Neuromodulation in Bonn:
TPS (Neurolith), tDCS & Vagus Nerve Stimulation
Summary: Gentle, non-invasive, outpatient. In my practice, I combine modern neuromodulatory procedures based on the approach of SOZOBRAINCENTER.COM to specifically influence dysregulated networks of the central and peripheral nervous system—with the goal of reducing symptoms and improving everyday function.
Typical indications (selection):
- Parkinson's disease
- Alzheimer’s disease and other dementias
- Amyotrophic lateral sclerosis (ALS)
- Epilepsy
- Depression (unipolar)
- Sleep disorders/insomnia
- Autism spectrum disorder
- Inflammatory bowel disease (IBD; Crohn’s disease, ulcerative colitis)
- Multiple sclerosis (MS)
- Tic disorders (incl. Tourette syndrome)
- (e.g., with central sensitization)
Why neuromodulation?
Neurological and psychiatric conditions are network dysfunctions—not just lesions of single areas. Neuromodulation uses electrical, pulsed-ultrasonic, or vagal stimuli to modulate neuronal excitability, synaptic plasticity (incl. meta-/homeostatic plasticity) and functional connectivity. This can lessen symptoms, open rehabilitation windows, and complement pharmacotherapy.
Our procedures
1) Transcranial Pulse Stimulation (TPS) with Neurolith® (Storz Medical)
Principle: Ultrashort acoustic pulses (pulsed ultrasound, non-thermal) are applied in a navigation-guided manner to cortical target regions. Mechanistic targets:
- neurovascular coupling
- BDNF-mediated plasticity
- network reconnection
Process:
– Precise target planning (history, findings, optionally imaging)
– 6–8 sessions of 30–45 min, typically 2×/week
– Monitoring: clinical assessment and standardized scales
Use cases:
– cognitive impairment/dementia
– Parkinson’s disease (akinesia/freezing, executive functions)
– depression
– chronic pain
– autism
Adverse effects: usually mild (brief head pressure, fatigue). No radiation exposure.
Evidence base: growing yet heterogeneous; biologically plausible, long-term data limited (emerging evidence).
2) Transcranial Direct Current Stimulation (tDCS, if needed HD-tDCS)
Principle: Weak direct currents (typically 1–2 mA) modulate cortical excitability (anodal, cathodal) and metaplasticity.
Process:
– Montage according to target network (e.g., DLPFC for depression, M1/S1 for pain, temporo-parietal for epilepsy/tics)
– 20–30 min per session; home-use devices after instruction; typically 2×/day per protocol
– Synergy with cognitive-motor training (state-dependency) recommended
Use cases:
– depression
– chronic (low back) pain
– epilepsy (add-on)
– Parkinson’s (motor/FoG)
– sleep regulation
– executive functions in autism
Adverse effects: tingling/itching under electrodes, rarely headache; no downtime.
Evidence base: moderate for some indications (depression/pain), exploratory for others. Protocoland outcome-driven.
3) Transcutaneous Vagus Nerve Stimulation (taVNS)
Principle: Activation of vagal afferents modulates LC-noradrenergic and cholinergic anti-inflammatory pathways (the inflammatory reflex).
Process:
– Individual parameterization (frequency, pulse width, duty cycle)
– 15–30 min, 3–7×/week, home protocols after instruction
– Monitoring: symptom scales, HRV, optionally inflammatory markers
Use cases:
– depression/anxiety
– sleep disorders
– IBD
– epilepsy (add-on)
– autonomic imbalance
– pain
Adverse effects: usually mild (skin irritation, tingling, rarely cough/throat irritation). Not with implanted stimulators/pacemakers without prior clearance.
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How we work
1. Medical evaluation (medication, comorbidities, contraindications, goal setting)
2. Network targeting (clinical, optionally EEG/functional measures)
3. Therapy plan (TPS, tDCS/HD-tDCS, taVNS—alone or combined)
4. Objective outcomes (e.g., UPDRS, MoCA, BDI-II, PSQI, HRV, pain NRS)
5. Follow-up & boosters depending on response pattern
Procedures with limited evidence are provided as individual therapeutic trials. No promise of cure. Benefits/risks are discussed in detail in advance; any off-label use is transparently communicated.
Who is not a good candidate?
– Pregnancy (relative, depending on procedure)
– Uncontrolled epilepsy for certain protocols, acute psychosis
– Active skin inflammation at electrode sites
– Implanted electronic devices (e.g., pacemaker), case-by-case clearance
Frequently asked questions (FAQ)
How quickly does treatment work?
First effects often after 3–6 sessions; consolidation with full cycles and adjunct training.
Can it be combined with medication?
Yes—dose adjustments are medically supervised.
Is it painful?
Generally no—occasional transient sensations may occur.
Will insurance cover it?
Mostly self-pay/private. Case-by-case reimbursement may be possible.
How do we measure success?
Standardized scales (UPDRS, MoCA, BDI-II, PSQI), HRV, pain NRS, and functional goals.
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