scholarly journals SUN-353 Physical and Cognitive Functioning Before and Six Months After Initiating Enzyme Replacement Therapy for an Adult with Hypophosphatasia: A Case Study

2020 ◽  
Vol 4 (Supplement_1) ◽  
Author(s):  
Kathryn Dahir ◽  
Christina Durrough ◽  
Margaret Hudson ◽  
Michael de Riesthal ◽  
Jiun-Ruey Hu ◽  
...  

Abstract We present changes on physical therapy (PT), occupational therapy (OT), and speech-language pathology (SLP) assessments for a patient pre- and 6 months post-initiation of recombinant alkaline phosphatase therapy for hypophosphatasia (HPP). Our patient is a 30-year-old male diagnosed with pediatric onset HPP at the age of 28. Features of his HPP include skull deformities and scoliosis noted as a toddler, early loss of primary dentition with the root intact prior to the age of 4, severe bone and muscle pain described as “severe growing pain”, and fatigue as a teenager. He was noted to have arthritis in his feet requiring surgical fusion, which was complicated by nonunion. By the age of 30, he required the use of assistive devices for ambulation due to fatigue and pain. Biochemistry was notable for ALP 17U/L (40-150), serum PLP 241 mcg/L (5-50), urine phosphethanolamine 47 nmolmgCr (0-27), and genetic testing demonstrated a variant of undetermined significance of ALPL genet (Het. C.1364G>A p.Gly455Asp). PT and OT assessments included a thorough musculoskeletal and neurologic examination, as well as functional testing of mobility, balance, motor control, and activity of daily living tasks. After 6 months of enzyme replacement therapy (ERT), the patient’s scores on measures of body structure and function were grossly unchanged or diminished (muscle strength). However, activity-based measures of functional performance generally improved on ERT. Performance on the Five Times Sit to Stand Test (FTSTS), gait speed, Functional Gait Assessment, Sensory Organization Test, and Six-Minute Walk Test (6MWT) improved. His most significant improvements were on the FTSTS and 6MWT; his FTSTS improved from 15.4 seconds to 9.1 seconds, surpassing the cut-off for falls risk (12s), while his 6MWT improved from 1,228 feet to 1,541 feet, surpassing the minimal detectable change for individuals with osteoarthritis (201 ft). Cognitive testing revealed improvement in delayed memory (e.g., word-list recognition, story-retell) on the Repeatable Battery of the Assessment of Neuropsychological Status from baseline (7%tile) to 6 months post therapy (47%tile). He also demonstrated improvement in Trail Making Part A [TM A, cognitive processing speed] & TM B (executive functioning) from baseline (45s, 49s) to 6 months post therapy (21s, 38s). Mean performance on TM A&B for adults 25-34 yrs is 24.4s±8.71 and 50.7s±12.4, respectively. Overall, the patient demonstrated improvement in delayed memory, cognitive processing speed and executive functioning on ERT. Additionally, while his performance on bedside impairment-based testing generally declined or remained unchanged, his performance on standardized functional assessments improved on ERT. These functional improvements in physical and cognitive domains likely enable the patient to more fully participate in life roles to improve quality of life.

2017 ◽  
Vol 31 (1) ◽  
pp. 44-51 ◽  
Author(s):  
Spencer W. Liebel ◽  
Erin C. Jones ◽  
Assaf Oshri ◽  
Emily S. Hallowell ◽  
Beth A. Jerskey ◽  
...  

2005 ◽  
Vol 36 (02) ◽  
Author(s):  
M Smitka ◽  
M von der Hagen ◽  
A Kaindl ◽  
C Gilitzer ◽  
J Dumontier ◽  
...  

2019 ◽  
Vol 22 (06) ◽  
pp. 103-117
Author(s):  
Mays Al-Tai ◽  
Deia Al-Asady ◽  
Rula Hamid

2021 ◽  
Vol 132 (2) ◽  
pp. S107-S108
Author(s):  
Nato Vashakmadze ◽  
Leyla Namazova-Baranova ◽  
Natalia Zhurkova ◽  
Olga Gordeeva ◽  
Nina Fedorova ◽  
...  

2021 ◽  
pp. 088307382198915
Author(s):  
Christoph Schwering ◽  
Gertrud Kammler ◽  
Eva Wibbeler ◽  
Martin Christner ◽  
Johannes K.-M. Knobloch ◽  
...  

Intracerebroventricular enzyme replacement therapy (ICV-ERT) for CLN2 disease represents the first approved treatment for neuronal ceroid lipofuscinosis (NCL) diseases. It is the first treatment where a recombinant lysosomal enzyme, cerliponase alfa, is administered into the lateral cerebral ventricles to reach the central nervous system, the organ affected in CLN2 disease. If untreated, CLN2 children show first symptoms such as epilepsy and language developmental delay at 2-4 years followed by rapid loss of motor and language function, vision loss, and early death. Treatment with cerliponase alfa has shown to slow the rapid neurologic decline. However, the mode of administration by 4 hour-long intracerebroventricular infusions every 14 days represents a potentially greater risk of infection compared to intravenous enzyme replacement therapies. The Hamburg NCL Specialty Clinic was the first site worldwide to perform intracerebroventricular enzyme replacement therapy in children with CLN2 disease. In order to ensure maximum patient safety, we analysed data from our center from more than 3000 intracerebroventricular enzyme replacement therapies in 48 patients over 6 years with regard to the occurrence of device-related adverse events and device infections. Since starting intracerebroventricular enzyme replacement therapy, we have also developed and continuously improved the “Hamburg Best Practice Guidelines for ICV–Enzyme Replacement Therapy (ERT) in CLN2 Disease.” Results from this study showed low rates for device-related adverse events and infections with 0.27% and 0.33%, respectively. Therefore, following our internal procedural guidelines has shown to improve standardization and patient safety of intracerebroventricular enzyme replacement therapy for CLN2 disease.


2018 ◽  
Vol 123 (2) ◽  
pp. S124-S125
Author(s):  
Roberto Sandobal Pacheco ◽  
Diana Espinosa Villanueva ◽  
Adriana Alcnatara Salinas ◽  
Jorge A. Romero Ramirez ◽  
Jose Antonio Vasquez Galeana ◽  
...  

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