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Antimicrobial
Resistance :
Hype or Fact?
Manju Puri
Director Professor & Former HOD
Department of Obstetrics & Gynecology
Lady Hardinge Medical College
New Delhi
AMR : Is it a
hype or fact?
For those who have experienced
the anxiety of an infection that
is drug-resistant, first-hand,
there is little that is needed to
prove the existence and the
importance of tackling AMR.
For majority of the people around the globe the threat of
drug resistance is either not known or seem a distant and
abstract risk
Obstetricians’ and AMR
• Rising antibiotic resistance will have
alarming secondary effects on safety
of child-birth including CS
• If AMR continues, much of the
progress, we have made in reducing
maternal and infant mortality in the
last century will be at a risk of being
undermined
We need to wake up before it is too late
Penicillin: An accidental discovery changed the course of medicine
1928
Antimicrobial Resistance is resistance of a microorganism to an antimicrobial agent
that was originally effective for treatment of infections caused by this microorganism
Antimicrobial resistance
2022
National Health Policy 2017
flagged AMR as a Key issue
WHO in 2001 declares AMR a
global public health problem
Magnitude of problem
• Deaths attributable to AMR every year as compared to other major causes of
deaths
300,000 Maternal
deaths per year
The Global Picture
Majority of deaths
will occur in Africa
and Asia – over 4
million in each
region.
10 million people a year
It is important to bridge the gap between global perceptions of AMR today
and how bad it is likely to become if the current trend is not altered
Rational Antimicrobial Therapy
Prevents
• Selection of pathogenic organisms like
Clostridium difficle
• Collateral damage and alteration of
patient’s microbiome especially GIT
• Toxicity or adverse effects of antibiotics
• Rising costs of treatment
• Discovery void of antibiotics
√
√
√
√
√
FACTS
Antibiotic Stewardship Programme Guidelines ( ICMR 2018)
Antibiotic void
> 35 years
Current
scenario…..
Smart of use of antimicrobials
• Intend to prevent infection
• Reduce colonization of
microorganisms at the time of
operation
• Needed for short duration (as
single preoperative shot)
Prophylactic
• Resolve an established infection
• Needed for longer duration
Therapeutic
Principles of
Optimal use of
Antibiotics:
For suspected
or proven
bacterial
infection
Initiating Empirical therapy*
• Choosing the right antibiotic
• Determine the optimum dose and route
• Initiate promptly
Tailoring therapy or Antibiotic time out
• Re-evaluation continuously; usually after 48-72 hrs
• Change to specific A/B; stop; adjust dose; add or subtract
Convert from intravenous to oral administration
Use for shortest effective dose
* Remember :
To take relevant cultures before starting A/B
5 D’s of
Appropriate
or Smart
Antibiotic
therapy
Right Diagnosis/ Indication
Right Drug
Right Dose
Right Duration
De-escalation to pathogen-targeted
therapy
Principles of Optimal
use of Antibiotics:
For Surgical prophylaxis
Antimicrobial prophylaxis is justified for most clean-contaminated procedures
Ann Surg. 2009 Apr;249(4):551-6. Surg Infect (Larchmt). 2013 Feb;14(1):73-156
Guidelines for prevention of Infection after Gynaecologic
procedures
• Laparoscopy (diagnostic, tubal sterilization, operative except for
hysterectomy)
• Other transcervical procedures:
• Hysteroscopy (diagnostic or operative)
• Intrauterine device insertion
• Endometrial biopsy
• HSG/SSG*(H/o of PID or damaged tubes on HSG or laparoscopy)
• Oocyte retrieval
• D&C for non-pregnancy indication
• Cervical tissue biopsy, including LEEP or endocervical curettage
• Cystoscopy
ACOG practice bulletin No. 195: Prevention of infection after gynecologic procedures. Obstet Gynecol 2018; 131:e172
NO ANTIBIOTIC REQUIRED
ACOG 2018
Guidelines for prevention of Infection after
Gynaecologic procedures
Uterine evacuation (including surgical
abortion, suction D&C, and D&E)
• Oral Doxycycline 200 mg
Metronidazole 1gm or Azithromycin
500mg single dose
Caesarean section
Hysterectomy
3rd and 4th degree perineal tears
Pelvic reconstructive surgery
colporrhaphy or vaginal sling or
mesh placement
• Cefazolin 2g I/V stat with in 60
min
• Metronidazole 500mg +
gentamicin 5mg/kg I/V
• Clindamycin 900 mg +gentamycin
5mg/Kg I/V
ACOG practice bulletin No. 195: Prevention of infection after gynecologic procedures. Obstet Gynecol 2018; 131:e172
ACOG 2018
ANTIBIOTIC PROPHYLAXIS
INDICATED
Antibiotic
Stewardship
It is a systematic measurement
and coordinated interventions
to promote optimal use of
antimicrobial agents
Antibiotic stewardship in Public Sector
Case study
25 yrs. Primigravida at term with preeclampsia underwent CS for Foetal distress
15/8/16
• Inj Ampicillin + Metronidazole
Day 2
Developed fever, tachycardia, tachypnoea, loose motions, discharge from wound;
blood and wound swab sent for C/S
• A/B stepped up: Meropenum and Ciprofloxacin
Day 6
BDCS coagulase negative staphylococcus (CoNS) sensitive to Vancomycin /Clindamycin ;
Pus C/S Methicillin sensitive (CoNS) sensitive to Linazolid/ Vancomycin/ Gentamycin;
• A/B changed : Vancomycin + Clindamycin added
Day 10
Pus C/S Acinobacter sensitive to Piptaz, Colistin,
• A/B changed: Piptaz added
Fever continued
Day 21
Exploratory laparotomy with peritoneal lavage
Day 26 (D6) breathlessness shifted to ICU intubated for assisted ventilation
Culture ET, central line Pseudomonas and Klebsiella Sensitive to Colistin.
• A/B stepped up to Colistin
Day 32 (D12) Extubated
Day 40 (D20) Discharged
Hospital acquired infection and Antimicrobial resistance
Key Messages
Prevention of infection is not about administering
antibiotics, antibiotics and antibiotics
AMR is a serious problem
It needs to be combated by Prudent or Smart use of antibiotics
Otherwise antibiotics will lose their efficacy
Return to the dark age of medicine……
It is more about use of aseptic precautions and rational use of antibiotics
Journey of Antibiotic
stewardship in the
Department of
Obstetrics &
Gynecology
LHMC
Point of Care Quality
Improvement Project on
Rational use of antibiotics
4 step approach
Steps in QI
Step IV Sustaining improvement
Step III
Developing and testing changes
PDSA cycle
Step II
Analyzing the problem and measuring
quality of care by identifying outcome
measure/s
Step I
Identifying a problem, writing an aim
statement, forming a team
Steps in QI
Step 1: Problem identification, forming a
team, and writing the aim statement
• AIM STATEMENT
We aim to increase the antibiotic prophylaxis (SSAB) in low-risk
patients undergoing elective major surgery from 0% to 60% by 8 weeks
QI TEAM MEMBERS
All consultants of Department of Obstetrics & Gynecology
Team leader
Communicator
Recorder
Step 2a: Analyzing and measuring quality of care
People
Place
Policy
Procedure
Major influence
Major influence
Minor influence
Minor influence
Problem
No dept antibiotic
policy in place
- No sensitization
- No awareness
- Reluctance to give SSAB
- Worried about asepsis
When to administer
Who will administer
Where to document
Non availability of
antibiotic in OT
Step 2b: Measuring quality of care:
Quality Indicators
Indicator Process indicator
Numerator No. of patients who received
SSAB
Denominator No of eligible patients who
underwent elective surgery
Frequency of
data analysis
Monthly
Data source (s) Case records
Indicator Outcome indicator
Numerator No. of patients who received
SSAB developing SSI
Denominator No of patients who received
SSAB
Frequency of
data analysis
Monthly
Data source (s) Case records
Act Plan
Study Do
Step 3 of Quality Improvement
Develop and test changes
Adopt
Adapt
Abandon
What are the results?
What did we learn?
What are we
going to do?
When and how
did we do it?
Step 3: Developing and testing changes
Change idea tested When was it done What was the result? What did we
learn?
1. • Formulation of AB policy,
detailed discussion,
finalization after agreement
• Sensitization Workshop for
residents on asepsis
• Roll it out in the department
July 1st, 2017 to Aug
30th , 2017
Build consensus of all involved
Not everyone was convinced due to fear of
sepsis
Adapt
Start small
2. • Implementation in one unit
• Sensitization workshop
conducted for residents and
NOs on AMR & asepsis
• Collected base line data on
outcome measure SSI
July 1st, 2017 to July
31st , 2017
35.6 % use
No ↑ SSI
Adapt
Sharing experience with other builds
confidence
3. Implementation in all units August 1st , 2017 Approx. 50% use Adopt
No ↑ SSI
Step 3: Developing and testing changes
Change idea tested When did you
try this? Date.
What was the result? What
did we learn?
4. Identified a coordinator
and nodal officers in each
unit with monthly
meeting in person with
presentation of data and
discussion of cases with
continuation of A/B
September 2017 SSAB use increased >60 %
Adopt
Increase in accountability and
ownership pays
SSAB remained above 60% Oct and Nov 17
↓ 59% in Dec 17 Need for Hardwiring
Change idea tested When did you
try this? Date.
What was the result? What
did we learn?
5.
6.
Addition of induction
training of residents and
regular sharing of data
by nodal officers with
coordinator
Hold meeting on fixed
day of the month with
nodal officers to review
data and have a WA
group with nodal officers
and unit heads as
members
March ’18
Sept ‘19
SSAB use increased 75% ADOPT
Lesson learnt
Wide dissemination and need for
continuous follow up is important
or sustenance
For a change to sustain it should
not be person centric but self
sustaining
Nov ‘18 to August ‘19 80 % - 90%
A meeting was missed in Aug and Sep ‘19 as the Coordinator
was on leave SSAB rate came down to 70-75%
Change idea tested When did you
try this? Date.
What was the result? What
did we learn?
7. Started sharing monthly
data during the monthly
statistics meeting
To show a ppt slide with
the SSAB usage and SSI
rate
Oct’19 Lesson learnt
Need for continuous follow up
for sustenance and sharing of
data keeps the momentum of
the change and everyone
interested
SSAB remained above 80% since Oct ’19 most of the months it is above 90%
Step 4: Sustaining
Improvement
• Continuous monitoring of process and outcome
indicator monthly
• Sharing of data
• Generate competition among units
• Appreciate those doing well
0 0
2 1 0 0 1 0 0 1 1 0
1.5
0 0 1 0 1 0 0.9 0 0 0 0 1 0 0 0 0 0 1 1.1
4.2
0 0 0 0 0 0 0 0 0 0 0
1.3
2.1
35.2
49.3
52.2
62.5
59.2
67.7
75
71
80
74
71
78
75
72
80 81 81
75
86
81
89
84
88
90
73
76
88
96
94 93 94
90 90
81
97.597.7
91.8
100
78.5
96.2 96 96.1
90.7
96
0
10
20
30
40
50
60
70
80
90
100
Jul-17
Aug-17
Sep-17
Oct-17
Nov-17
Dec-17
Jan-18
Feb-18
Mar-18
Apr-18
May-18
Jun-18
Jul-18
Aug-18
Sep-18
Oct-18
Nov-18
Dec-18
Jan-19
Feb-19
Mar-19
Apr-19
May-19
Jun-19
Jul-19
Aug-19
Sep-19
Oct-19
Nov-19
Dec-19
Jan-20
Feb-20
Mar-20
Apr-20
May-20
Jun-20
Jul-20
Aug-20
Sep-20
Oct-20
Nov-20
Dec-20
Jan-21
Feb-21
Mar-21
Apr-21
May-21
Jun-21
Jul-21
Aug-21
Sep-21
Oct-21
ANTIMICROBIAL STEWARDSHIP
SEPSIS-SAP % SAP % of all low risk (SAP/LOW RISK)
Implementation in one unit as pilot
Sensitizing workshop, Roll out to all units
Sharing of monthly data
Identification of unit nodals, Induction training of residents
Fixed day meeting , WA gp
Display of performance unitwise as bar charts
0
5
10
15
20
25
30
35
40
45
50
Jul-17
Aug-17
Sep-17
Oct-17
Nov-17
Dec-17
Jan-18
Feb-18
Mar-18
Apr-18
May-18
Jun-18
Jul-18
Aug-18
Sep-18
Oct-18
Nov-18
Dec-18
Jan-19
Feb-19
Mar-19
Apr-19
May-19
Jun-19
Jul-19
Aug-19
Sep-19
Oct-19
Nov-19
Dec-19
Jan-20
Feb-20
Mar-20
Apr-20
May-20
Jun-20
Jul-20
Aug-20
Sep-20
Oct-20
Nov-20
TOTAL SEPSIS % AND SEPSIS % IN SAP
Total Sepsis % SEPSIS-SSAP %
To conclude
If we do not act now AMR will take us back to
the dark age of Medicine
We should use antibiotics responsibly to
prevent AMR by observing 5Rs
Antibiotics are essential for prevention and
treatment of maternal infections for
reducing maternal and perinatal mortality
and morbidity.
Antimicrobial resistance is not a hype it is a
fact
Acknowledgements
• Prof. Sushila Rathee Mentor
• Prof. SS Trivedi Advisor
• Dr Jagdish Chandra Visionary
• Dr Aparna Sharma QI Buddy
• Dr Shilpi Nain Partner
• Dr Sonal Saxena 24x 7 AMR
Consultation line
• All consultants and residents
Department of Obs & Gynae LHMC
Antimicrobial Resistance Oration Abhilasha.pptx

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Antimicrobial Resistance Oration Abhilasha.pptx

  • 1. Antimicrobial Resistance : Hype or Fact? Manju Puri Director Professor & Former HOD Department of Obstetrics & Gynecology Lady Hardinge Medical College New Delhi
  • 2. AMR : Is it a hype or fact? For those who have experienced the anxiety of an infection that is drug-resistant, first-hand, there is little that is needed to prove the existence and the importance of tackling AMR.
  • 3. For majority of the people around the globe the threat of drug resistance is either not known or seem a distant and abstract risk
  • 4. Obstetricians’ and AMR • Rising antibiotic resistance will have alarming secondary effects on safety of child-birth including CS • If AMR continues, much of the progress, we have made in reducing maternal and infant mortality in the last century will be at a risk of being undermined We need to wake up before it is too late
  • 5. Penicillin: An accidental discovery changed the course of medicine 1928
  • 6. Antimicrobial Resistance is resistance of a microorganism to an antimicrobial agent that was originally effective for treatment of infections caused by this microorganism Antimicrobial resistance 2022 National Health Policy 2017 flagged AMR as a Key issue WHO in 2001 declares AMR a global public health problem
  • 7. Magnitude of problem • Deaths attributable to AMR every year as compared to other major causes of deaths 300,000 Maternal deaths per year
  • 8. The Global Picture Majority of deaths will occur in Africa and Asia – over 4 million in each region. 10 million people a year
  • 9. It is important to bridge the gap between global perceptions of AMR today and how bad it is likely to become if the current trend is not altered
  • 10.
  • 11. Rational Antimicrobial Therapy Prevents • Selection of pathogenic organisms like Clostridium difficle • Collateral damage and alteration of patient’s microbiome especially GIT • Toxicity or adverse effects of antibiotics • Rising costs of treatment • Discovery void of antibiotics √ √ √ √ √
  • 12. FACTS Antibiotic Stewardship Programme Guidelines ( ICMR 2018)
  • 15. Smart of use of antimicrobials • Intend to prevent infection • Reduce colonization of microorganisms at the time of operation • Needed for short duration (as single preoperative shot) Prophylactic • Resolve an established infection • Needed for longer duration Therapeutic
  • 16. Principles of Optimal use of Antibiotics: For suspected or proven bacterial infection Initiating Empirical therapy* • Choosing the right antibiotic • Determine the optimum dose and route • Initiate promptly Tailoring therapy or Antibiotic time out • Re-evaluation continuously; usually after 48-72 hrs • Change to specific A/B; stop; adjust dose; add or subtract Convert from intravenous to oral administration Use for shortest effective dose * Remember : To take relevant cultures before starting A/B
  • 17. 5 D’s of Appropriate or Smart Antibiotic therapy Right Diagnosis/ Indication Right Drug Right Dose Right Duration De-escalation to pathogen-targeted therapy
  • 18. Principles of Optimal use of Antibiotics: For Surgical prophylaxis
  • 19. Antimicrobial prophylaxis is justified for most clean-contaminated procedures Ann Surg. 2009 Apr;249(4):551-6. Surg Infect (Larchmt). 2013 Feb;14(1):73-156
  • 20. Guidelines for prevention of Infection after Gynaecologic procedures • Laparoscopy (diagnostic, tubal sterilization, operative except for hysterectomy) • Other transcervical procedures: • Hysteroscopy (diagnostic or operative) • Intrauterine device insertion • Endometrial biopsy • HSG/SSG*(H/o of PID or damaged tubes on HSG or laparoscopy) • Oocyte retrieval • D&C for non-pregnancy indication • Cervical tissue biopsy, including LEEP or endocervical curettage • Cystoscopy ACOG practice bulletin No. 195: Prevention of infection after gynecologic procedures. Obstet Gynecol 2018; 131:e172 NO ANTIBIOTIC REQUIRED ACOG 2018
  • 21. Guidelines for prevention of Infection after Gynaecologic procedures Uterine evacuation (including surgical abortion, suction D&C, and D&E) • Oral Doxycycline 200 mg Metronidazole 1gm or Azithromycin 500mg single dose Caesarean section Hysterectomy 3rd and 4th degree perineal tears Pelvic reconstructive surgery colporrhaphy or vaginal sling or mesh placement • Cefazolin 2g I/V stat with in 60 min • Metronidazole 500mg + gentamicin 5mg/kg I/V • Clindamycin 900 mg +gentamycin 5mg/Kg I/V ACOG practice bulletin No. 195: Prevention of infection after gynecologic procedures. Obstet Gynecol 2018; 131:e172 ACOG 2018 ANTIBIOTIC PROPHYLAXIS INDICATED
  • 22. Antibiotic Stewardship It is a systematic measurement and coordinated interventions to promote optimal use of antimicrobial agents
  • 23. Antibiotic stewardship in Public Sector
  • 24. Case study 25 yrs. Primigravida at term with preeclampsia underwent CS for Foetal distress 15/8/16 • Inj Ampicillin + Metronidazole Day 2 Developed fever, tachycardia, tachypnoea, loose motions, discharge from wound; blood and wound swab sent for C/S • A/B stepped up: Meropenum and Ciprofloxacin Day 6 BDCS coagulase negative staphylococcus (CoNS) sensitive to Vancomycin /Clindamycin ; Pus C/S Methicillin sensitive (CoNS) sensitive to Linazolid/ Vancomycin/ Gentamycin; • A/B changed : Vancomycin + Clindamycin added
  • 25. Day 10 Pus C/S Acinobacter sensitive to Piptaz, Colistin, • A/B changed: Piptaz added Fever continued Day 21 Exploratory laparotomy with peritoneal lavage Day 26 (D6) breathlessness shifted to ICU intubated for assisted ventilation Culture ET, central line Pseudomonas and Klebsiella Sensitive to Colistin. • A/B stepped up to Colistin Day 32 (D12) Extubated Day 40 (D20) Discharged Hospital acquired infection and Antimicrobial resistance
  • 26.
  • 27. Key Messages Prevention of infection is not about administering antibiotics, antibiotics and antibiotics AMR is a serious problem It needs to be combated by Prudent or Smart use of antibiotics Otherwise antibiotics will lose their efficacy Return to the dark age of medicine…… It is more about use of aseptic precautions and rational use of antibiotics
  • 28. Journey of Antibiotic stewardship in the Department of Obstetrics & Gynecology LHMC
  • 29. Point of Care Quality Improvement Project on Rational use of antibiotics 4 step approach
  • 30. Steps in QI Step IV Sustaining improvement Step III Developing and testing changes PDSA cycle Step II Analyzing the problem and measuring quality of care by identifying outcome measure/s Step I Identifying a problem, writing an aim statement, forming a team Steps in QI
  • 31. Step 1: Problem identification, forming a team, and writing the aim statement • AIM STATEMENT We aim to increase the antibiotic prophylaxis (SSAB) in low-risk patients undergoing elective major surgery from 0% to 60% by 8 weeks QI TEAM MEMBERS All consultants of Department of Obstetrics & Gynecology Team leader Communicator Recorder
  • 32. Step 2a: Analyzing and measuring quality of care People Place Policy Procedure Major influence Major influence Minor influence Minor influence Problem No dept antibiotic policy in place - No sensitization - No awareness - Reluctance to give SSAB - Worried about asepsis When to administer Who will administer Where to document Non availability of antibiotic in OT
  • 33. Step 2b: Measuring quality of care: Quality Indicators Indicator Process indicator Numerator No. of patients who received SSAB Denominator No of eligible patients who underwent elective surgery Frequency of data analysis Monthly Data source (s) Case records Indicator Outcome indicator Numerator No. of patients who received SSAB developing SSI Denominator No of patients who received SSAB Frequency of data analysis Monthly Data source (s) Case records
  • 34. Act Plan Study Do Step 3 of Quality Improvement Develop and test changes Adopt Adapt Abandon What are the results? What did we learn? What are we going to do? When and how did we do it?
  • 35. Step 3: Developing and testing changes Change idea tested When was it done What was the result? What did we learn? 1. • Formulation of AB policy, detailed discussion, finalization after agreement • Sensitization Workshop for residents on asepsis • Roll it out in the department July 1st, 2017 to Aug 30th , 2017 Build consensus of all involved Not everyone was convinced due to fear of sepsis Adapt Start small 2. • Implementation in one unit • Sensitization workshop conducted for residents and NOs on AMR & asepsis • Collected base line data on outcome measure SSI July 1st, 2017 to July 31st , 2017 35.6 % use No ↑ SSI Adapt Sharing experience with other builds confidence 3. Implementation in all units August 1st , 2017 Approx. 50% use Adopt No ↑ SSI
  • 36. Step 3: Developing and testing changes Change idea tested When did you try this? Date. What was the result? What did we learn? 4. Identified a coordinator and nodal officers in each unit with monthly meeting in person with presentation of data and discussion of cases with continuation of A/B September 2017 SSAB use increased >60 % Adopt Increase in accountability and ownership pays SSAB remained above 60% Oct and Nov 17 ↓ 59% in Dec 17 Need for Hardwiring
  • 37. Change idea tested When did you try this? Date. What was the result? What did we learn? 5. 6. Addition of induction training of residents and regular sharing of data by nodal officers with coordinator Hold meeting on fixed day of the month with nodal officers to review data and have a WA group with nodal officers and unit heads as members March ’18 Sept ‘19 SSAB use increased 75% ADOPT Lesson learnt Wide dissemination and need for continuous follow up is important or sustenance For a change to sustain it should not be person centric but self sustaining Nov ‘18 to August ‘19 80 % - 90% A meeting was missed in Aug and Sep ‘19 as the Coordinator was on leave SSAB rate came down to 70-75%
  • 38. Change idea tested When did you try this? Date. What was the result? What did we learn? 7. Started sharing monthly data during the monthly statistics meeting To show a ppt slide with the SSAB usage and SSI rate Oct’19 Lesson learnt Need for continuous follow up for sustenance and sharing of data keeps the momentum of the change and everyone interested SSAB remained above 80% since Oct ’19 most of the months it is above 90%
  • 39. Step 4: Sustaining Improvement • Continuous monitoring of process and outcome indicator monthly • Sharing of data • Generate competition among units • Appreciate those doing well
  • 40. 0 0 2 1 0 0 1 0 0 1 1 0 1.5 0 0 1 0 1 0 0.9 0 0 0 0 1 0 0 0 0 0 1 1.1 4.2 0 0 0 0 0 0 0 0 0 0 0 1.3 2.1 35.2 49.3 52.2 62.5 59.2 67.7 75 71 80 74 71 78 75 72 80 81 81 75 86 81 89 84 88 90 73 76 88 96 94 93 94 90 90 81 97.597.7 91.8 100 78.5 96.2 96 96.1 90.7 96 0 10 20 30 40 50 60 70 80 90 100 Jul-17 Aug-17 Sep-17 Oct-17 Nov-17 Dec-17 Jan-18 Feb-18 Mar-18 Apr-18 May-18 Jun-18 Jul-18 Aug-18 Sep-18 Oct-18 Nov-18 Dec-18 Jan-19 Feb-19 Mar-19 Apr-19 May-19 Jun-19 Jul-19 Aug-19 Sep-19 Oct-19 Nov-19 Dec-19 Jan-20 Feb-20 Mar-20 Apr-20 May-20 Jun-20 Jul-20 Aug-20 Sep-20 Oct-20 Nov-20 Dec-20 Jan-21 Feb-21 Mar-21 Apr-21 May-21 Jun-21 Jul-21 Aug-21 Sep-21 Oct-21 ANTIMICROBIAL STEWARDSHIP SEPSIS-SAP % SAP % of all low risk (SAP/LOW RISK) Implementation in one unit as pilot Sensitizing workshop, Roll out to all units Sharing of monthly data Identification of unit nodals, Induction training of residents Fixed day meeting , WA gp Display of performance unitwise as bar charts
  • 42. To conclude If we do not act now AMR will take us back to the dark age of Medicine We should use antibiotics responsibly to prevent AMR by observing 5Rs Antibiotics are essential for prevention and treatment of maternal infections for reducing maternal and perinatal mortality and morbidity. Antimicrobial resistance is not a hype it is a fact
  • 43. Acknowledgements • Prof. Sushila Rathee Mentor • Prof. SS Trivedi Advisor • Dr Jagdish Chandra Visionary • Dr Aparna Sharma QI Buddy • Dr Shilpi Nain Partner • Dr Sonal Saxena 24x 7 AMR Consultation line • All consultants and residents Department of Obs & Gynae LHMC

Editor's Notes

  1. Sir Alexander Fleming was a Scottish biologist, physician, microbiologist, and pharmacologist. Discovered Penicillin Howard Florey Australian pharmacologist and pathologist who shared the Nobel Prize in Physiology or Medicine in 1945 with Sir Ernst Chain German-born British biochemist, and their role in the development of penicillin Penicillin is now the most widely used antibiotic in the world
  2. Warnings about AMR are nothing new – Alexander Fleming reportedly warned about the development of drug-resistance in his 1945 Nobel Prize acceptance speech.
  3. Not to sterilize the tissues needed for a shorter duration. Reduce microbial load so that patient’s immune system can combat
  4. The primary goal is to optimize clinical outcomes while minimizing unintended consequences of antimicrobial use Improve susceptibility rates to targeted antimicrobials and optimizing resource utilization
  5. Highlight that this course is designed to teach a new skill – how to use quality improvement methods to improve service delivery at the point of care in your health facility We will spend Day 1 working through the four steps of QI using a hypothetical example On Day 2 we will help plan an initial QI project that you can carry out in your facility The first step is to pick something specific to work on, form a team and develop a precise aim statement to guide your efforts.