A COMPARATIVE STUDY OF SICKLE CELL DISEASE AND RHESUS FACTOR COMPARABILITY AMONG COUPLES IN YENEGOA AND PORT HARCOURT – Complete Project Material


ABSTRACT

The study on a
comparative study of sickle cell disease and Rhesus factor comparability among
couples in Yenegoa and Port Harcourt aimed at evaluating the media campaign in creating awareness on sickle cell and
Rhesus factor among couples in Yenegoa and port Harcourt, to examine whether
counseling before marriage will help control the prevalence of sickle cell and
Rhesus factor among couples in Nigeria, to determine whether low standard of
living will increase the mortality rate among children with sickle cell
disease, to determine the effect of Rhesus factor and sickle cell on child
mortality rate in Yenegoa and port Harcourt and to determine the extent to
which availability of drugs and medical facilities controls sickle cell disease
and Rhesus factor in Yenegoa and Port Harcourt. The study made use
of primary data which are gotten from the distribution of the research
questionnaires; the sample size for the study is 101. The study made use of the
Pearson correlation method and paired sample t-test for the analysis. However there is a statistically
significantly (0.00) strong
relationship (0.819) between the
responses of the respondents that said that Rhesus factor and sickle
cell have significant effect on child mortality rate in Yenegoa and Port
Harcourt and those
that said that broadcast media reaches higher number of audience in creating
awareness for sickle cell and Rhesus.The study therefore concluded that there
is significant the difference in effectiveness of media campaign on sickle cell
and Rhesus factor. The
study also made useful recommendation to assist the federal government in
decision making.

CHAPTER ONE

1.0 INTRODUCTION

1.1 BACKGROUND OF
STUDY

The prevalence
of sickle cell anemia and Rhesus factor comparability have increased overtime
time in Nigeria; thus causing an increase in mortality rate among children
especially those below twenty (20) years of age (Kulkarni, 2007). It is widely
believe that the causes of sickle cell anemia and Rhesus factor incompatibility
is due to a high level of ignorance on the dangers posed by these disease. The
federal government of Nigeria through the NGOs and the media has put in so much
effort on awareness campaign on how to control the occurrence of these diseases
especially for the young ones that are about the ages of getting married.

Sickle
cell disease (SCD) can simply be defined as a hereditary disorder in which an
individual has inherited two abnormal Hb genes, at least one of which is
responsible for the production of sickle Hb (HbS) (Creary et al., 2007). The
most common clinical phenotype is the homozygote, i.e. HbSS, also known as
sickle cell anaemia. Compound heterozygotes include HbSC, SD, SO-Arab and
Sbthal, which are all collectively (in addition to SS) referred to as SCD.

The
sickle-shaped red blood cells described by Herrick caused several
complications, including chronic anemia, vaso-occlusive pain episodes, ischemic
organ damage, infections, small stature, and delayed puberty (Barakat et al.,
2008). For many generations sickle cell disease has been a prevalent disorder
in Nigeria. Reports show that sickle cell disease was a well-known disorder in
most states in Nigeria and that the natives in Nigeria had several local names
for this disease before it was discovered in America (Reid & Rodgers,
2007).

According
to Modell B, (2007) stated that the HbS gene became prevalent in different
parts of the world following selective pressure because the heterozygote (HbAS)
is protected against some of the deleterious effects of malaria. Therefore, SCD
is found at its highest frequencies in parts of the world where malaria is or
was endemic. In the same vein, Fleming AF, (2008) stated that because of slave
trade and recent migrations, it is now found even more widely including in
Europe and the USA. Nonetheless, the prevalence is highest in tropical Africa
and, indeed, the country with the highest burden is Nigeria where the trait
occurs in 25–30% and sickle cell anaemia occurs in approximately 2% of all
births

The
most common features of SCD are chronic haemolytic anaemia and recurrent
vaso-occlusion. The latter is responsible for the painful crises that
characterise the disease. There is also a chronic vasculopathy triggered by
free heme resulting in nitric oxide scavenging and upregulation of adhesion
molecules in reticulocytes, neutrophils and endothelial cells (Wood KC, 2008).
This is further complicated by a procoagulant state following the activation of
platelets. There is smooth muscle dystonia and eventual hyperplasia, which
contributes to vascular occlusions (Morris CR, 2009). This explains the
plethora of features and complications seen in SCD. The major cause of
mortality in childhood is overwhelming bacterial infections especially due to
encapsulated organisms, principally pneumococcus.

On
the other hand Rh is short for Rhesus blood group system. The Rh blood type
contains parts called antigens including the D antigen. If the D antigen is
present, a person is considered to be Rh positive. If the D antigen is absent,
the person is said to be Rh negative. About 85% of Nigerians have an Rh
positive blood type, while the remaining 15% are Rh negative. The Rhesus factor
is very important to the human body; however there might variation in
compatibility which results to Rhesus disease.

A
study of Rh disease deepens our understanding of historical infant mortality in
general and perinatal mortality in particular. The decline of infant mortality
in Nigeria started around 1800, which is earlier than in most other countries.
At that time, rates were very high even if the Nigerians as well as other
African countries levels were low in international comparison (Edvinsson et al.
2008). However there have been several awareness campaigns on the sickle cell
disease and Rhesus factor comparability among couples in Nigeria. The use of
mass media and other medium may help in the dissemination of information on
sickle cell and Rhesus factor among couples in Nigeria.

1.2 STATEMENT OF
PROBLEM

Sickle cell
disease and Rhesus factor issue has been prevalent in Nigeria for a very long
time now. Families and friends have lost lives to these ailments as a result of
lack of awareness on the preventive measures to be taken to control the
ailments. The federal government of Nigeria has channeled lots of funds to the
medical centers in Nigeria to help salvage the situation but the incidence is
still on the increase. Take yenegoa and portharcourt for example, there are
several factors that can lead to the increase in sickle cell disease and Rhesus
factor disease; Viz:

1.  high
level of illiteracy

2.  lack
of awareness campaign on the effect of sickle cell disease and Rhesus factor
among couples

3.  low
standard of living  

4.  poor
medical facilities and

5.  lack
of counseling before marriage

 It is to this regard that the researcher
desire to carry out a comparative study on sickle cell disease and Rhesus
factor awareness campaign using mass media.

1.3 AIM AND OBJECTIVES
OF STUDY

The main aim of
the research work is to carry out a comparative study of sickle cell disease
and Rhesus factor comparability among couples in Yenegoa and Port Harcourt.
Other specific objectives of study are:

1.  to
examine whether media campaign has a role to play in the level of awareness on
sickle cell and Rhesus factor among couples in Yenegoa and port Harcourt

2.  to
examine whether counseling before marriage will help control the prevalence of
sickle cell and Rhesus factor among couples in Nigeria

3.  to
determine whether low standard of living will increase the mortality rate among
children with sickle cell disease

4.  to
determine the effect of Rhesus factor and sickle cell on child mortality rate
in Yenegoa and port Harcourt

5.  to
determine the extent to which availability of drugs and medical facilities
controls sickle cell disease and Rhesus factor in Yenegoa and Port Harcourt

1.4 RESEARCH QUESTIONS

The study came
up with research questions so as to ascertain the above stated objectives. The
research questions for the study are:

1.  What
is the difference in effectiveness of media campaign on sickle cell and Rhesus factor?

2.  Does
media campaign play a role in the level of awareness on sickle cell and Rhesus
factor among couples in Yenegoa and Port Harcourt?

3.  Does
counseling before marriage help control the prevalence of sickle cell and
Rhesus factor among couples in Nigeria?

4.  What
is the effect of standard of living on mortality rate among children with
sickle cell disease?

5.  to
determine the effect of Rhesus factor and sickle cell on child mortality rate
in Yenegoa and port Harcourt

6.  To
what extent does availability of drugs and medical facilities controls sickle
cell disease and Rhesus factor in Yenegoa and Port Harcourt?

1.5 STATEMENT OF RESEARCH HYPOTHESIS

Hypothesis 1

H0: there is no significant
the difference in effectiveness of media campaign on sickle cell and Rhesus
factor

H1: there is significant the
difference in effectiveness of media campaign on sickle cell and Rhesus factor

Hypothesis 2

H0: Rhesus factor and sickle
cell have no significant effect on child mortality rate in Yenegoa and port
harcourt

H1: Rhesus factor and sickle
cell have significant effect on child mortality rate in Yenegoa and port
harcourt

1.6 SIGNIFICANCE OF STUDY

The study on a
comparative study of sickle cell disease and Rhesus factor comparability will
be of immense benefit to couples in Yenegoa and Port Harcourt and the media
because the study will compare the effectiveness of media campaign on sickle cell
and that of Rhesus factor. The study will also serve as a source of literature
for other researchers that desire to carry out similar research on the above
topic. Finally the
study will contribute to the body of existing literature and knowledge in this
field of study and provide a basis for further research

1.7 SCOPE OF STUDY

The study on a
comparative study of sickle cell disease and Rhesus factor comparability will
be limited to the media house and the couples in Yenegoa and Port Harcourt. The
study will cover for a period of seventeen years (2000-2017).

1.8 LIMITATION OF
STUDY

The only problem the
researcher had in getting information from the respondents on sickle cell and
Rhesus factor was the unwillingness of the respondents to give information
about their health status. The might affect the information provided by the
respondents but the researchers however was able to get good information as
regard the research topic by making the respondents feel safe with whatever
information they provided to the researcher.

1.9 DEFINITION OF TERMS

Sickle cell: A group of
disorders among couples in Yenegoa and Port Harcourt that cause red blood cells
to become misshapen and break down

Rhesus factor: Rhesus factor in
accordance to the study isan
antigen occurring on the red blood cells of couples in Yenegoa and Port
Harcourt (around 85 per cent) and some other primates

Antigen: a toxin or other
foreign substance which induces an immune response in the body, especially the
production of antibodies

Genetic counseling:
Communication process between health care provider and client that emphasizes and
provides accurate and up-to-date information about a genetic disorder in a
sensitive and supportive, non-directive manner (SCDAA, 2005).

Hemoglobin: Chemical substance
(an iron containing protein) of the red blood cell, which carries oxygen to the
tissues, and gives the cell its red color (SCDAA, 2005).

Hemoglobin A (HbA): Hemoglobin
is composed of two alpha globins and two beta globins, normally produced by
children and adults (Jones, 2008, p. 119).

Hemoglobin C trait (AC):
Inheritance of one gene for the usual hemoglobin (A) and one gene for
hemoglobin (C). A person who has the hemoglobin C Trait (AC) is a carrier of
the hemoglobin C gene, and is not affected by the gene (SCDAA, 2005).

Hemoglobin C disease: A person
has both HbS and HbC and is often referred to as “HbSC.” Hemoglobin C causes
red blood cells to develop. Having just some hemoglobin C and normal
hemoglobin, a person will not have any symptoms of anemia. However, if the
sickle hemoglobin S is combined with the target cell, some mild to moderate
anemia may occur (UMMC, 2010).

Hemoglobin E disease: Similar to
sickle cell-C disease except that an element has been replaced in the
hemoglobin molecule under certain conditions, such as exhaustion, hypoxia,
severe infection, and/or iron deficiency

Sickle cell trait: A person
carrying the defective gene, HbS, but also has some normal hemoglobin HbA.
Persons with the sickle cell trait are usually without symptoms of the disease,
but mild anemia may occur under intense, stressful conditions, exhaustion,
hypoxia (low oxygen), and/or severe infection. The sickling of the defective
hemoglobin may occur and result in some complications associated with sickle
cell disease


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