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- QUESTION
Assignment 2: The Pathophysiology of Disorders
During the last 5 weeks, you have explored various body systems: neurological, cardiovascular, respiratory, and hematological. These four systems work together along with other body systems to complete a myriad of functions. For this reason, when disorders occur within one body system, it can create potentially devastating effects throughout the entire body. For instance, Parkinson’s disease is a disorder of the central nervous system, yet its alterations actually affect multiple body systems from the cardiovascular system to the gastrointestinal system. In this Assignment, you examine alterations associated with disorders, as well as the impact of the alterations on multiple body systems.To Prepare
From the list below, select a disorder of interest to you:
Alzheimer’s disease
Asthma in children
Chronic obstructive pulmonary disease (COPD)
Congestive heart failure
Hepatic disease (liver disease)
Hypertension
Hyperthyroidism and hypothyroidism
Seizures
Sepsis
Identify alterations associated with your selected disorder. Consider the pathophysiology of the alterations. Think about how these alterations produce pathophysiological changes in at least two body systems.
Reflect on how patient factors such as genetics, gender, ethnicity, age, and behavior might impact the pathophysiology of the alterations you identified, as well as the diagnosis and treatment of your selected disorder.
Review the “Mind maps—Dementia, Endocarditis, and Gastro-oesophageal Reflux Disease (GERD)†media in the Week 2 Learning Resources. Use the examples in the media as a guide to construct a mind map for the disorder you selected. Consider the epidemiology and clinical presentation of your selected disorder.
To CompleteDevelop a 5- to 10-slide PowerPoint presentation that addresses the following:
Describe your selected disorder, as well as associated alterations. Explain the pathophysiology of the alterations, including changes that occur in at least two body systems.
Explain how genetics, gender, ethnicity, age, and behavior might impact the pathophysiology of the alterations you identified, as well as diagnosis and treatment of your selected disorder.
Construct a mind map for the disorder you selected. Include the epidemiology, pathophysiology of alterations, risk factors, and clinical presentation, as well as the diagnosis and treatment of the disorder.
Subject | Nursing | Pages | 6 | Style | APA |
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Answer
- Chronic Obstructive Pulmonary Disease (COPD)
- Introduction
- COPD)is a common treatable and preventable disease (Qureshi, Sharafkhaneh, & Hanania, 2014).
- Mortality and morbidity globally (Qureshi et al., 2014; Scichilone et al., 2014).
- Social and economic burden (Qureshi et al., 2014).
- Pathophysiology of the Alterations
- Bacterial or viral respiratory infections (70 to 80s%) (Qureshi et al., 2014).
- Unknown etiologies or environmental pollutions (20 to 30%) (Qureshi et al., 2014).
- Persistent airflow obstruction or limitation (Qureshi et al., 2014).
- Caused by enhanced chronic inflammatory response in the airways and/or lungs by gases or noxious particles (Qureshi et al., 2014).
- Elevated white blood cell count and gastro-esophageal reflux are key predictors of COPD (Qureshi et al., 2014).
- Pathophysiology of the Alterations
- Dyspnea, sputum production, and a chronic cough (Qureshi et al., 2014).
- Congestive heart failure may mask COPD (Qureshi et al., 2014).
- Pulmonary embolism and deep venous thrombosis can contribute to acute exacerbations (Qureshi et al., 2014).
- Patients Factors
Genetics
Pathophysiology of COPD
- Interaction between genetic factors and environmental factors increases susceptibility of one to COPD (Han & Lazarus, 2016).
- Family history of disease increases the risk of COPD (Han & Lazarus, 2016).
- Mutation of A1AT protease increases the risk of loss of lung function given tobacco exposure (Han & Lazarus, 2016).
- Cholinergic nicotinic acetylcholine receptor HHIP, FAM13A, and CHRNA3/5 loci are linked to disease susceptibility (Han & Lazarus, 2016).
Diagnosis of COPD
- Interleukin-6 level, D dimer, prothrombin fragment, and von Willebrand’s factor are surrogate markers for inflammation, clotting activation, and endothelial damage (Qureshi et al., 2014).
Treatment
- Individuals who are genetically predisposed to COPD warrant regular medication (Qureshi et al., 2014).
- Patient Factors
Ethnicity
Pathophysiology of COPD
- Race determines distribution of COPD prevalence around the world (Han & Lazarus, 2016).
- African-Americans experience increased risk of COPD-associated mortality and prevalence rate compared to the general US population (Han & Lazarus, 2016).
Diagnosis of COPD
- COPD should be included into differential diagnoses when assessing African Americans who present with some signs and symptoms (Han & Lazarus, 2016).
Treatment of COPD
- Individuals with COPD from at risk populations should be given adequate treatment to reduce the risk of mortality (Han & Lazarus, 2016).
- Patient Factors
Age
Pathophysiology of COPD
- Young children and older people are at great risk of developing the disease (Celli & Augusti, 2018).
- The leading cause of death among people aged over 65 (Lowery et al., 2013).
Diagnosis of COPD
- Young children and older who present with breathing difficulties, chronic cough, and sputum should be assessed for COPD (Celli & Augusti, 2018).
Treatment of COPD
- Age may determine the choice of patient education strategies.
- Patient Factors
Behavior
Pathophysiology of COPD
- Smoking and cigarette smoke can exacerbate COPD (Qureshi et al., 2014).
- Prevalence of COPD is about 20% among smokers compared to 4% among nonsmokers (Han & Lazarus, 2016).
Diagnosis of COPD
- Patient history should be carefully taken during clinical investigation to put all behavioral risk factors into consideration (Celli & Augusti, 2018).
Treatment of COPD
- Patients at risk of COPD should be prevented from cigarette smoke exposure or should not smoke (Qureshi et al., 2014).
- Exacerbations of COPD should be promptly treated to reduce risk of exacerbations (Qureshi 2014).
- COPD MIND MAP
References
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