Unit-V Health information system MHA II Semester.pptxanjalatchi
This document discusses health informatics systems. It defines health informatics as the intersection of information science, computer science, and healthcare. The document outlines the objectives, requirements, components, sources, uses, and applications of health informatics. It discusses collecting and processing health-related data and information to organize healthcare services and conduct research. Some key benefits of health informatics systems include centralized data, increased efficiency, and improved security and access to patient information.
This document provides an overview of health information systems and descriptive statistics. It defines a health information system as a mechanism for collecting, processing, analyzing, and transmitting health data required for operating health services. Key components of health information systems include demography, health status, health resources, and service utilization. Sources of health information include censuses, vital event registration, sample registration systems, disease notification, and hospital and health service records. Descriptive statistics are used to organize and present health data in tables and graphs. Measures of central tendency and dispersion are discussed for describing key characteristics of health data.
Sources of health information in India.pptxMostaque Ahmed
1) Health information systems in India utilize various data sources including census data, vital statistics, sample registration systems, disease notification, hospital and health center records, surveys, and environmental records.
2) The sources are used to measure population health status, assess health programs and service delivery, conduct research, and inform health planning and policy decisions.
3) Key sources include the decennial national census, civil registration of vital events, sample registration system which provides annual health and demographic data, and population-based national health surveys.
This document discusses health information systems and the types of data and information they collect. It defines key terms like data, information, and intelligence in the context of health systems. It then outlines 14 common sources of health data, including vital statistics from censuses and disease registries, health surveys, health service and hospital records, and environmental health data. The goals of health information systems are described as measuring health status, enabling comparisons, and supporting planning, administration, management, and research.
Data collection is important for:
1. Diagnosis of community health problems and assessment of community needs.
2. Helps in the comparison of health status and disease status in different countries and in one country over the years.
3. Evaluation of health services and health programs.
A health information system is defined as a mechanism for organizing and operating health services, as well as research and training. The objectives of a health information system are to provide reliable and useful health information to administrators and officers, contribute to achieving health policy goals, increase efficiency and quality in health management, and provide information to amend health policies based on feedback. A health information system should be population-based, problem-oriented, and avoid unnecessary data aggregation, instead expressing information briefly and through formats like tables and charts. It should also allow for feedback and include data on demographics, health status, resource utilization, finances, and outcomes.
Vital statistics is accumulated data gathered on live births, deaths, migration, fetal deaths, marriages and divorces. The most common way of collecting information on these events is through civil registration, an administrative system used by governments to record vital events which occur in their populations.
Vital statistics is accumulated data gathered on live births, deaths, migration, fetal deaths, marriages and divorces. The most common way of collecting information on these events is through civil registration, an administrative system used by governments to record vital events which occur in their populations.
This document discusses key data sources and methods used in public health. It outlines several main sources of raw health data including births, deaths, hospital admissions, and prescriptions. These data are aggregated and linked to geography to measure population health indicators like mortality rates, life expectancy, and birth rates. Determinants of health like deprivation, lifestyle factors, and environment are also examined using surveys. The document explains methods like incidence, prevalence, crude rates, and age standardization used to analyze health data and measure the health of populations.
Unit-V Health information system MHA II Semester.pptxanjalatchi
This document discusses health informatics systems. It defines health informatics as the intersection of information science, computer science, and healthcare. The document outlines the objectives, requirements, components, sources, uses, and applications of health informatics. It discusses collecting and processing health-related data and information to organize healthcare services and conduct research. Some key benefits of health informatics systems include centralized data, increased efficiency, and improved security and access to patient information.
This document provides an overview of health information systems and descriptive statistics. It defines a health information system as a mechanism for collecting, processing, analyzing, and transmitting health data required for operating health services. Key components of health information systems include demography, health status, health resources, and service utilization. Sources of health information include censuses, vital event registration, sample registration systems, disease notification, and hospital and health service records. Descriptive statistics are used to organize and present health data in tables and graphs. Measures of central tendency and dispersion are discussed for describing key characteristics of health data.
Sources of health information in India.pptxMostaque Ahmed
1) Health information systems in India utilize various data sources including census data, vital statistics, sample registration systems, disease notification, hospital and health center records, surveys, and environmental records.
2) The sources are used to measure population health status, assess health programs and service delivery, conduct research, and inform health planning and policy decisions.
3) Key sources include the decennial national census, civil registration of vital events, sample registration system which provides annual health and demographic data, and population-based national health surveys.
This document discusses health information systems and the types of data and information they collect. It defines key terms like data, information, and intelligence in the context of health systems. It then outlines 14 common sources of health data, including vital statistics from censuses and disease registries, health surveys, health service and hospital records, and environmental health data. The goals of health information systems are described as measuring health status, enabling comparisons, and supporting planning, administration, management, and research.
Data collection is important for:
1. Diagnosis of community health problems and assessment of community needs.
2. Helps in the comparison of health status and disease status in different countries and in one country over the years.
3. Evaluation of health services and health programs.
A health information system is defined as a mechanism for organizing and operating health services, as well as research and training. The objectives of a health information system are to provide reliable and useful health information to administrators and officers, contribute to achieving health policy goals, increase efficiency and quality in health management, and provide information to amend health policies based on feedback. A health information system should be population-based, problem-oriented, and avoid unnecessary data aggregation, instead expressing information briefly and through formats like tables and charts. It should also allow for feedback and include data on demographics, health status, resource utilization, finances, and outcomes.
Vital statistics is accumulated data gathered on live births, deaths, migration, fetal deaths, marriages and divorces. The most common way of collecting information on these events is through civil registration, an administrative system used by governments to record vital events which occur in their populations.
Vital statistics is accumulated data gathered on live births, deaths, migration, fetal deaths, marriages and divorces. The most common way of collecting information on these events is through civil registration, an administrative system used by governments to record vital events which occur in their populations.
This document discusses key data sources and methods used in public health. It outlines several main sources of raw health data including births, deaths, hospital admissions, and prescriptions. These data are aggregated and linked to geography to measure population health indicators like mortality rates, life expectancy, and birth rates. Determinants of health like deprivation, lifestyle factors, and environment are also examined using surveys. The document explains methods like incidence, prevalence, crude rates, and age standardization used to analyze health data and measure the health of populations.
The document discusses health surveillance and informatics. It defines surveillance as the systematic collection and analysis of health data for decision making. The purposes of surveillance include monitoring disease trends, evaluating programs, and informing policy. Health informatics involves the management and analysis of health information and can include fields like nursing informatics, clinical informatics, and public health informatics. Sources of health data include censuses, vital statistics, disease notification systems, health surveys, and hospital records.
Surveillance involves the ongoing collection and analysis of health data to monitor diseases and detect outbreaks. The goals are to take action by responding to outbreaks, evaluating interventions, and planning prevention efforts. Data flows from clinical reporting through laboratories and regional networks to national and global levels for analysis and feedback. Indicators are established to measure progress towards objectives like reducing disease incidence. Overall, surveillance is meant to close the loop between data, decisions, and actions to improve public health.
Integrated Diseases Surveillance Project - IDSP IndiaRizwan S A
The document provides an overview of the Integrated Disease Surveillance Project (IDSP) in India. IDSP aims to establish a decentralized district-based system for surveillance of communicable and non-communicable diseases. Key aspects of IDSP include integrating existing disease surveillance, strengthening public health laboratories, using information technology, and developing human resources. IDSP implements syndromic, presumptive, and confirmed surveillance for various diseases. Information flows from the community level up through district, state, and national surveillance committees, which analyze data and coordinate response actions. New IDSP initiatives include an alert call center, e-learning modules, and a media scanning cell.
Vital statistics are records of life events like births, deaths, diseases, and marriages that help analyze community health and plan health services. They are collected through systems like censuses, registration of vital events, sample registration of births and deaths, disease notification, and population surveys. This data provides information on demography, health status, health resources, disease patterns, and more. It is used for purposes like evaluating health programs, assessing community health issues, informing legislation, and conducting research. Maintaining accurate and up-to-date vital statistics is important for effective public health management and policymaking.
The document discusses cancer registries and epidemiology in India. It notes that cancer cases are rising globally with Asia accounting for nearly half of new cases. The Indian Cancer Society was established in 1951 to address cancer issues in India. The National Cancer Registry Programme was launched in 1982 under ICMR to collect nationwide cancer incidence data through a network of population-based and hospital-based cancer registries. There are currently 29 population-based and 17 hospital-based cancer registries in India collecting data to analyze cancer trends and patterns to help address the growing cancer burden. Limitations include possible duplicate registrations and lack of unique patient identification numbers.
The document discusses public health surveillance, providing definitions and outlining its goals, history, uses, types, attributes, and process. It describes key public health surveillance programs in India, including the Integrated Disease Surveillance Program (IDSP) and National Surveillance Programme for Communicable Diseases (NSPCD). The goal of public health surveillance is to provide information to guide public health policies and programs by ongoing collection and analysis of health data. Effective surveillance systems aim to detect health issues, monitor trends, and link data to appropriate public health actions and interventions.
This ppt contains all information about Health statistics-Vital Statistics. It is useful for students of medical field learning preventive and social medicine, Swasthavritta (Ayurved), nursing and everyone who is interested in knowing about it.
The document provides information about the Integrated Disease Surveillance Programme (IDSP) in India. It discusses that IDSP aims to establish a decentralized disease surveillance system to detect early warning signals of outbreaks. Key elements of IDSP include detection and reporting of health events, investigation and confirmation of cases, collection and analysis of surveillance data, and feedback to initiate public health responses. IDSP implementation is organized at the national, state, and district levels with defined roles and reporting structures. The program coordinates surveillance of both communicable and non-communicable diseases using standardized reporting forms.
This document summarizes the results of comprehensive assessments of the civil registration and vital statistics (CRVS) system in the Philippines. The assessments found that (1) death registration completeness is only around 70% (2) there are various challenges hindering timely birth and death registration especially for out-of-facility births and deaths and in rural areas, and (3) improvements are needed in areas like data quality, storage, and dissemination. The document recommends strengthening partnerships between stakeholders and developing a strategic plan to address gaps identified in the assessments.
Chapter 5Sources of Data for Use in Epidemiology.docxketurahhazelhurst
Chapter 5
Sources of Data for Use in
Epidemiology
Learning Objectives
• Discuss criteria for assessing the quality
and utility of epidemiologic data
• Indicate privacy and confidentiality issues
that pertain to epidemiologic data
• Discuss the uses, strengths, and
weaknesses of various epidemiologic data
sources
Criteria for the Quality and
Utility of Epidemiologic Data
• Nature of the data
• Availability of the data
• Completeness of population
coverage
– Representativeness
– Generalizability (external validity)
– Thoroughness
• Strengths versus limitations
Nature of the Data
• Refers to the source of data, e.g.,
vital statistics, case registries,
physicians’ records, surveys of the
general population, or hospital and
clinic cases.
• Will affect the types of statistical
analyses and inferences that are
possible.
Availability of the Data
• Refers to investigator’s access to
data.
• For example, medical records and
other data with personal identifiers
may not be used without patients’
consent.
Completeness of Population
Coverage
• Representativeness—the degree to which
a sample resembles a parent population.
• Generalizability (external validity)— ability
to apply findings to a population that did
not participate in the study.
• Thoroughness—the care taken to identify
all cases of a given disease.
Strengths versus Limitations
• The utility of the data for various
types of epidemiologic research.
• Factors inherent in the data may limit
their usefulness.
– Incomplete diagnostic information.
– Case duplication.
Online Sources of Epidemiologic
Data
• Online bibliographic databases include
MEDLINE, TOXLINE, and commercial
databases.
• National Library of Medicine’s PubMed®
– MEDLINE is the main part of PubMed®
– Premier source of health-related literature
• TOXLINE—keyed to toxicology and includes
information on drugs and chemicals
Selected Internet Addresses
• American Public Health Association—
http://www.apha.org
• Centers for Disease Control and
Prevention—http://www.cdc.gov
• PubMed®—
http://www.ncbi.nlm.nih.gov/sites/entr
ez
Confidentiality
• Privacy Act of 1974
– Prohibits the release of confidential data
without the consent of the individual
• Freedom of Information Act
– Mandates the release of government
information to the public, except for personal
and medical files
• The Public Health Service Act
– Protects confidentiality of information
collected by some federal agencies, e.g.,
NCHS
The HIPAA Privacy Rule
• Refers to the Health Insurance Portability and
Accountability Act of 1996
• Sections of HIPAA “…require the Secretary of
HHS to publicize standards for the electronic
exchange, privacy and security of health
information…”
• Categories of protected health information
pertain to individually identifiable data re:
– The individual’s physical and mental health
– Provision of health care t ...
This document discusses health information systems (HISs). It defines health as the well-being of a person's physical, mental, and social condition. HISs gather, store, and transmit individuals' and organizations' health-related data, including hospitals, laboratories, and disease surveillance systems. This is done to increase the efficiency of health services and improve personal health. When establishing a HIS, many rules and regulations must be followed to protect individuals' privacy and ensure the accuracy of protected health information. Resources, indicators, data sources, data management, and dissemination and use are all important aspects of developing and maintaining an effective HIS.
This document discusses surveillance of risk factors for non-communicable diseases (NCDs) in India. It describes the need for NCD risk factor surveillance given the increasing burden of NCDs. Surveillance of risk factors like tobacco use, alcohol consumption, obesity, diet, physical activity and blood glucose/cholesterol levels is recommended through periodic sample surveys. The role of district surveillance officers includes organizing such surveys involving collection of demographic, behavioral and biological data on NCD risk factors from the community. Ensuring valid and reliable surveillance methods is important to generate accurate data on trends and patterns of NCD risk factors.
This document outlines an agenda and case studies for a healthcare analytics bootcamp. The bootcamp will use healthcare data to develop machine learning solutions to predict heart disease and identify high-risk patients. Case Study 1 will involve exploratory data analysis of tuberculosis data to analyze global trends, hotspots, and mortality rates. Case Study 2 will use a heart disease screening dataset and logistic regression to build a model to predict heart disease risk and develop treatment plans for high-risk patients. The document discusses the types of structured and unstructured healthcare data, sources of data, and applications of machine learning in healthcare analytics.
This document provides an outline for a lecture on introduction to statistics and demography. It begins with definitions of statistics, biostatistics, and related terms. It then discusses the role of statistics in clinical medicine and public health. Some basic statistical concepts are introduced such as population, sample, probability, and types of data. The document outlines the basic steps of statistical work including study design, data collection, sorting, and analysis. Finally, it discusses different methods of presenting data numerically, graphically, and mathematically.
Achieving UHC & equitable access to TB care in mixed public and private healt...Prashanth N S
Lecture delivered to the Engaging all health providers to End TB: Public-Private Mix (PPM) | May 21 and June 3-7, 2024 cohort at McGill Uniersity, Canada
Tribal health research examples based on work done under DBT/Wellcome Trust I...Prashanth N S
Presentation made based on work done under "Towards Health Equity & Transformative Action on Tribal Health" project under a clinica/public health intermediate fellowship from DBT/Wellcome Trust India Alliance to Prashanth N Srinivas. Presentation made at inauguration of Tribal Health Cell at Chamarajanagar Institute of Medical Sciences, Chamarajanagar, Karnataka at 2-day CME on Tribal health
More Related Content
Similar to Data sources for development professionals (India)
The document discusses health surveillance and informatics. It defines surveillance as the systematic collection and analysis of health data for decision making. The purposes of surveillance include monitoring disease trends, evaluating programs, and informing policy. Health informatics involves the management and analysis of health information and can include fields like nursing informatics, clinical informatics, and public health informatics. Sources of health data include censuses, vital statistics, disease notification systems, health surveys, and hospital records.
Surveillance involves the ongoing collection and analysis of health data to monitor diseases and detect outbreaks. The goals are to take action by responding to outbreaks, evaluating interventions, and planning prevention efforts. Data flows from clinical reporting through laboratories and regional networks to national and global levels for analysis and feedback. Indicators are established to measure progress towards objectives like reducing disease incidence. Overall, surveillance is meant to close the loop between data, decisions, and actions to improve public health.
Integrated Diseases Surveillance Project - IDSP IndiaRizwan S A
The document provides an overview of the Integrated Disease Surveillance Project (IDSP) in India. IDSP aims to establish a decentralized district-based system for surveillance of communicable and non-communicable diseases. Key aspects of IDSP include integrating existing disease surveillance, strengthening public health laboratories, using information technology, and developing human resources. IDSP implements syndromic, presumptive, and confirmed surveillance for various diseases. Information flows from the community level up through district, state, and national surveillance committees, which analyze data and coordinate response actions. New IDSP initiatives include an alert call center, e-learning modules, and a media scanning cell.
Vital statistics are records of life events like births, deaths, diseases, and marriages that help analyze community health and plan health services. They are collected through systems like censuses, registration of vital events, sample registration of births and deaths, disease notification, and population surveys. This data provides information on demography, health status, health resources, disease patterns, and more. It is used for purposes like evaluating health programs, assessing community health issues, informing legislation, and conducting research. Maintaining accurate and up-to-date vital statistics is important for effective public health management and policymaking.
The document discusses cancer registries and epidemiology in India. It notes that cancer cases are rising globally with Asia accounting for nearly half of new cases. The Indian Cancer Society was established in 1951 to address cancer issues in India. The National Cancer Registry Programme was launched in 1982 under ICMR to collect nationwide cancer incidence data through a network of population-based and hospital-based cancer registries. There are currently 29 population-based and 17 hospital-based cancer registries in India collecting data to analyze cancer trends and patterns to help address the growing cancer burden. Limitations include possible duplicate registrations and lack of unique patient identification numbers.
The document discusses public health surveillance, providing definitions and outlining its goals, history, uses, types, attributes, and process. It describes key public health surveillance programs in India, including the Integrated Disease Surveillance Program (IDSP) and National Surveillance Programme for Communicable Diseases (NSPCD). The goal of public health surveillance is to provide information to guide public health policies and programs by ongoing collection and analysis of health data. Effective surveillance systems aim to detect health issues, monitor trends, and link data to appropriate public health actions and interventions.
This ppt contains all information about Health statistics-Vital Statistics. It is useful for students of medical field learning preventive and social medicine, Swasthavritta (Ayurved), nursing and everyone who is interested in knowing about it.
The document provides information about the Integrated Disease Surveillance Programme (IDSP) in India. It discusses that IDSP aims to establish a decentralized disease surveillance system to detect early warning signals of outbreaks. Key elements of IDSP include detection and reporting of health events, investigation and confirmation of cases, collection and analysis of surveillance data, and feedback to initiate public health responses. IDSP implementation is organized at the national, state, and district levels with defined roles and reporting structures. The program coordinates surveillance of both communicable and non-communicable diseases using standardized reporting forms.
This document summarizes the results of comprehensive assessments of the civil registration and vital statistics (CRVS) system in the Philippines. The assessments found that (1) death registration completeness is only around 70% (2) there are various challenges hindering timely birth and death registration especially for out-of-facility births and deaths and in rural areas, and (3) improvements are needed in areas like data quality, storage, and dissemination. The document recommends strengthening partnerships between stakeholders and developing a strategic plan to address gaps identified in the assessments.
Chapter 5Sources of Data for Use in Epidemiology.docxketurahhazelhurst
Chapter 5
Sources of Data for Use in
Epidemiology
Learning Objectives
• Discuss criteria for assessing the quality
and utility of epidemiologic data
• Indicate privacy and confidentiality issues
that pertain to epidemiologic data
• Discuss the uses, strengths, and
weaknesses of various epidemiologic data
sources
Criteria for the Quality and
Utility of Epidemiologic Data
• Nature of the data
• Availability of the data
• Completeness of population
coverage
– Representativeness
– Generalizability (external validity)
– Thoroughness
• Strengths versus limitations
Nature of the Data
• Refers to the source of data, e.g.,
vital statistics, case registries,
physicians’ records, surveys of the
general population, or hospital and
clinic cases.
• Will affect the types of statistical
analyses and inferences that are
possible.
Availability of the Data
• Refers to investigator’s access to
data.
• For example, medical records and
other data with personal identifiers
may not be used without patients’
consent.
Completeness of Population
Coverage
• Representativeness—the degree to which
a sample resembles a parent population.
• Generalizability (external validity)— ability
to apply findings to a population that did
not participate in the study.
• Thoroughness—the care taken to identify
all cases of a given disease.
Strengths versus Limitations
• The utility of the data for various
types of epidemiologic research.
• Factors inherent in the data may limit
their usefulness.
– Incomplete diagnostic information.
– Case duplication.
Online Sources of Epidemiologic
Data
• Online bibliographic databases include
MEDLINE, TOXLINE, and commercial
databases.
• National Library of Medicine’s PubMed®
– MEDLINE is the main part of PubMed®
– Premier source of health-related literature
• TOXLINE—keyed to toxicology and includes
information on drugs and chemicals
Selected Internet Addresses
• American Public Health Association—
http://www.apha.org
• Centers for Disease Control and
Prevention—http://www.cdc.gov
• PubMed®—
http://www.ncbi.nlm.nih.gov/sites/entr
ez
Confidentiality
• Privacy Act of 1974
– Prohibits the release of confidential data
without the consent of the individual
• Freedom of Information Act
– Mandates the release of government
information to the public, except for personal
and medical files
• The Public Health Service Act
– Protects confidentiality of information
collected by some federal agencies, e.g.,
NCHS
The HIPAA Privacy Rule
• Refers to the Health Insurance Portability and
Accountability Act of 1996
• Sections of HIPAA “…require the Secretary of
HHS to publicize standards for the electronic
exchange, privacy and security of health
information…”
• Categories of protected health information
pertain to individually identifiable data re:
– The individual’s physical and mental health
– Provision of health care t ...
This document discusses health information systems (HISs). It defines health as the well-being of a person's physical, mental, and social condition. HISs gather, store, and transmit individuals' and organizations' health-related data, including hospitals, laboratories, and disease surveillance systems. This is done to increase the efficiency of health services and improve personal health. When establishing a HIS, many rules and regulations must be followed to protect individuals' privacy and ensure the accuracy of protected health information. Resources, indicators, data sources, data management, and dissemination and use are all important aspects of developing and maintaining an effective HIS.
This document discusses surveillance of risk factors for non-communicable diseases (NCDs) in India. It describes the need for NCD risk factor surveillance given the increasing burden of NCDs. Surveillance of risk factors like tobacco use, alcohol consumption, obesity, diet, physical activity and blood glucose/cholesterol levels is recommended through periodic sample surveys. The role of district surveillance officers includes organizing such surveys involving collection of demographic, behavioral and biological data on NCD risk factors from the community. Ensuring valid and reliable surveillance methods is important to generate accurate data on trends and patterns of NCD risk factors.
This document outlines an agenda and case studies for a healthcare analytics bootcamp. The bootcamp will use healthcare data to develop machine learning solutions to predict heart disease and identify high-risk patients. Case Study 1 will involve exploratory data analysis of tuberculosis data to analyze global trends, hotspots, and mortality rates. Case Study 2 will use a heart disease screening dataset and logistic regression to build a model to predict heart disease risk and develop treatment plans for high-risk patients. The document discusses the types of structured and unstructured healthcare data, sources of data, and applications of machine learning in healthcare analytics.
This document provides an outline for a lecture on introduction to statistics and demography. It begins with definitions of statistics, biostatistics, and related terms. It then discusses the role of statistics in clinical medicine and public health. Some basic statistical concepts are introduced such as population, sample, probability, and types of data. The document outlines the basic steps of statistical work including study design, data collection, sorting, and analysis. Finally, it discusses different methods of presenting data numerically, graphically, and mathematically.
Similar to Data sources for development professionals (India) (20)
Achieving UHC & equitable access to TB care in mixed public and private healt...Prashanth N S
Lecture delivered to the Engaging all health providers to End TB: Public-Private Mix (PPM) | May 21 and June 3-7, 2024 cohort at McGill Uniersity, Canada
Tribal health research examples based on work done under DBT/Wellcome Trust I...Prashanth N S
Presentation made based on work done under "Towards Health Equity & Transformative Action on Tribal Health" project under a clinica/public health intermediate fellowship from DBT/Wellcome Trust India Alliance to Prashanth N Srinivas. Presentation made at inauguration of Tribal Health Cell at Chamarajanagar Institute of Medical Sciences, Chamarajanagar, Karnataka at 2-day CME on Tribal health
Patterns, process & action on tribal health: Reflections from Towards Health ...Prashanth N S
Prashanth is a Faculty at IPH Bengaluru and is an MPH and PhD alumnus of ITM Antwerp. From May 2017-2022, through a fellowship from the DBT/Wellcome Trust India Alliance and with ITM Antwerp as his collaborator, he set up and expanded IPH Bengaluru’s ongoing work on health inequalities of indigenous peoples in India. A field station that he co-established with collaborators today continues to deepen community health, public health and social science inquiry into indigenous health through a recent grant from DBT/Wellcome trust to set up a Center for Training Research & Innovation in Tribal Health.
In this seminar Prashanth will share and reflect on the work accomplished in this fellowship and the field station and discuss possible areas for collaboration.
Equity in representation of rare diseases in IndiaPrashanth N S
Presentation made at a panel organised by the Department of Science & Technology Center for Policy Research, Indian Institute of Science Bengaluru in parternship with Ashoka University titled "Rare diseases in public health: The Indian Context" on February 19, 2022. Details here: https://dstcpriisc.org/2022/02/14/rare-diseases-in-public-health/
What’s in the method? Brief introduction to philosophy of science in public h...Prashanth N S
A long-ish interactive talk at the IPH Bangalore methods seminar giving an overview of the philosophy underlying methods choices in public health research especially as relevant to health policy and systems research
Patterns, process & action on tribal health: mapping of process & outcomes un...Prashanth N S
Presentation at the India Alliance Conclave 2021 based on the process and outcomes of THETA project. For more on THETA project, see https://wellcomeopenresearch.org/articles/4-202
Planetary Health Information Center at Pakke Tiger ReservePrashanth N S
Talk at the DBT/Wellcome Trust India Alliance Conclave by Nandini Velho & Prashanth N Srinivas based on the co-production of a planetary health information center that is being set up in collaboration with the Arunahcal Pradesh Forest Department and communities living around Pakke Tiger Reserve. The work is supported by a public engagement grant to Prashanth N Srinivas (2021-22)
Mental health in primary health care in India: The Gumballi experiencePrashanth N S
Invited panel presentation at the 10th European Conference on Tropical Medicine & International Health held at Antwerp (16-20 October 2017) by Prashanth N Srinivas. Presentation based on the book chapter by the same name by Prashanth N S, Sridharan V S, Seshadri T, Sudarshan H, Kishore Kumar K V & Murthy RS in the Palgrave Handbook on socio-cultural perspectives on Global Mental Health
Reflections from practice: Community engagement & COVID-19Prashanth N S
Slides used in the DBT/Wellcome Trust India Alliance Ask the Experts Webinar series 7 on community engagement. See full webinar details here: https://www.indiaalliance.org/news/434
Univeral health coverage and tribal health: Plenary talk at TRIBECON National...Prashanth N S
Plenary talk at the National Conference on Tribal Health held at Pravara Rural Medical College in September 2019 on healht inequities among Adivasi communities and the quest for Universal Health Coverage. Full talk video here: https://www.youtube.com/watch?v=8DCoJ2_yros
Corona in India: PHC Preparedness and lockdown effectsPrashanth N S
The 3rd in the ITM ALUMNI WEBINAR series. Talk by Dr. Prashanth Nuggehalli Srinivas, Faculty & DBT/Wellcome Trust India Alliance Fellow at Institute of Public Health Bangalore. Event details available here: https://www.itg.be/E/Event/itm-alumni-webinar-3-corona-in-india-phc-preparedness
Full recording here: https://youtu.be/nB5SYcRzRjM
Bird Brain: Open Bird Quiz finals by Prashanth & Shyamal (Bangalore Bird Day ...Prashanth N S
Slides from the Bird Brain: Open Bird Quiz finals at the 2019 Bangalore Bird day conducted by Prashanth N S & L Shyamal
See link on blog for details on the quiz: http://www.daktre.com/2020/01/bird-brains-open-quiz-2019/
Bird Brains: Open Bird Quiz at Bangalore Bird Day 2019 (Prelims)Prashanth N S
Quiz conducted at National College Jayanagar on the 2019 Bangalore Bird Day (see http://www.http://birdday.in). Quiz by Prashanth N S (http://www.daktre.com) & L Shyamal (http://www.muscicapa.blogspot.com)
Finals slides here: https://www.slideshare.net/PrashanthSrinivas/bird-brain-open-bird-quiz-finals-by-prashanth-shyamal-bangalore-bird-day-2019
Slides from a TEDx talk at TEDxOakridgeInternationalEinstein in Hyderabad on October 29, 2017. For video and description of talk, see http://www.daktre.com/2017/12/healthy-by-chance-or-by-choice/
Based on a bird quiz conducted at an annual meeting of birders/naturalists. Slides and content by Tanya Seshadri with inputs from Prashanth N S. For details of this quiz, see http://www.daktre.com/2017/11/quizzing-in-the-days-of-ebird/
Building the frontline health workers: Strengthening the role and training o...Prashanth N S
Presentation made at the All India People's medical and health education conference organised in February 2015 by the All India People's Science Network by Tanya Seshadri & Prashanth N S
Questioning improvements in health going beyond averagesPrashanth N S
Presentation made at EQUILOGS, webinar hosted by Shree Chitra Institute. See http://www.healthinequity.com/event/webinar-“questioning-improvements-health-–-going-beyond-averages” for details.
Presentation made at the First Karnataka Bird Festival held in Ranganathittu from 27-29 March 2015. In the presentation, I begin with an introduction to bird lore with a few examples from medieval Europe and going to examples of traditional names/knowledge/perspectives that have inspired Indian bird names. I finally end with examples of local bird names and lore of the Soliga people from southern Karnataka
Income inequalities in health presentationPrashanth N S
Presentation on socio-economic inequalities in health in India made at the National Seminar on Health Equity Evidence and Priorities for Research in India conducted by the Sree Chitra Tirunal Institute for Medical Sciences & Technology (SCTIMST), Trivandrum in 2015
The Building Blocks of QuestDB, a Time Series Databasejavier ramirez
Talk Delivered at Valencia Codes Meetup 2024-06.
Traditionally, databases have treated timestamps just as another data type. However, when performing real-time analytics, timestamps should be first class citizens and we need rich time semantics to get the most out of our data. We also need to deal with ever growing datasets while keeping performant, which is as fun as it sounds.
It is no wonder time-series databases are now more popular than ever before. Join me in this session to learn about the internal architecture and building blocks of QuestDB, an open source time-series database designed for speed. We will also review a history of some of the changes we have gone over the past two years to deal with late and unordered data, non-blocking writes, read-replicas, or faster batch ingestion.
ViewShift: Hassle-free Dynamic Policy Enforcement for Every Data LakeWalaa Eldin Moustafa
Dynamic policy enforcement is becoming an increasingly important topic in today’s world where data privacy and compliance is a top priority for companies, individuals, and regulators alike. In these slides, we discuss how LinkedIn implements a powerful dynamic policy enforcement engine, called ViewShift, and integrates it within its data lake. We show the query engine architecture and how catalog implementations can automatically route table resolutions to compliance-enforcing SQL views. Such views have a set of very interesting properties: (1) They are auto-generated from declarative data annotations. (2) They respect user-level consent and preferences (3) They are context-aware, encoding a different set of transformations for different use cases (4) They are portable; while the SQL logic is only implemented in one SQL dialect, it is accessible in all engines.
#SQL #Views #Privacy #Compliance #DataLake
4th Modern Marketing Reckoner by MMA Global India & Group M: 60+ experts on W...Social Samosa
The Modern Marketing Reckoner (MMR) is a comprehensive resource packed with POVs from 60+ industry leaders on how AI is transforming the 4 key pillars of marketing – product, place, price and promotions.
End-to-end pipeline agility - Berlin Buzzwords 2024Lars Albertsson
We describe how we achieve high change agility in data engineering by eliminating the fear of breaking downstream data pipelines through end-to-end pipeline testing, and by using schema metaprogramming to safely eliminate boilerplate involved in changes that affect whole pipelines.
A quick poll on agility in changing pipelines from end to end indicated a huge span in capabilities. For the question "How long time does it take for all downstream pipelines to be adapted to an upstream change," the median response was 6 months, but some respondents could do it in less than a day. When quantitative data engineering differences between the best and worst are measured, the span is often 100x-1000x, sometimes even more.
A long time ago, we suffered at Spotify from fear of changing pipelines due to not knowing what the impact might be downstream. We made plans for a technical solution to test pipelines end-to-end to mitigate that fear, but the effort failed for cultural reasons. We eventually solved this challenge, but in a different context. In this presentation we will describe how we test full pipelines effectively by manipulating workflow orchestration, which enables us to make changes in pipelines without fear of breaking downstream.
Making schema changes that affect many jobs also involves a lot of toil and boilerplate. Using schema-on-read mitigates some of it, but has drawbacks since it makes it more difficult to detect errors early. We will describe how we have rejected this tradeoff by applying schema metaprogramming, eliminating boilerplate but keeping the protection of static typing, thereby further improving agility to quickly modify data pipelines without fear.
Global Situational Awareness of A.I. and where its headedvikram sood
You can see the future first in San Francisco.
Over the past year, the talk of the town has shifted from $10 billion compute clusters to $100 billion clusters to trillion-dollar clusters. Every six months another zero is added to the boardroom plans. Behind the scenes, there’s a fierce scramble to secure every power contract still available for the rest of the decade, every voltage transformer that can possibly be procured. American big business is gearing up to pour trillions of dollars into a long-unseen mobilization of American industrial might. By the end of the decade, American electricity production will have grown tens of percent; from the shale fields of Pennsylvania to the solar farms of Nevada, hundreds of millions of GPUs will hum.
The AGI race has begun. We are building machines that can think and reason. By 2025/26, these machines will outpace college graduates. By the end of the decade, they will be smarter than you or I; we will have superintelligence, in the true sense of the word. Along the way, national security forces not seen in half a century will be un-leashed, and before long, The Project will be on. If we’re lucky, we’ll be in an all-out race with the CCP; if we’re unlucky, an all-out war.
Everyone is now talking about AI, but few have the faintest glimmer of what is about to hit them. Nvidia analysts still think 2024 might be close to the peak. Mainstream pundits are stuck on the wilful blindness of “it’s just predicting the next word”. They see only hype and business-as-usual; at most they entertain another internet-scale technological change.
Before long, the world will wake up. But right now, there are perhaps a few hundred people, most of them in San Francisco and the AI labs, that have situational awareness. Through whatever peculiar forces of fate, I have found myself amongst them. A few years ago, these people were derided as crazy—but they trusted the trendlines, which allowed them to correctly predict the AI advances of the past few years. Whether these people are also right about the next few years remains to be seen. But these are very smart people—the smartest people I have ever met—and they are the ones building this technology. Perhaps they will be an odd footnote in history, or perhaps they will go down in history like Szilard and Oppenheimer and Teller. If they are seeing the future even close to correctly, we are in for a wild ride.
Let me tell you what we see.
06-04-2024 - NYC Tech Week - Discussion on Vector Databases, Unstructured Data and AI
Discussion on Vector Databases, Unstructured Data and AI
https://www.meetup.com/unstructured-data-meetup-new-york/
This meetup is for people working in unstructured data. Speakers will come present about related topics such as vector databases, LLMs, and managing data at scale. The intended audience of this group includes roles like machine learning engineers, data scientists, data engineers, software engineers, and PMs.This meetup was formerly Milvus Meetup, and is sponsored by Zilliz maintainers of Milvus.
Predictably Improve Your B2B Tech Company's Performance by Leveraging DataKiwi Creative
Harness the power of AI-backed reports, benchmarking and data analysis to predict trends and detect anomalies in your marketing efforts.
Peter Caputa, CEO at Databox, reveals how you can discover the strategies and tools to increase your growth rate (and margins!).
From metrics to track to data habits to pick up, enhance your reporting for powerful insights to improve your B2B tech company's marketing.
- - -
This is the webinar recording from the June 2024 HubSpot User Group (HUG) for B2B Technology USA.
Watch the video recording at https://youtu.be/5vjwGfPN9lw
Sign up for future HUG events at https://events.hubspot.com/b2b-technology-usa/
Natural Language Processing (NLP), RAG and its applications .pptxfkyes25
1. In the realm of Natural Language Processing (NLP), knowledge-intensive tasks such as question answering, fact verification, and open-domain dialogue generation require the integration of vast and up-to-date information. Traditional neural models, though powerful, struggle with encoding all necessary knowledge within their parameters, leading to limitations in generalization and scalability. The paper "Retrieval-Augmented Generation for Knowledge-Intensive NLP Tasks" introduces RAG (Retrieval-Augmented Generation), a novel framework that synergizes retrieval mechanisms with generative models, enhancing performance by dynamically incorporating external knowledge during inference.
7. Where’s the data?
• Primary data
• Secondary data
– Routine system data: Quality issues,
– Closed systems: Lack of “Open”ness
– Data mindedness -> Data informs action?
(cf case study of B&D registration)
8. Case study: India’s civil registration
system
• System origin & structure
• Outputs
• Issues
• RTIable but…
• Dependence on surveys: Million death study
10. Sources of health data
1. Census
2. Registration of Vital Events
3. Sample Registration System (SRS)
4. Notification of Diseases
5. Hospital Records
6. Disease Registers
7. Record Linkage
8. Epidemiological Surveillance
11. 9. Other Health Service Records
10. Environmental Health Data
11. Health Manpower Statistics
12.Population Surveys
13. • SRS is based on a system of double recording
method. The first part of record collection is
done by a part time enumerator (usually the
local school teachers) in his or her area.
• In the second part, once in six months, an
official from the SRS department, who is a full
time enumerator independently collects data
on these aspects from all the households in the
sample villages and urban blocks.
• Matching done and unmatched records are
reverified
• The SRS is undertaken under the authority of
the Registrar General of India.
Sample registration system
14. • As of now, the SRS has more than 6670
sampling units, including 4435 in rural and
2235 in urban areas, covering a sample
population of almost 6 million population.
• Each rural sampling unit has a complete
village (subject to maximum population of
1500) while each urban sampling unit is
equivalent to an urban census enumeration
block with population of 750 to 1,000.
15. Other surveys
• National Sample Survey Organisation conducts
sample surveys at varying periods
– HH expenditure
– Nutritional intake
– Morbidity, healthcare and condition of aged
– Urban slums
– Disabled
16. • Usually diseases considered to be serious
public menace are notified.
• As per International Health Regulation ,
Cholera, Plague , Yellow Fever are to be
notified to WHO, Geneva.
• International Surveillance is required for
Louse borne Typhus, relapsing Fever,
Polio, Influenza, Malaria, Rabies,
Salmonellosis etc
• The primary purpose of notification is to effect
prevention & control of disease.
• Mainly Health workers at grass-root level
report the disease.
Notifiable diseases
17. Problems with notifiable diseases
• Huge/unregistered/unregulated private sector
• First point of care often not a formal health
provider
• Duplicate surveillance systems
(vertical/disease-oriented)
• Poor “response” to notifications – lack of
feedback & response
18. 1. Not comprehensive; only capture a
small part of disease burden in society
2. Admission determined by ability to
pay and other social factors
3. Hospitals (esp. private) do not have
catchment area
Hospital records
19. Other Health Service Records
1. Records of hospitals OPD .
2. Primary Health
Centres/CHCs/TH/DH
3. District-level offices:
DHO/DICDSO/Dsurv.O. DC office for
DSO etc
4. Private practitioners & hospitals
20. Disease registers
• A register is a permanent record & here the
cases can be followed-up.
• Morbidity registers exist only for Stroke, MI,
TB, Leprosy, Congenital Rubella &
congenital defects.
• If the reporting system is effective, & the
coverage is on national basis, than register
can provide useful data on disease specific
morbidity & mortality.
21. Surveillance systems
• HIV sentinel surveillance (since 1998)
• National Crime Records Bureau (1967)
• National Cancer registry – only city-based
• IDSP, NPSP, NVBDCP
• Behavioural surveillance – risk factors
• NNMB
22. Others
• NHA, SHA
• Modelling – NCMH (after WHO CMH by Jeff
Sachs) – looked at mortality, causes of death,
morbidity, health infrastructure
• Global burden of disease
23. Environmental Health Data
• It may be the data of air water &
noise pollution
• Industrial intoxicants.
• PCBs
24. Health Manpower Statistics
• State Medical/ dental / Nursing
Council can provide information of the
respective health manpower.
• Ministry of Health & Family Welfare ,
Govt. Of India publishes every year the
statistics data as “Health Information
of India.”
• Central Bureau of Health Information
42. DATA PORTAL INDIA : data.gov.in
• Facilitates Citizen Engagement
• Rate Data Sets
• Comment on quality of Datasets
• Embed Datasets in
Website, Blogs, Social Media Pages
• Provision to Suggest Datasets