The document discusses hospital antibiograms, which are periodic summaries of antimicrobial susceptibilities of bacterial isolates in a hospital. They are useful for clinicians to assess local susceptibility rates and monitor resistance trends over time. The document covers various topics related to antibiograms including how they are tested, interpreted, and documented. It emphasizes the importance of generating antibiograms using standardized methods and interpreting them carefully based on multiple factors.
The lecture describes the performance and presentation of the antibiograms by the hospitals based upon recommendations of CLSI and shows experience of some of our MOH hospitals with the advantages and pitfalls in them.
Antibiotics are most common therapeutic agents used in hospitals across world, however, microbial world is becoming resistant day by day, posing special challenges to clinicians specially working in ICU set ups. There are multiple ways to curb this menace, if approached together in antibiotic stewardship way, can bring about wonders and retain therapeutic potentials of these drugs.
The lecture describes the performance and presentation of the antibiograms by the hospitals based upon recommendations of CLSI and shows experience of some of our MOH hospitals with the advantages and pitfalls in them.
Antibiotics are most common therapeutic agents used in hospitals across world, however, microbial world is becoming resistant day by day, posing special challenges to clinicians specially working in ICU set ups. There are multiple ways to curb this menace, if approached together in antibiotic stewardship way, can bring about wonders and retain therapeutic potentials of these drugs.
Blood stream infections- clinical microbiologySijo A
Blood stream infections (BSI) refers to the presence of organisms in blood which are threat to every organ in the body.
It causes shock, multiple organ failure and DIC (Disseminated Intravascular Coagulation).
The presence of bacteria in blood is called Bacteremia.
The bacteria circulate and actively multiply in the blood stream is called Septicemia.
The presence of virus in blood is called Viremia.
The presence of parasite in blood is called Parasitemia.
The presence of fungi in blood is called Fungemia.
"Beyond Measure" is more than a tagline. It is at the core of what we do for our customers at SURVICE Metrology. It is the ability to look beyond a customer's request for support and provide further insight to both their requirements and the tools, techniques, and processes available to get the job done right the first time. Our diverse workforce at SURVICE Metrology brings experience and expertise from various industries, trades, and government institutions to our profession - and our reach back to internal resources at SURVICE Engineering's operations across the United States is unparalleled.
SURVICE Metrology provides innovative and integrated dimensional inspection services, 3-D modeling, and metrology application development. From our metrology facilities in Maryland, Florida and Michigan, as well as through our portable field measurement teams, we provide responsive support and quality products to our customers.
SURVICE Metrology is a division of the SURVICE Engineering Company (www.survice.com). SURVICE has been providing the DoD and industry customers with specialized products and services supporting the design, development, testing, and fielding of systems for more than 30 years. SURVICE's corporate headquarters is in Belcamp, MD, and has technical operations in Maryland, Virginia, Ohio, Alabama, Florida, and California.
We Employ:
• A suite of state-of-the-art metrology equipment – laser and structured-light scanning, portable and fixed CMMs, laser trackers, photogrammetry, x-ray computed tomography
• Advanced measurement and modeling tools
• Extensive measurement, modeling, reverse engineering, reality capture experience
• Unique custom application development capability – HawkEye, Enhanced Laser Radar, I-CARS, Structure From Motion
• Additive manufacturing – 3D printing and model prep services
Blood stream infections- clinical microbiologySijo A
Blood stream infections (BSI) refers to the presence of organisms in blood which are threat to every organ in the body.
It causes shock, multiple organ failure and DIC (Disseminated Intravascular Coagulation).
The presence of bacteria in blood is called Bacteremia.
The bacteria circulate and actively multiply in the blood stream is called Septicemia.
The presence of virus in blood is called Viremia.
The presence of parasite in blood is called Parasitemia.
The presence of fungi in blood is called Fungemia.
"Beyond Measure" is more than a tagline. It is at the core of what we do for our customers at SURVICE Metrology. It is the ability to look beyond a customer's request for support and provide further insight to both their requirements and the tools, techniques, and processes available to get the job done right the first time. Our diverse workforce at SURVICE Metrology brings experience and expertise from various industries, trades, and government institutions to our profession - and our reach back to internal resources at SURVICE Engineering's operations across the United States is unparalleled.
SURVICE Metrology provides innovative and integrated dimensional inspection services, 3-D modeling, and metrology application development. From our metrology facilities in Maryland, Florida and Michigan, as well as through our portable field measurement teams, we provide responsive support and quality products to our customers.
SURVICE Metrology is a division of the SURVICE Engineering Company (www.survice.com). SURVICE has been providing the DoD and industry customers with specialized products and services supporting the design, development, testing, and fielding of systems for more than 30 years. SURVICE's corporate headquarters is in Belcamp, MD, and has technical operations in Maryland, Virginia, Ohio, Alabama, Florida, and California.
We Employ:
• A suite of state-of-the-art metrology equipment – laser and structured-light scanning, portable and fixed CMMs, laser trackers, photogrammetry, x-ray computed tomography
• Advanced measurement and modeling tools
• Extensive measurement, modeling, reverse engineering, reality capture experience
• Unique custom application development capability – HawkEye, Enhanced Laser Radar, I-CARS, Structure From Motion
• Additive manufacturing – 3D printing and model prep services
The Program file is created from various peer reviewed, and world standard protocols in implantation of Safe Operation theater standards for wider use in the world, In India still we do not have any set standards and practices, As good beginning is half done, I wish all my professional friends go through the article, your opinions and comments are highly appreciated for future developments,
Dr.T.V.Rao MD
For more Info visit www.healthlibrary.com "What is Medical Negligence" by Dr. Ghazala Shaikh held on 23rd Mar 2016.
Public awareness of medical negligence in India has increased but the 'term' is till misunderstood by the common man. Its medical negligence is needs to be explained and understood in legal perspective and merits of the case has to be find out by the medico legal consultants.
Here I am trying to explain how Medical Negligence and Medical Ethics are interlinked and why doctors must do all they can to defend our ethics. I am sharing case history, every day clinical examinations and management of common illness to explain why they are unethical medical practice.
Since I published a letter in 1996, critisising the use of preprinted assessment sheet, allowing nurses to work like doctors in the NHS(UK), the number of deaths, complications and wrong doings has escalated to catastrophic proportions. Doctors who continue to work are suffering in silence. The ones who raised concern were systamatically harassed, bullied and ostracised.
The institutions, associations, nursing council and the Royal Colleges and the WMA have ignored their duty to protect fellow human. I do not think we can claim to be members of a "Noble Profession" if we allow this un-ethical medical practice continues.
The General Medical Has not only ignored their duty to protect fellow human but also discriminated doctors passing out from Non-European medical schools by allowing nurses to work like doctors. This institution has failed to define the word "Doctor" and has inflicted pain and suffering to doctors who defend their moral and ethical duty.
Our profession and our lives are threatened by emerging and antibiotic resistant infections. We must join hands and defend our profession. By allowing nurses with no medical school training or skill to clinically examine patients to diagnose and prescribe drugs, we have failed to protect fellow human who trust our profession. This is substandard, un-ethical medical practice that has brought us shame must be stopped.
Please leave your comments and criticise me if I am wrong. As a Hindu Brahmin, it is my religious duty to defend "Dharma", protect the sick and vulnerable. Please watch this presentation and ask your self have you fulfilled your promise and are you defending your faith?
In this presentation it has been tried to give a glimpse of different type of consent, how it should be taken, how the patient to be explained, when consent is must and conditions where consent is not required, so as to guide you in your every day practice.
Antibiotic sensitivity test PPT by Dr.C.P.PRINCEDR.PRINCE C P
Antibiotic sensitivity test: in vitro testing of bacterial cultures with antibiotics to determine susceptibility of bacteria to antibiotic therapy.
A laboratory test which determines how effective antibiotic therapy is against a bacterial infections.
Antibiotic sensitivity testing will control the use of Antibiotics in clinical practice
Testing will assist the clinicians in the choice of drugs for the treatment of infections.
Helps to guide the Physician in choosing Antibiotics
The accumulated results on different pathogens their sensitivity will guide the physician in choosing empirical treatment in serious patients before the individual’s laboratory results are analyzed in the Microbiology laboratory.
Reveals the changing trends in the local isolates.
Helps the local pattern of antibiotic prescribing.
PPT Prepared by
Dr.Prince.C.P
Department of Microbiology
Mother Theresa PG&RIHS
Pondicherry
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
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Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
2. Different methods to Test
Antibiotic Sensitivity patterns
03-08-2016 Dr.T.V.Rao MD 2
3. What is an
antibiogram
•An antibiogram is a
laboratory test used to
determine the
sensitivity pattern of a
given microorganism
to a range of
antibiotics.
03-08-2016 Dr.T.V.Rao MD 3
4. What is a Hospital
Antibiogram
•The hospital antibiogram is a periodic summary
of antimicrobial susceptibilities of local bacterial
isolates submitted to the hospital's clinical
microbiology laboratory. Antibiograms are often
used by clinicians to assess local susceptibility
rates, as an aid in selecting empiric antibiotic
therapy, and in monitoring resistance trends
over time within an institution
03-08-2016 Dr.T.V.Rao MD 4
5. Helps in identifying the Antibiotic
Resistance patterns
•Antibiograms can
also used to
compare
susceptibility rates
across institutions
and track
resistance trends03-08-2016 Dr.T.V.Rao MD 5
6. Why we need An Antibiogram
•Antimicrobial-resistant bacterial infections
are a challenging problem in the hospital
setting. Infections caused by resistant- and
multidrug-resistant (MDR) bacteria not
only increase morbidity and mortality, but
also increase overall healthcare costs,
primarily by prolonging hospital length of
stay.03-08-2016 Dr.T.V.Rao MD 6
7. Hospital Associated Infections can
be Monitored with Antibiograms
• In situations when
hospital-acquired
infections do occur, the
preponderance of MDR
bacteria as the causative
pathogen challenges
clinicians in selecting
appropriate therapy and
treatment regimens.
03-08-2016 Dr.T.V.Rao MD 7
8. We need better methods to monitor
Antibiotic Therapy
•Inappropriate
therapy can have
significant
clinical and
economic
consequences
03-08-2016 Dr.T.V.Rao MD 8
9. Wrong Antibiograms add to
MDR Strains
• Inappropriate
antimicrobial
selection also has
the potential to
increase the risk for
resistance
development.03-08-2016 Dr.T.V.Rao MD 9
10. Antibiograms are also
used to
•Check if the causative agent belongs to a
species capable of exhibiting resistance to
commonly used antibiotics.
•Study the epidemiology of resistance
•Evaluate the efficacy of a new antibiotics
03-08-2016 Dr.T.V.Rao MD 10
11. Hospital Antibiograms are essential
tools
• Hospital antibiograms can be an
essential tool to monitor local
epidemiology and emerging
resistance trends.
Antibiograms, if generated and
utilized appropriately, can
monitor resistance at
healthcare facilities by
reporting susceptibility rates of
common pathogens over a
period of time03-08-2016 Dr.T.V.Rao MD 11
12. Selecting an Appropriate Antibiotic
a Priority
•They can, therefore,
serve as an invaluable
guide in selecting
appropriate empiric
therapy and influence
institutional
antimicrobial use
policies
03-08-2016 Dr.T.V.Rao MD 12
13. Growing Importance of
Antibiograms
•Over the last twenty
years, new categories
of antibiotics have
entered the market
and numerous forms
of resistance have
appeared and
multiplied
03-08-2016 Dr.T.V.Rao MD 13
14. Antibiograms are also used to
• Check if the causative agent
belongs to a species capable
of exhibiting resistance to
commonly used antibiotics.
• Study the epidemiology of
resistance
• Evaluate the efficacy of a
new antibiotic
03-08-2016 Dr.T.V.Rao MD 14
15. Why should you develop and use
an antibiogram at your Hospital
facility?
• Antibiograms encourage responsible use of antibiotics
throughout facilities. Prescribing clinicians—physicians,
nurse practitioners, and physician assistants—can consult
these tools before initiating empiric antibiotic therapy, which
may improve outcomes among patients with infections.
• Antibiograms are a good way to detect changes in resistance
patterns for an entire facility or for locations within a facility.
• Antibiograms can be inexpensive to develop and maintain.
The results are easily accessible to health care providers.
03-08-2016 Dr.T.V.Rao MD 15
16. How to begin our Work with
Antibiograms
• Isolation, identification of the
pathological Microbe and
antibiogram of a pathogenic
agent are normally carried out
when a bacterial disease has
produced a problem
• We have specific and
General methods to identify
the pathogenic bacterial
isolate
03-08-2016 Dr.T.V.Rao MD 16
17. Mechanism in Testing the
Antibiograms
• The basic idea of
diffusion assays is as
follows: the tested
antibiotics are
impregnated in paper
discs which are placed on
plate of agar medium
inoculated with the
bacteria in question.
03-08-2016 Dr.T.V.Rao MD 17
18. Mechanism in Testing the
Antibiograms
• Following diffusion of the
compounds through the
agar, a "halo" or zone of
inhibition forms where a
concentration of the
specific diffused
antibiotic is sufficient to
inhibit that microbial
growth
03-08-2016 Dr.T.V.Rao MD 18
19. Interpreting an
antibiogram• The correct
interpretation of the
antibiogram will be of
interest to
Microbiologists and
laboratory technicians
alike. Standardized
methods are established
and can be found in the
WHO manuals.
03-08-2016 Dr.T.V.Rao MD 19
20. Still we have not
Understood Problems with
Antibiograms
• One of the most frequently
asked questions relates to in-
vitro (in the lab)/in-vivo (in
the field) relationships. Why is
it that satisfactory in vitro or
laboratory test results can
translate into poor clinical
efficacy In these situations,
thought should be given to:
clinical and laboratory
coordination
03-08-2016 Dr.T.V.Rao MD 20
21. To have a better Understanding of
Antibiograms
•a) Whether or not the diagnosis correct?
•b) Whether the problem is really caused by the isolated
bacteria?
•c) Whether the product was administered correctly, at the
right dose level, for the correct number of days?
•d) Whether the activity level of the drug coincides with
label specifications
03-08-2016 Dr.T.V.Rao MD 21
22. Factors influencing the
interpretation of an antibiogram
• Based on this reasoning, the
diffusion method is sometimes
mistakenly interpreted as a
quantitative method. The more
potent an antimicrobial
compound, the less
concentrated it need be, and
consequently at points further
from the disc with consequently
lower concentrations, microbial
growth will still be inhibited
03-08-2016 Dr.T.V.Rao MD 22
24. Basic Interpretation of
Zone Sizes
•Therefore, it is often
assumed that the
larger the diameter
of the zone of
inhibition, the more
potent the
antimicrobial
03-08-2016 Dr.T.V.Rao MD 24
25. Why Concentration of the Antibiotic
matters
• A number of factors however,
may interfere with this
interpretation. Firstly, the
concentration of the antibiotic in
the disc must be taken into
account. The higher the
concentration in the disc, the
more concentrated the
compound will be at a given
distance from the disc itself.
03-08-2016 Dr.T.V.Rao MD 25
26. Time too matters in optimal
Reading of Antibiograms
• Also, the length of time
allowed for the process to
occur can greatly influence
the diameter of the zone of
inhibition as the longer
diffusion is allowed to take
place the higher the
concentrations at any given
point in the gradient will be.
03-08-2016 Dr.T.V.Rao MD 26
27. Zone sizes are Interpreted with
consideration of many factors
• Related to this, the infusibility of
the antimicrobial compound
through the agar can greatly
impact on the observed zone of
inhibition, such that a very
potent inhibitor may produce a
relatively small "halo" simply
because it is unable to diffuse
adequately through the
medium. In addition, the extent
of the growth of the microbe
03-08-2016 Dr.T.V.Rao MD 27
28. Outcome of Antibiograms
depend on many factors
• In relation to the
degree of diffusion,
can influence the
resulting zone of
inhibition, such that
the timing of both
factors, microbial
growth and
diffusion, interplay.
03-08-2016 Dr.T.V.Rao MD 28
29. What are the Isolates to be Taken for
Reporting Antibiograms
•Only the first isolate from the patient is to
be included in the analysis. The analysis
should be done on the basis of patient
location and specimen type. The percentage
susceptibility of the most frequently
isolated bacteria should be presented in the
antibiogram, preferably in a tabular form
03-08-2016 Dr.T.V.Rao MD 29
30. Basis of Choosing
Antibiotic Discs
•The selection of the most appropriate antibiotics
to test is a decision best made by each clinical
laboratory in consultation with the field
veterinarian. To avoid unnecessary duplication,
only one antibiotic from each family should be
used. Agents of the same family have similar
clinical efficacy, show nearly the same spectrum
of activity and have similar cross-resistance and
cross-susceptibility.03-08-2016 Dr.T.V.Rao MD 30
31. How to prepare the inoculum for
Testing the Antibiograms
•At least three to five well-
isolated colonies of the
same morphological type
bacteria are selected from a
primary agar plate culture
and transferred into a tube
containing 4-5 ml of broth
medium.
03-08-2016 Dr.T.V.Rao MD 31
32. Preparing inoculum for
Testing Antibiograms• This is incubated at 35°C for
2-6 hours and then applied
with a sterile cotton swab on a
dried surface of a Mueller-
Hinton agar plate.
Alternatively the inoculums
can be prepared by making a
direct broth or saline
suspension of isolated colonies
selected from a primary agar
plate03-08-2016 Dr.T.V.Rao MD 32
33. Placement of Antibiotic Discs for Optimal
Antibiograms
• The predetermined battery of
anti-microbial disks is dispensed
onto the surface of the
inoculated agar plate. Each disk
must be pressed down to ensure
complete contact with the agar
surface. The disk must be
distributed evenly no closer than
24mm from Center to centre.
The plates are inverted and
placed in an incubator at 35°C.
03-08-2016 Dr.T.V.Rao MD 33
34. Reading the Zones of
Inhibition
• After 16-18 hours of
incubation, each plate is
examined. The resulting
zones of inhibition (halo) will
be uniformly circular and
there will be a confluent
lawn of growth. The
diameters of the zone of
complete inhibition are
measured, including the
diameter of the disk03-08-2016 Dr.T.V.Rao MD 34
35. Measuring Zone Sizes in
Antibiograms
• The measurement can be
done using a sliding calliper,
ruler or compass as
demonstrated in picture .
The zone margin should be
taken as the area showing
no obvious, visible growth
that can be detected by the
naked eye.
03-08-2016 Dr.T.V.Rao MD 35
36. Formulating the Concentration of
Antibiotic and relevance of zones
depend on
•Comparing zone diameters to
minimum inhibitory
concentrations (MICs) of a
large number of isolates,
including those with known
mechanisms of resistance
relevant to the particular
class of drug
03-08-2016 Dr.T.V.Rao MD 36
37. Pharmaco kinetics play a Major
Role
•Analysing the MICs
and correlated zone
sizes in relation to
the pharmaco-
kinetics of the drug
from normal dose
range schedules
03-08-2016 Dr.T.V.Rao MD 37
38. Choosing Antibiotics to the
effectiveness of isolated
pathogens
•Analysing whenever
possible the tentative
in vitro interpretive
criteria in relation to
studies of clinical
efficacy in the
treatment of specific
pathogens
03-08-2016 Dr.T.V.Rao MD 38
39. What is Susceptible
• This category implies that an
infection due to this
bacterium may be
appropriately treated with
the dosage of antibiotic
recommended for that type
of infection and infecting
species, unless otherwise
contraindicated
03-08-2016 Dr.T.V.Rao MD 39
40. Intermediate
• This category implies that an
infection due to this
bacteria, may be treated
when possible with higher
than normal dosage of this
antibiotic, or when the drug
is physiologically
concentrated in certain body
sites, like Quinolones in
urine03-08-2016 Dr.T.V.Rao MD 40
41. Resistant
•Resistant strain will
probably not respond to
any treatment, as they
are not inhibited by the
usually achievable
systemic concentrations
of the antibiotic when
normal dosage schedules
are used.
03-08-2016 Dr.T.V.Rao MD 41
42. How we express the
Results
• Because of these
complexities in the
diffusion method, it is
perhaps best to consider
the results of the
diffusion assay as
qualitative only,
expressed as: Sensitive,
Intermediate and
Resistant03-08-2016 Dr.T.V.Rao MD 42
43. Do not Process the specimens
Directly for Antibiotic Sensitivity
testing•The practice of
conducting susceptibility
tests directly with clinical
material should be
avoided except in clinical
emergencies when direct
gram staining suggests
the presence of a single
pathogen03-08-2016 Dr.T.V.Rao MD 43
44. Document Antibiograms with
WHONET
• Some hospitals have
adequate support from
the computer
department to be able to
extract data from their
reporting module. The
WHONET software can
be freely downloaded
and used for analysis.
03-08-2016 Dr.T.V.Rao MD 44
46. WHONET AND CLSI HELPS IN
ANALYSIS OF THE ANTIBIOGRAMS
Consensus guidelines have
been developed by the
Clinical and Laboratory
Standards Institute (CLSI) to
standardise methods used in
constructing antibiograms.
These guidelines can be
incorporated into the
WHONET software for
analysis
03-08-2016 Dr.T.V.Rao MD 46
48. How to modernized Hospital
Antibiograms
• The antibiogram must be
printed or put up in the
intranet for easy access to
all clinicians. Antibiotic
policy is one of the
mandatory requirements
for accreditation, and
making an antibiogram is
the first step before framing
the antibiotic policy.
03-08-2016 Dr.T.V.Rao MD 48
49. Critical Thinking on
Antibiograms
•Antibiograms only
capture the aggregate
proportion of
susceptible isolates for a
given organism-
antibiotic combination.
They do not provide the
prevalence resistance to
multiple antibiotics.
03-08-2016 Dr.T.V.Rao MD 49
50. Antibiograms helps for taking decisions on
Empiric Antibiotics
•Antibiograms provide
guidance for empiric
antibiotic use in patients,
but other factors including
patient characteristics and
prevalence of other risk
factors should be
incorporated when making
therapeutic decisions
03-08-2016 Dr.T.V.Rao MD 50
51. Future of
Antibiograms•The future of
antibiograms would
be the incorporation
of patient related
data to make
information more
reliable and for
predicting outbreaks03-08-2016 Dr.T.V.Rao MD 51
52. Mobile Application on Iphone and IPad
• Antibiograms help healthcare
professionals and clinical
microbiologists choose the most
effective antibiotics to
empirically treat infections,
based on local susceptibility
patterns. Now this valuable
information can be available to
them on iPhone/iPad mobile
devices.
03-08-2016 Dr.T.V.Rao MD 52
53. Antibiogram app
•With the
Antibiograms app,
you simply select a
bacterium, select a
patient group, and you
are given the proportion
of susceptible organisms
for each antibiotic tested
in your local laboratory.
03-08-2016 Dr.T.V.Rao MD 53
54. For Better Understanding on
Antibiograms
• For more detailed information, look at the WHO's
technical manual.
• Ref 1 The Facts about Antibiogram - Dr Yonatan Segal
• 2 Hospital antibiogram: a necessity. Joshi PubMed . Indian J
Med Microbiol. 2010 Oct-Dec;28(4):277-80. doi:
10.4103/0255-0857.71802
• 3 Concise Antibiogram Toolkit - EFwww.ahrq.gov/NH-ASP
Guide • May 2014 AHRQ Pub. No. 14-0012-1-EFwww
03-08-2016 Dr.T.V.Rao MD 54
55. • Program Created By Dr.T.V.Rao MD for basic understanding
on Creation and Documentation of Hospital Antibiograms
for New Generation of Medical Microbiologists practicing
World Wide for better health care
•Email
•doctortvrao@gmail.com
03-08-2016 Dr.T.V.Rao MD 55