As you continue reflecting back on your journey the past eight weeks in N705, what was helpful to your learning and what hindered your learning?

As you continue reflecting back on your journey the past eight weeks in N705, what was helpful to your learning and what hindered your learning?  What are some ways I could have further supported you in the process as your professor?  What would be your parting advice to future N705 students?

At least 150 words with at least 1 scholarly article reference within the past 5 years.

Cystic Fibrosis

The role genetics plays in the disease.

Cystic Fibrosis is a genetic disease characterized by hypochloremia and autosomal recessive inheritance tendencies. CF occurs in 1 in 2500 births, and 1 out of 25 whites carry one copy of the specific gene that causes cystic Fibrosis. When one of 2 or more alternative forms of a gene in the DNA sequence is at a genomic location with embryos inheriting two alleles, one from each parent, the individual is homozygous (having identical genome markers found at the same place on the chromosome). . (McCance & Huether, 2019

Homozygous individuals must have a recessive allele to deliver the disease. (National Human Genome Research Institute, 2023) These genes or alleles are classified as normal, wild-type, abnormal, or mutant. If the allele is different, defined as heterozygous, or has two versions of the genomic marker. (Dutra, Ph.D., 2023) The CF gene encodes a protein product that forms chloride channels in the membranes of specialized epithelial cells.
Defective transport of chloride ions leads to a salt imbalance, resulting in secretions of abnormally thick, dehydrated mucus. Some digestive organs, particularly the pancreas, become obstructed, causing malnutrition, and the lungs become clogged with mucus making them highly susceptible to bacterial infections (Pseudomonas). With the progression of the disease, lung disease and heart failure develop, and by age 40, death is expected. Consanguinity or two individuals from the same bloodline (second cousins or closer) becoming pregnant with both carrying the same recessive genes,  contributing to the inheritance of CF. (Dutra, Ph.D., 2023, Chapter four)

Why is the patient presenting with the specific symptoms described?

The symptoms: of crying after eating, not gaining weight, having a swollen belly, and skin that tastes like salt are consistent with CF. Presenting due to the baby’s disease progresses. Newborns can and may be asymptomatic, and with age, symptoms develop. CF affects the pancreas and liver, resulting in pancreatic insufficiency leading to malabsorption and malnutrition. Babies with CF can be born with intestinal obstruction (Meconium ileus). The baby is eating, but his body is not metabolizing the nutrients from his food. The baby cannot digest the food, so the food does not move through the GI tract resulting in abdominal swelling. The baby cries after he eats due to the discomfort and pain accompanying his stomach filling and the food being unable to move through the GI tract. Other symptoms reported are swelling in the rectum that can create an intestinal blockage and an inflated colon. (Egan MD et al., n.d.) As a mutated gene, the CFTR modifies the protein that helps transport sodium across the cell membrane. This action results in losing more sodium through sweating and affects how sodium and water move through channels in the body.

CF patients may require specialized vitamins A, D, E, and K due to the inability to metabolize these vitamins, thus creating greater gastrointestinal developments.

The mother reported that her other son had had multiple episodes of chest congestion and pneumonia, symptoms of CF also. This is a clue that the mother was familiar with CF. Cystic Fibrosis creates thickened mucous, allowing mucous buildup within the respiratory tract, resulting in bronchiectasis and infections. Impaired bronchioles/ damaged airways cannot move the mucus up and out of the body.

CF is the most diagnosed genetic disorder presenting symptoms of advancing obstructive lung disease, sinusitis, exocrine pancreatic insufficiency leading to malabsorption and malnutrition, liver and pancreatic dysfunction, and male infertility. Lung infections, breathing problems, wheezing and prolonged coughing, salty-tasting skin and sweat, nose or sinuses (polyps) growth, swelling in the rectum and rectal prolapse, and clubbing of toes or fingers. (Egan MD et al., n.d.)

The physiologic response to the stimulus presented in the scenario and why you think this response occurred.

The physiological response to the stimulus presented resulted from the infant born receiving the recessive gene pattern for Cystic Fibrosis (CF) development from his parents. The child eating is experiencing abdominal pain after eating and therefore cries. The mother offers that she also has a 23-month-old son experiencing symptoms of CF, chest congestion, and pneumonia and has received some information related to CF. the mother is now questioning what CF is and whether she should have any more children. The mother has some knowledge of CF, a hereditary disease. (Dickinson MD, MPH & Collaco, MD, Ph.D., 2021)

The cells that are involved in this process.

CF originates from a specific mutation of the recessive gene pattern, a mutation. They are establishing what specific CF mutation resulted in the disease development. CF results from a misfolded or improperly functioning protein called the Cystic Fibrosis conductance regulator (CFTR). CFTR works in the membrane of the epithelial cells of organs throughout the body as a chloride ion channel. This channel allows chloride to move in and out of the body. The movement of the chloride across the membrane attracts sodium ions across the cell membrane, followed by a subsequent follow of water to the cell’s exterior. The chloride and sodium exchange is the process of hydration and thins mucous. In CF, the dysfunctioning CFTR channel inhibits the water flow, leaving the mucous thickened and without sufficient water, making it difficult for the mucous to move with ciliary clearance. The thickened mucous buildup creates a perfect atmosphere for bacterial growth and the breakdown of normal respiratory functions. The thickened mucous also creates problems in organs such as the sinuses, liver, pancreas, intestines, and male reproductive tract. (Stephen [Shannon], 2015)

How would another characteristic (e.g., gender, genetics) change your response?

CF, an auto-recessive inherited disease, affects males and females equally proportionately. Other factors occur within closely related parents, have a very high probability of having a CF offspring, seen in siblings but not the parents, and one-fourth of the children of parents that are CF carriers will be affected. Questioning the parent’s biological relationship could offer some valuable information. To answer the mother’s question if she should have more children, I recommend genomic testing before conceiving to make an informed decision.

References

Dickinson MD, MPH, K. M., & Collaco, MD, Ph.D., J. M. (2021). Cystic Fibrosis. Pediatrics in Review42(2). Retrieved February 26, 2023, from https://pubmed.ncbi.nlm.nih.gov/33526571/Links to an external site.

Dutra, Ph.D., A. (2023). HETEROZYGOUS (Talking Glossary of Genomic and Genetic Terms) [Heterozygous]. National Human Genome Research Institute. Retrieved February 26, 2023, from https://www.genome.gov/genetics-glossary/heterozygousLinks to an external site.

Egan MD, M., Koff MD, J., & Britto-Leon MD, C. (n.d.). Cystic Fibrosis in Children. Yale Medicine. Retrieved February 26, 2023, from  https://www.yalemedicine.org/conditions/cystic-fibrosis-in-children#:~:text=In%20addition%20to%20losing%20more%20salt%20through%20sweat,kissing%20their%20babies%2C%20that%20their%20skin%20tastes%20salty.%29Links to an external site.

McCance, K., & Huether, S. (2019). Pathophysiology: The biologic basis for disease in adults and children (8th ed.). Louis, MO: Mosby Elsevier.

National Human Genome Research Institute. (2023). ALLELE (Talking Glossary of Genomic and Genetic Terms) [Allele]. Retrieved February 26, 2023, from  https://www.genome.gov/genetics-glossary/AlleleLinks to an external site.

Stephen. (2015). The Cellular Mechanism of CF: The Basics. Cystic Fibrosis News Today.

https://cysticfibrosisnewstoday.com/news/the-cellular-mechanism-of-cf-the-basics/Links to an external site.

This is a write-up of respiratory exam. I need you to expand on the information with in-text citation.

This is a write-up of respiratory exam. I need you to expand on the information with in-text citation.

I need two high-level scholarly references within the last 5 years in APA format with in text citations.

 

Write up for Cardiovascular Physical Examination

 

Blood pressure: upright and supine position to compare the blood pressure. When going from supine to sitting position, there is no changes or decrease in blood pressure or dizziness.

 

Neck veins: patient turned her head to the right, no jugular vein distention observed at 30-35 degrees. Jugular venous pressure measured at 30-45 degrees, under 3 cm which is normal.

Carotid pulses palpated bilateral: no thrill. Auscultation with bell and diaphragm, no bruit.

 

Chest and trunk:

Inspection:

no visualized chest wall abnormalities. Sternum at midline. No precordial pulsations. No aortic abdominal pulsations.

 

Palpation:

No thrill, heaves or lifts in the aortic, pulmonary, Erbs point, tricuspid and mitral area.

Point of maximum intensity (PMI) : 5th intercostal space at the left midclavicular line.

Aortic valve: 2nd right intercostal space. Pulmonic valve : 2nd left intercostal space. Erb’s point: 3rd left intercostal space. Tricuspid: 4th left , mitral 5th left intercostal space.

 

Auscultation:

S1 and S2 present. Regular rhythm and rate. Auscultation of Aortic, Pulmonary, Erb’s Point, tricuspid and mitral valves no bruits.

Physiologic splitting of S2 occurs due to unsynchronized closure of pulmonary and aortic valves during inspiration

Abdominal aorta: no thrills/bruits.

 

Peripheral exam:

Extremities without visual abnormalities, skin is warm, no jaundice, no edema, no varicose veins. Radial pulse: bilateral equal grade 3+. Brachial pulse: bilateral equal grade 3+. Femoral pulse: bilateral: bilateral equal grade 3+. Popliteal pulse bilateral equal grade 3+ Dorsalis pedis pulse bilateral equal grade 3+. Posterior tibial pulse bilateral equal grade 3+

Capillary refill in finger and toes:< 2 sec

Fingers: No clubbing, cyanosis, tar staining or splinter hemorrhages.

 

Expectations

Initial Post:

Everything in APA format with intext citations

References: 2 high-level scholarly references within the last 5 years in APA format.

Plagiarism free.

Turnitin receipt.

The role genetics plays in the disease.

The role genetics plays in the disease.

Cystic Fibrosis is a genetic disease characterized by hypochloremia and autosomal recessive inheritance tendencies. CF occurs in 1 in 2500 births, and 1 out of 25 whites carry one copy of the specific gene that causes cystic Fibrosis. When one of 2 or more alternative forms of a gene in the DNA sequence is at a genomic location with embryos inheriting two alleles, one from each parent, the individual is homozygous (having identical genome markers found at the same place on the chromosome). . (McCance & Huether, 2019

Homozygous individuals must have a recessive allele to deliver the disease. (National Human Genome Research Institute, 2023) These genes or alleles are classified as normal, wild-type, abnormal, or mutant. If the allele is different, defined as heterozygous, or has two versions of the genomic marker. (Dutra, Ph.D., 2023) The CF gene encodes a protein product that forms chloride channels in the membranes of specialized epithelial cells.
Defective transport of chloride ions leads to a salt imbalance, resulting in secretions of abnormally thick, dehydrated mucus. Some digestive organs, particularly the pancreas, become obstructed, causing malnutrition, and the lungs become clogged with mucus making them highly susceptible to bacterial infections (Pseudomonas). With the progression of the disease, lung disease and heart failure develop, and by age 40, death is expected. Consanguinity or two individuals from the same bloodline (second cousins or closer) becoming pregnant with both carrying the same recessive genes,  contributing to the inheritance of CF. (Dutra, Ph.D., 2023, Chapter four)

Why is the patient presenting with the specific symptoms described?

The symptoms: of crying after eating, not gaining weight, having a swollen belly, and skin that tastes like salt are consistent with CF. Presenting due to the baby’s disease progresses. Newborns can and may be asymptomatic, and with age, symptoms develop. CF affects the pancreas and liver, resulting in pancreatic insufficiency leading to malabsorption and malnutrition. Babies with CF can be born with intestinal obstruction (Meconium ileus). The baby is eating, but his body is not metabolizing the nutrients from his food. The baby cannot digest the food, so the food does not move through the GI tract resulting in abdominal swelling. The baby cries after he eats due to the discomfort and pain accompanying his stomach filling and the food being unable to move through the GI tract. Other symptoms reported are swelling in the rectum that can create an intestinal blockage and an inflated colon. (Egan MD et al., n.d.) As a mutated gene, the CFTR modifies the protein that helps transport sodium across the cell membrane. This action results in losing more sodium through sweating and affects how sodium and water move through channels in the body.

CF patients may require specialized vitamins A, D, E, and K due to the inability to metabolize these vitamins, thus creating greater gastrointestinal developments.

The mother reported that her other son had had multiple episodes of chest congestion and pneumonia, symptoms of CF also. This is a clue that the mother was familiar with CF. Cystic Fibrosis creates thickened mucous, allowing mucous buildup within the respiratory tract, resulting in bronchiectasis and infections. Impaired bronchioles/ damaged airways cannot move the mucus up and out of the body.

CF is the most diagnosed genetic disorder presenting symptoms of advancing obstructive lung disease, sinusitis, exocrine pancreatic insufficiency leading to malabsorption and malnutrition, liver and pancreatic dysfunction, and male infertility. Lung infections, breathing problems, wheezing and prolonged coughing, salty-tasting skin and sweat, nose or sinuses (polyps) growth, swelling in the rectum and rectal prolapse, and clubbing of toes or fingers. (Egan MD et al., n.d.)

The physiologic response to the stimulus presented in the scenario and why you think this response occurred.

The physiological response to the stimulus presented resulted from the infant born receiving the recessive gene pattern for Cystic Fibrosis (CF) development from his parents. The child eating is experiencing abdominal pain after eating and therefore cries. The mother offers that she also has a 23-month-old son experiencing symptoms of CF, chest congestion, and pneumonia and has received some information related to CF. the mother is now questioning what CF is and whether she should have any more children. The mother has some knowledge of CF, a hereditary disease. (Dickinson MD, MPH & Collaco, MD, Ph.D., 2021)

The cells that are involved in this process.

CF originates from a specific mutation of the recessive gene pattern, a mutation. They are establishing what specific CF mutation resulted in the disease development. CF results from a misfolded or improperly functioning protein called the Cystic Fibrosis conductance regulator (CFTR). CFTR works in the membrane of the epithelial cells of organs throughout the body as a chloride ion channel. This channel allows chloride to move in and out of the body. The movement of the chloride across the membrane attracts sodium ions across the cell membrane, followed by a subsequent follow of water to the cell’s exterior. The chloride and sodium exchange is the process of hydration and thins mucous. In CF, the dysfunctioning CFTR channel inhibits the water flow, leaving the mucous thickened and without sufficient water, making it difficult for the mucous to move with ciliary clearance. The thickened mucous buildup creates a perfect atmosphere for bacterial growth and the breakdown of normal respiratory functions. The thickened mucous also creates problems in organs such as the sinuses, liver, pancreas, intestines, and male reproductive tract. (Stephen [Shannon], 2015)

How would another characteristic (e.g., gender, genetics) change your response?

CF, an auto-recessive inherited disease, affects males and females equally proportionately. Other factors occur within closely related parents, have a very high probability of having a CF offspring, seen in siblings but not the parents, and one-fourth of the children of parents that are CF carriers will be affected. Questioning the parent’s biological relationship could offer some valuable information. To answer the mother’s question if she should have more children, I recommend genomic testing before conceiving to make an informed decision.

References

Dickinson MD, MPH, K. M., & Collaco, MD, Ph.D., J. M. (2021). Cystic Fibrosis. Pediatrics in Review42(2). Retrieved February 26, 2023, from https://pubmed.ncbi.nlm.nih.gov/33526571/Links to an external site.

Dutra, Ph.D., A. (2023). HETEROZYGOUS (Talking Glossary of Genomic and Genetic Terms) [Heterozygous]. National Human Genome Research Institute. Retrieved February 26, 2023, from https://www.genome.gov/genetics-glossary/heterozygousLinks to an external site.

Egan MD, M., Koff MD, J., & Britto-Leon MD, C. (n.d.). Cystic Fibrosis in Children. Yale Medicine. Retrieved February 26, 2023, from  https://www.yalemedicine.org/conditions/cystic-fibrosis-in-children#:~:text=In%20addition%20to%20losing%20more%20salt%20through%20sweat,kissing%20their%20babies%2C%20that%20their%20skin%20tastes%20salty.%29Links to an external site.

McCance, K., & Huether, S. (2019). Pathophysiology: The biologic basis for disease in adults and children (8th ed.). Louis, MO: Mosby Elsevier.

National Human Genome Research Institute. (2023). ALLELE (Talking Glossary of Genomic and Genetic Terms) [Allele]. Retrieved February 26, 2023, from  https://www.genome.gov/genetics-glossary/AlleleLinks to an external site.

Stephen. (2015). The Cellular Mechanism of CF: The Basics. Cystic Fibrosis News Today.

https://cysticfibrosisnewstoday.com/news/the-cellular-mechanism-of-cf-the-basics/Links to an external site.

Respond to two of your colleagues who selected a different patient than you, using one or more of the following approaches:

Respond to two of your colleagues who selected a different patient than you, using one or more of the following approaches:

  • Share additional interview and communication techniques that could be effective with your colleague’s selected patient.
  • Suggest additional health-related risks that might be considered.
  • Validate an idea with your own experience and additional research

APA Format

Min 2 resources

history of morbid obesity with disabilities in rural setting:

Peer 1

Amanda Surujbali

35 year-old white male with history of morbid obesity with disabilities in rural setting:

It is important to take the time to get to know each patient you may come across and develop a rapport with them, helping them feel more comfortable with the care they may receive from you as well as communication amongst both you and the patient. Asking questions that show patient centered care to figure out how to make them feel better is always key as well as showing courtesy, comforting them, connecting, and showing confirmation at the end (Ball et al, 2019). Getting to know them and connecting on a personal level is important in making them feel safe to even continue to answer questions, open up, and speak with you. Communication would differ from patient to patient depending on the factors you may observe with them. Some of them are age, acuity of illness, education level, tradition/ religious beliefs, and ethnicity.

Depending on the patient’s social determinants I would be able to know whether to use task oriented, clinician centered, behavior centered, or patient centered model since there are different levels of information sharing between patients and healthcare professionals (Diamond-Fox, 2021). For my patient, I may target things to help me gather perhaps why he is disabled and what may have caused this, as well as what could have caused him to come in to get seen/ get help. If this patient can speak with me, I would use a patient centered model since Diamond-Fox explains that a clinician centered model is geared toward the disease framework. He discusses the patient centered model is geared toward illness and depending on the situation one would use which ever works more in their benefit (Diamond-Fox, 2021). Since Morbid Obesity is a condition that can stem from lots of different reasons, it made sense to go with the patient centered approach in order to gain knowledge on factors that may be aiding in the illness for this patient.  Asking if he has certain conditions and if he takes medications can also help me to learn if his medication is causing the morbid obesity versus the obesity being a result of a sedentary lifestyle, or something else. According to Sullivan, getting a list of all medications that are prescribed and even over-the-counter medications can also be a crucial part of the medical history (Sullivan, 2018).

With my 35 year-old white male with history of morbid obesity with disabilities in rural setting, the appropriate risk assessment instrument would be the functional assessment since he has disabilities. This assessment will help to determine the variety of disability he has so I would cover all areas of this assessment in order to get a clear picture of how disabled this patient is in order to get proper management plans on board.This can help him with becoming more independent or less disabled/ get the help he needs at home to continue living in conditions that would not make his conditions worse. The Functional assessment covers mobility, upper extremity function, household chores, activities of daily living, and instrumental activities of daily living (Ball et al, 2019). A health related risk this patient has is his morbid obesity that is potentially causing him to have disabilities at the age of 35.

To begin building a health history for this specific patient I would let him know I was going to ask questions regarding his activities of daily living at home/ on a usual basis in order to be able to put a plan together with him to help facilitate the care he may need or for him to have a chance at healing and getting better. Some of the questions I would ask are do you try to take the stairs or use steps and if yes how many can he do, if he has issues walking from his bedroom to the bathroom or one room in the house to another, if he is able to get the mail walking to the mailbox, if he is able to reach things on shelves above him or not, if he takes part in any chores at home and if he does what does he do (in order to gauge if he does heavy or light activities), is he able to eat without gasping for air, how does he transition onto the toilet in order to use the bathroom, who helps him with his medications, are they easy to get to, and if he is able to understand how he should take his medications in case it’s a med he needs to draw up and give himself, cut a pill in half, or mix a solution to drink. There are much more questions that I can ask to help build my health history, but these are some of the pertinent ones that stood out to me from the Functional Assessment tool mentioned above.

References:

Ball, J. W., Dains, J. E., & Flynn, J. A. (2019).  Seidel’s Guide to Physical Examination (9th ed.). Elsevier Health Sciences (US). Retrieved from                        https://mbsdirect.vitalsource.com/books/9780323481953Links to an external site. .

Diamond-Fox, S. (2021). Undertaking consultations and clinical assessments at advanced level.  British Journal of Nursing,  30(4), 238–243.                      Retrieved from  https://doi.org/10.12968/bjon.2021.30.4.238Links to an external site. .

Sullivan, D. D. (2018).  Guide to Clinical Documentation (3rd ed.). F. A. Davis Company. Retrieved from                                                                                     https://mbsdirect.vitalsource.com/books/9780803694194Links to an external site. .

 

 

Peer 2

Maricela Leiva

Building a Health History

Effective patient management is dependent on comprehensive and effective history collection by the healthcare provider. A comprehensive and accurate history collection is specifically crucial in enhancing an accurate diagnosis and enhancing employment of effective treatment interventions (Karaca & Durna, 2019). Effective communication is crucial in enhancing the process of health history collection. Consideration of patient specific factors such as gender, age, environmental setting and ethnicity is also crucial in promoting an individualized care plan (Ebrahimi. et al 2021). This discussion aims to highlight a summary of an interview involving a case scenario of a 35-year-old patient who presents with a history of morbid obesity with difficulty in the rural setting. The targeted questions will also be outlined.

Summary of the interview

            The interview of the 35-year-old patient who presented with the case involves the process of consideration of the patient specific factors to dictate techniques employed. Some of the techniques employed in the case scenario to enhance communication and information collection include practicing active listening, asking open ended questions, demonstrating empathy, and employment of non-verbal cues.

Through employing open ended questions, the healthcare providers allow for collection of comprehensive information from the healthcare provider. Showing empathy is also crucial in promoting compliance to the interview.

Risk Assessment Instrument

The most applicable risk assessment tool in this case scenario would involve the Framingham Risk Score. The Framingham Risk Score is crucial in investigating for an individual’s risk profile of experiencing a cardiovascular disease within a 10-year timeframe (Petruzzo,.et al, 2021). This risk assessment tool focuses on investigating for potentially underlying risk factors such as smoking, hypertension, sex, age, and cholesterol levels.

Targeted Questions

The targeted questions that may be employed in the case scenario include:

· Give a description of your daily diet and physical activity

· Describe any significant changes in mental status and mood

· Give a medical history related to the underlying factors as dictated by the Framingham Risk Score.

· Any history of cardiovascular disease.

· Describe your common pain and discomfort management interventions and their efficacy.

Reference

Karaca, A., & Durna, Z. (2019). Patient satisfaction with the quality of nursing care. Nursing

open, 6(2), 535-545.

Petruzzo, M., Reia, A., Maniscalco, G. T., Luiso, F., Lanzillo, R., Russo, C. V., … & Moccia, M.

(2021). The Framingham cardiovascular risk score and 5‐year progression of multiple sclerosis. European Journal of Neurology, 28(3), 893-900.

Ebrahimi, Z., Patel, H., Wijk, H., Ekman, I., & Olaya-Contreras, P. (2021). A systematic review

on implementation of person-centered care interventions for older people in out-of-hospital settings. Geriatric Nursing, 42(1), 213-224.

Grading Rubric for Reaction Paper

Perioperative/Operating Room Reaction Paper (Grading Rubric for Reaction Paper) Student Name: ______________________________________ Evaluation of each area as: (Objectives Met, Not Met, and insufficient information). Objectives Met Not Met Insufficient Information Title Page: Name, title and author Title Page (e.g. Trinitas School of Nursing, NURE132, Peri-operative Reaction Paper, Name of Adjunct Faculty, all centered). Introduction: States purpose of the paper and incorporates personal objectives for the experience. Pre-operative Stage: Explains the preoperative diagnosis, consents, medications, laboratory results, and teaching (if known). Incorporates evidence of the National Patient Safety Goals (Patient Identification, Universal Precaution – “Time Out”, infection prevention, sterility, fall, pressure ulcer prevention, etc.). Surgical infection prevention prophylaxis (antibiotic), CAUTI (Foley cath removal postop), etc. Intraoperative Stage: Describes the roles of Surgical Team Members (surgeon, scrub and circulating nurses, OR techs, anesthesia, etc.). Discusses how teamwork and collaboration was demonstrated during surgical procedure and the relationship to patient safety. Post-operative Stage: Role of the Nurse and Anesthesia in the recovery process: Management of airway, vital signs, etc. Discussion of the RNs’ Roles in Caring for the Perioperative Patient: Incorporates nursing care and the client’s reactions. 1. How the nurse functions in this setting. 2. How the nurse cares for the specific needs of the patient (pain, airway, etc.) Evaluation of the Experience: Your reaction to the experience and how it may or may not accomplish your goals. Rate the value of this learning activity and explain what was the most important or surprising thing you learned. Writing style, correct APA, grammar, spelling Grade: Pass/Fail/Pass with revision (circle one) Comments: ______________________________________

Respond to  at least two of your colleagues  on 2 different days who selected a different patient than you, using one or more of the following approaches:

Respond to  at least two of your colleagues  on 2 different days who selected a different patient than you, using one or more of the following approaches:

· Share additional interview and communication techniques that could be effective with your colleague’s selected patient.

· Suggest additional health-related risks that might be considered.

· Validate an idea with your own experience and additional research

 

Peer 1

 

Introduction

The case study analysis assigned to me involves an 85-year-old white female living alone with no family who is in declining health. In expanding upon the case study, I utilized the SOAP note format, which is presented below:

Subjective (S): JD is an 85-year-old white woman who presents to the emergency department with concerns about declining health due to multiple falls and pain in the left hip. The falls began about a year ago and have increased in frequency and severity in the past three months. The most recent fall was today when the patient fell while getting up to use the bathroom, and she fell to the floor and landed on her left side. She immediately called 911. She states that pain in the left hip increases with weight-bearing activities, and she has been unable to put weight on the left side. She has not taken anything for the pain. She states that pain is 10/10 with any weight-bearing or ROM activities. She does not use any assistive devices for mobility. She eats one meal daily and tries to have a Boost supplemental shake daily. Patient has intermittent urine incontinence. She does not have relatives or friends available to assist her. She still drives, though she avoids driving at night.

She has a history of osteoporosis, hypertension, dyslipidemia, anxiety, and depression. Her medications include: metoprolol tartrate 50 mg twice daily, atorvastatin 20 mg daily, sertraline 50 mg daily, multivitamin daily, and vitamin D3 25 mcg daily.

Objective (O): JD is an older white woman who appears frail, malnourished, and anxious. Alert and oriented x 3. VS: 143/94, P 101, RR 20, 97% on room air at rest, and T 97.8F. Weight 91 pounds and height 5’1”. BMI is 17.2. Significant bruising was noted in the LLE from the lateral aspect of the hip that extends medially towards the groin and distally above the knee. X-rays demonstrate a left femoral neck fracture.

Assessment (A): 1.) Traumatic fracture of the left femoral neck 2.) falls 3.) malnourishment 4.) hypertension 5.) osteoporosis 6.) dyslipidemia 7.) anxiety 8.) depression.

Plan (P): Patient is being admitted to the hospital for immediate surgery for a traumatic left femoral neck fracture. Referral and transfer to orthopedics are planned. Patient was provided education on proper nutritional requirements and how to maintain a healthy weight via teach-back and literature. The provider had a conversation with the patient regarding the safety of living within her home, and the patient plans to return home accordingly. Patient is to follow up with the orthopedic surgeon, primary care provider, and cardiologist upon discharge. A discussion for plans to discharge from the hospital to a skilled nursing facility was had, and the patient agreed with this plan. Medication additions include: hydrocodone-acetaminophen 5-325 every 4-6 hours as needed. No medications were discontinued.

Communication and Interview Techniques

Providers must efficiently use several communication and interview techniques with various populations. In this case study, the patient is an elderly 85-year-old woman. One study provides evidence that the elderly population does not tend to seek out emergency department care unless severe or life-threatening injuries occur (Lutz et al., 2018). She has no hearing or visual concerns; therefore, the provider does not need to make adjustments. The provider should position themselves near the patient with as few obstacles in between as possible (Ball et al., 2019). Maintaining eye contact, having an open posture, using appropriate non-verbal cues, and utilizing appropriate follow-up questions are necessary to gain the patient’s trust (Ball et al., 2019). Since the interview is occurring in the emergency department, the interview must be focused and timely. The provider should begin with open-ended questions to ascertain the patient’s chief concern and follow up with appropriate questions to gain the patient’s trust (Ball et al., 2019). Once rapport is developed and the patient is more at ease, the provider can ask more personal questions, such as about lifestyle and socioeconomic status (Ball et al., 2019). Questions should occur one at a time and in a manner that allows for the patient to respond fully before proceeding. Though the patient’s care will be transferred to the orthopedic surgeon, education should be provided to the patient. Since the patient is in a heightened emotional state, it is necessary to provide educational materials in the form of literature for the patient to reference later (Hoek et al., 2020). Keeping the patient informed at every step of care is imperative to ease the patient’s anxiety and ensure safe outcomes.

Risk Assessment Instrument

Several risk assessment instruments would be beneficial in this case study. A fall risk assessment tool is the most common and pertinent tool for the patient in this case study. A widely used tool is the Johns Hopkins Fall Risk Assessment Tool, which consists of 7 questions about age, fall history, elimination, bowel and urine, medications, patient care equipment, mobility, and cognition (Johns Hopkins Medicine, n.d.). Scores between 6-13 are a moderate fall risk, and greater than 13 points are a high fall risk (Johns Hopkins Medicine, n.d.). Patient in this case study is a high-fall risk as demonstrated by her age (85), fall in the past six months, incontinence, medications (antihypertensive, opiate), and impaired mobility.

Another risk assessment tool that should be utilized in this case study should involve nutritional status. Significant evidence suggests that malnourishment is a risk factor for falls and should be addressed at every point of care (Adly et al., 2019). Since the patient in this case study is below the recommended BMI and only eats one meal/daily with the occasional supplemental beverage, it is necessary to provide extensive education to inform the patient of the importance of maintaining a healthy diet to prevent future falls and fractures. One of the most commonly used nutritional risk screening tools for the elderly is the Mini Nutritional Assessment Short-Form (MNA). The MNA includes various components such as loss of appetite, altered sense of taste and smell, loss of thirst, frailty, and depression, all of which are relevant in the older population (Reber et al., 2019). Information gathered from this tool allows for timely nutritional intervention. Maintaining an optimal nutritional status could lead to fewer falls.

Health Risk Interview Summary

· What is your past medical history?

· What is your living situation?

· Do you live alone? Have any relatives or friends that would be able to assist you?

· What obstacles within your home make it difficult for you to complete daily activities? Do you use an assistive device for mobility?

· Take me through a typical day.

· How many meals are you eating? What do the meals consist of?

· What are your bowel and urinary habits? Do you wake up at night to use the bathroom?

· Are you able to shower/bathe yourself? Do you use any assistive devices? Do you feel safe and steady when doing these activities?

· How do you manage your medications? Do you always take them as they are prescribed? How do you pick up your medications?

· How often do you fall in a week, month, or year?

· Is there a specific time of day when you fall? Is there a specific activity that you are doing when you fall?

 

 

 

Peer 2

he Comprehensive History and Physical

When gathering a comprehensive history and physical (H&P), several areas need to be addressed (Sullivan, 2019). Components of an H&P include the chief complaint with history of present illness, past medical history, family history, social history, review of systems, physical examination, laboratory data, problem list with assessments and differential diagnoses, and the treatment plan (Sullivan, 2019). There is not a one size fits all technique to completing a H&P meaning that the patient’s situation should lead the conversation (Ball et al., 2019). Communication is paramount; therefore, healthcare providers need to make sure they are being understood by using non-medical jargon as well as clarifying what the patient states (Ball et al., 2019). If the patient is presenting in an emergency setting, the emergency care is provided prior to the H&P as needed (Ball et al., 2019). This paper will address working with a 4-year-old male African American child.

One of the first things to address when working with children is if a consenting adult is present with the patient (Ball et al., 2019). It cannot be assumed that the person in the room with the child has guardianship (Ball et al., 2019). Asking a direct question such as their name and their relation to the child, plus if they have the right to consent to care should be asked upon initial meeting (Ball et al., 2019). The child should be a part of the introductions as well and can be included by getting down to their level to be able to look into their eyes and speak to them (Ball et al., 2019). Asking the guardian and child how they would like to be addressed helps establish a respectful relationship while clarifying the relationship between the patient and person in the room (Ball et al., 2019). The 4-year-old child should be able to answer some questions with the guardian being able to expand on the answers (Ball et al., 2019). The patient is best able to answer what something feels like to them (Ball et al., 2019). Letting the guardian expand on their observations helps to clarify the symptoms and situation that is beyond the understanding of a 4-year-old (McCance & Huether, 2019). Asking direct open-ended questions such as “what prompted you to seek care today” or “when was the child’s last know well day” can allow for the person to tell the narrative of the condition without being prompted by the health care professional (Ball et al., 2019). Also, by asking last know well day rather than first sick day, it opens up the idea of really when the symptoms started (Ball et al., 2019). Allowing for a narrative enables many questions to be answered without having to ask them and they will be in the patient or guardian’s own words (Ball et al., 2019). The healthcare provider can listen to the narrative without interrupting, getting a sense of the chief complaint, then ask directed follow up questions (Ball et al., 2019).

Children may be anxious or nervous about being in the office so they should be allowed to sit where they are comfortable when able (Ball et al., 2019). For example, in the lap of a parent (Ball et al., 2019). Having a sick child can be stressful so emotions maybe running high (Ball et al., 2019). The health care professional should use respectful candor to gain trust of the patient and guardian (Ball et al., 2019). It is also important to run a risk assessment for maltreatment when a vulnerable population, such as a child, is being seen (van der put et al., 2017). van der put et al. (2017) found that ancillary staff assessments, such as social work, had a better risk assessment tool than clinical tools being used. Van der put et al. (2017) suggest combining aspects of both type of assessments to limit patients falling through the cracks. Healthcare providers are assessing the guardian in the room as well, looking for signs of stress from caregiving (van der put et al., 2017). Ball et al. (2019) also highlights that witnessing violence as a child can hinder appropriate growth and development. Asking a direct question like “has something scared you” or “do you ever have bad dreams about something that you have seen” can help to open a discussion on the situation that occurred (Ball et al., 2019). Getting feedback from the guardian on how they addressed the situation can also assist in gathering information on how this is affecting the child (Ball et al., 2019).

Asking what a typical day looks like for the child can help gather information (Ball et al., 2019). For example, when asked if there are pets in the home the answer may be no, but there may be pets in the home of a babysitter which could trigger allergies (Ball et al., 2019). Running through a typical day can help determine the patient’s social determinants of health from the environments that the child is exposed to (Ball et al., 2019). Some information can be gathered based on where the patient lives (Ball et al., 2019). For example, if the patient lives in an area with high known child asthma cases due to air quality, then the child should be checked for signs and symptoms of asthma and the guardian educated on the risks and what signs to look for (Ball et al., 2019).

Part of a child’s H&P should include if the child is hitting developmental milestones (Ball et al., 2019). A four-year-old child could be in preschool in which case the information could be gathered as to how the child in doing in a social school environment (Ball et al., 2019). History of milestone development is important as well; did the child hit developmental markers up to this age (Ball et al., 2019)? In preschool aged children, gross motor skills can be especially meaningful for other developmental functions (Amemiya et al., 2018). Gross motor skills can affect physical and psychological functions, but also social participation for children (Amemiya et al., 2018).  Monitoring the gross motor skills in the preschool years can help to see developmental delays or deficits (Amemiya et al., 2018).

Gathering a family history is especially important for children as many genetic diseases can be seen by tracing the family (Ball et al., 2019). The child is African American. Some diseases are more prevalent in populations with ancestors from Africa (McCance & Huether, 2019). For example, if the family has a history of sickle cell disease, the child may need to be checked for the disease (McCance & Huether, 2019). Gathering cultural and religious practices that may affect care is also imperative as it may guide the direction of care in a different route (Ball et al., 2019).

If medications are being prescribed two key factors need to be addressed. Can the patient’s guardian afford the medication and do they understand how the medication is to be taken (Rosenthal & Burchum, 2021)? Practitioners throw around the word noncompliance easily but what is behind the noncompliance (Rosenthal & Burchum, 2021)? If the patient’s guardian does not understand the importance of the medication or they cannot afford the medication, it is the job of the healthcare professional to remedy these situations (Rosenthal & Burchum, 2021). If they cannot afford the top tier medication, can they afford a second-tier medication? These medications may not have as high of efficacy but it may be better than the patient being without anything (Rosenthal & Burchum, 2021). Guardians also need to understand that children process medications differently than adults due to immature organ systems and that many medications are not studied in children so they are being written off label (Rosenthal & Burchum, 2021). Teaching the importance of monitoring the child after medication doses should be part of the education in the visit (Rosenthal & Burchum, 2021).

In conclusion, a comprehensive history and physical is just that, comprehensive. Obtaining the history and physical is just as important as the physical exam (Sullivan, 2019). Documentation is also key as the record is often used as a base throughout the patient’s entire clinical course (Sullivan, 2019). As a healthcare provider it is our goal to provide above adequate care to our patients, which all begins with the initial H&P (Sullivan, 2019).

You have had the opportunity to review thermoregulation as is pertains to the human body. With this discussion, you will need to explain what thermoregulation is and why is it important?

You have had the opportunity to review thermoregulation as is pertains to the human body. With this discussion, you will need to explain what thermoregulation is and why is it important?

 

Please make an initial post by midweek, and respond to at least two other student’s posts with substantial details that demonstrate an understanding of the concepts, and critical thinking. Remember that your posts must exhibit appropriate writing mechanics including using proper language, cordiality, and proper grammar and punctuation. If you refer to any outside sources or reference materials be sure to provide proper attribution and/or citation.

Soap Note

Soap Note # ____ Main Diagnosis ______________

 

PATIENT INFORMATION

Name:

Age:

Gender at Birth:

Gender Identity:

Source:

Allergies:

Current Medications:

1.

PMH:

Immunizations:

Preventive Care:

Surgical History:

Family History:

Social History:

Sexual Orientation:

Nutrition History:

 

Subjective Data:

Chief Complaint:

Symptom analysis/HPI:

The patient is …

 

Review of Systems (ROS) (This section is what the patient says, therefore should state Pt denies, or Pt states….. )

CONSTITUTIONAL:

NEUROLOGIC:

HEENT:

RESPIRATORY:

CARDIOVASCULAR:

GASTROINTESTINAL:

GENITOURINARY:

MUSCULOSKELETAL:

SKIN:

 

Objective Data:

VITAL SIGNS:

 

GENERAL APPREARANCE:

NEUROLOGIC:

HEENT:

CARDIOVASCULAR:

RESPIRATORY:

GASTROINTESTINAL:

MUSKULOSKELETAL:

INTEGUMENTARY:

 

ASSESSMENT:

(In a paragraph please state “your encounter with your patient and your findings ( including subjective and objective data)

Example : “Pt came in to our clinic c/o of ear pain. Pt states that the pain started 3 days ago after swimming. Pt denies discharge etc… on examination I noted this and that etc.)

Main Diagnosis

(Include the name of your Main Diagnosis along with its ICD10 I10. (Look at PDF example provided) Include the in-text reference/s as per APA style 7th Edition.

Differential diagnosis (minimum 4)

PLAN:

Labs and Diagnostic Test to be ordered (if applicable)

1. –

1. –

Pharmacological treatment:

Non-Pharmacologic treatment:

Education (provide the most relevant ones tailored to your patient)

 

Follow-ups/Referrals

References (in APA Style)