The knowledge level and attitudes of pregnant women in passing on Research Paper

The knowledge aim and attitudes of pregnant women in catch up withing on reap hook cell disease - Research Paper showcaseThe paper tells that sickle cell anemia is an inherited stemma disease where the body makes sickle-shaped florid blood cells containing abnormal hemoglobin. Sickle cells are stiff and sticky and tend to block blood string up in the blood vessels of the limbs and organs. Blocked blood flow causes serious infections, disturb, and organ damage. Patients are born with it. wad who inherit a normal gene from one of the parent and sickle hemoglobin gene from the different parent exhibit a sickle cell attribute. People with a sickle cell trait do not have Sickle cell anemia but have one gene that causes the disease. Approximately 2,500 people have sickle cell anaemia. This disease is now prevalent among pregnant women. A deal on sickle cell anaemia in pregnant women is very significant for it pull up stakes impart knowledge on this condition in relation to th e womans and the in-born childs health. However, the study is challenging as people have very little knowledge on this disease. The study seeks the relevance between the level of knowledge and the attitudes of pregnant women with the sickle cell trait from the disseminated sclerosis Delta and the sickle cell disease. To achieve this, the researcher will rely on an interview done in Mississippi Delta on Africa-American pregnant women and other relevant literature. Age, marital status, economic status, occupation, and level of education are well-nigh of the demographic variables the researcher used. According to the interview, only 20% of the respondents have enough knowledge about the sickle cell trait. ... This implies that there is very little knowledge on the sickle cell trait thence the increased spread of sickle cell anaemia from pregnant women to their inborn children. Contents Contents 4 Background 6 Problem Statement 7 Purpose 8 Research Questions 8 philosophical Basis 8 D efinitions 10 Summary 11 Introduction 12 Concept Development 14 Major Related Studies 15 Summary 17 Study Design 19 Sample 19 Inclusion criteria 19 Interviews 20 information Collection Plan 20 Ethical Considerations 21 Data Analysis Plan 22 story 1 22 Stage 2 22 Stage 3 22 Stage 4 23 Stage 5 23 Stage 6 23 Stage 7 23 Strategies for Rigor and Validity 24 Summary 25 REFERENCES 26 Introduction 32 Demographics of the Sample 32 Major Themes 33 Summary 35 Introduction 37 Limitations 39 Summary 41 REFERENCES 43 DEMOGRAPHIC TOOL 44 INTERVIEW QUESTIONS 46 have FOR PARTICIPATION IN RESEARCH subject field 47 ASSENT TO PARTICIPATE IN RESEARCH STUDY 49 CHAPTER 1 INTRODUCTION Background Sickle cell disease is a disorder of the blood that is genetic in nature. Defective hemoglobin molecules that aggregate to form sickle-shaped, elongated, and inflexible rod-like structures that are unable to pass through teeny-weeny blood vessels (Papadakis et al, 2006) characterize it. As they are unable to p ass through these small vessels, these sickle-shaped cells pile up together leading to blockages and starving tissues and organs of oxygenated blood. This results in regular periods of pain and is associated with damage to important body organs and tissues and can cause serious medical problems. Blockage may cause problems such as vaso-occlusive, hemolytic, splenic sequestration, and aplastic crises. Other medical conditions that may result include infections, stroke, priapism,