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Duodenal Levodopa Treatment in advanced Parkinson’s Disease

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Presentation on theme: "Duodenal Levodopa Treatment in advanced Parkinson’s Disease"— Presentation transcript:

1 Duodenal Levodopa Treatment in advanced Parkinson’s Disease
Baciu Diana, MG, VI Scientific Advisor: Lecturer: Dr. Szász József-Attila UMF Târgu Mureș, Neurology II, Târgu Mureș Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

2 Parkinson’s Syndrome:
Hypo-kinetic hypertonic, extrapyramidal motor syndrome Progressive, neurodegenerative disease Heterogenous etiology Rather affects middle-age people The onset-age plays an important role in further evolution of the disease Parkinson’s Syndrome: Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

3 Pathophysiology: Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

4 Pathophysiology: Two major pathological mechanism:
Loss of pigmented dopamine neurons The presence of Lewy bodies and Lewy neurites Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

5 Clinical Presentation:
Classic Symptoms Rest Tremor Bradykinesia/Hypokinesia/Akinesia Stiff Rigidity Early Symptoms Tremor at rest Muscle rigidity Stooped posture Expressionless face Slow movement Poor balance and coordination Advanced Symptoms Complications of L-Dopa therapy -Motor fluctuations -Dyskinesia and Dystonia Depression Dementia Psychosis Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

6 Parkinson’s Disease: Diagnostic
I. Clinical: Hoehn and Yahr Staging Scale: motor symptoms quantification Schwab and England activities of daily living (ADL)-scale Unified Parkinson´s Disease Rating Scale (MDS-UPDRS) : Therapy monitoring I: non-motor experiences of daily living II: motor experiences of daily living III: motor examination IV: motor complications Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

7 Parkinson’s Disease: Diagnostic
II. Imaging: SPECT/PET CT/MRI for Diff. Dg. Transcranial Doppler- Sonography Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

8 Motor Fluctuations incidence increase with use of Levodopa
Treatment: Mild/Youg PD Patient Levodopa-Low Dose: MAOB Inhibitor/Dopamine Agonist ModeratePD.Pat. Monotherapy: Higher Doses of L-Dopa Combination: L-Dopa+ Dopa-Agonists/I-MAOB Severe/Od PD Pat. Duodopa: L-Dopa/Carbidopa intestinal delivery Deep Brain Stimulation Monotherapy >5 years of L-Dopa: 50% P.D.Pat-MF Motor Fluctuations incidence increase with use of Levodopa Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

9 Complications of treatment with L-DOPA
Chorea, Benign Hereditary; Chorea, Chronic Progressive; Chorea, Rheumatic; Chorea, Senile; Chorea, Sydenham; Dyskinesias, Paroxysmal; Neuroacanthocytosis; Paroxysmal Dyskinesias; Senile Chorea; Sydenham Chorea) Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

10 Motor Fluctuations: Hypokinetic symptoms: “wearing off ”
end of dose akinesia “sudden off” “delayed on” “no on” “early morning akinesia” “peak-dose akinesia” “on-off” “freezing” Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

11 Aim of the Study Material and Methods
The follow-up of the patients who suffer motor fluctuations , with advanced Parkinson’s disease Which person requires treatment with intestinal gel Patients monitoring before and after Duodopa-medication Comparing performance of motor fluctuations Material and Methods The therapeutic method with intestinal gel Levodopa/Carbidopa has been firstly used in the Neurology Clinic II Tg. Mures in June 2011 Until December 2013 , 21 patients with advanced P.D and hypokinetic motor fluctuations were assesed with Duodopa-treatment Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

12 Results I. Distribution according to risc factors
Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

13 Results I. Distribution according to risc factors
Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

14 Results II. Distribution on motor fluctuations
Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

15 Results III. Patient distribution of oral medications
Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

16 Treatment with Duodopa: Intestinal Gel
Ideal Patient Advanced P.D with max. therapeutic dose Onset Dose Good response, without adverse effects: individualized doses Tester Test Period: Duodopa-effect was investigated in hospital Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

17 Results: Treatment with Duodopa
Generally, most of the patients presented a decrease in the number of “off-hours” Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

18 Results IV. Clinical Quantification of motor fluctuations
Daily activities of patients and motor symptoms were measured using international scales Hoehn-Yahr Scale Before and UPDRS II+III After Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

19 Results: Clinical Quantification of motor fluctuations:
UPDRS II (Daily Activity): The amount of the grade scale for measuring daily activity before treatment was compared with the one after treatment. Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

20 Results: Clinical Quantification of motor fluctuations:
UPDRS III (Motor System):The total amount of the grade scale for measuring motor performance during “ON” before treatment was compared with the one after treatment Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

21 Conclusions: Main causes in the occurrence of M.F are:
Progressive degeneration of dopamine terminals Short Half-Life of L-Dopa, which produces a discontinous dopamine stimulation Gastric inactivation of L-Dopa or low absorbtion Duodopa – Intestinal Gel Administration can solve this issues - maintaining a constant level of dopamine in the blood Objectively, all 21 patients experienced a significant reduction in the fluctuations, while achieving a better gait function Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion

22 Thank you for your attention!
Introduction-Pathophysiology-Diagnostic-Treatment-Material and Methods-Results-Conclusion


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