Alzheimer's disease resident survival guide: Difference between revisions
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{{WikiDoc CMG}}; {{AE}}{{Fs}} | {{WikiDoc CMG}}; {{AE}}{{Fs}}, [[User:MoisesRomo|Moises Romo M.D.]] | ||
{{SK}}Alzheimer's disease ''management, Alzheimer's disease workup, Alzheimer's disease approach, approach to Alzheimer's disease, Alzheimer's disease treatment'' | {{SK}}Alzheimer's disease ''management, Alzheimer's disease workup, Alzheimer's disease approach, approach to Alzheimer's disease, Alzheimer's disease treatment'' | ||
==Overview== | ==Overview== | ||
'''Alzheimer's disease''' is the most common cause of dementia among older people. Dementia is a loss of thinking, remembering, and reasoning skills that interfere with a person's daily life and activities. The diagnosis of Alzheimer's disease (AD) is made on the basis of clinical criteria described by either the National Institute on Aging and the Alzheimer's Association (NIA-AA) or DSM-V (Diagnostic and Statistical Manual of Mental Disorders, fifth edition). There is no known cure for Alzheimer's disease (AD). Available treatments offer relatively small symptomatic benefit but remain palliative in nature. Current treatments can be divided into pharmacological, psychosocial, and caregiving. | '''[[Alzheimer's disease]]''' is the most common cause of dementia among older people. [[Dementia]] is a loss of thinking, remembering, and [[reasoning]] skills that interfere with a person's daily life and activities. The [[diagnosis]] of [[Alzheimer's disease|Alzheimer's disease (AD)]] is made on the basis of [[clinical]] criteria described by either the National Institute on Aging and the Alzheimer's Association (NIA-AA) or DSM-V (Diagnostic and Statistical Manual of [[Mental Disorders]], fifth edition). There is no known cure for [[Alzheimer's disease|Alzheimer's disease (AD)]]. Available [[treatments]] offer relatively small [[symptomatic]] benefit but remain [[Palliative care|palliative]] in nature. Current [[treatments]] can be divided into [[pharmacological]], [[psychosocial]], and [[Caregiving and dementia|caregiving]]. | ||
==Causes== | ==Causes== | ||
===Life Threatening Causes=== | ===Life Threatening Causes=== | ||
Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated. | Life-threatening causes include conditions that may result in death or permanent [[disability]] within 24 hours if left untreated. | ||
*Alzheimer's disease is not a life-threatening condition that may result in death or permanent disability within 24 hours if left untreated. | *Alzheimer's disease is not a life-threatening condition that may result in death or permanent [[disability]] within 24 hours if left untreated. | ||
===Common Causes=== | ===Common Causes=== | ||
While there is no direct cause for the development of Alzheimer's disease, there are several factors that may contribute to its acquisition: | While there is no direct cause for the [[development]] of [[Alzheimer's disease]], there are several [[Risk factors|factors]] that may contribute to its acquisition: | ||
*Chromosomal | *[[Chromosomal]] | ||
**'''Down syndrome''' | **'''Down syndrome''' | ||
***Trisomy 21 | ***[[Trisomy 21]] | ||
***Overexpression of amyloid precursor protein (APP) on chromosome 21 | ***[[Overexpression]] of [[Amyloid precursor protein|amyloid precursor protein (APP)]] on [[chromosome 21]] | ||
***Develop the neuropathologic hallmarks of AD after age 40 years | ***Develop the neuropathologic hallmarks of [[Alzheimer's disease|AD]] after age 40 years | ||
*Familial | *[[Familial]] | ||
**'''Late-onset familial (AD2)''' | **'''Late-onset familial (AD2)''' | ||
***APOE gene: | ***[[APOE]] gene: | ||
***TREM2 gene: | ***[[TREM2]] gene: | ||
***PLD3 gene | ***[[PLD3]] gene | ||
***UNC5C gene | ***[[UNC5C]] gene | ||
***AKAP9 gene (in African-Americans only) | ***[[AKAP9]] gene (in African-Americans only) | ||
**'''Early-onset familial AD (AD1, AD3, AD4)''' | **'''Early-onset familial AD (AD1, AD3, AD4)''' | ||
***PSEN1 gene: | ***[[PSEN1]] gene: | ||
***PSEN2 gene: | ***[[PSEN2]] gene: | ||
***APP gene: | ***[[APPI|APP]] gene: | ||
*Unknown (includes genetic/environment interactions) | *Unknown (includes genetic/environment interactions) | ||
**'''Multifactorial''' | **'''Multifactorial''' | ||
***Aging | ***[[Aging]] | ||
***Genetic predisposition | ***[[Genetic]] predisposition | ||
***Exposure to one or more environmental agents including head trauma, low education | ***Exposure to one or more environmental agents including [[head trauma]], low level of education, [[viruses]], and/or [[toxins]] | ||
==Diagnosis== | ==Diagnosis== | ||
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{{familytree/end}} | {{familytree/end}} | ||
== Treatment == | ==Treatment== | ||
Shown below is an [[algorithm]] summarizing the | Shown below is an [[algorithm]] summarizing the [[treatment]] of [[Alzheimer's disease]] according to the the American Academy of Neurology guidelines:<ref name="GrossbergTong2019">{{cite journal|last1=Grossberg|first1=George T.|last2=Tong|first2=Gary|last3=Burke|first3=Anna D.|last4=Tariot|first4=Pierre N.|last5=Fink|first5=Anne|title=Present Algorithms and Future Treatments for Alzheimer’s Disease|journal=Journal of Alzheimer's Disease|volume=67|issue=4|year=2019|pages=1157–1171|issn=13872877|doi=10.3233/JAD-180903}}</ref><br /> | ||
<br> | <br> | ||
{{Family tree/start}} | {{Family tree/start}} | ||
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*Perform [https://www.wikidoc.org/index.php/Laboratory laboratory testing] to exclude potentially reversible causes of [https://www.wikidoc.org/index.php/Amnesia amnesia]. Initial tests should include a [https://www.wikidoc.org/index.php/CBC CBC], [https://www.wikidoc.org/index.php/Toxicology_screen urine toxicology], [https://www.wikidoc.org/index.php/Thyroid_function_tests thyroid function], [https://www.wikidoc.org/index.php/Folate_deficiency folate], and [https://www.wikidoc.org/index.php/Vitamin_B12 vitamin B12] level. | *Perform [https://www.wikidoc.org/index.php/Laboratory laboratory testing] to exclude potentially reversible causes of [https://www.wikidoc.org/index.php/Amnesia amnesia]. Initial tests should include a [https://www.wikidoc.org/index.php/CBC CBC], [https://www.wikidoc.org/index.php/Toxicology_screen urine toxicology], [https://www.wikidoc.org/index.php/Thyroid_function_tests thyroid function], [https://www.wikidoc.org/index.php/Folate_deficiency folate], and [https://www.wikidoc.org/index.php/Vitamin_B12 vitamin B12] level. | ||
*When pereforming cognitive assesment, use tests such as [https://www.wikidoc.org/index.php/MMSE MMSE], Mini-cog, [https://www.wikidoc.org/index.php/MoCA MoCA], SIB-8, and AD8.<ref name="pmid1202204">{{cite journal |vauthors=Folstein MF, Folstein SE, McHugh PR |title="Mini-mental state". A practical method for grading the cognitive state of patients for the clinician |journal=J Psychiatr Res |volume=12 |issue=3 |pages=189–98 |date=November 1975 |pmid=1202204 |doi=10.1016/0022-3956(75)90026-6 |url=}}</ref><ref name="pmid14511167">{{cite journal |vauthors=Borson S, Scanlan JM, Chen P, Ganguli M |title=The Mini-Cog as a screen for dementia: validation in a population-based sample |journal=J Am Geriatr Soc |volume=51 |issue=10 |pages=1451–4 |date=October 2003 |pmid=14511167 |doi=10.1046/j.1532-5415.2003.51465.x |url=}}</ref><ref name="pmid15817019">{{cite journal |vauthors=Nasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I, Cummings JL, Chertkow H |title=The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment |journal=J Am Geriatr Soc |volume=53 |issue=4 |pages=695–9 |date=April 2005 |pmid=15817019 |doi=10.1111/j.1532-5415.2005.53221.x |url=}}</ref><ref name="pmid19571727">{{cite journal |vauthors=Schmitt FA, Saxton JA, Xu Y, McRae T, Sun Y, Richardson S, Li H |title=A brief instrument to assess treatment response in the patient with advanced Alzheimer disease |journal=Alzheimer Dis Assoc Disord |volume=23 |issue=4 |pages=377–83 |date=2009 |pmid=19571727 |doi=10.1097/WAD.0b013e3181ac9cc1 |url=}}</ref> | *When pereforming [[cognitive]] assesment, use tests such as [https://www.wikidoc.org/index.php/MMSE MMSE], Mini-cog, [https://www.wikidoc.org/index.php/MoCA MoCA], SIB-8, and AD8.<ref name="pmid1202204">{{cite journal |vauthors=Folstein MF, Folstein SE, McHugh PR |title="Mini-mental state". A practical method for grading the cognitive state of patients for the clinician |journal=J Psychiatr Res |volume=12 |issue=3 |pages=189–98 |date=November 1975 |pmid=1202204 |doi=10.1016/0022-3956(75)90026-6 |url=}}</ref><ref name="pmid14511167">{{cite journal |vauthors=Borson S, Scanlan JM, Chen P, Ganguli M |title=The Mini-Cog as a screen for dementia: validation in a population-based sample |journal=J Am Geriatr Soc |volume=51 |issue=10 |pages=1451–4 |date=October 2003 |pmid=14511167 |doi=10.1046/j.1532-5415.2003.51465.x |url=}}</ref><ref name="pmid15817019">{{cite journal |vauthors=Nasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I, Cummings JL, Chertkow H |title=The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment |journal=J Am Geriatr Soc |volume=53 |issue=4 |pages=695–9 |date=April 2005 |pmid=15817019 |doi=10.1111/j.1532-5415.2005.53221.x |url=}}</ref><ref name="pmid19571727">{{cite journal |vauthors=Schmitt FA, Saxton JA, Xu Y, McRae T, Sun Y, Richardson S, Li H |title=A brief instrument to assess treatment response in the patient with advanced Alzheimer disease |journal=Alzheimer Dis Assoc Disord |volume=23 |issue=4 |pages=377–83 |date=2009 |pmid=19571727 |doi=10.1097/WAD.0b013e3181ac9cc1 |url=}}</ref> | ||
*When determining level of independence and level of disability, use test such as ADCS–ADL.<ref name="pmid195717272">{{cite journal |vauthors=Schmitt FA, Saxton JA, Xu Y, McRae T, Sun Y, Richardson S, Li H |title=A brief instrument to assess treatment response in the patient with advanced Alzheimer disease |journal=Alzheimer Dis Assoc Disord |volume=23 |issue=4 |pages=377–83 |date=2009 |pmid=19571727 |doi=10.1097/WAD.0b013e3181ac9cc1 |url=}}</ref> | *When determining level of independence and level of [[disability]], use test such as ADCS–ADL.<ref name="pmid195717272">{{cite journal |vauthors=Schmitt FA, Saxton JA, Xu Y, McRae T, Sun Y, Richardson S, Li H |title=A brief instrument to assess treatment response in the patient with advanced Alzheimer disease |journal=Alzheimer Dis Assoc Disord |volume=23 |issue=4 |pages=377–83 |date=2009 |pmid=19571727 |doi=10.1097/WAD.0b013e3181ac9cc1 |url=}}</ref> | ||
*When determining the level of [https://www.wikidoc.org/index.php/Behavioral behavioral] [https://www.wikidoc.org/index.php/Symptoms symptoms], use the NPI-Q test.<ref name="pmid11001602">{{cite journal |vauthors=Kaufer DI, Cummings JL, Ketchel P, Smith V, MacMillan A, Shelley T, Lopez OL, DeKosky ST |title=Validation of the NPI-Q, a brief clinical form of the Neuropsychiatric Inventory |journal=J Neuropsychiatry Clin Neurosci |volume=12 |issue=2 |pages=233–9 |date=2000 |pmid=11001602 |doi=10.1176/jnp.12.2.233 |url=}}</ref> | *When determining the level of [https://www.wikidoc.org/index.php/Behavioral behavioral] [https://www.wikidoc.org/index.php/Symptoms symptoms], use the NPI-Q test.<ref name="pmid11001602">{{cite journal |vauthors=Kaufer DI, Cummings JL, Ketchel P, Smith V, MacMillan A, Shelley T, Lopez OL, DeKosky ST |title=Validation of the NPI-Q, a brief clinical form of the Neuropsychiatric Inventory |journal=J Neuropsychiatry Clin Neurosci |volume=12 |issue=2 |pages=233–9 |date=2000 |pmid=11001602 |doi=10.1176/jnp.12.2.233 |url=}}</ref> | ||
*Identify primary caregiver and assess his health, as well as adequacy of family and other support systems.<ref name="pmid25815358">{{cite journal |vauthors=Cummings JL, Isaacson RS, Schmitt FA, Velting DM |title=A practical algorithm for managing Alzheimer's disease: what, when, and why? |journal=Ann Clin Transl Neurol |volume=2 |issue=3 |pages=307–23 |date=March 2015 |pmid=25815358 |doi=10.1002/acn3.166 |url=}}</ref> | *Identify primary caregiver and assess his health, as well as adequacy of family and other support systems.<ref name="pmid25815358">{{cite journal |vauthors=Cummings JL, Isaacson RS, Schmitt FA, Velting DM |title=A practical algorithm for managing Alzheimer's disease: what, when, and why? |journal=Ann Clin Transl Neurol |volume=2 |issue=3 |pages=307–23 |date=March 2015 |pmid=25815358 |doi=10.1002/acn3.166 |url=}}</ref> |
Revision as of 06:13, 16 January 2021
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D., Moises Romo M.D.
Synonyms and keywords:Alzheimer's disease management, Alzheimer's disease workup, Alzheimer's disease approach, approach to Alzheimer's disease, Alzheimer's disease treatment
Overview
Alzheimer's disease is the most common cause of dementia among older people. Dementia is a loss of thinking, remembering, and reasoning skills that interfere with a person's daily life and activities. The diagnosis of Alzheimer's disease (AD) is made on the basis of clinical criteria described by either the National Institute on Aging and the Alzheimer's Association (NIA-AA) or DSM-V (Diagnostic and Statistical Manual of Mental Disorders, fifth edition). There is no known cure for Alzheimer's disease (AD). Available treatments offer relatively small symptomatic benefit but remain palliative in nature. Current treatments can be divided into pharmacological, psychosocial, and caregiving.
Causes
Life Threatening Causes
Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated.
- Alzheimer's disease is not a life-threatening condition that may result in death or permanent disability within 24 hours if left untreated.
Common Causes
While there is no direct cause for the development of Alzheimer's disease, there are several factors that may contribute to its acquisition:
- Chromosomal
- Down syndrome
- Trisomy 21
- Overexpression of amyloid precursor protein (APP) on chromosome 21
- Develop the neuropathologic hallmarks of AD after age 40 years
- Down syndrome
- Familial
- Unknown (includes genetic/environment interactions)
- Multifactorial
- Aging
- Genetic predisposition
- Exposure to one or more environmental agents including head trauma, low level of education, viruses, and/or toxins
- Multifactorial
Diagnosis
Shown below is an algorithm summarizing the diagnosis of amnesia according to the the American Academy of Neurology guidelines:[1]
Treatment
Shown below is an algorithm summarizing the treatment of Alzheimer's disease according to the the American Academy of Neurology guidelines:[2]
Patient with diagnosed Alzheimer's disease | |||||||||||||||||||||||||||||||||||||||||
Mild to moderate | Moderate to severe | ||||||||||||||||||||||||||||||||||||||||
Initiate therapy •Donepezil. 5 mg once daily; titrate 10 mg once daily •Galantamine (solution). 4 mg twice daily; titrate to 8 mg twice daily •Galantamine (ER capsules). 8 mg once daily; titrate to 16 mg once daily •Rivastigmine (patch). 4.6 mg once daily; titrate to 9.5 mg once daily •Rivastigmine (oral). 1.5 mg twice daily; titrate to 6 mg twice daily | |||||||||||||||||||||||||||||||||||||||||
Adverse event Considere switch to a different ChEI | Disease progression Considere high dose or switch to a different ChEI | Initiate therapy •Donepezil. 5 mg once daily; titrate 10 mg once daily •Rivastigmine (patch). 4.6 mg once daily; titrate to 9.5 mg once daily •Memantine. 5 mg once daily; titrate to 10 mg twice daily or Memantine XR. 7 mg once daily; titrate to 28 mg once daily •Combination ChEI+ Memantine. 7 mg twice daily or 10 mg once daily (ER); titrate to 10 mg twice daily or 28 mg once daily (ER) | |||||||||||||||||||||||||||||||||||||||
Monitor and reevaluate therapy Monitor every 3-4 months and titrate dose as needed | |||||||||||||||||||||||||||||||||||||||||
Adverse event Considere switch to a different therapy | Disease progression Considere higher dose or switch to a different therapy | ||||||||||||||||||||||||||||||||||||||||
Discontinue therapy When all cognitive function and functional abilities are lost at terminal stages of AD | |||||||||||||||||||||||||||||||||||||||||
Recommendations for maintaining brain health in elderly patients with and without Alzheimer's Disease |
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Do's
- Perform laboratory testing to exclude potentially reversible causes of amnesia. Initial tests should include a CBC, urine toxicology, thyroid function, folate, and vitamin B12 level.
- When pereforming cognitive assesment, use tests such as MMSE, Mini-cog, MoCA, SIB-8, and AD8.[3][4][5][6]
- When determining level of independence and level of disability, use test such as ADCS–ADL.[7]
- When determining the level of behavioral symptoms, use the NPI-Q test.[8]
- Identify primary caregiver and assess his health, as well as adequacy of family and other support systems.[9]
- Neuroimaging may diagnose vascular disease, normal pressure hydrocephalus, tumors, abscess.[10]
- Perform a minimental status test on physical examination and pay especial attention in concentration domain. Minimental testing has the potential distinguish mild cognitive impairment from dementia.[11]
- Always have in mind depression as a possible cause of memory impairmant. Depression is common cause of amnesia; a SIGE CAPS evaluation may disclose an underlying mood disorder.[12].
Don'ts
- If alcoholism and thiamine deficiency is suspected, do not administer glucose before thiamine. Administration of glucose before thiamine may lead to Wernicke encephalopathy.[13]
References
- ↑ Jahn H (December 2013). "Memory loss in Alzheimer's disease". Dialogues Clin Neurosci. 15 (4): 445–54. PMC 3898682. PMID 24459411.
- ↑ Grossberg, George T.; Tong, Gary; Burke, Anna D.; Tariot, Pierre N.; Fink, Anne (2019). "Present Algorithms and Future Treatments for Alzheimer's Disease". Journal of Alzheimer's Disease. 67 (4): 1157–1171. doi:10.3233/JAD-180903. ISSN 1387-2877.
- ↑ Folstein MF, Folstein SE, McHugh PR (November 1975). ""Mini-mental state". A practical method for grading the cognitive state of patients for the clinician". J Psychiatr Res. 12 (3): 189–98. doi:10.1016/0022-3956(75)90026-6. PMID 1202204.
- ↑ Borson S, Scanlan JM, Chen P, Ganguli M (October 2003). "The Mini-Cog as a screen for dementia: validation in a population-based sample". J Am Geriatr Soc. 51 (10): 1451–4. doi:10.1046/j.1532-5415.2003.51465.x. PMID 14511167.
- ↑ Nasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I, Cummings JL, Chertkow H (April 2005). "The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment". J Am Geriatr Soc. 53 (4): 695–9. doi:10.1111/j.1532-5415.2005.53221.x. PMID 15817019.
- ↑ Schmitt FA, Saxton JA, Xu Y, McRae T, Sun Y, Richardson S, Li H (2009). "A brief instrument to assess treatment response in the patient with advanced Alzheimer disease". Alzheimer Dis Assoc Disord. 23 (4): 377–83. doi:10.1097/WAD.0b013e3181ac9cc1. PMID 19571727.
- ↑ Schmitt FA, Saxton JA, Xu Y, McRae T, Sun Y, Richardson S, Li H (2009). "A brief instrument to assess treatment response in the patient with advanced Alzheimer disease". Alzheimer Dis Assoc Disord. 23 (4): 377–83. doi:10.1097/WAD.0b013e3181ac9cc1. PMID 19571727.
- ↑ Kaufer DI, Cummings JL, Ketchel P, Smith V, MacMillan A, Shelley T, Lopez OL, DeKosky ST (2000). "Validation of the NPI-Q, a brief clinical form of the Neuropsychiatric Inventory". J Neuropsychiatry Clin Neurosci. 12 (2): 233–9. doi:10.1176/jnp.12.2.233. PMID 11001602.
- ↑ Cummings JL, Isaacson RS, Schmitt FA, Velting DM (March 2015). "A practical algorithm for managing Alzheimer's disease: what, when, and why?". Ann Clin Transl Neurol. 2 (3): 307–23. doi:10.1002/acn3.166. PMID 25815358.
- ↑ Knopman DS, DeKosky ST, Cummings JL, Chui H, Corey-Bloom J, Relkin N, Small GW, Miller B, Stevens JC (May 2001). "Practice parameter: diagnosis of dementia (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology". Neurology. 56 (9): 1143–53. doi:10.1212/wnl.56.9.1143. PMID 11342678.
- ↑ Petersen RC, Stevens JC, Ganguli M, Tangalos EG, Cummings JL, DeKosky ST (May 2001). "Practice parameter: early detection of dementia: mild cognitive impairment (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology". Neurology. 56 (9): 1133–42. doi:10.1212/wnl.56.9.1133. PMID 11342677.
- ↑ Squire LR, Zouzounis JA (December 1988). "Self-ratings of memory dysfunction: different findings in depression and amnesia". J Clin Exp Neuropsychol. 10 (6): 727–38. doi:10.1080/01688638808402810. PMID 3235647.
- ↑ Hack, Jason B.; Hoffman, Robert S. (1998). "Thiamine Before Glucose to Prevent Wernicke Encephalopathy: Examining the Conventional Wisdom". JAMA. 279 (8): 583. doi:10.1001/jama.279.8.583a. ISSN 0098-7484.