A. Cooksey: ALS Presentation

AC
by Alicia Cooksey0 views·Updated Nov 16, 2020

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  1. Hi, everyone.
  2. My name's Alicia Cooksey, and I'm doing my presentation on
  3. amyotrophic lateral sclerosis, also known as a less or Lou
  4. Gehrig's disease, after the baseball player from the 19 twenties
  5. and 19 thirties who had this disease.
  6. Okay, right, And Ailes is a progressive and fatal muscular
  7. disease. Um, it causes a degeneration of motor neurons to
  8. stop sending messages to the muscles, which causes the muscles
  9. to weaken and waste away.
  10. And then it eventually it affects the respiratory muscles, which
  11. causes death within 2 to 5 years.
  12. One suspected cause is too much glutamate, which is a
  13. chemical that's responsible for relaying messages between the motor neurons.
  14. But researchers actually don't know the real cause.
  15. Um, according to the Neurological Disorders Institute from 2000 and
  16. 16, it's approximated that 14 to 15,000 Americans have this
  17. disease 5 to 10% inherited from their parents, and most
  18. will die within 3 to 5 years.
  19. Um, Ailes affects persons of all races.
  20. However, white males persons older than 60 those with the
  21. family history are more likely to develop ales.
  22. And there's some studies from the National Institute of Neurological
  23. Disorders that suggest that veterans are two times more likely
  24. to develop a less.
  25. Researchers are looking into environmental toxins.
  26. Pesticides lead as suspects as to why the veterans are
  27. getting a less more than the regular population.
  28. Um, and genetics is another point of research signs and
  29. symptoms. Um, in the beginning, signs and symptoms are pretty
  30. subtle. Um, sometimes muscle twitches, cramps real vague.
  31. Um, sometimes that'll bring people into their primary care, doctor.
  32. Um, and many times it's a ruling out of all
  33. other diseases.
  34. Want to make a diagnosis of, um, and then eventually
  35. the This weakness progresses into weakness, slurred speech and usually
  36. the well, inevitably, the inability to walk, swallow or breathe.
  37. Um, one interesting, uh, trial said that heavier people have
  38. a longer survival rate than those who have a B
  39. M I of less than 18.5.
  40. So probably the only disease were a little extra weight
  41. could benefit you.
  42. Although the disease can strike at any age, it most
  43. commonly strikes people ages 55 to 75.
  44. These people are in the prime of their lives working
  45. supporting families.
  46. Um, sometimes they just maybe made it to retirement.
  47. Finally have some time and money toe do some fun
  48. things, and they're just not prepared for the complete devastation
  49. of this disease.
  50. Um, it's a very expensive disease process.
  51. Um, actually, any disease that needs home health care.
  52. But I spoke Thio unity point, um, companion care service
  53. is and Pekin, Illinois.
  54. And they said that for 24 hour service for one
  55. year, it cost $197,424.
  56. That's just toe.
  57. Have a sienna in your home that doesn't you know,
  58. all the other expenses, Um, that come with this?
  59. Um, And in my 30 years of healthcare, I've had
  60. three private duty, A less patients totally in about three
  61. years. Care for all three of them?
  62. I always say that I won't take another a less
  63. patient because it, to me, is one of the hardest
  64. diseases. Um, it's very, very draining.
  65. It's very devastating to walk with these families through this,
  66. um, all my patients I was with from the very
  67. beginning to the end.
  68. Um, they it was usually about a year and a
  69. half or so that I was with each patient.
  70. Um, I think one of the most difficult things for
  71. me was that they didn't lose any of their cognitive
  72. abilities. Some patients may, but they usually, um, stay sharp.
  73. And they just kind of become entombed in their body.
  74. Um, on I have seen houses mortgaged.
  75. Um ah, lot of family burn out in a lot
  76. of family stress because of this disease process.
  77. Now, let's go to our nursing process.
  78. So first, we're going to start with assessment.
  79. Um, it's really important to get a baseline with these
  80. patients s so we can track the progression of the
  81. disease. We need to watch for their motor strength, skin
  82. integrity, urinary and bowel function, swallowing lung sounds and communication
  83. and do a safety assessment of the home.
  84. We also need to assess their emotional mental health and
  85. the families coping, um, skills and the support needed in
  86. any respite needed.
  87. We need to talk faster here.
  88. Okay. Nursing diagnosis is risk for aspiration.
  89. Um, this is actually while I got hired into my
  90. first, a less patient was just to come in and
  91. spend two hours at each meal for feeding because of
  92. the big aspiration risk.
  93. And it takes a very, very long time for these
  94. guys. Thio thio eat their meals We also need thio
  95. Watch for risk of skin breakdown is they lose weight
  96. as they're incontinent We need Thio watch their skin and
  97. then also be really aware of caregiver strain And I'm
  98. calling in support staff and respite What?
  99. They need it.
  100. Okay, moving on to planning The nurse needs to keep
  101. in mind who their audiences when they're planning care.
  102. Um, it's usually going to be the patient and caregivers
  103. And we need to remember to recognize health, literacy and
  104. of the emotional state, um of everyone when we're teaching
  105. them this.
  106. Alright, interventions aspiration We need to teach about medications to
  107. decrease section or secretions feeding and swallowing techniques Positioning food
  108. consistency Um, communication signals are really important to talk about
  109. before communication is lost and to make sure that everybody
  110. knows about suctioning.
  111. Um, we also need thio skin protection and skin breakdown.
  112. Uh, really telling the family and caregivers how important turning
  113. is and dry and how quickly breakdown can happen.
  114. Um, usually, they're just not aware of that, and I
  115. think they can leave them for a few hours.
  116. And you really have to tell them that you know,
  117. No turning frequently is very, very important.
  118. Um, keeping them dry.
  119. No wrinkles, proper nutrition and safe transfer to prevent the
  120. friction on dhe.
  121. Then caregiver strain.
  122. Um, you can't completely eliminate it.
  123. But if you can teach them about support groups, social
  124. workers that can help with insurance home health agencies to
  125. call in for respite meal delivery and to really let
  126. them know it's okay to get help.
  127. Okay, how do we evaluate this?
  128. Teach back is always important.
  129. Any skills that you have taught, whether it's turning suctioning
  130. feeding, have them teach that back to you.
  131. Make sure as a nurse you having frequent follow up
  132. visits. And also I found really important that you have
  133. a communication log in the home so that everyone's on
  134. the same page.
  135. Um, and that we can so we can give consistent
  136. care. So, in conclusion, this is such a difficult disease
  137. process for everyone involved.
  138. Um, but as a nurse, by giving immaculate care, using
  139. evidence based nursing techniques and really giving great compassion to
  140. everyone involved, we can help, um, ease the burden of
  141. the family and the patient through this disease process.
  142. Uh, here's my references.
  143. And thank you, everyone