Ghiduri actuale pentru monitorizarea progresiei bolii1
General
Complete history and physical examination including family history and evaluation of quality of life, gastrointestinal symptoms, work/study performance, level of depression/anxiety
Every clinic visit
α-Gal A enzyme activity and GLA mutation analysis.
If not previously determined
Renal
Renal Glomerular filtration rate (measured GFR [preferred] or estimated [eGFR] using appropriate formulae)
Annually if low risk, every 6 months if moderate risk, and every 3 months if high to very high risk; a measured GFR only once yearly because of complexity
Albuminuria (preferred, more sensitive) and/or proteinuria (24-h or spot urine for total protein/creatinine and albumin/creatinine ratios)
Annually if low risk, every 6 months if moderate risk, and every 3 months if high to very high risk
25 OH vitamin D
As clinically indicated; vitamin D levels in late fall/early winter
Kidney biopsy
As clinically indicated. Podocyte foot process effacement may precede pathological albuminuria
Cardiac
Blood pressure and cardiac rhythm
Every clinic visit
ECG and echocardiography
Annually, and as clinically indicated
48-h Holter monitoring to detect intermittent rhythm abnormalities; implantable loop recorder recommended for patients with significant hypertrophic cardiomyopathy
Annually, but may be assessed more or less frequently depending on age and other risk factors; if arrhythmias detected, more frequent/detailed rhythm surveillance should be instituted (schedule determined individually)
Cardiac MRI with gadolinium
If available, whenever there is evidence of clinical progression of disease or regularly at an interval > 2 years
Cardiac MRI with T1 mapping
Investigational tool, should be interpreted with caution
Cerebrovascular
Brain natriuretic peptide
At least annually for patients with cardiomyopathy or bradycardia
Brain MRI (TOF MRA at first assessment in male patients aged over 21 and female patients over 30, then according to the clinical picture)
Every 3 years and when clinically needed (e.g., presence of neurological changes that could potentially relate to stroke)
CT imaging
In case of acute stroke and only if MRI is contraindicated due to cardiac pacing
Peripheral nervous system
Pain evaluation and history: pain measurement scale such as the Neuropathic Pain Symptom Inventory or Brief Pain Inventory
Annually
Cold and heat intolerance, vibratory thresholds (quantitative sensory testing, if available)
Annually (less frequently in older patients)
Autonomic symptom evaluation by orthostatic blood pressure
Annually
Skin biopsy (for IENFD assessment, if available)
Consider
ENT
Audiometry [17]
As required [17]
Pulmonary
Spirometry, including response to bronchodilators, treadmill exercise testing, oximetry, chest X-ray
Every 2 years or more frequently for clinical indications; chest X-ray according to clinical indications
Gastrointestinal
Referral to gastroenterology specialist for endoscopic or radiographic evaluation
If symptoms persist or worsen despite treatment
Overall glycolipid burden
Plasma and urinary sediment lyso-GL-3, GL-3
At baseline and then annually (at the moment, this is for research purposes only); biobanking of plasma/serum samples recommended if feasible
Skeletal
Bone dual-energy X-ray absorptiometry (DEXA)
Consider
Ophthalmological
Ophthalmological screening
Ophthalmological screening as clinically indicated
Complete history and physical examination including family history and evaluation of quality of life, gastrointestinal symptoms, work/study performance, level of depression/anxiety
Every clinic visit
α-Gal A enzyme activity and GLA mutation analysis.
If not previously determined
Renal Glomerular filtration rate (measured GFR [preferred] or estimated [eGFR] using appropriate formulae)
Annually if low risk, every 6 months if moderate risk, and every 3 months if high to very high risk; a measured GFR only once yearly because of complexity
Albuminuria (preferred, more sensitive) and/or proteinuria (24-h or spot urine for total protein/creatinine and albumin/creatinine ratios)
Annually if low risk, every 6 months if moderate risk, and every 3 months if high to very high risk
25 OH vitamin D
As clinically indicated; vitamin D levels in late fall/early winter
Kidney biopsy
As clinically indicated. Podocyte foot process effacement may precede pathological albuminuria
Blood pressure and cardiac rhythm
Every clinic visit
ECG and echocardiography
Annually, and as clinically indicated
48-h Holter monitoring to detect intermittent rhythm abnormalities; implantable loop recorder recommended for patients with significant hypertrophic cardiomyopathy
Annually, but may be assessed more or less frequently depending on age and other risk factors; if arrhythmias detected, more frequent/detailed rhythm surveillance should be instituted (schedule determined individually)
Cardiac MRI with gadolinium
If available, whenever there is evidence of clinical progression of disease or regularly at an interval > 2 years
Cardiac MRI with T1 mapping
Investigational tool, should be interpreted with caution
Brain natriuretic peptide
At least annually for patients with cardiomyopathy or bradycardia
Brain MRI (TOF MRA at first assessment in male patients aged over 21 and female patients over 30, then according to the clinical picture)
Every 3 years and when clinically needed (e.g., presence of neurological changes that could potentially relate to stroke)
CT imaging
In case of acute stroke and only if MRI is contraindicated due to cardiac pacing
Pain evaluation and history: pain measurement scale such as the Neuropathic Pain Symptom Inventory or Brief Pain Inventory
Annually
Cold and heat intolerance, vibratory thresholds (quantitative sensory testing, if available)
Annually (less frequently in older patients)
Autonomic symptom evaluation by orthostatic blood pressure
Annually
Skin biopsy (for IENFD assessment, if available)
Consider
Audiometry [17]
As required [17]
Spirometry, including response to bronchodilators, treadmill exercise testing, oximetry, chest X-ray
Every 2 years or more frequently for clinical indications; chest X-ray according to clinical indications
Referral to gastroenterology specialist for endoscopic or radiographic evaluation
If symptoms persist or worsen despite treatment
Plasma and urinary sediment lyso-GL-3, GL-3
At baseline and then annually (at the moment, this is for research purposes only); biobanking of plasma/serum samples recommended if feasible
Bone dual-energy X-ray absorptiometry (DEXA)
Consider
Ophthalmological screening
Ophthalmological screening as clinically indicated
Baseline values should always be obtained; longer intervals between more complex organ assessments can be considered in asymptomatic female patients with a normal initial evaluation and/or favorable X chromosome inactivation pattern. CKD, chronic kidney disease; CT, computed tomography; ECG, electrocardiography; eGFR, estimated glomerular filtration rate; ENT, ear, nose, and throat; GFR, glomerular filtration rate; IENFD, intra-epidermal nerve fiber density; MRI, magnetic resonance imaging; TOF MRA, time-of-flight magnetic resonance angiography (head and neck).
A risk levels based on KDIGO 2012 chronic kidney disease classification scheme. Low risk, CKD Stage G1/2 A1; moderate risk, CKD stage G3a A1, G1/2 A2; high to very high risk CKD
Stage G4 or 5, G3b A1, G3 A3.
Această listă conține o selecție de publicații recente despre boala Fabry, nu o listă exhaustivă.
Molecular Genetics and Metabolism. 2023;139(2):107585.
Nephrology Dialysis Transplantation. 2023:gfad164.
Molecular Genetics and Metabolism. 2022;137(1-2):49-61.
Clinical genetics. 2019;96(2):107-117.
Molecular genetics and metabolism. 2018;124(3):189-203.
Molecular Genetics and Metabolism. 2021;132(4):234-243.
Dacă aveți mai multe întrebări sau doriți să solicitați mai multe informații, vă rugăm să nu ezitați să ne contactați la ro.medinfo@chiesi.com
Referințe:
Pentru pacienți - „În cazul în care trebuie să raportați o reacție adversă la medicament, vă rugăm să vă adresați medicului dumneavoastră, solicitându-i să completeze și să transmită raportul de caz relevant autorității sanitare în cauză, în conformitate cu cerințele de farmacovigilență în vigoare în țara dumneavoastră. Cu toate acestea, vă reamintim că fiecare pacient poate raporta orice astfel de cazuri direct în sistemul național de raportare.
Pentru profesioniștii din domeniul sănătății: „în cazul în care doriți să raportați o reacție adversă la medicament de care aveți cunoștință, vă rugăm să o raportați autorității sanitare în conformitate cu cerințele stabilite de legislația referitoare la farmacovigilență” https://www.anm.ro/medicamente-de-uz-uman/farmacovigilenta/raporteaza-o-reactie-adversa/
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