Video-Directly Observed Therapy (V-DOT) is a promising solution for monitoring TB and HIV
treatment adherence for binational patients in the U.S.-Mexico border region.
Anti Tubercular Drugs - Mechanism of Action and Adverse effects Thomas Kurian
A brief outline of the mechanism of action and adverse effects of anti tubercular drugs
Only First line and second line drugs are dealt with.First line drugs may be useful for MBBS students and the rest is directed for postgraduate students.
Hope you find it useful.
The bacteria that cause tuberculosis (TB) can develop resistance to the antimicrobial drugs used to cure the disease. Multidrug-resistant TB (MDR-TB) is TB that does not respond to at least isoniazid and rifampicin, the 2 most powerful anti-TB drugs.
The 2 reasons why multidrug resistance continues to emerge and spread are mismanagement of TB treatment and person-to-person transmission. Most people with TB are cured by a strictly followed, 6-month drug regimen that is provided to patients with support and supervision. Inappropriate or incorrect use of antimicrobial drugs, or use of ineffective formulations of drugs (such as use of single drugs, poor quality medicines or bad storage conditions), and premature treatment interruption can cause drug resistance, which can then be transmitted, especially in crowded settings such as prisons and hospitals.
In some countries, it is becoming increasingly difficult to treat MDR-TB. Treatment options are limited and expensive, recommended medicines are not always available, and patients experience many adverse effects from the drugs. In some cases even more severe drug-resistant TB may develop. Extensively drug-resistant TB, XDR-TB, is a form of multidrug-resistant TB with additional resistance to more anti-TB drugs that therefore responds to even fewer available medicines. It has been reported in 117 countries worldwide.
Drug resistance can be detected using special laboratory tests which test the bacteria for sensitivity to the drugs or detect resistance patterns. These tests can be molecular in type (such as Xpert MTB/RIF) or else culture-based. Molecular techniques can provide results within hours and have been successfully implemented even in low resource settings.
New WHO recommendations aim to speed up detection and improve treatment outcomes for MDR-TB through use of a novel rapid diagnostic test and a shorter, cheaper treatment regimen. At less than US$ 1000 per patient, the new treatment regimen can be completed in 9–12 months. Not only is it less expensive than current regimens, but it is also expected to improve outcomes and potentially decrease deaths due to better adherence to treatment and reduced loss to follow-up.
Solutions to control drug-resistant TB are to:
cure the TB patient the first time around
provide access to diagnosis
ensure adequate infection control in facilities where patients are treated
ensure the appropriate use of recommended second-line drugs.
In 2015, an estimated 480 000 people worldwide developed MDR-TB, and an additional 100 000 people with rifampicin-resistant TB were also newly eligible for MDR-TB treatment. India, China, and the Russian Federation accounted for 45% of the 580 000 cases. It is estimated that about 9.5% of these cases were XDR-TB.
Anti Tubercular Drugs - Mechanism of Action and Adverse effects Thomas Kurian
A brief outline of the mechanism of action and adverse effects of anti tubercular drugs
Only First line and second line drugs are dealt with.First line drugs may be useful for MBBS students and the rest is directed for postgraduate students.
Hope you find it useful.
The bacteria that cause tuberculosis (TB) can develop resistance to the antimicrobial drugs used to cure the disease. Multidrug-resistant TB (MDR-TB) is TB that does not respond to at least isoniazid and rifampicin, the 2 most powerful anti-TB drugs.
The 2 reasons why multidrug resistance continues to emerge and spread are mismanagement of TB treatment and person-to-person transmission. Most people with TB are cured by a strictly followed, 6-month drug regimen that is provided to patients with support and supervision. Inappropriate or incorrect use of antimicrobial drugs, or use of ineffective formulations of drugs (such as use of single drugs, poor quality medicines or bad storage conditions), and premature treatment interruption can cause drug resistance, which can then be transmitted, especially in crowded settings such as prisons and hospitals.
In some countries, it is becoming increasingly difficult to treat MDR-TB. Treatment options are limited and expensive, recommended medicines are not always available, and patients experience many adverse effects from the drugs. In some cases even more severe drug-resistant TB may develop. Extensively drug-resistant TB, XDR-TB, is a form of multidrug-resistant TB with additional resistance to more anti-TB drugs that therefore responds to even fewer available medicines. It has been reported in 117 countries worldwide.
Drug resistance can be detected using special laboratory tests which test the bacteria for sensitivity to the drugs or detect resistance patterns. These tests can be molecular in type (such as Xpert MTB/RIF) or else culture-based. Molecular techniques can provide results within hours and have been successfully implemented even in low resource settings.
New WHO recommendations aim to speed up detection and improve treatment outcomes for MDR-TB through use of a novel rapid diagnostic test and a shorter, cheaper treatment regimen. At less than US$ 1000 per patient, the new treatment regimen can be completed in 9–12 months. Not only is it less expensive than current regimens, but it is also expected to improve outcomes and potentially decrease deaths due to better adherence to treatment and reduced loss to follow-up.
Solutions to control drug-resistant TB are to:
cure the TB patient the first time around
provide access to diagnosis
ensure adequate infection control in facilities where patients are treated
ensure the appropriate use of recommended second-line drugs.
In 2015, an estimated 480 000 people worldwide developed MDR-TB, and an additional 100 000 people with rifampicin-resistant TB were also newly eligible for MDR-TB treatment. India, China, and the Russian Federation accounted for 45% of the 580 000 cases. It is estimated that about 9.5% of these cases were XDR-TB.
advanced drug delivery system of miconazole nitratemahbub alam
A liposome is a tiny bubble (vesicle), made out of the same material as a cell membrane.
Liposomes were first described by British hematologist Dr. Alec.
LIPOSOME derives from two Greek words: lipo("fat") and soma ("body"); it is so named because its composition is primarily of phospholipid.
This word document deals with the drug profile of amikacin. Important headings, with respect to its pharmacology, along with a note on important dosage regimens and antimicrobial spectrum, have also been mentioned, with reference to standard textbooks, guidelines and relevant articles.
Immunosuppressant are drugs or medicines that lower the body's ability to reject a transplanted organ. Another term for these drugs is anti-rejection drugs. There are 2 types of immunosuppressants: Induction drugs: Powerful antirejection medicine used at the time of transplant.
cancer chemotherapy
Introduction,Types of cancer,Aetiology of cancer,Pathogenesis of cancer,Diagnosis of cancer,Treatment of cancer,Novel drugs for cancer,Future prospects
advanced drug delivery system of miconazole nitratemahbub alam
A liposome is a tiny bubble (vesicle), made out of the same material as a cell membrane.
Liposomes were first described by British hematologist Dr. Alec.
LIPOSOME derives from two Greek words: lipo("fat") and soma ("body"); it is so named because its composition is primarily of phospholipid.
This word document deals with the drug profile of amikacin. Important headings, with respect to its pharmacology, along with a note on important dosage regimens and antimicrobial spectrum, have also been mentioned, with reference to standard textbooks, guidelines and relevant articles.
Immunosuppressant are drugs or medicines that lower the body's ability to reject a transplanted organ. Another term for these drugs is anti-rejection drugs. There are 2 types of immunosuppressants: Induction drugs: Powerful antirejection medicine used at the time of transplant.
cancer chemotherapy
Introduction,Types of cancer,Aetiology of cancer,Pathogenesis of cancer,Diagnosis of cancer,Treatment of cancer,Novel drugs for cancer,Future prospects
The following presentation is only for quick reference. I would advise you to read the theoretical aspects of the respective topic and then use this presentation for your last minute revision. I hope it helps you..!!
Mayur D. Chauhan
"What Will It Take To Control TB?" Richard Chaisson, MDUWGlobalHealth
Dr. Richard Chaisson, Professor of Medicine, Epidemiology and International Health and Director of the Center for Tuberculosis Research at the Johns Hopkins University in Baltimore was the keynote Jan. 19 as part of the Washington Global Health Discovery Series. His talk was on ""What Will It Take To Control TB?"
Non tubercular mycobacterial infection following surgery- Dr Keyur BhattDrKeyurBhattMSMRCSEd
Atypical Tuberculosis following surgery or laparoscopy. How to diagnose how to quantify and how to treat.
This is a very important presentation for the discovery and management of atypical tuberculosis infection any surgery.
this can happen after any laparoscopy or any interventional procedures.
• Much is still unknown regarding the markers of disease and recovery process for SARS-CoV-2, including if and what immunity arises and which tests or markers can be useful in assessing immunity status
• A multi-phased plan is required to reopen the economy post-COVID-19, with significantly daily testing capacity (millions) required at all stages
o Challenges with scientific validation, regulatory, manufacturing, and ongoing logistics must be overcome to successfully ramp up testing capacities in the US
o Hundreds of molecular and serology tests are now available, but many have limited accuracy (high false positive/negative rates) due to the rapid development and lack of validation of these tests
• In this edition of Demystifying COVID-19 Testing, we highlight what is required now and in the future to move to a “new normal” and why it is challenging to get this testing up and running at volumes needed in the US
New faces of tuberculosis: new chellenges requiring new solutionsJean Jacques Bernatas
TB reflects poverty, and while it accompanies Humankind for 70,000 years, this disease presents new faces for which new solutions must be implemented to move towards TB elimination by 2030. Finally a better coordination between all stakeholders is instrumental for winning this fight.
Joseph Eron, M.D., of University of North Carolina at Chapel Hill, presents "The State of the Art in HIV Cure Research – Hope or Hype: What Does It Mean for Patients" at AIDS Clinical Rounds
Richard Garfein, PhD, MPH
Professor
Herbert Wertheim School of Public Health and Human Longevity Science
Adjunct Professor
Division of Infectious Disease and Global Public Health
Department of Medicine
University of California, San Diego
Keynote address by Dr. Eric Goosby of UCSF, presented at CFAR HIV Research in International Settings (CHRIS) meeting in San Diego, October 1, 2014. Dr. Goosby discussed. "Global Health Delivery and Diplomacy: The Long Road to Sustainable Programs."
Fifth Annual Mitchell Memorial Lecture, October 6, 2014, at UC San Diego, featuring Dr. Jonathan Karn of Case Western Reserve University speaking on "Lessons Learned from models for HIV latency helping to formulate virus eradication strategies."
A mixed methods approach to understanding injection drug‐related HIV risk among female sex workers and their non‐commercial partners: A case study from Northern Mexico
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Title: Sense of Taste
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 structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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
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ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the 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 lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
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. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Video Directly Observed Therapy for HIV and TB patients
1. TB
“Video-Directly Observed Therapy:
A promising solution for monitoring TB and HIV
treatment adherence for binational patients in the
U.S.-Mexico border region”
Muñoz F., Collins K., Moser K., Cerecer-Callú P., Sullivan M.,
Chockalingam G., Rios P., Zúñiga M.L., Burgos J.L., Rodwell T., Rangel
M., Patrick K., Garfein R.
Division of Global Public Health
School of Medicine
University of California, San Diego
Sixth Annual CFAR International HIV/AIDS Research Day
San Diego, CA
September 18th, 2012
2. TB/HIV Syndemic TB
Human immunodeficiency virus (HIV) and tuberculosis (TB)
syndemic that cause high morbidity and mortality worldwide
TB is the leading cause of
death among persons
with HIV (PWHIV)
TB disease in PWHIV can
be prevented with
effective treatment
MMWR, CDC, 2012; WHO, 2012; Kwan & Ernst, 2011; Garfein 2010
3. Tuberculosis Burden TB
TB
A bacterial infection caused by M. tuberculosis (Mtb)
TB usually affects the lungs but can spread to other
parts of the body
TB is the 2nd leading cause of death from infectious
diseases worldwide
— 1/3 of the world’s population is
infected with Mtb
— Worldwide there are 9 million new
cases and 1.4-2 millions deaths from
TB annually
— Each infected person will spread TB
to 10-15 other individuals before
death or cure
Estimated number of persons
infected with TB –worldwide,
WHO 2010 MMWR, CDC, 2012; WHO, 2012 &2010
4. Mexico and U.S. TB Incidence Rates*
By State
Cases Rate*
NATIONAL 13,142 4.2
BORDER 4,180 6.8
CA
7.0 AZ
NM
San Diego: 8.4 3.5
3.0
Tijuana: 46.1 40.5 TX
B.C. 6.2
26.4
SON 17.1
16.5
CHI
Cases Rate* COH
NATIONAL 15,649 14.1 NL
TAM
BORDER 4,290 25.7 19.9 31.9
CDC, 2008; CDPH, 2008; DGEPI Mexico, 2008; INEGI, 2005; SINAVE, 2007.
* Rate = cases per 100,000 population Adapted from: Schneider E, et al. Rev Panam Salud Publica. 2004;16(1):23–34.
5. TB treatment
• Curable with antibiotics, but takes >6 months to treat
– Side effects common
– Contraindicated with other medications and alcohol
– Careful monitoring is necessary to assure medication
adherence
• Poor adherence drug resistance (MDR/XDR-TB)
– Delayed resolution or worsening symptoms
– Resistant strains can be transmitted
– Drastically increases treatment costs
– Increase probability of death
MMWR, CDC, 2012; WHO, 2012 &2010
6. Directly Observed Therapy (DOT)
• Preferred treatment strategy for all
patients
– Improves adherence
– Reduce acquired drug resistance,
treatment failure, and relapse
Provider visits the patient
– DOT saved 6.8 million lives in 1995-2010
• Care provider observes patient
taking every medication dose until
treatment is completed
Patient goes to the clinic
CDC, 2007; WHO, 2012
7. TB treatment: DOT
However, DOT is …
o Costly
o Labor intensive and time consuming
o Limit patient mobility
o Logistically difficult to administer for binational patients
o May not be feasible for patients in rural areas
o Potentially jeopardizes patient privacy and
confidentiality
o Patient stigmatization
8. Technology to Improve Medication
Adherence
• New opportunities to reach and improve the level of
care for underserved population worldwide
• Previous studies
• Monitoring medication adherence, patient education,
motivation and health messaging, frequent communication
with patient, reminder system and data gathering.
• Broader range of diseases (TB, HIV/AIDS, Diabetes)
• Technology previously used
• MEMS caps
• short message system (SMS)
• text messages
• phone reminders
Pellowski & Kalichman, 2012; Hoffman et al, 2010
9. 1st Generation Technology
• Count the number of doses dispensed
(MEMS Caps, GlowCap, etc.)
2nd Generation Technology
• Drug metabolite testing (blood, urine, hair, toenails)
• Patient-facilitated tracking (Adhere.IO, Pill Apps)
• Embedded sensors (Proteus, SmartPill)
10. Video Phone Experiment
• Landline-based system
• First 33 patients in 9 months
• Advantages:
– High patient acceptance
– Saved $$$
– 27,840 miles saved ($10,161)
– 795 hours saved ($15,000)
• Disadvantages:
– Limited to business hours
– Must take meds while at home
– Won’t work for San Diego’s binational patients
12. Objectives
• To develop and pilot test the mobile phone-
based video direct observed therapy (VDOT)
program among TB patients in a bi-national
border region.
• To assess the feasibility and acceptability of
VDOT among patients, providers, and health
officials.
13. Methods
Two phased pilot study in San Diego, CA and
Tijuana, BC, Mexico (4/1/2009-10/1/2012)
Phase I: Focus Groups
Phase II: Pilot VDOT trial
Both phases conducted in San Diego and
Tijuana to evaluate VDOT simultaneously in
high and low economic resource areas.
Pilot study approved by the UCSD Human
Research Protection Program and the Bioethics
Committee of COLEF.
13
14. Phase I: Focus Group Design
• Participants: TB patients who recently completed in-person
DOT, TB care providers and health officials.
• Explored feasibility, acceptability and general perceptions of
VDOT.
San Diego Tijuana
# of # of # of # of
Groups Participants Groups Participants
Providers 2 14 1 19
Patients 4 14 1 9
Promotores 0 1 14
– Participants’ ages ranged from 24-88 years (mean 47) and did not
differ by city.
– In both cities, approximately half (49% overall) of the patients and
providers were male; over half (67% overall) were Hispanic.
15. Focus Groups Results
Providers Patients
• Solve transportation problems, • Save transportation cost as well
save patients money, as alleviate stigma.
Feasibility • Protect patient privacy from “With the demonstration that’s
neighbors and friends, been shown I think it’s really easy.”
• Alleviate risk of stigma.
‐Both providers and patients felt they could easily do it.
• Wait to eat until his “promotor“
• Better option than the current showed up, which sometimes
system of “in‐person” DOT and did not happen until 2pm.
Acceptability “landline” video‐DOT. “You’re not locked to your house,
and you’re not locked to the time of
the day that you have to take your
medication.”
‐Both providers and patients had a little concern about using cell phones.
17. Phase II: Pilot Study Design
• Population:
– Newly diagnosed pulmonary TB patients selected by TB Control Program
– San Diego (n=40) and Tijuana (n=10)
• Patients provide informed consent
• Patients taught to use phone by DOT case worker
• Videos observed and tracked by TB Program staff
• Patient interviews conducted pre and post treatment
• $25 given for each interview, but nothing for doing VDOT
• Planned to follow patients for 4-9 months on VDOT
• Data Collection:
– Interviews assessed demographics, attitudes about TB, study
satisfaction and experience/comfort using technology including
smart phones, number of doses observed by VDOT
18. Results
San Diego Tijuana
Number enrolled 43 9
Number of bi-national participants* 6 0
Cell phones lost/stolen/broken 2 2
18
*Participants reported spent time in both cities
19. Pilot study: Patient characteristics
San Diego Bi‐national Tijuana
Socio‐demographics
n=37 (%) n=6 (%) n=9 (%)
Age: Mean (range) 39 (18‐86) 37.5 (22‐50) 28 (19‐65)
Gender 20 (54.1) 3 (50.0) 5 (55.6)
Male 17 (45.9) 3 (50.0) 4 (44.5)
Female
Hispanic or Latino 12 (32.4) 6 (100) 9 (100)
Race
Asian 13 (35.1) 0 (0) 0 (0)
African American/Black 3 (8.1) 0 (0) 0 (0)
Caucasian/White 10 (27.0) 0 (0) 3 (33.4)
Other/Mixed Race 11 (29.7) 6 (100) 6 (66.6)
Educational Attainment
Illiterate 0 (0) 0 (0) 1 (11.1)
< High School 6 (16.2) 2 (33.3) 3 (33.3)
> High School 28 (75.7) 4 (66.7) 5 (55.6)
Had employment (last 3 months) 35 (94.6) 3 (50.0) 4 (44.4)
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20. Pilot Study:
Medication Doses by VDOT
San Diego Bi‐national Tijuana
Medication doses by VCP‐DOT n=37 n=6 n=9
Mean (range) Mean (range) Mean (range)
Total medication doses expected 88.4 (10‐202) 107 (40‐107) 92.5 (2‐168)
Total medication doses observed 84 ( 9‐200) 96.1(21‐153) 88.4 (2‐165)
Proportion of total medication
94% (50‐100) 84% (52‐96) 95%(88‐100)
observed/ total medication expected (%)
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21. Pilot Study:
Post-test survey results
San Diego Bi‐national Tijuana
Experience with VDOT
n=35 (%)* n=6 (%) n=9 (%)
>½ the Time 3 ( 8.6) 0 (0) 1 (11.1)
Had problems recording a video Rarely 17 (48.6) 5 (83.3) 5 (55.6)
Never 15 (42.9) 1 (16.7) 3 (33.3)
>½ the Time 6 (17.1) 0 (0) 1 (11.1)
Had problems sending a video Rarely 23 (65.7) 5 (83.3) 6 (66.7)
Never 6 (17.1) 1 (16.7) 2 (22.2)
Unable to send a video due to poor reception 10 (28.6) 4 (66.7) 5 (55.6)
Yes, Always 6 (17.1) 4 (66.7) 2 (22.2)
Able to send videos while
Yes, Sometimes 2 (5.7) 2 (33.3) 1 (11.1)
traveling outside of SD or TJ Never Tried 27 (77.2) 0 (0) 6 (66.7)
1 20 (57.1) 5 (83.3) 1 (11.1)
Days practicing with a DOT worker 2 6 (17.1) 0 (0) 0 (0)
before recorded a video alone 3 2 (5.7) 0 (0) 3 (33.4)
>4 6 (17.1) 1 (16.7) 5 (55.6)
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22. Pilot Study:
Post-test survey results
San Diego Bi‐national Tijuana
Convenience of VDOT n=35 (%) n=6 (%) n=9 (%)
More 27 (77.1) 7 (77.8) 6 (100)
VDOT more confidential that In‐
No Difference 6 (17.1) 2 (22.2) 0 (0)
Person DOT Less 2 (5.8) 0 (0) 0 (0)
VDOT 33 (94.4) 8 (88.9) 5 (83.3)
To redo TB treatment, they choose In‐person DOT 1 (2.8) 1 (11.1) 0 (0)
No Preference 1 (2.8) 0 (0) 1 (16.7)
Inconvenient 3 (8.6) 0 (0) 0 (0)
Convenience using VDOT compared Neutral 0(0) 0 (0) 0 (0)
with In‐person DOT Convenient 32 (91.4) 6 (100) 9 (100)
Concern of people watching take a video 11 (31.4) 2 (33.3) 6 (66.7)
Recommend VDOT to other TB patients 35 (100) 6 (100) 9 (100)
VDOT allowed more freedom to travel outside of
31 (88.6) 6 (100) 8 (88.9)
home than in‐person DOT 22
23. Opportunities, Challenges
and Observations
Patients, nurses, DOT workers/promotor and health officials
considered VDOT to be highly feasible and acceptable
High patient satisfaction and appreciation for mobility that VDOT
allows
Considerable savings in staff time and travel reported in both
cities
SMS reminders lapse when cell/WiFi was unavailable
Some video uploads delayed by cell/WiFi limitations
2 patients preferred in-person DOT
23
24. Conclusions
- Results showed VDOT to be feasible and acceptable in
both high and low resource settings
- VDOT allows all doses taken by bi-national patients to be
counted, even when they were traveling
- VDOT is a promising mobile solution to monitoring TB and
other conditions such as HIV that require strict treatment
adherence
- Future research is needed to test VDOT among patients
with TB/HIV co-infection
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25. Acknowledgements
UCSD Division of Global Public Health
Richard Garfein (PI), Jazmine Cuevas-Mota , Kelly
Collins, Fatima Munoz, Maria Luisa Zuniga, Jose Luis
Burgos, Timothy Rodwell, Maureen Clark
UCSD Department of Family and Preventive
Medicine
Kevin Patrick
UCSD Calit2
Kevin Patrick, Fredric Raab, Mark Sullivan, Phillip
Rios, Alison Flick, Ganz Chockalingam
San Diego County Health and Human Services
Agency
Kathleen Moser, Christine Kozik, Krystal Liang,
Deborah McIntosh
ISESALUD, Tijuana, BC, Mexico
Paris Cerecer, Cristhian Ambriz
El Colegio de la Frontera Norte, BC, Mexico
Maria Gudelia Rangel
* Funded by the National Institutes of Health (R21-AI088326) and Alliance Healthcare Foundation.
* Premium QIK membership accounts provided at no cost by QIK.COM.
26. GRACIAS
Fátima Muñoz, M.D., M.P.H.
Email: famunoz@ucsd.edu
Phone: 619-534-9670
Division of Global Public Health
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