1. What are the similarities of the concepts/metaparadigms of Sister Callista Roy, Betty Neuman, Imogene King and Hildegard Peplau? Explain these similarities. 2. What are the diferrences of the concepts/metaparadigms of Sister Callista Roy, Betty Neuman, Imogene King and Hildegard Peplau? Discuss how it differs from others.
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- Hello good day, I am having a problem answering this question and I need your help on this. Hoping for a response and thank you In each chosen disease, pls. supply the information below: So I've chosen "Congenital Hypothyroidism", so I need a short description, its pathophysiology, laboratory diagnosis, and Treatment and Prevention of my chosen disease. a. Short Description b. Pathophysiology c. Laboratory Diagnosis d. Treatment and Preventionindividuals relationship Dwarf or normal I-2 and III-6 II-1 and II-6 III-1 and II- 8 8. A woman has normal blood clotting but testing indicated that she is a carrier of hemophilia. Her parents have normal blood clotting and her brother has hemophilia. She marries a normal man and they have a daughter with normal blood clotting. What are the chances, if they have a son, that he will have hemophilia?Match the STD with their descriptions. Question 24 options: leading cause of PID; bacteria ~95% of all USA infected leading cause of cervical cancer prior to vaccine and ~79,100,000 (~30%) of USA infected or newly infected each year; basically, 50% of USA infected leads to AIDS; 1,144,500 people infected in the USA ~20% of all USA infected, (~1 in 5 people) 1. HIV 2. HSV-1 3. HSV-2 4. HPV 5. Chlamydia trachomatis and Neisseria gonorrhoeae
- Please help me to answer ALL the letters with the correct answer. NO MORE EXPLANATION 1. When asked by the mother why she had a large baby, as a nurse how will you explain this? A. You had eaten a lot when you were pregnant which caused the baby to become large B. You have a familial tendency because LGA is genetically predetermined to become large C. You may had excessive production of growth hormone that is why you had a large baby D. The medications that you had taken during pregnancy caused it to become large2. A child with hyperbilirubinemia is exposed to phototherapy. As you do this intervention to the baby, as at nurse you need to assess the baby frequently for: A. assess level of consciousness B. assess motor strength and reflexes C. assess skin turgor and intake and output ~ D. assess bowel sounds and frequency of bowel movement." 3. Situation: A neonate born prematurely via NSD with apgar score of 6. AOG is 34 weeks. The nurse anticipates that the child is at high risk due…From NTSA case study https://static.nsta.org/case_study_docs/case_studies/cystic_fibrosis.pdf Please help with questions 2, 3 and 4 of part two 2. What is the chance that Nancy passed on the CF allele to her baby? 3. What is the chance that Jake passed on the allele if he is a carrier? 4. What is the chance that their baby will have CF if they are both carriers? If their first child has CF, what is the chance that their second child will have CF? What is the chance that the baby will inherit CF if only Nancy is a carrier?Make a 1 FDAR. Use any focus from the given case except "boggy uterus". Case: Date/Time: 9/13/2022 @ 10:30 AM Admitted at 9:00AM a case of D.A.M., 30 years old, G2P1T1P0A0L1M0, at 39 weeksage of gestation, singleton from Balamban, Cebu, with chief complaints of stronguterine contractionsand severe labor pains. Upon IE, it was noted that cervix is fully dilated, 100% effaced and ruptured bag of water. After a while, she shouted: “Help, the baby is coming”. D.A.M. was immediately transferred tothe delivery room, mounted in the delivery table and prepared for imminent delivery. After 1 hour, she delivered per vagina a healthy baby boy. Oxytocin given 10 “IU” at right upper arm within 1 minute after delivery of the baby. 5 minutes after, fetal surface of the placenta was presented at the birth canal. Intact perineum. Vital signs within normal range. Uterus boggy (“not firm”) with fundus palpable at 1cm below umbilicus. Lochia rubra moderate. Patient appears sleepy.
- case study: C was a six year old boy who passed away at the Lady Cilento Children’s Hospital on14 January 2017. He was a generally healthy and happy child. C’s treating team at the Lady Cilento Children’s Hospital attributed his death to overwhelming sepsis due to melioidosis. His death was not discussed with the coroner at that time. No autopsy was performed. C’s death was first reported to the State Coroner on 3 May 2018 due to the family’s concerns about the care C received from a remote hospital over several days leading up to his admission on 10 January 2017 and subsequent transfer to a regional hospital by which time he was seriously ill. The family also lodged a complaint with the Office of the Health Ombudsman. The Health Ombudsman considered the family’scomplaint potentially identified broader systemic issues and undertook a systemicinvestigation. The family’s concerns related to failure by remote hospital staff to correctly diagnoseand investigate the cause of C’s worsening…This is homework not a test! From NTSA case study https://static.nsta.org/case_study_docs/case_studies/cystic_fibrosis.pdf Please help with questions 2, 3 and 4 of part four 2. "The successful use of gene therapy to cure SCID syndrome (2000) is hoped to be a permanent cure for those patients because a good copy of the problem gene was inserted into the patients' blood stem cells in the bone marrow (hematopoietic stem cells). Once white blood cells enter the blood stream they have a limited life span, on the order of a few week to months. The blood stem cells are the cells that create more white blood cells to replace those that are lost. If the gene was only inserted into the circulating mature white blood cells, the patient would only be temporarily cured until those cells were used up or died." The current gene therapy approaches to cure CF involve inserting a functional CFTR gene into the mature epithelial cells of the lungs. In light of the preceding paragraph, do you think that…hi, can I please get help on a case study on nueroanatomy I have been struggling for a couple of hours now and can't seem to understand the study to answer the following questions. is there any way or format that i can get help. I would really appreciate it. thanks! 1. Based on the information in the case, what is the most likely neuroanatomic location for a single lesion that can explain all of the patient’s symptoms and signs? In your own words, explain how you arrived at that localization. 2.What are some possibilities for the nature of the lesion (e.g., stroke, tumor, trauma, etc.)? In your own words, explain your rationale for these options. 3. How does the laboratory data and neuroimaging demonstrate the actual lesion for the patient? Describe how you interpret the data in your own words. 4.How was the patient was treated, and how did they subsequently fare? Describe the treatment plan in your own words.
- Please read the case study, Giving Birth to Someone Else's Children? A Case of Disputed Maternity, and then answer the following questions: From Part I, Karen needs a kidney transplant and her sons are being tested for possible donors. However, it seems that the blood test have indicated that neither of her sons are her children based on HLA matching. 1. What is HLA? How is HLA determined and inherited? How is this used to match a donor and recipient for a tissue transplantation? 2. What are some possible explanations for Karen's situation? How would you test these hypotheses?JUST ANSWER the NUMBER 5. Three pregnant women due to give birth were admitted to a hospital, accompanied by their partners on the same night. Given that the hospital staff forgot to put name tag on the babies, to be able to identify which baby goes with which couple, a blood test was performed with the following results:2. 356 Q7. Haemophiliacs possess a non-functional form of the gene responsible for the production of blood clotting factors. Shown below is the occurrence of haemophilia in one family. Completed forms to be made available for external moderation. 4. = male = female = male haemophiliac 8. 1. 5. 6 3. 4. 11 12 Using the following symbols: H= dominant allele h = recessive allele 1) State the genotypes of the following individuals. Individual Genotype 1. HH ЧАН HH 9. 6. 2) On the basis of the information provided, is the inheritance of haemophilia: 1) autosomal or sex-linked? Sex-linked (ii) dominant or recessive? Recessive 3) State the probability of individual 8 being a carrier of haemophilia. Individual 8 is a female and is a daughter of individual 1 and 2. Individual 1 x individual 2