Dr gunturu revathi

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Hands-on Session: Analyzing and Understanding Hospital-level Resistance Data Dr.G.Revathi, Associate Professor & Consultant Microbiologist, The Aga Khan University Hospital Nairobi, KENYA

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Hands-on Session: Analyzing and Understanding Hospital-level

Resistance Data

Dr.G.Revathi,

Associate Professor & Consultant Microbiologist,

The Aga Khan University Hospital

Nairobi, KENYA

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Objective of this presentation l  To describe the collection, analysis and

use of the cumulative bacterial identification and antimicrobial susceptibility data in The Aga Kahn University hospital Nairobi.

l To show examples of different data sets that are usually derived from this source

l Examples of different clinical applications

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l The Aga khan University Hospital Microbiology division – A well equipped modern facility

l Blood cultures – Automated Fluorogenic system Bactec 9050

l Bacterial identification by commercial API and automated Vitek Compact 2

l The unit generates about 30 - 45 bacterial susceptibility results on an average working day

l The division includes a TB culture lab

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HIS and LIS are in place since 2007. But LIS has limited capacity to store or

analyze data All bacterial identification susceptibility

data Captured on spread sheets on daily basis.

Data is entered on separate sheet for each organism.

Certain organisms are grouped together- Enterobacter & Citrobacter

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l  Locally developed data entry and management system is used to analyze cumulative microbiological test data.

l  Patient demographic information, specimen information are manually entered in LIS

l  Test results are exported from Vitek compact 2 to laboratory information system. Can be down loaded into spread sheets.

l  Detection of duplicate isolates is based on patients’ names and identification numbers, organism identification and susceptibility patterns.

l  Isolates from screening specimens excluded and analyzed as separate set of data

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l TB lab data is captured separately l Two different technologists counter check

the entries for accuracy. l Residents / consultants audit accuracy of

data at random.

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l  Listing of identification and antibiotic susceptibility test results are generated once in two month.

l  All species are presented, regardless of the number isolated.

Specific subsets tabulated such as

l  Different locations of hospital (e.g. inpatient, outpatient, surgical ward, New born unit, intensive care unit),

l  Specimen types (blood, urine) l  Special patient groups - Renal clinic, Chest clinic,

Diabetic clinic

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Other applications are l  Listings of all patients with bacteraemia, l  Daily listings of patients with resistant or highly

transmissible micro-organisms l  Detection of patients with possible nosocomial infection.

l  Cumulative antimicrobial susceptible data of relevant species are presented in tabular form.

l  Separate tables for specific subsets if needed. graphs a to follow accumulated data over several years.

l  These data are used to update empiric therapy schemes.

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Data reports percent susceptible and does not include percent intermediate in the statistics. l • The data presented in separate subgroups in the report (e.g. gram positive vs. gram negative, l inpatient vs. outpatient, and antibiotics tested on urine). l • Multidisciplinary approach - review by physician, infection control personnel and pharmacist prior to publication. Usually clinical audits and chart reviews complement the conclusions

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Repeat isolates from same patient are handled by episode and phenotype based approach.

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l Enterococcus faecium % decrease in susceptibility -Nitrofurantoin (urine) 26

l Staphylococcus, coag neg % decrease in susceptibility -Moxifloxacin 21

Examples of interpretations

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SALMONNELPHI/SPP.

AGE SEX OP/IP SPECIMENORGANISM Pus cells AMPCIPRO NALID CEFTRI CHLORA COTRI1.9yrs m 11463 Stool Sal spp Nil S S S S S S9yrs ? 1738 Lavin stool Sal spp Nil S S S S S S4.3yrs m 12246 Stool Sal spp 2/hpf S S S S S S3.9yrs f 12801 Stool Sal spp 15/hpf S S S S S S10yrs f 13248 Stool Sal spp Nl S S S S S S1.5yrs ? 1834 Stool Sal spp Nil S S S S S S3.11 f 14686 stool Sal spp 15/hpf S R R S S S9yrs f 26384 Blood Ctr Sal spp R S S R S1day f Blood Ctr Sal spp R S S S S7m f 2155 Stool Sal spp Nil S S R S R1yr m othaya Stool Sal spp R S S S2.4 yrs f 370 Othay Stool Sal spp S S S S7m m 32705 Stool Sal spp S S S S S3.9yrs f 32533 Stool Sal spp S S S S9yrs m 9594 Stool Sal spp 10 hpf S S S S S S9m m 2182 stool salspp nil S S S S R S14yrs f 15053 stool salspp 8 hpf S S S S S S1yr m 15821 Stool salspp 2 hpf S S S S S S

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Clinically significant UTI cases from data base

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Colistin usage information from pharmacy

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l Limitations of this data collection l  It is not possible all the time to ascertain

Pathogen vs. colonizer in certain specimens. l Manual entries are checked and audited but

errors may happen l  Large number of isolates from satellite

clinics do not have clinical information l Data needs lot of filtering before it can

make sense – eg. Sputum vs. pneumonia, Urine vs UTI Clinical validation not possible in all specimens

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Trends of resistance to anti TB Drugs at AKHUN

Trends of resistance to tested TB Drugs at AKHUN

0.00%

5.00%

10.00%

15.00%

20.00%

25.00%

30.00%

2007 2008 2009 2010 2011

Years

Freq

. in

%ag

es STREPTOMYCINISONIAZIDRIFAMPCINETHAMBUTOLPZA

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Trends of MDR TB at the AKUHN in 2007- 2011

Trends of MDR occurence at the AKUHN in 2007- 2011

02468101214

1 2 3 4 5

Years

Fre

q. o

f M

DR

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Multi-drug resistant gram negative bacilli isolated from nosocomial pneumonias during

2001 – 2003

TOTAL 552 ISOLATES 21%

24%

10% 7%

24%

14% E. Coli = 108 Klebsiella spp = 126 Proteus spp = 54 Enterobacter spp = 36 Pseudomonas spp = 126 Miscellaneous = 72

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Meropenem/Imipenem

100 100 100 100 100 83.2

16.8 0 0 0 0 0

Organism

0

20

40

60

80

100

Perce

ntage

Sensitivity Resistance

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ANALYSIS OF PSEUDOMONAS SUSCEPTIBILITY 2011

0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

CIP CEF

CAZ

IMIP AMI

TAZ

GENTA

CRO PIP TIM MER

ANTIBIOTICS

PERC

ENTA

GE

Series1

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l Hospital antibiogram cannot be used alone to select the optimal empiric therapy in an individual patient-

l  specific patient factors to be considered, the type and severity of infection,

l  the infecting organism, l  the patient's medical history, comorbid

factors l Previous hospitalisations, past antibiotic

use.

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ESCHERICHIA COLI Approximately 14% of isolates produce extended spectrum beta lactamases in 2003, 22% in 2005

2001 960 isolates

2003 828 isolates

2004 – 2005 1158 isolates

Antibiotic Susceptible Susceptible Susceptible

Augmentin 91% 88% 87%

Gentamicin 85% 86% 88%

Amikacin 93% 89% 90%

Chloramphenicol 67% 53% 58%

Cefuroxime 90.5% 89% 82%

Ceftazidime 96% 89% 91%

Ceftriaxone 96% 89% 91%

Cefaclor 96% 89% 82%

Cotrimoxazole 63% 50% 57%

Ciprofloxacin 93% 90% 92%

Nitrofurantoin 79% 80% 87%

Nalidixic acid 81% 75% 68%

Cefepime - 91% 86%

Meropenem/Imipenem - 98% 100%

Tazo/Piperacillan - 99% 99%

Ticarcillin/Clavulanate 100% 100% 100%

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