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CHAPTER ONE

INTRODUCTION
1.0 Introduction
This chapter provides the background of the study, the statement of the problem, the
objectives of the study, the research questions, the significance of the study, the scope
and limitation of the study.
1.1 Background of the tud!
The advancement in medical research is aimed at enhancing diagnosis of various
diseases. Over the last several years focus has been on achieving sustainable diagnosis of
several genetically transmitted, non-atherosclerotic cardiovascular diseases. Diagnostics
are an integral and critical part of a health care system of any country as the results of
these tests inform a wide range of medical decision making. rom the genetic tests that
inform personali!ed cancer treatment to the microbial culture that identifies the right
antibiotic to fight an infection, diagnostic tests. The identification of the sequence of the
human genome and of human genes has changed our understanding of health and
pathogenesis. "t is now recogni!ed that virtually all diseases may have a genetic
component. Thus, molecular genetics could become a powerful diagnostic and screening
tool. The comple# interplay between genetic predisposition and environmental
influences, however, limits the predictive power of genetic testing.
$s the traditional laboratory remains a mainstay for diagnostic testing while significant
testing is done outside the laboratory, in such point of care settings as hospitals,
physicians% offices, and clinics, and for personnel in the field, such as emergency
responders and soldiers. &regnancy tests and diabetes test strips are familiar e#amples of
diagnostics that are available directly to consumers. The main categories of diagnostics
are clinical chemistry, immunology, hematology, microbiology and molecular
diagnostics. The diagnostics industry continues to innovate in all of these important areas,
and molecular diagnostics has captured particular attention in recent years because of the
deep insights these types of tests bring to diagnosis and treatment.
'
The emergence of nucleic acid amplification and detection is a shift from the past and has
resulted in a change from conventional laboratory methods that rely on phenotypic
e#pression of antigens or biochemical products, to molecular methods for the rapid
identification of a number of infectious agents. These new methods have become
increasingly incorporated into the clinical microbiology laboratory, particularly for the
detection and characterisation of virus infections and for the diagnosis of diseases due to
fastidious bacteria.
The advantages of rapid turn-around time and high sensitivity and specificity are
appealing but must be matched by rigorous validation and quality control. (uch
diagnoses have mostly come to the clinical microbiology laboratory in the form of &)*
technology, initially involving single round or nested procedures with detection by gel
electrophoresis. +owever, with the introduction of automation for the various stages of
D,$ or *,$ e#traction, amplification and product detection together with real-time
&)*, molecular laboratories will continue to become more efficient and cost-effective.
-icro-array technology such as the D,$ chip will likely further increase the utility of
molecular detection in the clinical microbiology laboratory.
1." tate#ent of the Pro$%e#
Dissecting a patient%s fundamental constitutional makeup also raises psychological,
ethical and professional questions. -olecular diagnostics is a dynamic and transformative
area of diagnostics, leading to insights in research and treatment in many disease states
that are revolutioni!ing health care. -olecular diagnostics detect and measure the
presence of genetic material or proteins associated with a specific health condition or
disease, helping to uncover the underlying mechanisms of disease and enabling clinicians
to tailor care at an individual level facilitating the practice of .personali!ed medicine.
-olecular techniques using antibodies and molecular probes will be analysed in detail.
-ethods employing differential hybridisation of nucleic acids will be discussed. $
variety of inherited gene defects and D,$ sequence changes that ultimately result in
diseases such as cancer will be studied. The ethics of such molecular analysis will be
/
discussed. Therefore, accurate diagnosis of infections is crucial to reduce morbidity and
mortality in tropical areas. $vailable literature on epidemiology and immunity depend on
accurate detection, diagnosis, and density estimation. Traditionally, light microscopy
01-2 e#amination of blood smears has been considered the gold standard for the
diagnosis of diseases. 1- has clear advantages since it incurs low costs, allows species
identification and quantification and neither comple# sample preparation nor advanced
technology is required. +owever, the role of 1- as gold standard has been questioned
due to false negative results at low levels of parasitaemia, with a predicted limit of
detection of five to /3 parasites per microlitre of blood and frequent errors in species
identification in mi#ed infections. "n this sense, microscopy seems to be an imperfect
reference standard.
Therefore, it is difficult to estimate its true sensitivity and specificity or to evaluate new
diagnostic methods. (everal molecular methods based on the amplification of D,$ have
been developed for the detection of malarial infections in humans. The semi-nested
multiple# malaria &)* 0(n--&)*2 is a widely used method and it is considered a
molecular gold standard due to its good performance in the detection of mi#ed species
infection and the ability to differentiate disease causing species of bacteria and viruses.
"n recent years, new molecular methods have been developed for the detection of various
species, mostly based on real time quantitative &)*s 0q&)*2. These new molecular
methods have been promoted as an automated, quantitative, and closed system that
reduces the risk of cross-contamination inherent in conventional &)*. (everal real-time
&)* methods for malaria have been described and validated within a research setting
with high sensitivity and specificity values. +owever, some advantages should be
considered such as their ability to detect mi#ed &lasmodium infections but also some
limitations, such as their application in rural areas without adequate laboratory
conditions.
$lternative methods sensitive enough to detect low levels of parasitaemia in
asymptomatic infections are required to complement or replace parasitological
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e#amination with light microscopy. This would allow minimi!ation of errors in diagnosis
0false positives, false negatives and species misidentification2 that may lead to biased
estimates of protective efficacy against the parasite.
The incorporation of molecular tools for the characteri!ation of parasite infections has
allowed increase sensitivity in the detection of human malarial parasites in blood. The
aim of the present study was to compare different malaria diagnostic methods and to
broaden the knowledge of malaria prevalence in a hospital in -oi Teaching and *eferral
+ospital 0-T*+2 5ldoret Town, 6enya.
1.& O$'ecti(e) of the tud!
The general objective of this study was to investigate the effects of -olecular 7iology on
Diagnosis of "nfectious Diseases in 1aboratory Testing.
The specific objectives of the study were as follows8
i2 To e#amine the usefulness of molecular biology on treatment of diseases
ii2 To e#amine the effects of effects of molecular biology on screening of diseases
iii2 To determine the influence of molecular lab test on risk assessment of diseases
iv2 To e#amine the effects of molecular biology on staging and prognosis of diseases
1.* Re)earch +ue)tion)
The study sought to answer the following questions8
i2 To what e#tent has molecular biology enhanced accuracy in treatment of detected
diseases9
ii2 :hat are the effects of molecular biology on early identification of high-risk
diseases on patient9
iii2 +ow has molecular biology influenced diagnostic tests to complement traditional
risk factors9
iv2 :hat the effects of molecular biology on assessing severity and risk of recurrence
of diseases9
;
1., ignificance of the tud!
$ thorough understanding of the e#tent to which molecular biology has revised
traditional diagnostic criteria is essential. The role of genetic testing in assessing
prognosis and identifying high-risk subgroups or in defining basic disease mechanisms
and pathophysiology. Demonstrating the presence of the infecting organism, or a
surrogate marker of infection, is often crucial for effective clinical management and for
selecting other appropriate disease control activities such as contact tracing. $
diagnostic tests have multiple uses, including8 patient management, especially when
clinical symptoms are not specific for a particular infection< screening for asymptomatic
infections< surveillance< epidemiological studies< evaluating the effectiveness of
interventions, including verification of elimination< and detecting infections with markers
of drug resistance.
The findings of this study will be useful in facilitating the setting of appropriate standards
for test evaluation< to provide best-practice guidelines for assessing the performance and
operational characteristics of diagnostic tests for infectious diseases< to help those
designing evaluations at all levels, from test manufacturers to end-users< and to facilitate
critical review of published and unpublished evaluations, with a view to selecting or
approving tests that have been appropriately evaluated and shown to meet defined
performance targets.
The target audience for this document includes institutions and research groups that are
planning trials of diagnostic tests< organi!ations that fund or conduct trials of diagnostic
tests< agencies responsible for the procurement of diagnostic tests< diagnostic test
manufacturers< and regulatory authorities. The results and findings of this study will
confirm major achievements in the laboratory diagnosis of diseases enabling medical
practitioners in the country to utili!e the literature from this study. "t will also be useful in
determining the effective methods of patient management, disease detection enabling
simplicity of medical treatment.
=
1.- co.e and /i#itation) of the tud!
There are the scope and limits within which this study was carried out and its
generali!ation applicable. These areas are covered in the section that follows8
1.-.1 co.e of the tud!
The study focused mainly on the infectious diseases that can be diagnosed in the lab from
patients visiting the -T*+ in 5ldoret town. This facility was the only one used as a case
study hence many other pubic and private hospitals were not investigated minimi!ing the
generali!ation of the findings making their applicability to within the under said scope.
1.-." /i#itation) of the tud!
The study faced several limitation first several participants had to be convinced of their
importance and the ethical use of the information obtained from them in the study as
purely for academic purposes. There are many factors that influence the performance of
tests in different settings. They include differences in the characteristics of the population
or the infectious agent, including the infection prevalence and genetic variation of the
pathogen or host, as well as the test methodology. Therefore, wherever possible, test
evaluations had to be performed under the range of conditions in which they are likely to
be used in practice. "n some situations, it forced the evaluations to be facilitated through
multi-centre trials. (econdly, many specimens testing required a lot of accuracy hence a
lot of time was needed to carry out the tests over a repeated period of time. (ome devices
were also not easily available hence a compromise was made although the outcomes were
not compromised.
1ack of resources and e#pertise limited the performance of adequate evaluations of
diagnostic tests, and many new tests are marketed directly to end-users who lack the
ability to assess their performance. The onus is therefore on those who perform the
evaluations to ensure that the quality of the methods and the documentation used is such
that the findings add usefully to the pool of knowledge on which others can draw.
>
CHAPTER T0O
/ITERATURE RE1IE0
".0 Introduction
This chapter reviews the study on the related field, acknowledgement the contribution
made various scholars publication, medic journal, te#t and periodicals, its identifies the
gap and provide the way forward a critical review is done to identify gaps, thereafter a
summery is made on the study .
".1 The Conce.t of Di)ea)e Diagno)i)
"n any health care system, the performance of practitioner can be based on their ability to
accurately detect and diagnose a medical problem. This enhances an accurate response to
medication and management of the problem as may early be detected. $ diagnostic test
for an infectious agent can be used to demonstrate the presence or absence of infection, or
to detect evidence of a previous infection. Demonstrating the presence of the infecting
organism, or a surrogate marker of infection, is often crucial for effective clinical
management and for selecting other appropriate disease control activities such as contact
tracing.
The usefulness of diagnostic methods lies on their accuracy, simple and affordability for
the population for which they are intended. They must also provide a result in time to
institute effective control measures, particularly treatment. or some infections, early
diagnosis and treatment can have an important role in preventing the development of
long-term complications or in interrupting transmission of the infectious agent. "n a
broader conte#t, diagnostic tests can have multiple uses, including8 patient management,
especially when clinical symptoms are not specific for a particular infection 0as is often
the case2< screening for asymptomatic infections< surveillance< epidemiological studies
0for e#ample, rapid assessments of disease burden or outbreak investigations2< evaluating
the effectiveness of interventions, including verification of elimination< and detecting
infections with markers of drug resistance.
?
The other important measures of test performance are positive predictive value 0&&@2,
the probability that those testing positive by the test are truly infected, and negative
predictive value 0,&@2, the probability that those testing negative by the test are truly
uninfected. 7oth of these measures are often e#pressed as percentages. &&@ and ,&@
depend not only on the sensitivity and specificity of the test, but also on the prevalence of
infection in the population studied. The reproducibility of a test is an assessment of the
e#tent to which the same tester achieves the same results on repeated testing of the same
samples, or the e#tent to which different testers achieve the same results on the same
samples, and is measured by the percentage of times the same results are obtained when
the test is used repeatedly on the same specimens.
*eproducibility can therefore be measured between operators or with the same operator,
or using different lots of the same test reagent. The accuracy of a test is sometimes used
as an overall measure of its performance and is defined as the percentage of individuals
for whom both the test and the reference standard give the same result 0that is, the
percentage of individuals whom both tests classify as infected or uninfected2. ,ote that
the use of this measure of diagnostic accuracy is of limited value and is often difficult to
interpret, as it depends on sensitivity, specificity and the prevalence of infection.
Operational characteristics include the time taken to perform the test, its technical
simplicity or ease of use, user acceptability and the stability of the test under user
conditions. The ease of use will depend on the ease of acquiring and maintaining the
equipment required to perform the test, how difficult it is to train staff to use the test and
to interpret the results of the test correctly, and the stability of the test under the e#pected
conditions of use. $ll of these characteristics are important for determining the settings in
which a diagnostic test can be used and the level of staff training required.
*ecent technological developments have led to the proliferation of new, rapid diagnostic
tests that hold promise for the improved management and control of infectious diseases.
:hether these tests are useful in a given setting and, if so, which test is most appropriate
A
are questions that can be answered only through evaluations in the appropriate laboratory,
clinical or field settings.
"." 2o%ecu%ar Bio%og!
-olecular methods have become increasingly incorporated into the clinical microbiology
laboratory, particularly for the detection and characterisation of virus infections and for
the diagnosis of diseases due to fastidious bacteria. The advantages of rapid turn-around
time and high sensitivity and specificity are appealing but must be matched by rigorous
validation and quality control.
-olecular biology tools are aimed at bringing a very sophisticated level of sensitivity and
specificity to diagnostics. These tools are e#pected to detect a bacterium, virus, yeast,
parasite or genetic marker through the presence of D,$ or *,$ genetic sequences in a
blood sample. Tests are performed directly on a clinical sample and make it possible to
obtain results in just a few hours.

These tests are used to detect pathogens 0bacteria, viruses, yeasts2, identify antibiotic
resistance mechanisms, and measure the quantity of a virus, such as +"@, in the blood.
They thus allow choices to be made about a specific treatment, monitor its effectiveness,
and determine how human cells react to a disease or infection. "dentifying patients who
will be responsive to a given treatment, and those for whom such therapy may cause
significant side effects, represents a recent application for molecular biology.
-olecular detection has mostly come to the clinical microbiology laboratory in the form
of &)* technology, initially involving single round or nested procedures with detection
by gel electrophoresis. +owever, with the introduction of automation for the various
stages of D,$ or *,$ e#traction, amplification and product detection together with
real-time &)*, molecular laboratories will continue to become more efficient and cost-
effective. -icroarray technology such as the D,$ chip will likely further increase the
utility of molecular detection in the clinical microbiology laboratory.
B
-olecular biology usage includes the discipline of virology where it has been applied to
resistance testing, genotyping and viral load quantification in addition to routine viral
detection. "n the area of bacteriology molecular methods have been applied to resistance
testing, the detection of infection due to fastidious bacteria, the more rapid detection of
serious bacterial infections compared to conventional methods and the detection of
bacterial infection after antibiotics have been administered. $dvances into the areas of
parasitology and mycology have also been made such as more rapid diagnosis of fungal
infection in neutropenic patients. Other applications include detection of biosecurity
agents< applications to epidemiology and infection control together with the potential
pitfalls with molecular methods.
".& Techni3ue) u)ed in Detection and Diagno)i) of Di)ea)e)
There are many techniques used in modern diagnostics to detect and quantify specific
D,$ or D,$ sequences, as well as proteins. The fundamental of these techniques
include the polymerase chain reaction, which is used to amplify specific sequences of
D,$ or *,$. (ubsequent reports will elaborate on additional genetic test methods, such
as in situ hybridi!ation or whole genome sequencing, and such protein detection tests as
mass spectrometry.
One of the essential methods underlying many molecular diagnostics is amplification, the
process of making copies of a specific D,$ or *,$ sequence found in a sample until
there are so many copies that they can be detected and measured.
There are a number of different amplification technologies, but polymerase chain reaction
0&)*2 testing is the most widely used and is considered a work horse in molecular
diagnostics. &)* is a powerful tool for locating short segments of a gene where known
critical mutations or variances can lead to altered cell functions associated with disease or
altered function. &)* tests for the presence of a portion of D,$ that has a known base
sequence, employing the same en!ymatic process used by natural D,$ replication to
rapidly amplify, or copy, that sequence until there are thousands or millions of copies.
'3
7ecause &)* relies on amplification, it is highly sensitive, meaning it can detect specific
D,$ segments that may be present at very low levels in the sample.
The past studies developed ways to detect the presence of &)*-amplified D,$ by how
far it traveled in a gel in relation to other, different-si!ed, pieces of D,$ when all the
pieces were pulled by an electric current. Cel electrophoresis can still be used, but now
the use of fluorescent dyes, that bind to the target D,$ segment as it is amplified, enable
automated instruments to monitor the resulting fluorescence without using gels. "n this
manner, technologies such as quantitative real-time &)* not only can detect the presence
of the target D,$ segment, but also quantify the amount of target D,$ that was
originally present in the sample. This can be used, for e#ample, to determine the
prevalence of an infectious agent in the body.
".* E#.irica% Re(ie4
Diagnosis of several other communicable diseases has come to rely heavily on molecular
diagnostic tests. $n important case is the use of molecular kits for the detection of -D*
T7. 6eeping in mind the steady rise in cases with drug resistant T7, and limitations of
drug susceptibility testing, rapid molecular tests appear promising. $n increasing number
of laboratories are adopting the techniques, especially in developing countries with a
heavy burden of the disease. "t has been reported that mutations outside the region of a
specific gene may not be detected by some assays designed to detect drug resistance.
These strains could still be resistant, with the risk of the patient being subjected to
ineffective treatment with the drug. $nother scenario is the highly mutable +uman
"mmunodeficiency @irus 0+"@2.
(imilar to the case of many other infectious diseases, nucleic acid amplification methods
provide an alternative approach in the detection of microorganisms and thus offer new
possibilities for a more rapid and accurate diagnosis of tuberculosis. $s mentioned
before, rather than to increase the number of microorganisms by culture, amplification
methods, like &)*, directly increase the amount of nucleic acid target in vitro.
''
*apid mutations in a drug-resistant strain can impact the potential for detection 4.
$nother major drawback is that the mere presence of resistance genes may not correlate
with e#pressed resistance and vice versa. The absence of the gene does not rule out
resistance, which could be by another mechanism. (imilarly, resistance genes may be
present but une#pressed due to mutational or regulatory silencing. $s much as it is
necessary to use rapid molecular tests, it is also important to be vigilant towards
emergence of mutants which might escape the detection limit. $wareness and vigilance
are required to avoid this pitfall in addition to looking out for new and emerging mutants.
The clinical benefit of genetic testing for +,&)) has been demonstrated, but it is not
part of standard management. The identification of mutations in families fulfilling
clinical criteria makes genetic testing an important option in the management of +,&)).
-orbidity and mortality can be reduced in individuals at the risk for +,&)) by using
early and intensive screening. "n patients who are carriers of mutations associated with
+,&)), prophylactic colectomy is the most effective method of reducing the risk of
colorectal cancer. $ decision analysis model shows that the benefits of intervention range
from '4.= years of gains in life e#pectancy for endoscopic surveillance to '=.> years for
prophylactic colectomy compared with no intervention
$lternative methods sensitive enough to detect low levels of parasitaemia in
asymptomatic infections are required to complement or replace parasitological
e#amination with light microscopy. This would allow minimi!ation of errors in diagnosis
0false positives, false negatives and species misidentification2 that may lead to biased
estimates of protective efficacy against the parasite. The incorporation of molecular tools
for the characteri!ation of parasite infections has allowed increase sensitivity in the
detection of human malarial parasites in blood.
Traditionally, light microscopy 01-2 e#amination of blood smears has been considered
the gold standard for the diagnosis of malaria. 1- has clear advantages since it incurs
low costs, allows species identification and quantification and neither comple# sample
preparation nor advanced technology is required. +owever, the role of 1- as gold
'/
standard has been questioned due to false negative results at low levels of parasitaemia,
with a predicted limit of detection of five to /3 parasites per microlitre of blood and
frequent errors in species identification in mi#ed infections.
$ total of ;?' samples, selected as defined above, were included in the cross-sectional
malaria study. 7ased on &)* results, weighted parasite prevalence was estimated at ?D
0B=D )"8 ;.?EB.42. The prevalence of &. falciparum was /.'D 0B=D )"8 3.A'E4.;2 while
that of &. viva# was =D 0B=D )"8 /.BE>.?2. &lasmodium viva# was the dominant species
detected and the difference was statistically significant 0F/ G =.'/' pH3.3=2. -alaria
prevalence in children was lower than in adults and the difference was statistically
significant 0F / G =.B4 pH3.3=2 0Table /2. $mong tested adult individuals, infection
frequently occurred before 43 years of age and only in three adults were parasiti!ed at an
age over 43 years old. The highest prevalence of the parasite 0'3.BD2 was observed in
age groups under '= years old with a mean age of five years.
Testing for autoantibodies provides a cornerstone of diagnosis of these diseases,
especially &7). -olecular biological methods have made possible the identification of
some of the intracellular protein antigens and the predominant epitopes recogni!ed by
some of the disease-specific autoantibodies. This work has led to development of assays
that can be used in the clinical laboratory. $ssays utili!ing recombinant proteins should
make tissue-based immunofluorescence assays obsolete in cases where the auto antigen is
known. "n &7), cD,$s for several of the major mitochondrial and nuclear auto antigens
have been cloned and sequenced, and recombinant proteins have been used to detect
autoantibodies.
(creening of bacteriophage lcD,$ e#pression libraries with autoantibodies from affected
patients identified the 5/ subunits of the pyruvate dehydrogenase comple#, the branched-
chain /-o#oacid dehydrogenase comple#, and the /-o#oglutarate dehydrogenase comple#
as the major mitochondrial auto antigens in &7). 51"($s utili!ing e#pressed
recombinant proteins or designer polypeptides have been devised that are sensitive and
specific for detection of antibodies against these proteins. Determination of the
'4
immunodominant epitopes on these three proteins has allowed construction of a
.designer hybridI clone that contains the major epitope of each. $n immunoassay
utili!ing a designer polypeptide e#pressed from this clone is highly sensitive and specific
for the diagnosis of &7).
"n addition to antibodies against mitochondrial o#oacid dehydrogenase 5/ subunits, some
individuals with &7) also have other specific autoantibodies. The cD,$ cloning of
gp/'3 made possible the identification of its immunodominant epitope, which was
mapped to a stretch of '= amino acids. Two 51"($s have been developed for detection
of autoantibodies against the predominant autoepitope of gp/'3.
$part from the high-sensitive detection of bacterial pathogens, amplified D,$ segments
can be used for a variety of purposes. The number and position of repetitive D,$
elements present in the genome of M. tuberculosis, for e#ample, are representing strain-
specific markers and the information has been used in epidemiologic studies of
tuberculosis.
"., Critica% Re(ie4 of /iterature and 5no4%edge 6a.
The basis for effective treatment and cure of a patient is the rapid diagnosis of the disease
and its causative agent, which is founded on the analysis of the clinical symptoms
coupled with laboratory tests. $s we approach the /'st century, clinicians are becoming
increasingly able to diagnose and treat diseases at the molecular level. The rapid
development of new methods and techniques in the area of molecular biology has gained
new insights into the genetic and structural features of a considerable number of human
pathogens. These results obtained by intensive basic research are currently leading to
improved diagnostic procedures.
The alarming trend of coinfection of T7 with +"@, has been associated with the
worsening of the urban and social conditions, and changes in immigration patterns.
:idespread emergence of multidrug-resistant tuberculosis 0-D*-T72, especially in
institutional settings, has made it difficult to control the spread of T7 0/32. The
';
emergence of multidrug-resistant strains has reduced the efficacy of treatment almost to
the level of the pre-antibiotic era 0/'2. *ecent -D*-T7 outbreaks have been
characteri!ed by mortality rates of =3 -A3D and a duration of only ;-'> weeks from the
time of diagnosis to the time of death. *esistance to rifampin, for e#ample, involves
alterations of the *,$ polymerase.
"mprovements in antibiotic and antiviral therapy for specific microorganims will require
development of increasingly more accurate method of diagnosis. ,ucleic acid-based
technology has the potential to become one of the most powerful tools in clinical
microbiology since it essentially circumvents the necessity for the microorganism to be
isolated in pure culture prior to its definitive identification.
"n the face of the current problems in laboratory diagnosis of infectious diseases, it is
apparent that the continued use of older and slower methods of detection is unacceptable.
5specially in the case of severe infections, the diagnostic capabilities of molecular
biology-based techniques will have major positive impact on health care costs, as well as
on the associated morbidity and mortality. "f, for e#ample, generation of a report that a
given patient is infected with an antibiotic-resistant pathogen, can help the physician to
better tailor therapy to that personJs needs.
These advances in molecular biology have enhanced our understanding of the primary
defects and basic mechanisms responsible for the pathogenesis of these conditions and
their phenotypic e#pression, and in the process, new perspectives on cardiac diagnosis
have been formulated. "n the course of this scientific evolution, a certain measure of
uncertainty has also arisen regarding the implications of genetic analysis for clinical
diagnostic criteria.
Despite the rapid development of new molecular techniques, the implementation of
genetic testing for many disorders in standard clinical management has not been justified.
:ith their high costs, their variable analytical and clinical validity and their limited
availability, genetic tests for many types of hereditary cancers are far from satisfactory.
'=
1egal, social and ethical issues also affect the integration of genetic testing into the health
care system. ,ew subgroups of genetically affected individuals without conventional
clinical diagnostic findings have been identified solely by virtue of access to molecular
laboratory techniques, creating a number of medical and ethical concerns regarding the
possible clinical implications.
"ndeed, the e#tent to which such individuals should receive sequential evaluations andKor
therapy or be subjected to employment or insurance discrimination, psychological harm,
loss of privacy, or unnecessary withdrawal from competitive athletics is uncertain but
remains a legitimate source of concern. "t is therefore particularly timely and appropriate
to analy!e these issues in detail, specifically the e#tent to which molecular biology has
revised traditional diagnostic criteria. The role of genetic testing in assessing prognosis
and identifying high-risk subgroups or in defining basic disease mechanisms and
pathophysiology is, however, largely beyond the scope of this scientific statement.
'>
CHAPTER THREE
REEARCH 2ETHODO/O67
&.0 Introduction
This chapter outlines the research design and methodology adopted for the purpose of
this study. "t gives a detailed description of how the study was conducted. The chapter is
divided into sections as follows8 The geographical locale of study area, research design,
target population, sampling si!e, sampling procedure and design, data collection and data
analysis and interpretation.
&.1 Re)earch De)ign
The research design employed in this study was the evaluation trial that depended on its
purpose and the population for which the test is intended. "n general, a diagnostic test
should be evaluated using methods and equipment that are appropriate for that purpose.
The staff performing the evaluation should be appropriately trained so that they are
proficient in performing the test being evaluated and the comparator tests.
&." The tud! Area
The study was carried out in -oi Teaching and referral +ospital in 5ldoret town from
among the patients who visited the clinics in the second week of ebruary.
&.& Target Po.u%ation
Target population in statistics is the specific population about which information is
desired 0leedy and Ormond, /33=2. 6othari 0/33;2 defines a population as a set of people,
elements, events, group of things that are being investigated. The target population in
which the diagnostic test was done included all patients attending clinic in week two of
ebruary. This totaled to about /333 participants e#pected to visit the clinic in that week.
This population had the reliable information for a replacement to an e#isting test, use of a
triage instrument to identify those in need of further investigation, and used as an
'?
additional test in a diagnostic strategy. "t is of little value to evaluate tests that are
unlikely to be affordable or accessible to the target population, or which yield results that
are unlikely to influence patient care or public health practice.
&.* a#.%e i8e and a#.%ing Techni3ue
The study group consisted of all subjects who satisfy the criteria for inclusion and are not
disqualified by one or more of the e#clusion criteria. "n this case, a consecutive series of
subjects were included. This also included the sub-selection, for e#ample, only those who
test negative by the reference test. +owever, this can lead to biased estimates if the
sample is not truly random. :here possible, all tests under evaluation should were
compared with a reference 0gold2 standard. The choice of an appropriate reference
standard is crucial for the legitimacy of the comparison. $ serological assay was not
compared with an assay that detects a microorganism directly, as clinically defined
reference standards are not appropriate when clinical presentation is not sensitive or
specific. The results from the assays were combined to produce a composite reference
standard.
The key question to be addressed before embarking on a study, and the question that is
often hardest to answer, is what level of performance is required of the test. The levels
that might be acceptable in one setting might be inappropriate in another. The indications
for performing the test can vary. The level and availability of healthcare resources and
disease prevalence all have a bearing on setting the acceptable performance of a test.
"ncreasing the sample si!e reduces the uncertainty regarding the estimates of sensitivity
and specificity 0the e#tent of this uncertainty is summari!ed by the confidence interval2.
The narrower the confidence interval, the greater the precision of the estimate. $ B=D
confidence interval is often used that is, we can be B=D certain that the interval contains
the true values of sensitivity 0or specificity2.
'A
The formula for calculating the B=D confidence interval is given by equation '
where p G sensitivity 0or specificity2 measured as a proportion 0not a percentage2 and n G
number of samples from infected people 0or, for specificity, from uninfected people2.
"n the study B? samples are positive by the gold standard test and B3 of these are positive
by the test under evaluation, then the sensitivity of the test is estimated by p G B3KB? G
3.B/A and the confidence interval, using the formula above, is given in equation /.
This means that the study was B=D sure that the interval A?.?D to B?.BD contains the
true sensitivity of the test under evaluation. "n considering sample si!e, it is important to
consider the desired precision with which the sensitivity of the test was measured. "n this
order, a rough estimate of what was e#pected to be the sensitivity is made. (ince the
study e#pected the sensitivity of the test under evaluation is appro#imately p03.A 0A3D22
and aimed to measure the sensitivity to within L x 0where x is e#pressed as a proportion
rather than a percentage< 3.'3 rather than '3D2 and choose n so that the confidence
interval is L x 0for e#ample L '3D2. This is shown in equations 4E=.
which translates to8
Thus, if p G 3.A3 and x G 3.'3, then
'B
Therefore, to measure the sensitivity to within L '3D the study required at least >/
samples that are positive by the gold standard test. $ sensitivity of a new test is A3D and
a confidence interval of L >D, the study required to recruit or have archived specimens
from, '?3 infected study subjects by the reference standard test. $gain with the
prevalence of infection in the study population as '3D, then there were '3 infected
subjects per '33 patients seen at the clinic. (o, to have '?3 infected subjects, the study
recruited ',?33 patients 0'33K'3 M '?32.
&., Data Co%%ection Procedure
Two common circumstances in which diagnostic tests are deployed are8 (creening people
presenting to a clinic who have symptoms that might be caused by the infection to
identify those who are truly infected 0for e#ample, persons presenting with a fever that
might be caused by malaria2 and Distinguishing infected people from non-infected people
in a population, irrespective of whether or not they have any symptoms that might be
characteristic of the infection.
"n the first situation, tests with high sensitivity was required so that a high proportion of
all truly infected patients are identified for treatment and in the second case, if the
infection is rare, high specificity was required or else a high proportion of those who test
positive could be false positives 0that is, the test will have a poor &&@2. "n either
circumstance it is necessary to identify a group of truly infected and truly uninfected
individuals to assess sensitivity and specificity, respectively.
$ common design for an evaluation study is to enroll consecutive subjects who are
clinically suspected of having the target condition. The suspicion of infection can be
based on presenting symptoms or on a referral by another healthcare professional. These
participants then undergo the test under evaluation as well as the reference standard test.
"n studies in which only a small proportion of those tested are likely to be infected, all
subjects can be subjected to the reference standard test first. $ll positives and only a
random sample of test negatives can then be subjected to the test under evaluation. This
can lead to more efficient use of resources if the target condition is rare.
/3
Tests were evaluated using stored specimens collected from those with known infection
status. (uch studies are rapid and can be of great value but there is a risk that they can
lead to inflated estimates of diagnostic accuracy 0when the stored samples have been
collected from the Jsickest of the sickJ and the Jhealthiest of the wellJ2. The estimate of
specificity could be biased, for e#ample, the negative samples relate only to a group with
one alternative condition, rather than a group including the full range of conditions that
presented symptoms that are similar to the infection under study hence the study
considered minimi!ing biasness in the results.
The setting where patients were recruited and where the evaluation was conducted
defined. This might was done in a clinic or laboratory, a remote health post or a hospital
in this case all tests were done at -T*+. Tests were performed differently in a primary
care setting compared with a secondary or tertiary care setting. The spectrum of endemic
infections and the range of other conditions observed varied from setting to setting, due
to referral mechanism. Other factors that affected test performance and differ between
sites included climate, host genetics and the local strains of pathogens. 7ecause the test
characteristics varied in different settings, hence it was valuable to conduct multi-centre
studies.
&.- Data Co%%ection In)tru#ent)
The data was collected using a lab schedule that included a list of specimen taken form
the participants. This was supported by a simple questionnaire to help obtain some
demographic information from the participant.
&.9 Pi%ot tud!
7efore subjecting the respondents to the questionnaires, a pre-test was conducted. The
pre-test conducted reviewed the designed questionnaires for reliability. The respondents
were conveniently selected since statistical conditions are not necessary in the pilot study
0)ooper and (chindler, /3342.The purpose of the pilot was to refine the questionnaires to
improve reliability. The participants of the pre-test were from the Turbo health centre.
/'
The sample si!e of the pre-test was 43. Out of the 43 participants, =3 percent were male
and =3 percent were female.
&.9.1 Re%ia$i%it! of the Re)earch In)tru#ent)
-ugenda and -ugenda 0/33>2, defines reliability as a measure of the degree to which a
research instrument yields consistent results or data after repeated trials. $ re-test method
assessing reliability of data involves administering the same instrument twice to the same
subjects. $ccording to 6umar 0/33>2, the ratio between the test and the re-test scores is
an indication of the reliability of the instrument.
&earson%s product moment correlation was used to find the coefficient of correlation.
)hronbach%s $lpha tests of multiple questionnaires following each profile were
calculated to test the reliability of responses for each individual. The level of .?33 or
greater is suggested as an indication of the internal consistency 0,unnally, 'B?A2.
&.9." 1a%idit! of the In)tru#ent)
(mith 0'BB'2 defines validity as the degree to which the researcher has measured what he
Kshe has set out to measure. -ugenda and -ugenda 0/33>2, defines validity as the
accuracy and meaningfulness of inferences, which are based on the research results. The
instruments were rated in terms of how effective its samples are in significant aspects of
the purpose of the study. @alidity involves content, face, and construct. @alidity was
determined using e#pert help from my supervisor and other e#perienced members.
The content validity of the instruments was determined in two ways. irst, the researcher
discussed the items in the instruments with the supervisor. $dvice given helped the
researcher to determine the validity of the research instruments. The advice included
suggestions, clarifications and other inputs in order. These suggestions were used to make
necessary changes. (econdly content validity of the instruments was determined through
piloting, where the responses of the subjects were checked, against the research
objectives. This gave a reason as to why content was used. or a research instrument to
//
be considered valid, the content selected and included in the questionnaires must be
relevant to the variable being investigated argues 0,euman /3332.
&.: Data Ana%!)i)
This study adopted both qualitative and quantitative analysis in order to achieve the aims
and objectives of the study. Descriptive methods were employed. The data was organi!ed
in tabular form and represented in frequency distribution tables and percentage
distribution of the respondents. The data collected, from the students, college
administrators and the lecturers was treated separately, then the information analy!ed and
compared. This study analysed the research questions in relations to the objectives
described in the previous chapter, the variables in relation to the dependent variable.
(tatistical &ackage for (ocial (ciences 0(&((2 version '> was used to assist in obtaining
the output for the techniques of analysis such as the )ronbach%s for the analysis.
Nualitative techniques 0frequency tables and charts2 were used for the presentation of
quantifiable data that was presented te#tually using descriptive statistics and inferential
statistics 0regression models2. This was used as a strategy for analysis between study
variables. -ean scores, standard deviations were used in analy!ing items that adopt a
1ikert format.
/4
CHAPTER ;OUR
REU/T ANA/7I AND INTERPRETATION
*.0 Introduction
This chapter is presented under the following headings8 descriptive statistics of effects of
molecular biology on diagnosis of infectious diseases, and multiple linear regression
analyses with the necessary assumptions.
*.1 De#ogra.hic Characteri)tic)
The demographic information of this study included gender, age, level of education,
position held, and duration in the post. The participants were asked to the most
appropriate and accurate feature of demographic characteristics.
*.1.1 6ender of Re).ondent)
Ta$%e *.1< 6ender Di)tri$ution of Re).ondent)
;re3uenc! Percent 1a%id Percent
6ender
1a%id -ale ;/ 4=.B 4=.B
emale ?= >;.' >;.'
Tota% 119 100.0 100.0
The result in table ;.' indicates that female accounted for >;.'D 0?=2 while male were
4A.BD 0;/2. This means that male were the majority participants in this study. This can be
attributed to the fact that the hospital is a case for women as mostly many women visit
hospitals than men, however, in some cases today gender parity has not been
e#perienced, and gender factor was in influencing e#ploratory variables in this study.
*.1." Age Bracket of Re).ondent)
6nowing the age bracket of the participants was important as there may be some
influence age may pose on the clinical testing and the diagnosis of the problem within the
selected sampled population.
/;
Ta$%e *."< Age Di)tri$ution of Re).ondent)
Age Bracket ;re3uenc! Percent 1a%id Percent
1a%id /3-/= '= '/.A '/.A
/=-43 =/ ;;.; ;;.;
43-;3 'A '=.; '=.;
;3-=3 '/ '3.4 '3.4
=3->3 '3 3A.= 3A.=
>3 $bove '3 3A.= 3A.=
Tota% 119 100.0 100.0
The research sought to find out the age bracket of the respondents. rom the results in
table ;./ and figure ;./ above, /3-/= represented '/.AD 0'=2, /=-43 ;;D 0=/2, 43-;3
'=.;D 0'A2, ;3-=3 '3.4D 0'/2, =3->3 3A.=D 0'32 and lastly >3 above years accounted for
3A.=D 0'32. This indicated that majority of participants were aged between age bracket
/=-43 years old. This is true since the larger percentage of participants were youthful
female individuals.
*.1.& /e(e% of Education of Re).ondent)
Ta$%e *.&< Highe)t Education Achie(ed
/e(e% of Education ;re3uenc! Percent 1a%id Percent
1a%id Certificate /? /4.' /4.'
DiplomaK+igher Diploma 4A 4/.= 4/.=
Degree /; /3.= /3.=
-asters Degree 'A '=.; '=.;
Others '3 3A.= 3A.=
Tota% 119 100.0 100.0
The study sought to find out the highest level of education of the respondents. rom the
results in table ;.4 and figure ;.4 above, those with certificate qualification accounted for
/4.'D 0/?2, diploma or higher diploma 4/.=D 04A2, degree /3.=D 0/;2, masters '=.;D
0'A2 while others accounted for 3A.=D 0'32. This showed that many participants in this
/=
study had diploma or higher diploma level of education, followed by the certificate and
then degree, at the same time masters also accounted for a significant proportion of the
respondents.
*." De)cri.ti(e tati)tic) Re)u%t) of Diagno)i) of Infectiou) Di)ea)e)
Ta$%e *.*< De)cri.ti(e tati)tic)
N Mean Std. Dev
Diagnosis is $ccurate in its test results ''? 4.3?>B '.;3B3=
The Diagnosis is simple to use ''? 4.;B=? '.4>//3
The Diagnosis &rovide a result in time
to institute effective control measures ''? 4.3>A; '.;/;?3
5arly diagnosis and treatment ''? 4.>4/= './;BA/
Diagnosis has positive predictive value ''? 4.AAAB '.3;34?
Diagnosis enhances responses to medication
and management ''? 4.B3>3 '.4A4/B
The results in table ;.;, the descriptive statistics of variables indicated that the mean
scores of Diagnosis enhances responses to medication and management is moderately
stable at highest score of mean 4.B3>3 and standard deviation of '.4A4/B with the least
mean score of 4.3>A; and standard deviation of '.;3B3=. This is an indication that
generally the testing and diagnosis of infectious diseases provide avenues for responses to
medication and management.
*.& tati)tic) and ;re3uenc! Di)tri$ution) for the Traditiona% Diagno)i) !)te#
This section presents all the items used to measure the Traditional Diagnosis (ystem
0TD(2 of Diagnosis of infectious diseases in -T+ measured on a 1ikert scale of =
ranging from =G(trongly $gree, ;G$gree, 4G,eutral, /GDisagree, 'G(trongly Disagree.
-olecular biology tools bring a very sophisticated level of sensitivity and specificity to
diagnostics. These tools can detect a bacterium, virus, yeast, parasite or genetic marker
through the presence of D,$ or *,$ genetic sequences in a blood sample. Tests are
performed directly on a clinical sample and make it possible to obtain results in just a few
/>
hours. These tests are used to detect pathogens 0bacteria, viruses, yeasts2, identify
antibiotic resistance mechanisms, and measure the quantity of a virus, such as +"@, in the
blood. They thus allow choices to be made about a specific treatment, monitor its
effectiveness, and determine how human cells react to a disease or infection. "dentifying
patients who will be responsive to a given treatment, and those for whom such therapy
may cause significant side effects, represents a recent application for molecular biology.
*.&.1 O.inion on 5no4%edge of U)e of Diagno)i) Te)ting
To find out if the if diagnosis is 5#tracting, $mplification and Detection of diseases,
participants were asked to state yes or no.
Ta$%e *.,< ;re3uenc! Di)tri$ution of O.inion on U)e of Diagno)i)
O.inion ;re3uenc! Percent 1a%id Percent
@alid Oes ?A >>.? >>.?
,o 4B 44.4 44.4
Tota% 119 100.0 100.0
The result indicates that >>.?D 0?A2 of participants answered yes to the question and
44.4D 04B2 declined. "t was an indication that more than half of the sampled population
agreed that the diagnosis enhance 5#tracting, $mplification and Detection of diseases.
*.* Diagno)i) 2ethod) of 2o%ecu%ar Bio%og!
The study e#plored the form of methods that are applied in the molecular diagnosis
testing. The results were ass shown in table ;.> below.

The results indicated that the most method used is in the area of virology as there are
many methods applied in the virus diagnoses. This included +erpes simple# virus,
cytomegalovirus, 5pstein-7arr virus, varicella !oster virus, human herpes virus type >, ?,
A respiratory viruses 0such as influen!a virus, respiratory syncytial virus, parainfluen!a
virus, adenovirus, rhinovirus2, ($*(-)o@, avian influen!a virus, +"@, hepatitis 7,
hepatitis ), human papilloma virus, enterovirus and orf virus, mulloscum contagiosum.
/?
Ta$%e *.-< 2o%ecu%ar Bio%og! Diagno)i) 2ethod) for Infectiou) Di)ea)e)
Area 2ethod ;re3 =>?
1iro%og!
+erpes simple# virus, cytomegalovirus, 5pstein-7arr
virus,
'3 A.>
varicella !oster virus, human herpes virus type >, ?, A '3 A.>
respiratory viruses 0such as influen!a virus, respiratory
syncytial virus,
A >.A
parainfluen!a virus, adenovirus, rhinovirus2 '/ '3.4
($*(-)o@, avian influen!a virus > ;.?
+"@, hepatitis 7, hepatitis ) '/ '3.4
human papilloma virus, enterovirus = ;.4
orf virus, mulloscum contagiosum = ;.4
rotavirus, norovirus, enteric adenoviruses > =.'
Bacterio%og!
C. trachomatis, N. gonorrhoeae, B. pertussis, M.
tuberculosis, nontuberculous
'' B.;
mycobacteria, T. whipplei, B. henselae, genital
mycoplasmata, C. burnettii M. pneumoniae, C.
pneumoniae, Legionella spp., N. meningitidis, S.
pneumoniae
'/ '3.4
Para)ito%og! Plasmodium spp., T. gondii '3 A.>
2!co%og! P. iroveci, !spergillus spp. '3 A.>
Tota% 119.0 100.0
+"@, hepatitis 7, hepatitis ) and para-influen!a virus, adenovirus, rhinovirus2 both
accounted for '3.4D0'/2 each as the highest reported methods of virus diagnosis and was
followed by +erpes simple# virus, cytomegalovirus, 5pstein-7arr virus and varicella
!oster virus, human herpes virus type >, ?, A at A.>D0'32. The least method reported in
virus diagnosis was human papilloma virus, enterovirus and orf virus, mulloscum
contagiosum both at ;.4D0=2.
*., I#.ortance of 2o%ecu%ar Bio%og! /a$ Diagno)i)
The study also sought to establish the benefits of using molecular biology lab testing in
diagnosing infectious disease. The results were as shown in table ;.? below.
Ta$%e *.9< Benefit) of 2o%ecu%ar Bio%og! /a$ Te)ting
/A
Benefit ;re3 =>?
aster results and accurate ;= 4A.=
(creening and "dentify selected serotypes associated with disease /= /'.;
5liminates bacterial overgrowth as a problem '? ';.=
Nuantitates bacteria more readily 'A '=.;
)onfirm bacterial invasion '/ '3./
Tota% 119.0 100.0
The result in table ;.? indicate that the benefits of molecular biology form of diagnosis
included aster results and accurate, identify selected serotypes associated with disease,
eliminates bacterial overgrowth as a problem, quantitates bacteria more readily and
confirm bacterial invasion. The most reported was 4A.=D0;=2 representing faster results
and accuracy, which was followed by identify selected serotypes associated with disease
at /'.;D0/=2. The least reported was '3./D0'/2 representing confirm bacterial invasion.
This means that importance of molecular biology diagnosis of infectious diseases is
placed on its accuracy, screening and identifying selected serotypes associated with
disease.
*.- Effect) of 2o%ecu%ar Bio%og! Diagno)i)
To help achieve the objectives of this study, four questions were asked and the study
sought for their solutions. The results in table ;.B were obtained.
"t was indicated that indicated the enhanced accuracy in treatment of detected diseases,
early identification of high-risk diseases on patient, diagnostic tests to complement
traditional risk factors and assessing severity and risk of recurrence of diseases were key
to the influence of this diagnosis formula and their influence were in that order
respectively.
Ta$%e *.:< 2o%ecu%ar Bio%og! Effect) on Infectiou) Di)ea)e Diagno)i)
Effect) on /a$ Diagno)i) of Infectiou) Di)ea)e) ;re3 =>?
5nhanced accuracy in treatment of detected diseases ;A ;'.3
5arly identification of high-risk diseases on patient 4= /B.B
Diagnostic tests to complement traditional risk factors 'B '>./
$ssessing severity and risk of recurrence of diseases 'A '=.;
Tota% 119.0 100.0
/B
-ajority indicated that enhanced accuracy in treatment of detected diseases was most
common, and the least was in assessing severity and risk of recurrence of diseases.
"n summary the result of the test performed indicated varying results but confirmed the
similarities of the studies done in other parts of the world.
CHAPTER ;I1E
DICUION O; ;INDIN6@ CONC/UION AND RECO22ENDATION
,.0 Introduction
This chapter presents the discussions of findings, conclusions and recommendations as
well as some suggested areas of consideration for future studies.
,.1 Di)cu))ion) of finding)
The findings were that majority of the participants were female at >;.'D, this is a
common phenomenon in the patients visiting hospitals and clinics in particular the
43
government health centres, it is however, not clear whether this general perception
attributed to the problem of study is influenced by this female dominancy.
The majority of the participants were aged between /=-43 ;;D 0=/2, followed by 43-;3
'=.;D. These were the average age of the participants. $ prime age for introduction of
change that can result in e#perienced medical challenges, yet it is not clear if there is a
formed opinion of this age that has influenced the study about the outcomes reported in
chapter four above. Those with diploma education were the majority at 4/.=D followed
by the degree holder at /3.=D.
The study found out that Diagnosis enhanced responses to medication and management is
so important in the use of molecular biology test. This means that it was difficult to have
the stability of accurate result with the traditional methods used before. This is an
indication that generally the testing and diagnosis of infectious diseases provide avenues
for responses to medication and management. &riority is placed in diagnosis accuracy ass
this would facilitate the proper treatment and management of infectious diseases.
Tests are performed directly on a clinical sample and make it possible to obtain results in
just a few hours. These tests are used to detect pathogens 0bacteria, viruses, yeasts2,
identify antibiotic resistance mechanisms, and measure the quantity of a virus, such as
+"@, in the blood. They thus allow choices to be made about a specific treatment,
monitor its effectiveness, and determine how human cells react to a disease or infection.
"dentifying patients who will be responsive to a given treatment, and those for whom
such therapy may cause significant side effects, represents a recent application for
molecular biology.
The conclusion made on the findings of the benefits was that molecular biology use has
been implemented and its benefits are being e#perienced in the laboratories of -T*+
and hopefully in other health facilities in the country. These benefits are able to correct
misdiagnosis of problems resulting in wrong medication and management care of
infectious diseases. "t provides quick and accurate results from the lab to enhance
4'
treatment of the patients. This will enable unnecessary deaths due to improper diagnosis
or delayed results from eventual occurrences.
There are four main areas of application of molecular biology in diagnosis of infectious
diseases. These include8 @irology, 7acteriology, &arasitology and -ycology. The
virology problem has several methods used in its diagnosis. The remainder tow areas of
infectious microbes don%t portray wider usage in the diagnosis. "t is important to note the
number of methods used in each area.
The findings indicted that the benefits of molecular biology was its accuracy and faster in
producing results. This means that importance of molecular biology diagnosis of
infectious diseases is placed on its accuracy, screening and identifying selected serotypes
associated with disease.
"t was found out that the enhanced accuracy in treatment of detected diseases, early
identification of high-risk diseases on patient, diagnostic tests to complement traditional
risk factors and assessing severity and risk of recurrence of diseases were key to the
influence of this diagnosis formula and their influence were in that order respectively.
-ajority indicated that enhanced accuracy in treatment of detected diseases was most
common, and the least was in assessing severity and risk of recurrence of diseases.
,.1.1 Achie(ing the O$'ecti(e) of the tud!
The objective one intended to e#amine the usefulness of molecular biology on treatment
of diseases. The findings indicated that the methodology is essential in screening for
detection of high level risk problems so that early detections can be made for proper
management and treatment to start at its earliest time possible. "t is also useful in its
accuracy in the result from the lab test. This included both objectives one, three and four
the findings in the usefulness and screening provided the solutions to these objectives.
4/
The study also e#amined the effects of molecular biology on screening of diseases. These
findings indicated that early detection, isolation of infected cases is some of the functions
of molecular biology. "t implies that molecular biology can enhance detection, selection,
amplification of diseases hence influencing proper screening of infectious diseases to
produce accurate results. This is also made possible as the method will screen deeply into
the sample specimen to ensure nothing is left unnoticed for the result to be accurate, even
the lowest level of microbes in a specimen will be detected.
,." Conc%u)ion)
in the findings it was indicated that majority of the participants were female, conclusions
drawn form this findings is that gender disparity is common in the visits, diagnosis and
treatment and management of infectious diseases in the public health centres especially
-T*+.
The other conclusion drawn was that main individuals visiting these health centres are the
youth, a situation resulting from the current state of young generations leading with
challenges requiring hospitalisation. There was no highest level of education as majority
was in the diploma levels. "t is therefore concluded that lack of highest level of education
may hinder proper diagnosis, treatment and management of infectious diseases. This is
true where majority of patients with lower education levels fail to observe dosage
requirements.
The findings has revealed that the level of acceptance of the variables e#plored is on
averagely about A3D, this is similar to a conclusion made on the past studies on use of
modern diagnosing methods such as molecular biology. The conclusion is that the same
trend of state of change is reported however, it important to note that the limitations of
this method is huge that the other traditional ones cannot be replaced hence it is intended
for integration into the conventional ones. The study would conclude that there is a
general state of perception in the laboratory tests of infectious diseases that would
encourage these findings. That means molecular biology lab testing at -T*+ is
approved as on going with majority approval.
44
The study found out that Diagnosis enhanced responses to medication and management is
so important in the use of molecular biology test. This means that it was difficult to have
the stability of accurate result with the traditional methods used before. This is an
indication that generally the testing and diagnosis of infectious diseases provide avenues
for responses to medication and management. &riority is placed in diagnosis accuracy ass
this would facilitate the proper treatment and management of infectious diseases.
These tools can detect a bacterium, virus, yeast, parasite or genetic marker through the
presence of D,$ or *,$ genetic sequences in a blood sample. Tests are performed
directly on a clinical sample and make it possible to obtain results in just a few hours.
These tests are used to detect pathogens 0bacteria, viruses, yeasts2, identify antibiotic
resistance mechanisms, and measure the quantity of a virus, such as +"@, in the blood.
They thus allow choices to be made about a specific treatment, monitor its effectiveness,
and determine how human cells react to a disease or infection. "dentifying patients who
will be responsive to a given treatment, and those for whom such therapy may cause
significant side effects, represents a recent application for molecular biology.
The findings from the result show that the diagnosis enhances 5#tracting, $mplification
and Detection of diseases. "t implies that these three areas represent main benefit of
molecular biology use. There are cases where diseases have been diagnosed for the
wrong symptoms and treatment and management is given for wrong diagnosis hence
complicating the whole situation. This has resulted in many deaths therefore the concern
by introducing molecular biology is to enhance clear detection, e#tracting and
amplification of the diseases so that proper medicine can be provided and tools for
management be given properly.
There are four main areas of application of molecular biology in diagnosis of infectious
diseases. These include8 @irology, 7acteriology, &arasitology and -ycology. The
virology problem has several methods used in its diagnosis. The remainder tow areas of
4;
infectious microbes don%t portray wider usage in the diagnosis. "t is important to note the
number of methods used in each area.
The findings indicted that the benefits of molecular biology was its accuracy and faster in
producing results. This means that importance of molecular biology diagnosis of
infectious diseases is placed on its accuracy, screening and identifying selected serotypes
associated with disease.
"t was found out that the enhanced accuracy in treatment of detected diseases, early
identification of high-risk diseases on patient, diagnostic tests to complement traditional
risk factors and assessing severity and risk of recurrence of diseases were key to the
influence of this diagnosis formula and their influence were in that order respectively.
-ajority indicated that enhanced accuracy in treatment of detected diseases was most
common, and the least was in assessing severity and risk of recurrence of diseases.
,.& Reco##endation)
There are some areas reported as requiring support in terms of resources. These areas if
not addressed would make it hard for the process to be completely successful< therefore
the study makes the following recommendations8
The training of personnel to handle the molecular biology instruments to be provided at
all the times especially during the implementation period of this newly discovered
method of diagnosis. This will enable the urgency of access to important facilities thus
reducing time wastage.
The study also recommends that professionally qualified human resource be recruited
where there are such shortages.
There is also a need to ensure appropriate budget support so that priorities are achieved
today other than being suspended for future period due to financial shortages.
4=
The last important recommendation is to ensure that this molecular biology method of
diagnosis is successfully implemented and that this level of performance be increased.
,.* ugge)tion) for ;urther tudie)
$ study is needed to investigate on the factors influencing an informed opinion in change
introduction and implementation modern diagnosis methods in lab testing process.
$ longitudinal survey study is also required to investigate on the reasons why the
implementation of modern methods does not immediately result into long term solutions
to medical problems faced in health centres in the country.
Reference)
Ceisterfer-1owrance $$, 6ass (, Tanigawa C, @osberg +-&, -c6enna :, (eidman )5,
(eidman PC. $ molecular basis for familial hypertrophic cardiomyopathy8 a b-cardiac
myosin heavy chain gene missense mutation. Cell. 'BB3<>/8BBB E'33>.
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6eller +, (eidman PC, (eidman )5. -apping a gene for familial hypertrophic
cardiomyopathy to chromosome ';q'. N "ngl # Med. 'BAB<4/'8'4?/E'4?A.
(chwart! 6, )arrier 1, Cuicheney &, 6omajda -. -olecular basis of familial
cardiomyopathies. Circulation. 'BB=<B'8=4/E=;3.
4>
-arian $P, *oberts *. *ecent advances in the molecular genetics of hypertrophic
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(olomon (D, Parcho P$, -c6enna :P, Ceisterfer-1owrance $, Cermain *, (alerni *,
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