas
  • 36. Peri-operative Prophylaxis • Choice of AMA: - Dictated by the most common pathogen encountered - Skin pathogens are usual targets: 1st Generation Cephalosporins - H/o allergy to penicillins: Vancomycin/Clindamycin • Timing of administration: - Before skin incision - All agents 30-60 mins prior - Vancomycin and Flouroquinolones 120mins prior
  • 37. Peri-operative Prophylaxis • Route of administration: - Intravenous • Dosage: - Same as therapy • Duration: - No longer than 24hrs - Single dose as effective as multiple doses - Multiple doses assoc with a higher risk of Resistance & Colitis • Re-dosing: - If duration of surgery exceeds 2 x half lives - Blood loss > 1500ml or Haemodilution> 15ml/kg
  • 40. AMA Guidelines for Skin & Soft tissue infections
  • 41. AMA Guidelines for Skin & Soft tissue infections
  • 42. Dosages of AMA’s active against MDR organisms