Scrambler Therapy May Relieve Chronic Neuropathic Pain More Effectively Than Guideline-Based Drug Management: Results of a Pilot, Randomized, Controlled Trial
An Internet questionnaire to predict the presence or absence of organic patho...Nelson Hendler
The Pain Validity Test, developed by a team of physicians from Johns Hopkins Hospital, is available over the Internet, at www.MarylandClinicalDiagnostics.com. The test can predict, with 95% accuracy, which patient will have abnormalities on medical tersting, i.e. who has a valid complaint of pain. The test takes only 5 minutes to set up a patient, 15 minutes for a patient to take the test, and results are available immediately after completion. The test has been admitted as evidence in court cases in over 30 cases in 8 states.
The paper lists the correct method of diagnosing chronic pain, and matching the proper medication to tissue damage without the use of narcotics or opioids.
An Internet questionnaire to predict the presence or absence of organic patho...Nelson Hendler
The Pain Validity Test, developed by a team of physicians from Johns Hopkins Hospital, is available over the Internet, at www.MarylandClinicalDiagnostics.com. The test can predict, with 95% accuracy, which patient will have abnormalities on medical tersting, i.e. who has a valid complaint of pain. The test takes only 5 minutes to set up a patient, 15 minutes for a patient to take the test, and results are available immediately after completion. The test has been admitted as evidence in court cases in over 30 cases in 8 states.
The paper lists the correct method of diagnosing chronic pain, and matching the proper medication to tissue damage without the use of narcotics or opioids.
Current opiate prescription treatment has led to increased deaths, patients with marginal improvement in pain with minimal improvement in quality of life and high system utilization.
The integrated high-risk patient pain management clinics have been established to increase quality of pain care, stabilize high-risk patients and reduce impact of on primary care physicians and clinic utilization. These clinics are one aspect of a comprehensive plan to increase high quality pain care and reduce opiate deaths.
Mental Health – In this current period of data collection rates of
depression in all groups were reduced number of patients with mild MDD < 10%, number of patients with moderate < 7%, number of patients with severe depression < 7% and # of patients with all levels of MDD by 23%. The change in sample depression was significant with p =.01. 37% of patients had a score that indicates a likely full diagnosis of PTSD.
Via Christi Women's Connection presentation on advance in depression treatment by Matthew Macaluso, DO, medical director of Via Christi Psychiatric Clinic.
The experience of pain is a
normal sensation existing as an
expedient mechanism for
preservation of life, reduction of
injury and/or the initiation of
healing. It is formally defined in
many research studies as an
unpleasant sensory and emotional
experience associated with real or
potential tissue damage (Merskey
& Bogduk, 1994)...........
Scrambler Therapy Theory...
The MC-5A, which received broad FDA 510(k) clearance in February, 2009, is a computerized medical device that applies a low amperage electric signal which transmits synthetic non-pain information through disposable surface electrodes on the skin (similar to an EKG) to surface nerve receptors of the c-fibers. Scrambler Therapy synthesizes 16 different types of nerve action potentials similar to endogenous ones, assembles them into sequences, and uses algorithms to determine patient-specific cutaneous electrostimulation to reduce and eliminate pain. ST attempts to replace the “pain” information with artificial “non-pain” information
Scrambler Therapy is:Non - Invasive,Non - Narcotic,Pain free without known side effects.
Clinically proven effective by scientific research:
http://bit.ly/1dXrMos
What is the difference between TENS and Scrambler Therapy?
Scrambler Therapy is provided to patients through the use of an innovative, revolutionary MC-5A medical device for the treatment of severe, chronic, neuropathic pain.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Marineo + smith jan 2012 scrambler therapy better than drugs marineo 2012
1. Vol. 43 No. 1 January 2012
Journal of Pain and Symptom Management
87
Original Article
Scrambler Therapy May Relieve Chronic
Neuropathic Pain More Effectively Than
Guideline-Based Drug Management: Results
of a Pilot, Randomized, Controlled Trial
Giuseppe Marineo, PhD, Vittorio Iorno, MD, Cristiano Gandini, MD,
Vincenzo Moschini, MD, and Thomas J. Smith, MD
Delta Research & Development (G.M.), Centro Ricerche Bioingegneria Medica, University of Rome
‘‘Tor Vergata,’’ Rome, Italy; Centro di Medicina del Dolore ‘‘Mario Tiengo’’ (V.I., C.G., V.M.), IRCCS
Fondazione Ospedale Maggiore Policlinico, Mangiagalli and Regina Elena, Milan, Italy; and
Division of Hematology/Oncology and Palliative Care (T.J.S.), Massey Cancer Center, Virginia
Commonwealth University, Richmond, Virginia, USA
Abstract
Context. Neuropathic pain is common, disabling, and often difficult to treat.
Objectives. To compare guideline-based drug management with Scrambler
therapy, a patient-specific electrocutaneous nerve stimulation device.
Methods. A clinical trial with patients randomized to either guideline-based
pharmacological treatment or Scrambler therapy for a cycle of 10 daily sessions
was performed. Patients were matched by type of pain including postsurgical
neuropathic pain, postherpetic neuralgia, or spinal canal stenosis. Primary
outcome was change in visual analogue scale (VAS) pain scores at one month;
secondary outcomes included VAS pain scores at two and three months, pain
medication use, and allodynia.
Results. Fifty-two patients were randomized. The mean VAS pain score before
treatment was 8.1 points (control) and 8.0 points (Scrambler). At one month, the
mean VAS score was reduced from 8.1 to 5.8 (À28%) in the control group, and from
8 to 0.7 points (À91%) in the Scrambler group (P < 0.0001). At two and three
months, the mean pain scores in the control group were 5.7 and 5.9 points,
respectively, and 1.4 and 2 points in the Scrambler group, respectively (P < 0.0001).
More relapses were seen in polyradicular pain than monoradicular pain, but
retreatment and maintenance therapy gave relief. No adverse effects were observed.
Conclusion. In this pilot randomized trial, Scrambler therapy appeared to
relieve chronic neuropathic pain better than guideline-based drug
management. J Pain Symptom Manage 2012;43:87e95. Ó 2012 U.S. Cancer Pain
Relief Committee. Published by Elsevier Inc. All rights reserved.
Address correspondence to: Giuseppe Marineo, PhD,
Delta Research & Development, Via di Mezzocammino, 85 00187 Rome, Italy. E-mail: g.marineo@
mclink.it, or Thomas J. Smith, MD, Duffy Palliative
Care Service, Sidney Kimmel Cancer Center, Johns
Ó 2012 U.S. Cancer Pain Relief Committee
Published by Elsevier Inc. All rights reserved.
Hopkins, 600 North Wolfe Street, Blaylock 369,
Baltimore, MD 21287-0005. E-mail: tsmit136@
jhmi.edu
Accepted for publication: March 15, 2011.
0885-3924/$ - see front matter
doi:10.1016/j.jpainsymman.2011.03.015
2. 88
Marineo et al.
Vol. 43 No. 1 January 2012
Key Words
Chronic neuropathic pain, analgesics, refractory pain, Scrambler therapy, electroanalgesia
Introduction
Methods
Neuropathic pain is common, chronic, disabling, and often difficult to effectively treat.1
Common types of neuropathic pain include
postsurgical pain, postherpetic neuralgia
(PHN), spinal cord stenosis (SCS) (also known
as narrow canal syndrome), and chemotherapyinduced peripheral neuropathy.2 Although
conventional treatments such as opioids, neuroleptics, and other drugs help, all have side
effects and limited effectiveness.3
Scrambler therapy is a novel approach to
pain control that attempts to relieve pain
by providing ‘‘nonpain’’ information via cutaneous nerves to block the effect of pain information. Scrambler therapy synthesizes 16
different types of nerve action potentials similar to endogenous ones, assembles them into
sequences, and uses algorithms to determine
a patient-specific cutaneous electrostimulation
to reduce pain. Scrambler therapy has relieved
refractory chronic pain in uncontrolled clinical trials. In the pilot trial, 11 cancer patients
with abdominal pain received 10 daily onehour treatment sessions.4 Pain was reduced
from 8.6 to 2.3, on a numeric rating scale
from 0 to 10, after the first treatment and to
<0.5 (P < 0.0001) at the end of 10 sessions.
In the second trial, 226 patients with neuropathic pain, including failed back surgery
pain, brachial plexus neuropathy, and others,
were treated.5 Eighty percent of patients
had greater than 50% pain relief. Smith
et al.6 treated 16 patients with refractory
chemotherapy-induced neuropathic pain with
10 daily hour-long sessions to the painful areas.
Pain scores were reduced by 58% from the
start of treatment to the end. No toxicity has
been observed in any trial. However, all these
trials were single-arm trials with no control
group.
The purpose of this study was to directly compare management of chronic refractory neuropathic pain by Scrambler therapy with
management using current guideline-based
drug treatment7 in a randomized controlled
trial.
Study Population
Patients were eligible if they had chronic
neuropathic pain rated as 6 or more on a visual
analogue scale (VAS) on at least four days each
week, for the prior three months despite treatments including antidepressants, anticonvulsants, and opioids. Patients were treated at
Ospedale Maggiore, Policlinico Mangiagalli
and Regina Elena of Milan at the Centre for
Pain Medicine ‘‘Mario Tiengo.’’ Most of the recruited patients were already undergoing treatment in this facility and had been given the
standard treatment for neuropathic pain by
their physicians. The inclusion and exclusion
criteria are listed in Table 1.
The monitoring of patients during and after
treatments always took place at the same facility, the Centre for Pain Medicine in Milan. Two
research assistants performed the Scrambler
therapy under the direction of the treating
physicians. These two research assistants collected the pain assessments in both arms of
the study.
Informed consent was obtained from all patients. The Scrambler therapy device had been
granted Ministry of Health approval for hospital and ambulatory use. The hospital’s scientific and health unit, acting as the
institutional review board, approved and monitored the study.
Randomization and Stratification
For this trial at one center, the patients who
were eligible (pain $6 for at least three
months, despite treatment according to local
practice) were classified according to their
pain diagnosis (postsurgical, PHN, SCS).
They were then assigned to a treatment group:
alternative drug therapy according to the
European Federation of Neurological Societies (EFNS) guidelines and in standard practice at this center, or Scrambler therapy with
no change in the ineffective drug regimen.
They were assigned consecutively in the order
they were enrolled in the trial, for example,
the first PHN patient to drug treatment, the
3. Vol. 43 No. 1 January 2012
Scrambler Therapy for Chronic Neuropathic Pain
89
Table 1
Inclusion and Exclusion Criteria
Inclusion
Exclusion
Presence of mainly neuropathic pain
VAS pain intensity $6 in the preceding
three months
Failure to respond to currently used pharmacologic
treatment of neuropathic pain (antidepressants,
anticonvulsants, and opioids)
Absence of significant responses to TENS or other
similar electroanalgesic methods
In addition to pain, presence of related sensitivity
symptoms: allodynia, hyperpathia, hyperesthesia
Presence of pain for at least six months
Cancer-related pain
Presence of serious psychiatric disorder (schizophrenia, manicdepressive psychosis, primary major depression)
Presence of dermatologic conditions that preclude application of
skin electrodes
Uncontrolled seizures
Use of antiseizure medications
Any form of medical ‘‘metal’’ device (e.g., pacemakers, defibrillators,
vascular clips or stents, cardiac valve or joint replacements)
Frequency of pain more than four days per week
Age >18 years
Consent to Scrambler therapy treatment
second PHN patient to Scrambler therapy, the
third PHN patient to drug treatment, and so
forth. The assignment was done in order by
the research assistants, with no exceptions.
Allocation was not concealed (Fig. 1).
Standardized Control Treatment
The control group patients were managed
by the same team of pain specialists using the
most up-to-date EFNS guidelines. The most
common baseline therapy (typically amitriptyline, gabapentin, and tramadol) before randomization, which had resulted in a baseline
VAS pain score of 8.1, was switched to
All patients, n=56
Assessed for eligibility
Randomized;
stratified by type
of pain
Control Group, n=26
Start new drugs, e.g.,
amitriptyline,
clonazepam, oxycodone
Scrambler Group, n=26
Start Scrambler therapy;
stay on prior drugs
Control Group,
Evaluable n=26
Scrambler Group,
Evaluable n=26
Fig. 1. Assignment of patients to treatment groups.
a potentially more effective one (typically
amitriptyline, clonazepam, and oxycodone).
Low-dose clonazepam is classified as an anticonvulsant, has documented efficacy in case
series,8e10 and is the standard practice at this
center when gabapentin has not been
effective.
Standardized Scrambler Treatment
The Scrambler attempts to deliver ‘‘nonpain’’ information to the area in pain by simulating five external artificial neurons. Action
potentials that resemble normal nerve impulses are digitally synthesized, assembled
into packets of information strings, and delivered using standard silver gel electrodes similar to electrocardiogram electrodes. Each
new packet is created with an algorithm that
takes into account the previous outputs,
dynamically modifying four main variables.
These variables include the following: 1) type
of action potential to use (16 different possible
combinations); 2) packet-associated frequency
(from 43 to 52 Hz); 3) packet time duration
(0.7e10 seconds); and 4) the amplitude of
modulation. The system quickly tries different
combinations until pain relief is achieved.
(The technology details are described in patent number PCT/IT2007/000647.) The impulses are transmitted by surface electrodes
placed on the skin in the dermatome areas
of pain above and below the dermatome.
The electrical charge used in Scrambler therapy is low, and the U.S. Food and Drug Administration has approved it as safe. At the highest
setting, ‘‘70’’ on the dial from 10 to 70, the
4. 90
Marineo et al.
amperage (A) is 3.50e5.50 mA, and the
maximum current density is only 0.0002009
W/cm2.
Each Scrambler therapy patient was given
a 45-minute daily treatment for 10 consecutive
days, Monday through Friday. The stimulus
was increased to the maximum intensity individually bearable by the patient that did not
cause any additional pain or discomfort. The
principal investigator (V. I.) chose the best
treatment areas during the first visit, which
were then replicated daily. The Scrambler therapy group maintained their starting drug
treatment with no changes. Normally the electrodes are never applied directly on the painful area but in the dermatomes above and
below the pain affected area. For example, if
the pain involves L3, the first electrode is positioned close to but outside of the painful area
in dermatome L2 or L3 and the other on the
opposite side of the pain area in zone L3 or
L4. Once the electrodes are positioned, the
operator slowly raises the stimulation level until pain relief is obtained; if not obtained, the
operator can add or move channels to increase
the coverage. There are a total of five channels, or paired sets of electrodes. If pain is
not relieved, the electrode placement or stimulus is changed.
Data and Statistical Considerations
The primary endpoint was the change in
pain VAS scores11 from entry to the scores at
one, two, and three months. Pain intensity
was measured by an unmarked 10-cm long
VAS.12 The patients were classified as having
‘‘monoradicular pain’’ if they had one dominant area of pain, for example, one area of
Vol. 43 No. 1 January 2012
PHN, and ‘‘polyradicular pain’’ if they had
multiple areas of pain.13 Allodynia was tested
with von Frey elements by the research assistants and recorded as ‘‘present’’ or ‘‘not present.’’ The sample size of 26 in each arm was
determined using an anticipated effect size of
À1.59, with a starting VAS pain score of 6
and a standard deviation of 2 to give a 5%
alpha error margin and 80% power. All statistical calculations were done with StatMate 2
(GraphPad Software, Inc., La Jolla, CA;
http://www.graphpad.com/StatMate/statmate.
htm).
For the primary endpoint of pain, a repeatedmeasures analysis of variance (ANOVA) was
done with the VAS score as the dependent variable and time (baseline, one month, etc.), treatment (treated or control), and treatment by
time interaction terms as the independent variables. The repeated-measures model accounts
for the correlations that might arise from the
same individuals being observed over time. Secondary endpoints included change in pain
scores by the type of pain and mono- or polyradicular nature of the pain, change in allodynia,
and change in medication use and doses; all
were measured at entry, one, two, and three
months. Changes in pain intensity over time
were analyzed with one-way ANOVA and the
Tukey-Kramer Multiple Comparisons Test.
The difference in medication type and in dosage, and in allodynia, was evaluated using
repeated-measures ANOVA.
Results
The randomized patients were similar in
both groups, as shown in Table 2. The study
Table 2
Demographic Comparison of the Groups
Control Group (n ¼ 26), n (%)
Scrambler Therapy Group (n ¼ 26), n (%)
Sex
Male
Female
10 (38.46)
16 (61.53)
9 (34.61)
17 (65.38)
Age, mean (SD), years
53 (16.14)
56 (16.26)
Diagnoses
Postsurgical neuropathic pain
PHN
SCS
14 (53.84)
8 (30.76)
4 (15.38)
14 (53.84)
8 (30.76)
4 (15.38)
8.11/10 Æ 1.03
8.01 Æ 1.12
Patient Description
Pain score at entry, after six months
of standard treatment
SD ¼ standard deviation.
5. Vol. 43 No. 1 January 2012
Scrambler Therapy for Chronic Neuropathic Pain
sample statistical validity was confirmed with
the normality test of Kolmogorov and Smirnov
(P > 0.1).
The primary endpoint results are shown in
Fig. 2. The VAS pain score in the control group
fell by 28% at one month. Average VAS pain
intensity in the Scrambler therapy group
decreased from entry to T1 (one month),
T2 (two months), and T3 (three months)
(ANOVA P < 0.0001). The treatment by time
interaction term was significant (P < 0.0001)
suggesting that the decline in the VAS score
over time in the treated group was significantly
steeper than the control group (Fig. 2.) The
comparison between the two arms of the study
at monthly intervals confirmed this significance (P < 0.001, Tukey-Kramer Multiple
Comparisons Test). Results shown in Table 3
document that pain scores were reduced significantly with Scrambler therapy compared
with the control group (all results P < 0.001
by ANOVA). Pain was reduced in all groups:
postsurgical neuropathic pain (P < 0.0001 by
ANOVA), PHN (P < 0.0001), and SCS
(P ¼ 0.0108). Fig. 3 shows the effect in the different diagnoses.
Scrambler therapy appeared to be effective
in both mono- and polyradicular pain, but
more patients relapsed in the polyradicular
Fig. 2. Effect of treatment on pain scores over time.
A repeated-measures ANOVA with the VAS score as
the dependent variable and time (baseline, one
month, etc.), treatment (treated or control), and
treatment by time interaction terms as the independent variables. The repeated-measures model
accounts for the correlations that might arise from
the same individuals being observed over time. The
treatment by time interaction term was significant
(P < 0.0001), suggesting that the decline in the VAS
score over time in the treated group was significantly
steeper than that in the control group.
91
Table 3
Mean Variation in Pain Intensity (by VAS) Over
Time
Time of Assessment
(months)
T0,
T1,
T2,
T3,
entry
one month
two months
three months
Group
Control
Scrambler Therapy
8.11/10 Æ 1.03
5.84/10 Æ 1.34
5.76/10 Æ 1.40
5.91/10 Æ 1.44
8.01 Æ 1.12
0.78 Æ 1.78
1.49 Æ 2.39
2.03 Æ 3.14
All results statistically significant, P < 0.001 by ANOVA.
group, as shown in Fig. 4. These pain relapses
at three months were statistically significant in
the Scrambler therapy group (P < 0.001,
Tukey-Kramer Multiple Comparisons Test)
but not in the control group (P > 0.05). This
relapse was observed only in patients with polyradicular neuropathy, compared with those
with mononeuropathy (P < 0.001, ANOVA
test by Tukey-Kramer Multiple Comparisons
Test). The control group changes had no difference in the relapse rate when comparing
the type of pain (P > 0.05).
Scrambler therapy appeared to have a positive effect on allodynia. Allodynia was reduced
at one and three months in the Scrambler
therapy group (Fig. 5). The changes were statistically significant comparing the Scrambler
therapy group with the control group at one
month (P ¼ 0.0017, Fisher’s Exact Test), two
months (P ¼ 0.0094), and three months
(P ¼ 0.0644). However, given the simple
method of assessment (‘‘yes’’ or ‘‘no’’) done
in this pilot trial, further work is needed to
confirm this effect.
Scrambler therapy was associated with significant pain medication dose reductions, as
shown in Fig. 6. The percentage reduction
was calculated compared with the initial dose
at entry, then reassessed at times T2 and T3.
Fig. 3. Effect of treatment by type of pain.
PSP ¼ postsurgical pain.
6. 92
Marineo et al.
Vol. 43 No. 1 January 2012
Fig. 4. Effect of therapy by mono- or polyneuropathy.
At T3, opioids were totally eliminated in 11 of
17 cases, halved in one case, and unvaried in
five cases. Anticonvulsants were eliminated in
17 of 24 cases, reduced in one case, and unvaried in six cases. Lastly, antidepressants were
eliminated in nine of 19 cases, reduced in
four cases, and unvaried in six cases. Dosage
variation was statistically significant (repeatedmeasures ANOVA: P < 0.0001).
Discussion
In this small, randomized, controlled trial,
Scrambler therapy appeared to reduce pain, allodynia, and pain drug use significantly better
than guideline-based drug therapy. In 21 of 26
patients, pain could be relieved entirely.
Scrambler therapy was associated with a 91%
pain reduction compared with a 28% reduction using new medications.
Chronic pain syndromes can be helped by
patient-specific (adjusted to the tolerance of
the individual patient) direct nerve stimulation.14e16 The mechanisms by which direct
patient-specific nerve stimulation reduce pain
Fig. 5. Effect of treatment on allodynia. Allodynia
was assessed as present or absent. The graph shows
the percentage of subjects in each arm that had
allodynia at each time point.
include raising the ‘‘gate’’ threshold for pain
at the spinal cord, reducing ‘‘wind up’’ (central
sensitization of the spinal cord and brain that
amplifies the abnormal feelings), reducing impulses from the damaged nerve, and reducing
psychological maladaptation to pain.17 Spinal
cord stimulation gave a 50% pain reduction
in small nonrandomized series for chronic
pain from complex regional pain syndrome I
(median change in VAS 10 to 0e2, P < 0.01,
sustained)18 and PHN (median change in
VAS 9 to 1, sustained).19 Spinal cord stimulation gave over 50% pain reduction in a randomized trial compared with conventional
medical management in patients with failed
back syndrome (mean scores fell from 7.6 to
3.8 or less, sustained for 24 months,
P < 0.001).20 This same >50% effect size has
been observed in randomized trials of intraspinal drug delivery systems compared with conventional pain management, when opioids
and local anesthetics can be infused21 to act
directly on nerves. However, spinal cord stimulation and intrathecal drug delivery involve
invasive expensive technology with the possibility of serious complications.
Scrambler therapy differs from transcutaneous electrical nerve stimulation (TENS) in
Fig. 6. Effect of treatment on pain medication use.
7. Vol. 43 No. 1 January 2012
Scrambler Therapy for Chronic Neuropathic Pain
many aspects, although both provide stimulation via peripheral nerves. Clinically, TENS therapy has been shown effective in postoperative
pain and musculoskeletal pain, but the number
and quality of randomized controlled trials are
often inadequate for particular conditions.22
We were not able to find any randomized trials
of TENS for SCS or chronic postsurgical pain.
As reviewed by Niv et al.,23 the TENS effect in
PHN has been limited in randomized trials
and disappears a few hours after treatment.
TENS provides an on-off biphasic current without variation, whereas Scrambler therapy provides continuously changing variable nonlinear
waveforms. Recent studies with TENS units
have used a continuous pulse pattern, pulse
width of 200 microseconds, and a pulse frequency of 80 Hz, increased until the patient feels
a strong sensation. The Scrambler therapy average charge per phase is 38.8 microcoulombs,
similar to conventional TENS devices. The phase
duration is 6.8e10.9 microseconds, and the
pulse rate is 43e52 Hz. Because the frequency
delivered by the device never exceeds 52 Hz,
the mean energy delivered per second is generally less than most standard TENS devices, which
deliver a square wave with frequencies greater
than 52 Hz.
How Scrambler therapy causes pain relief
requires further study, but our observations
may inform mechanisms. First, Scrambler therapy gives new ‘‘nonpain’’ information such
that patients report new sensations in the
pain area (pressure, itching, ‘‘bee sting’’ sensations, and a flow of impulses). Second, it is not
simple C-fiber electrical stimulation, which
would produce pain. Third, Scrambler therapy
is not producing paresthesias because the
patient does not feel numbness and can still
feel other noxious stimuli. Fourth, Scrambler
therapy analgesia occurs quickly, suggesting
that the receptors are transmitting the
‘‘nonpain’’ information. Fifth, the sustained
pain relief for days or months suggests either
resetting of calcium channels (as with ziconotide) or remodulation of the pain system’s
response. Finally, the patient feels the sensation throughout the dermatome, not just
under the electrode patch, suggesting the
spread of ‘‘nonpain’’ information along the
lines of nerve transmission. Clearly, more study
is needed to define the effect and the
mechanisms.
93
There are limitations to this study. First, this is
a well-balanced, randomized, controlled study
similar to that done comparing implantable
drug delivery systems with guideline-based
care,24 but it is not a ‘‘sham’’ trial. Some researchers will insist that the only proof of efficacy is a randomized, double-blind, believable
placebo, or sham-controlled trial, but these
may be difficult to perform.25 It has been
hard to devise appropriate blinded studies because Scrambler therapy requires adjustments
of the electrode placement and dose, titrated
to pain relief, before the actual daily treatment
is begun. Alternative methods to control for
placebo effect include two strategies done
here: first, to set a pain relief goal that would
likely be unobtainable with placebo, and second, to allow an effective comparison control
group. Here, the reduction in pain was 91%,
much higher than typically seen with placebo.
For example, in a randomized trial of electrostimulation for back pain, the sham group had
a 9% reduction in back pain,26 and a study involving various nonpharmacological therapies
in low back pain showed that the placebo effect
was less than two points on a normalized 0e10
scale.27 The second alternative to a placebocontrolled trial allows an effective control comparison group. Here, the control group had
a 28% reduction in pain by the end of the first
month, consistent with the 14%e20% reduction seen in worst and usual pain in the
guideline-managed group of a large randomized trial,28 and the 39% reduction in pain
seen in the guideline-managed control group
of a cancer pain trial.20,25 A second limitation
to the study is the type of treatment provided
to the control group. Although some clinicians
would suggest alternative drug treatments, this
was the current practice at this Italian pain center, and the control group had a very reasonable
28% reduction in pain. A third limitation is the
small sample size, but the study was powered to
detect a relatively large difference in pain control and accomplished this.
There are strengths to this study, in addition
to the limitations. The patients were well balanced in the two arms. The patient-reported
outcomes are all standard, reproducible,
and valid. The magnitude of the pain relief
effect is large, persistent, consistent with the
reduction in pain medication use, and consistent with the size of the pain relief in the
8. 94
Marineo et al.
single-arm uncontrolled Scrambler therapy
studies. The comparison group had good relief of pain from standard guideline-based
measures applied by the expert group, as
noted above. The pain relief was well beyond
the 50%29 and 33%30 reductions proposed as
being clinically important for chronic pain.
In conclusion, the pain relief obtained in
this small, pilot, randomized trial encourages
further development of both treatment and
of knowledge regarding Scrambler therapy.
This knowledge will provide a better understanding of the mechanisms of action and
new opportunities for the treatment of all
forms of pain. It also provides more knowledge
of effect size for further randomized placeboor sham-controlled trials, which are underway.
Disclosures and Acknowledgments
Dr. Giuseppe Marineo holds property rights
to the Scrambler Therapy basic research
and international patent to its technology
development.
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