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case study

Patient Background: A 68-year-old married man with vocational education, living in a city, experienced his first ischemic stroke. Six months later, he was diagnosed with moderate mixed aphasia. This condition often lowers quality of life across physical, psychological, and environmental domains.

Family History: No specific hereditary link to stroke or aphasia was reported. However, his marital status aligns with evidence that family support can aid stroke recovery and improve well-being.

Assessment and Diagnosis: Stroke was diagnosed via brain imaging (CT/MRI). A speech-language pathologist confirmed moderate mixed aphasia using the SODA scale and Jadwiga Szumska’s Aphasia Test Method.

Suggested Treatment Plan: A multidisciplinary plan, including individualized speech-language therapy, is essential. Interventions tailored to his needs aim to improve communication and overall functioning in moderate aphasia.

Patient education: Aphasia impairs communication, reading, writing, and numeracy. Patients and caregivers were educated on consistent therapy, coping strategies, and the importance of social interaction in recovery.

Follow-up: The WHOQOL-BREF tool at six months post-discharge helped monitor progress. Ongoing reassessment remains vital to adjust therapy and enhance outcomes.

  1. How can interdisciplinary teams support recovery in moderate aphasia post-stroke? Answer Team-based care with early speech therapy, counseling, occupational therapy, and social work improves communication and quality of life.
  2. Why is early, tailored speech therapy key for moderate mixed aphasia? Answer Early diagnosis and individualized SODA-guided therapy improve function and help maintain quality of life.
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case study

Patient Background: Mrs. Green, a 72-year-old woman, presented to her GP with concerns about progressive memory decline. She was undergoing evaluation as part of routine cognitive screening for older adults.

Assessment and Diagnosis: Initial clinical evaluation through physical and cognitive assessments in primary care has shown only 61% diagnostic accuracy for Alzheimer’s disease. A blood test (PrecivityAD2) measuring p-tau217 was used, predicting Alzheimer’s with 88–92% accuracy. CSF and PET scans, while highly accurate, are less accessible in primary care.

Suggested Treatment Plan: Following a positive test result, FDA-approved anti-amyloid therapy was initiated to help slow disease progression.

  1. How could blood-based biomarker tests reshape Alzheimer’s diagnosis in primary care? Answer Blood-based biomarkers enhance early detection, reduce reliance on specialty imaging, and improve access to timely treatment.
  2. Beyond being less invasive, what role does the Lumipulse plasma ratio test play in Alzheimer’s diagnosis? Answer It helps identify amyloid plaques in adults 55+ with cognitive symptoms, aiding diagnosis in specialized care. Not for screening—results must be interpreted with clinical findings.
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Measuring efficacy for myasthenia gravis treatments: A review of biomarkers used in clinical trials - PubMed

Measuring efficacy for myasthenia gravis treatments: A review of biomarkers used in clinical trials - PubMed

Source : https://pubmed.ncbi.nlm.nih.gov/40639531/

Myasthenia gravis is an autoimmune disease that impairs neuromuscular transmission through autoantibodies, most commonly targeting acetylcholine receptors (AChR). While clinical scores like the Quantitative Myasthenia Gravis Score (QMGS) and the...

This review analyzes biomarker use in gMG clinical trials, revealing inconsistent measurement practices and lack of standardization. It urges consensus guidelines to improve efficacy assessments and future trial comparability.

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The 2025 APA Resource Document explores catatonia’s history, prevalence, diagnostics, differential diagnoses, and treatment—including benzodiazepines and ECT. It also addresses special populations like pediatrics, pregnancy, dementia, and outlines ethical/legal concerns.

Review APA’s latest guidance on catatonia