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ASSIGNMENT ON HEALTH ADMINISTRATION

Q.1 a. Identify the reasons that led to the implementation of the


Revised National Tuberculosis Programme?
Solution-

Tuberculosis (TB) is an infectious disease caused by a Bacterium, Mycobacterium


tuberculosis. It is spread through the air by a person suffering from TB. A single patient
can infect 10 or more people in a year. India has a long and distinguished tradition of
research in TB. Studies from the Tuberculosis Research Centre in Chennai and the
National Tuberculosis Institute in Bangalore provided key knowledge to improve
treatment of TB patients all around the world. Modern anti-TB treatment can cure
virtually all patients. It is, however, very important that treatment be taken for the
prescribed duration, which in every case is a minimum of 6 months. Because treatment
is of such a long duration and patients feel better after just 1-2 months, and because
many TB patients face other problems such as poverty and unemployment, treatment is
often interrupted. Therefore, just providing anti-TB medication is not sufficient to
ensure that patients are cured. The DOTS strategy ensures that infectious TB patients are
diagnosed and treated effectively till cure, by ensuring availability of the full course of
drugs and a system for monitoring patient compliance to the treatment.

Directly Observed Treatment, Short-course


The DOTS strategy along with the other components of the Stop TB strategy,
implemented under the Revised National Tuberculosis Control Programme (RNTCP) in
India, is a comprehensive package for TB control. The DOTS strategy is cost-effective
and is today the international standard for TB control programmes. To date, more than
180 countries are implementing the DOTS strategy. India has adapted and tested the
DOTS strategy in various parts of the country since 1993, with excellent results, and by
March 2006 nationwide DOTS coverage has been achieved.

DOTS is a systematic strategy which has five components

• Political and administrative commitment. TB is the leading infectious cause of


death among adults. TB kills more men than women, yet more women die of TB
than all causes associated with childbirth combined. Since TB can be cured and
the epidemic reversed, it warrants the topmost priority, which it has been
accorded by the Government of India. This priority must be continued and
expanded at the state, district and local levels.
• Good quality diagnosis. Good quality microscopy allows health workers to see
the tubercle bacilli and is essential to identify the infectious patients who need
treatment the most.
• Good quality drugs. An uninterrupted supply of good quality anti-TB drugs must
be available. In the RNTCP, a box of medications for the entire treatment is
earmarked for every patient registered; ensuring the availability of the full course
of treatment the moment the patient is initiated on treatment. Hence in DOTS,
the treatment can never interrupt for lack of medicine.

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• Supervised treatment to ensure the right treatment, given in the right way. The
RNTCP uses the best anti-TB medications available. But unless treatment is
made convenient for patients, it will fail. This is why the heart of the DOTS
programme is "directly observed treatment" in which a health worker, or another
trained person who is not a family member, watches as the patient swallows the
anti-TB medicines in their presence.
• Systematic monitoring and accountability. The programme is accountable for the
outcome of every patient treated. This is done using standard recording and
reporting system, and the technique of ‘cohort analyses. The cure rate and other
key indicators are monitored at every level of the health system, and if any area
is not meeting expectations, supervision is intensified. The RNTCP shifts the
responsibility for cure from the patient to the health system.

The new Stop TB Strategy published by WHO in 2006 has DOTS in the core with
additional components to address TB/HIV and MDR-TB, health system strengthening,
involvement of all care providers, engaging people with TB and affected communities,
and enabling/promoting research. RNTCP is already implementing/ plans to implement
the activities recommended under the new Stop TB Strategy.

DOTS in India

Controlling TB in India is a tremendous challenge. The TB burden in India is still


staggering. Every year, 1.8 million persons develop the disease, of which about 800,000
are infectious; and, until recently, 370,000 died of it annually —1,000 every day. The
disease is a major barrier to social and economic development. An estimated 100 million
workdays are lost due to illness. Society and the country also incur a huge cost due to
TB—nearly US$ 3 billion in indirect costs and US$ 300 million in direct costs.

The Revised National Tuberculosis Control Programme (RNTCP), based on the DOTS
strategy, began as a pilot in 1993 and was launched as a national programme in 1997.
Rapid RNTCP expansion began in late 1998. By the end of 2000, 30%of the country’s
population was covered, and by the end of 2002, 50%of the country’s population was
covered under the RNTCP. By the end of 2003, 778 million populations were covered,
and at the end of year 2004 the coverage reached to 997 million. By December 2005,
around 97% (about 1080 million) of the population had been covered, and the entire
country was covered under DOTS by 24th March 2006.

Every day in India, under the RNTCP, more than 15,000 suspects are being examined
for TB, free of charge. The diagnosis of these patients and the follow-up of patients on
treatment are achieved through the examination of more than 50,000 laboratory
specimens. As a result of these examinations, each day, about 3,500 patients are started
on treatment, stopping the spread of TB in the community. In order to achieve this, more
than 600,000 health care workers have been trained and more than 11,500 designated
laboratory Microscopy Centres have been upgraded and supplied with binocular
microscopes since the inception of the RNTCP. As a result of rapid expansion in
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diagnostic facilities, the proportion of sputum- positive cases confirmed in the


laboratory are doubles that of the previous programme and is on par with international
standards. Despite the rapid expansion, overall performance remains good and in many
areas is excellent. Treatment success rates have tripled from 25%in the earlier
programme to 86%in RNTCP.

DOTS Expansion in India

In 1992, the Government of India, together with the World Health Organization (WHO)
and Swedish International Development Agency (SIDA), reviewed the National TB
Programme and concluded that it suffered from managerial weakness, inadequate
funding, over-reliance on x-ray, non-standard treatment regimens, low rates of treatment
completion, and lack of systematic information on treatment outcomes. Programme
review showed that only 30% of patients were diagnosed and only 30% of those treated
successfully. Based on the findings and recommendations of the review in 1992, the
GOI evolved a revised strategy and launched the Revised National TB Control
Programme (RNTCP) in the country. Starting as pilots in October 1993, the RNTCP
was implemented in a population of 2.35 million in 5 sites in different states (Delhi,
Kerala, West Bengal, Maharashtra, and Gujarat). The programme was expanded to a

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population of 13.85 million in 1995 and 16 million in 1996. Having proved both its
technical and operational feasibility, a soft loan of US $ 142 million was negotiated with
the World Bank in December 1996 and the credit agreement was signed with IDA in
May 1997. In 1997 RNTCP was launched as a national programme. It was envisaged to
implement RNTCP in 102 districts of the country covering a population of 271 million
in a phased manner. Another 203 SCC districts with a population of 447 million were
envisaged to be strengthened as a transitional step for introduction of revised strategy at
a later stage. Having started in 1997, rapid scale-up began in late 1998, when another
100 million populations was covered under RNTCP. Over the years RNTCP has
expanded rapidly as shown below:

March
Year 1998 1999 2000 2001 2002 2003 2004 2005
2006
Population
18 130 287 450 530 775 947 1080 1114
Covered *
* cumulative, in millions

Starting in 1997, the project was implemented in a phased manner to ensure that quality
of services is maintained. By March 2006, entire country has been covered under the
programme.

Revised National TB Control Programme and its recent progress in DOTS expansion
have been encouraging. As per Global TB Report 2003, 2/3rd of the additional sputum
positive cases reported under DOTS in 2001, were found in India. In 2002, over 620,000
cases were placed on treatment of which nearly 250,000 were new smear positive cases.
In the year 2003, more than 900,000 cases were placed on treatment. In the year 2004
alone more than 1100,000 cases were placed on treatment, and in the 2005, more than
1290,000 cases were placed on treatment - largest cohort of cases, more than any other
country in the world. By December 2009, more than 11 million patients have been
initiated on treatment, saving more than 2 million additional lives. The success of DOTS
in India has contributed substantially to the success of TB control in the world.

RNTCP has consistently achieved treatment success rate of more than 85%, and case
detection close to the global target. However, in 2007 RNTCP for the first time has
achieved the global target of 70% case detection while maintaining the treatment
success rate of more than 85%.

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Multi-drug-Resistant Tuberculosis (MDRTB)

MDRTB refers to strains of the bacterium which are proven in a laboratory to be


resistant to the two most active anti-TB drugs, ionized and rifampicin. Treatment of
MDRTB is extremely expensive, toxic, arduous, and often unsuccessful. DOTS have
been proven to prevent the emergence of MDRTB, and also to reverse the incidence of
MDRTB where it has emerged. MDRTB is a tragedy for individual patients and a
symptom of poor TB management. The best way to confront this challenge is to
improve TB treatment and implement DOTS. Beginning 1999, the Tuberculosis
Research Centre, Chennai in collaboration with the National Tuberculosis Institute,
Bangalore, initiated drug resistance surveys in different parts of the country using the
WHO/IUATLD guidelines. The table below provides information about primary ionized
resistance and primary multi-drug resistance based on analyses completed to date.

Table: Primary drug resistance, India (1999-2002)

Primary
Intake Number of Primary multi-drug
District (Zone) isoniazid
period patients resistance %
resistance %
2.8
North Arcot
1999 282 23.4
(South)
f

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Raichur (South) 1999-2000 278 18.7 2.5


Wardha (West) 2000-2001 197 15 0.5
Jabalpur (West) 2001-2002 273 17 1.0
Hoogly (East) 2000-2001 350 10.3 3.0
Mayurbanj (East)2000-2002 343 2.5 0.7

Currently large scale representative drug resistance surveys are on-going in 2 States and
3 (Andhra Pradesh, Orissa, and Uttar Pradesh) other States are likely to conduct these
surveys.

RNTCP is planning to introduce second line anti-TB treatment for MDR-TB cases,
starting in early 2007. For this purpose State level Intermediate Reference Laboratories
are being established to provide quality assured culture and drug susceptibility testing
facilities. The guidelines for management of MDR-TB under DOTS-Plus strategy have
been developed.

Second Phase of RNTCP

In the first phase of RNTCP (1998-2005), the programme’s focus was on ensuring
expansion of quality DOTS services to the entire country. There are many challenges
remaining that are to be addressed in order to achieve the TB-related targets set by the
Millennium Development Goals for 2015 and to achieve TB control in the longer term.

The RNTCP has now entered its second phase in which the programme aims to firstly
consolidate the gains made to date, to widen services both in terms of activities and
access, and to sustain the achievements for decades to come in order to achieve ultimate
objective of TB control in the country.

All components of new Stop TB Strategy are incorporated in the second phase of
RNTCP. These are:

1. Pursue quality DOTS expansion and enhancement, by improving the case


finding are cure through an effective patient-centred approach to reach all
patients, especially the poor.
2. Address TB-HIV, MDR-TB and other challenges, by scaling up TB-HIV joint
activities, DOTS Plus, and other relevant approaches.
3. Contribute to health system strengthening, by collaborating with other health
programmes and general services
4. Involve all health care providers, public, nongovernmental and private, by
scaling up approaches based on a public-private mix (PPM), to ensure adherence
to the International Standards of TB care.
5. Engage people with TB, and affected communities to demand, and contribute to
effective care. This will involve scaling-up of community TB care; creating
demand thorough context-specific advocacy, communication and social
mobilization.

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6. Enable and promote research for the development of new drugs, diagnostic and
vaccines. Operational Research will also be needed to improve programme
performance.

The Revised National TB Control Programme now aims to widen the scope for
providing standardized, good quality treatment and diagnostic services to all TB patients
in a patient-friendly environment, in which ever health care facility they seek treatment
from. Recognizing the need to reach to every TB patient in the country, the programme
has made special provisions to reach marginalized sections of the society, including
creating demand for services through specific advocacy, communication and social
mobilization activities.

b. Explain the need for International Health Regulations?


Solution-

The International Health Regulations 2005 are legally binding regulations (forming
international law) that aim to a) assist countries to work together to save lives and
livelihoods endangered by the spread of diseases and other health risks, and b) avoid
unnecessary interference with international trade and travel. The purpose and scope of
IHR 2005 are to prevent, protect against, control and provide a public health response to
the international spread of disease in ways that are commensurate with and restricted to
public health risks, and which avoid unnecessary interference with international traffic
and trade.

The International Health Regulations Evolution

The International Health Regulations originated with the International Sanitary


Regulations adapted at the International Sanitary Conference in Paris in 1851. The
cholera epidemics that hit Europe in 1830 and 1847 made apparent the need for
international cooperation in public health. In 1948, the World Health Organization
Constitution came about. The Twenty-Second World Health Assembly (1969) adopted,
revised and consolidated the International Sanitary Regulations, which were renamed
the International Health Regulations (1969).

The Twenty-Sixth World Health Assembly in 1973 amended the IHR (1969) in relation
to provisions on cholera. In view of the global eradication of smallpox, the Thirty-fourth
World Health Assembly amended the IHR (1969) to exclude smallpox in the list of
notifiable diseases. During the Forty-Eighth World Health Assembly in 1995, WHO and
Member States agreed on the need to revise the IHR (1969). The revision of IHR (1969)
came about because of its inherent limitations, most notably:

• Narrow scope of Notifiable diseases (cholera, plague, yellow fever).[1] The past
few decades have seen the emergence and re-emergence of infectious diseases.
The emergence of “new” infectious agents Ebola Hemorrhagic Fever and the re-
emergence of cholera and plague in South America and India, respectively;

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• Dependence on official country notification; and


• Lack of a formal internationally coordinated mechanism to prevent the
international spread of disease.

These challenges were placed against the backdrop of the increased travel and trade
characteristic of the 20th century. The IHR (2005) entered into force, generally, on 15
June 2007, and are currently binding on 194 countries (States Parties) across the globe,
including all 193 Member States of WHO.

The Principles Embodying the IHR (2005)

The implementation of IHR (2005) shall be:

1. With full respect for the dignity, human rights and fundamental freedom of
persons;
2. Guided by the Charter of the United Nations and the Constitution of the World
Health Organization;
3. Guided by the goal of their universal application for the protection of all people
of the world from the international spread of disease;
4. States have, in accordance with the Charter of the United Nations and the
principles of international law, the sovereign right to legislate and to implement
legislation in pursuance of their health policies. In doing so, they should uphold
the purpose of these Regulations. (Art 3. IHR (2005))

Q.2 a. Write short notes on the Executive Board of WHO and


UNICEF?
Solution-

Executive Board of WHO

The Executive Board is composed of 34 individuals technically qualified in the field of


health, each one designated by a Member State elected to do so by the World Health
Assembly. Member States are elected for three-year terms.

The Board meets at least twice a year; the main meeting is normally in January, with a
second shorter meeting in May, immediately after the
Health Assembly. The main functions of the Executive
Board are to give effect to the decisions and policies of the Health Assembly, to advise
it and generally to facilitate its work.

a. Chairman of the Executive Board.


b. Executive Board members.
c. Composition of the Executive Board.
d. Documentation of Executive Board sessions and Health Assemblies.
e. Executive Board Committees.
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f. Ad-hoc open-ended Intergovernmental Working Group to Review the Working


Methods of the Executive Board.

Executive Board of UNICEF

The Executive Board is the governing body of UNICEF, providing intergovernmental


support and oversight to the organization, in accordance with the overall policy
guidance of the United Nations General Assembly and the Economic and Social
Council.

Comprising 36 members, representing the five regional groups of Member States at the
United Nations, the Executive Board reviews UNICEF activities and approves its
policies, country programmes and budgets. Its work is coordinated by the Bureau,
comprising the President and four Vice-Presidents, each officer representing one of the
five regional groups.

The Office of the Secretary of the Executive Board supports and services the Executive
Board. It is responsible for maintaining an effective relationship between the Executive
Board and the UNICEF secretariat.

The Executive Board’s annual term is identical to a calendar year, running from 1
January to 31 December. The Executive Board meets three times each year, in a first
regular session (January/February), annual session (May/June) and second regular
session (September). Executive Board sessions are held at the United Nations
headquarters in New York.

b. How useful is digital imaging in the field of medicine?


Solution-

Digital Imaging and Communications in Medicine (DICOM) is a standard for handling,


storing, printing, and transmitting information in medical imaging. It includes a file
format definition and a network communications protocol. The communication protocol
is an application protocol that uses TCP/IP to communicate between systems. DICOM
files can be exchanged between two entities that are capable of receiving image and
patient data in DICOM format. The National Electrical Manufacturers Association
(NEMA) holds the copyright to this standard.[1] It was developed by the DICOM
Standards Committee, whose members [2] are also partly members of NEMA.[3]

DICOM enables the integration of scanners, servers, workstations, printers, and network
hardware from multiple manufacturers into a picture archiving and communication
system (PACS). The different devices come with DICOM conformance statements
which clearly state the DICOM classes they support. DICOM has been widely adopted
by hospitals and is making inroads in smaller applications like dentists' and doctors'
offices.

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DICOM is known as NEMA Standard PS3, and as ISO Standard 12052.

DICOM Data Format

DICOM differs from some, but not some other, data formats in that it groups
information into data sets. That means that a file of a chest X-Ray image, for example,
actually contains the patient ID within the file, so that the image can never be separated
from this information by mistake. This is similar to the way that image formats such as
JPEG can also have embedded tags to identify and otherwise describe the image.

A DICOM data object consists of a number of attributes, including items such as name,
ID, etc., and also one special attribute containing the image pixel data (i.e. logically, the
main object has no "header" as such - merely a list of attributes, including the pixel
data). A single DICOM object can only contain one attribute containing pixel data. For
many modalities, this corresponds to a single image. But note that the attribute may
contain multiple "frames", allowing storage of cine loops or other multi-frame data.
Another example is NM data, where an NM image by definition is a multi-dimensional
multi-frame image. In these cases three- or four-dimensional data can be encapsulated in
a single DICOM object. Pixel data can be compressed using a variety of standards,
including JPEG, JPEG Lossless, JPEG 2000, and Run-length encoding (RLE). LZW
(zip) compression can be used for the whole data set (not just the pixel data) but this is
rarely implemented.

DICOM uses three different Data Element encoding schemes. With Explicit Value
Representation (VR) Data Elements, for VRs that are not OB, OW, OF, SQ, UT, or UN,
the format for each Data Element is: GROUP (2 bytes) ELEMENT (2 bytes) VR (2
bytes) LengthInByte (2 bytes) Data (variable length). For the other Explicit Data
Elements or Implicit Data Elements, see section 7.1 of Part 5 of the DICOM Standard.

The same basic format is used for all applications, including network and file usage, but
when written to a file, usually a true "header" (containing copies of a few key attributes
and details of the application which wrote it) is added.

Q.3. Outline the impact of:

a. Impact on Health-

Research focusing on individuals has found a very robust relationship


between an adult Individual’s income and that individual’s health, using a
range of measures for both. Regardless of how measures of health status
and measures of SES are combined, there is little doubt that poverty leads
to ill health. For example, in a recent review of the literature, Benzeval and
Judge provide evidence from 16 studies using eight different data sets from
four different countries. Health status outcome measures include: subjective
self-reports, mortality, emotional stability, chronic conditions, general life
satisfaction and physical functioning. Socio-economic status measures

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include: current income level, recent income change, poverty flags, current
earnings, multi-period averaged incomes, relative position in the income
distribution and number of spells of poverty. In summing up their review, the
authors conclude: .All of the studies that include measures of income level
find that it is significantly related to health outcomes.

Similarly, Mullah and colleagues conclude: Voluminous empirical studies and


reviews demonstrate a robust association between income and morbidity
and mortality, using various measures of both income and health, across
samples, and at various time points. An important research issue in the
study of poverty and health is the possibility for ill health to limit an
individual’s ability to engage in paid work and hence reduce his or her
income, even if he or she comes from an affluent background.

Further important conclusions from this body of work include the following:
• The relationship between individual income and health is non-linear (i.e.
low-income individuals suffer larger negative health consequences than
high-income individuals reap health benefits, though high-income individuals
do reap benefits).
• Longer-term measures of average income have larger associations with
health than measures of current income, which can be highly volatile.

b. Health on economic growth

Although the health of individuals in a country can only be roughly approximated in


national averages, the models showed significant effects of adult survival rate (ASR) on
economic growth for low income countries. Thus, for example, for the poorest countries,
a 1% change in ASR was associated with an approximate 0.05% increase in growth rate.
While the magnitude of this coefficient was small, a similar increase of 1% in
investment/GDP ratio was associated with a 0.014% increase in growth rate. A novel
aspect of the analysis was that we were able to estimate the threshold point beyond
which ASR had a negligible effect on growth rates; confidence intervals for the net
impact of ASR on economic growth highlighted the asymmetries for poor and rich
countries. The specification tests based on instrumental variables estimates showed that
the explanatory variables lagged ASR, investment/GDP ratio, GDP, and the interaction
between ASR and GDP, should be treated as simultaneously determined with growth
rates.

From the viewpoint of the conceptual issues addressed in the paper, it is important that
future research compile more elaborate data on health indicators. Thus, for example,
ASR in poor countries reflects the levels of nutrition, smoking prevalence rates,
infectious diseases, health infrastructure, and factors such as accidents leading to
premature deaths. By contrast, differences in ASR in middle and high income countries
may be strongly influenced by genetic factors and by the timeliness and costs of
preventive health care. Because investments in skill acquisition in poor countries depend
on the ASR, the years for which skilled labour remains productive is likely to be
important for explaining economic productivity.
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It would be useful to augment statistics such as percentages of skilled and unskilled


labour in countries by measures of physical and mental health. For example, work days
lost due to ill health can be estimated from household surveys or using other
methodologies (e.g. Murray and Lopez, 1996). Measures of cognitive function in
different age cohorts may also be useful for explaining economic performance of
countries. Analyses based on elaborate data sets would afford sharper insights into the
likely impact of health on economic growth.

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