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21. Noninvasive electrical bone growth stimulators for spinal fusion or foot and ankle indications

Noninvasive electrical bone growth stimulators for spinal fusion or foot and ankle indications Noninvasive electrical bone growth stimulators for spinal fusion or foot and ankle indications Noninvasive electrical bone growth stimulators for spinal fusion or foot and ankle indications HAYES, Inc. Record Status This is a bibliographic record of a published health technology assessment. No evaluation of the quality of this assessment has been made for the HTA database. Citation HAYES, Inc (...) .. Noninvasive electrical bone growth stimulators for spinal fusion or foot and ankle indications. Lansdale: HAYES, Inc.. Directory Publication. 2016 Authors' objectives Noninvasive electrical bone growth stimulators (EBGS) are external devices that deliver electrical energy to a fracture or bone fusion site. The goal is to induce osteogenesis, stimulate bone growth, and promote healing of fresh, delayed, or nonunion bone fractures and surgical joint fusions. Controversy: Controversial issues related

2017 Health Technology Assessment (HTA) Database.

22. Electrical bone growth stimulation, invasive

Electrical bone growth stimulation, invasive Electrical bone growth stimulation, invasive Electrical bone growth stimulation, invasive HAYES, Inc. Record Status This is a bibliographic record of a published health technology assessment. No evaluation of the quality of this assessment has been made for the HTA database. Citation HAYES, Inc.. Electrical bone growth stimulation, invasive. Lansdale: HAYES, Inc.. Directory Publication. 2016 Authors' objectives Invasive bone growth stimulators (...) are fully implanted battery-operated devices that deliver electrical energy to bone sites to which cathodes are applied. They are intended to induce osteogenesis, stimulate bone growth, and promote healing in nonhealing fractures or a bone fusion site. Controversy: Surgical implantation and constant delivery of electrical stimulation may pose safety hazards. Limited evidence is available to enable evaluation of efficacy and safety. Relevant Questions: For patients undergoing arthrodesis or treatment

2017 Health Technology Assessment (HTA) Database.

23. ODFS Pace and Pace XL functional electrical stimulation devices for treating drop foot

ODFS Pace and Pace XL functional electrical stimulation devices for treating drop foot ODFS P ODFS Pace and P ace and Pace XL functional electrical ace XL functional electrical stimulation de stimulation devices for treating drop foot vices for treating drop foot Medtech innovation briefing Published: 11 March 2016 nice.org.uk/guidance/mib56 pathways Summary Summary The Odstock Dropped Foot Stimulator (ODFS) Pace and Pace XL devices are functional electrical stimulators indicated for treating (...) . Subject to Notice of rights (https://www.nice.org.uk/terms-and- conditions#notice-of-rights). Page 1 of 51Product summary and lik Product summary and likely place in ely place in ther therap apy y The Odstock Dropped Foot Stimulator (ODFS) Pace and Pace XL are portable functional electrical stimulation (FES) devices, which are used to help people with drop foot walk. The ODFS devices are used as part of an integrated rehabilitation system as an alternative, or in addition to, a foot orthosis or other

2016 National Institute for Health and Clinical Excellence - Advice

24. Electric stimulation therapy (EST) in patients with gastroesophageal reflux disease

Electric stimulation therapy (EST) in patients with gastroesophageal reflux disease Electric stimulation therapy (EST) in patients with gastroesophageal reflux disease Electric stimulation therapy (EST) in patients with gastroesophageal reflux disease Stanak M, Hawlik K Record Status This is a bibliographic record of a published health technology assessment from a member of INAHTA. No evaluation of the quality of this assessment has been made for the HTA database. Citation Stanak M, Hawlik K (...) . Electric stimulation therapy (EST) in patients with gastroesophageal reflux disease. Vienna: Ludwig Boltzmann Institut fuer Health Technology Assessment (LBIHTA). Decision Support Document. 2017 Authors' conclusions Overall, three studies with the total of 70 patients were included in the assessment of safety, however no study could answer the question of efficacy. The quality of evidence was very low and the overall risk of bias was considered moderate. Hence, no conclusion could be made about

2017 Health Technology Assessment (HTA) Database.

25. Functional electrical stimulation for rehabilitation following spinal cord injury

Functional electrical stimulation for rehabilitation following spinal cord injury Functional electrical stimulation for rehabilitation following spinal cord injury Functional electrical stimulation for rehabilitation following spinal cord injury HAYES, Inc Record Status This is a bibliographic record of a published health technology assessment. No evaluation of the quality of this assessment has been made for the HTA database. Citation HAYES, Inc. Functional electrical stimulation (...) , the current average age at injury is 42.0 years. Cases are reported predominately in men (80%). Technology Description: Functional electrical stimulation (FES) is the direct application of safe levels of electric current to intact nerve fibers in a coordinated fashion to cause involuntary, but purposeful, muscle contraction. FES has 2 primary clinical applications in patients with SCI – therapeutic and functional. Therapeutic FES enables exercise, typically resistive, with the goal of preventing muscular

2017 Health Technology Assessment (HTA) Database.

26. Percutaneous electrical nerve stimulation for treatment of low back pain

Percutaneous electrical nerve stimulation for treatment of low back pain Percutaneous electrical nerve stimulation for treatment of low back pain Percutaneous electrical nerve stimulation for treatment of low back pain HAYES, Inc Record Status This is a bibliographic record of a published health technology assessment. No evaluation of the quality of this assessment has been made for the HTA database. Citation HAYES, Inc. Percutaneous electrical nerve stimulation for treatment of low back pain (...) : Percutaneous electrical nerve stimulation (PENS) is a conservative, minimally invasive treatment for pain in which acupuncture-like needles connected through a cable to an external power source are inserted into the skin. Needle placement is near the area of pain and are percutaneous instead of cutaneous, as in transcutaneous electrical nerve stimulation (TENS). PENS electrodes are not permanently implanted as in spinal cord stimulation. The mechanism of action of PENS is theorized to modulate

2017 Health Technology Assessment (HTA) Database.

27. The effect of combined transcranial direct current stimulation and peripheral nerve electrical stimulation on corticospinal excitability. Full Text available with Trip Pro

The effect of combined transcranial direct current stimulation and peripheral nerve electrical stimulation on corticospinal excitability. Transcranial direct current stimulation (tDCS) and peripheral nerve electrical stimulation (PES) can change corticospinal excitability. tDCS can be used to non-invasively modulate the cerebral cortex's excitability by applying weak current to an electrode attached to the head, and the effect varies with the electrode's polarity. Previous studies have reported (...) the effect of combined tDCS and PES on corticospinal excitability; when compared to single stimulation, combined stimulation increases cortical excitability. In contrast, another study reported that the effect of tDCS is attenuated by PES; hence, there is no consensus opinion on the effect on combined stimulation. Therefore, this study aimed to clarify the effect of combined tDCS and PES on corticospinal excitability. In Experiment 1, the combined stimulation of anodal tDCS and PES (anodal tDCS + PES

2019 PLoS ONE

28. Efficiency of Neuromuscular Electrical Stimulation and Transcutaneous Nerve Stimulation on Hemiplegic Shoulder Pain: A Randomized Controlled Trial (Abstract)

Efficiency of Neuromuscular Electrical Stimulation and Transcutaneous Nerve Stimulation on Hemiplegic Shoulder Pain: A Randomized Controlled Trial To compare the efficacy of neuromuscular electrical stimulation (NMES) and transcutaneous nerve stimulation (TENS) on hemiplegic shoulder pain (HSP).This is a prospective randomized controlled trial.A rehabilitation hospital.Participants (N=90) were randomized into NMES (n=36), TENS (n=36), or control groups (n=18).NMES (15Hz, pulse width 200μs (...) ) was applied to supraspinatus and deltoids (medial and posterior parts), whereas TENS (100Hz, pulse width 100μs) was used on the same areas. The surface electrodes were placed near the motor points of the supraspinatus and medial or posterior bundle of deltoids. The 4-week treatment consisted of 20 sessions, each session composed of 1 hour of stimulation per day. Routine rehabilitation program without any stimulation was administered to the control and the NMES/TENS groups. Numerical rating scale (NRS

2018 EvidenceUpdates

29. Comparison of transcutaneous electrical nerve stimulation (TENS) and functional electrical stimulation (FES) for spasticity in spinal cord injury - A pilot randomized cross-over trial. Full Text available with Trip Pro

Comparison of transcutaneous electrical nerve stimulation (TENS) and functional electrical stimulation (FES) for spasticity in spinal cord injury - A pilot randomized cross-over trial. Spasticity following spinal cord injury (SCI) can impair function and affect quality of life. This study compared the effects of transcutaneous electrical nerve stimulation (TENS) and functional electrical stimulation (FES) on lower limb spasticity in patients with SCI.Double blind randomized crossover (...) design.Neuro-rehabilitation unit, Manipal University, India.Ten participants (age: 39 ± 13.6 years, C1-T11, 1-26 months post SCI) with lower limb spasticity were enrolled in this study.Participants were administered electrical stimulation with TENS and FES (duration - 30 minutes) in a cross over manner separated by 24 hours.Spasticity was measured using modified Ashworth scale (MAS) [for hip abductors, knee extensors and ankle plantar flexors] and spinal cord assessment tool for spastic reflexes (SCATS

2018 The journal of spinal cord medicine Controlled trial quality: uncertain

30. Effectiveness of Functional Electrical Stimulation (FES) versus Conventional Electrical Stimulation in Gait Rehabilitation of Patients with Stroke. (Abstract)

Effectiveness of Functional Electrical Stimulation (FES) versus Conventional Electrical Stimulation in Gait Rehabilitation of Patients with Stroke. To compare the effectiveness of functional electrical stimulation (FES) versus conventional electrical stimulation in gait rehabilitation of patients with stroke for finding the most appropriate problem-oriented treatment for foot drop patients in a shorter time period.Randomized controlled trial.Armed Forces Institute of Rehabilitation Medicine (...) , Rawalpindi, from July to December 2016.Subjects with foot drop due to stroke were allotted randomly into 1 of 2 groups receiving standard rehabilitation with Functional Electrical Stimulation (FES) or Electrical Muscle Stimulation (EMS). FES was applied on tibialis anterior 30 minutes/day, five days/week for six weeks. EMS was also applied on the tibialis anterior five days/week for six weeks. Outcome measures included Fugl-Meyer Assessment Scale, Modified Ashworth Scale, Berg Balance Scale (BBS), Time

2018 Journal of the College of Physicians and Surgeons--Pakistan : JCPSP Controlled trial quality: uncertain

31. Effects of the combination therapy of tilt sensor functional electrical stimulation and integrated volitional control electrical stimulation on brain activity during the subacute phase following stroke: a feasibility study. Full Text available with Trip Pro

Effects of the combination therapy of tilt sensor functional electrical stimulation and integrated volitional control electrical stimulation on brain activity during the subacute phase following stroke: a feasibility study. [Purpose] The aim of this study was to investigate whether the combination of integrated volitional control functional electrical stimulation and tilt sensor functional electrical stimulation training affected brain activation during the subacute phase following a stroke (...) . [Participant and Methods] The patient was a 60-year-old male with right hemiparesis, secondary to stroke in the left thalamus. Conventional intervention was performed for 60 minutes per day during the first two weeks of treatment (the control condition). Functional electrical stimulation intervention, including integrated volitional control functional electrical stimulation and tilt sensor functional electrical stimulation training, was then performed for 60 minutes per day for two weeks (the experimental

2018 Journal of physical therapy science Controlled trial quality: uncertain

32. Gastric Electrical Stimulation Reduces Refractory Vomiting in a Randomized Crossover Trial Full Text available with Trip Pro

Gastric Electrical Stimulation Reduces Refractory Vomiting in a Randomized Crossover Trial Gastric Electrical Stimulation Reduces Refractory Vomiting in a Randomized Crossover Trial - PubMed This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features! Welcome to the new PubMed. For legacy PubMed go to . Clipboard, Search History, and several other advanced features are temporarily unavailable. National Institutes of Health U.S. National (...) Permalink Copy Page navigation Gastroenterology Actions . 2020 Feb;158(3):506-514.e2. doi: 10.1053/j.gastro.2019.10.018. Epub 2019 Oct 21. Gastric Electrical Stimulation Reduces Refractory Vomiting in a Randomized Crossover Trial , , , , , , , , , , , , , , , , , , , , , , , , Collaborators, Affiliations Expand Collaborators ENTERRA Research Group : , , , , , , , , , , , , , , , , , , Affiliations 1 Rouen University Hospital-Inserm UMR 1073/Inserm CIC-CRB 1404, Rouen, France. 2 Paris-HP Louis Mourier

2020 EvidenceUpdates

33. Effect of footplate neuromuscular electrical stimulation on functional and quality-of-life parameters in patients with peripheral artery disease: pilot, and subsequent randomized clinical trial (Abstract)

Effect of footplate neuromuscular electrical stimulation on functional and quality-of-life parameters in patients with peripheral artery disease: pilot, and subsequent randomized clinical trial Supervised exercise programmes for intermittent claudication have poor access and limited compliance. Neuromuscular electrical stimulation (NMES) may be an effective alternative. A proof-of-concept study and RCT were conducted.In study 1, eligible patients underwent baseline assessment; treadmill testing (...) for initial (ICD) and maximum (MCD) claudication distance; EuroQoL Five Dimensions five-level instrument (EQ-5D-5L™) and Intermittent Claudication Questionnaire (ICQ) assessment; and measurement of ultrasound haemodynamics of the superficial femoral artery. After familiarization with the NMES device, participants underwent a 30-min session of stimulation with concomitant recording of haemodynamic measures at 15 min, and after device cessation. Measurements were repeated after 6 weeks of daily use of NMES

2020 EvidenceUpdates

34. The complementary effects of galvanic current electrical stimulation associated with conservative treatment to increase vasodilation in patients with Raynaud`s phenomenon: a randomized trial

The complementary effects of galvanic current electrical stimulation associated with conservative treatment to increase vasodilation in patients with Raynaud`s phenomenon: a randomized trial The Complementary Effects of Galvanic Current Electrical Stimulation Associated With Conservative Treatment to Increase Vasodilation in Patients With Raynaud's Phenomenon: A Randomized Trial - PubMed This site needs JavaScript to work properly. Please enable it to take advantage of the complete set (...) Optional text in email: Save Cancel Create a file for external citation management software Create file Cancel Actions Cite Share Permalink Copy Page navigation Clin Rehabil Actions . 2020 May;34(5):595-606. doi: 10.1177/0269215520907652. Epub 2020 Mar 6. The Complementary Effects of Galvanic Current Electrical Stimulation Associated With Conservative Treatment to Increase Vasodilation in Patients With Raynaud's Phenomenon: A Randomized Trial , , , , , Affiliations Expand Affiliations 1 Instituto de

2020 EvidenceUpdates

35. High frequency electrical stimulation induces a long-lasting enhancement of event-related potentials but does not change the perception elicited by intra-epidermal electrical stimuli delivered to the area of increased mechanical pinprick sensitivity. Full Text available with Trip Pro

High frequency electrical stimulation induces a long-lasting enhancement of event-related potentials but does not change the perception elicited by intra-epidermal electrical stimuli delivered to the area of increased mechanical pinprick sensitivity. High frequency electrical stimulation (HFS) of the skin induces increased pinprick sensitivity in the surrounding unconditioned skin. The aim of the present study was to investigate the contribution of A-fiber nociceptors to this increased pinprick (...) sensitivity. For this we assessed if the perception and brain responses elicited by low-intensity intra-epidermal electrical stimulation (IES), a method preferentially activating Aδ-fiber nociceptors, are increased in the area of HFS-induced increased pinprick sensitivity. HFS was delivered to one of the two forearms of seventeen healthy volunteers. Mechanical pinprick stimulation and IES were delivered at both arms before HFS (T0), 20 minutes after HFS (T1) and 45 minutes after HFS (T2). In all

2018 PLoS ONE

36. The Effectiveness and Risks of Cranial Electrical Stimulation

The Effectiveness and Risks of Cranial Electrical Stimulation Management Briefs eBrief-no120 -- Enter search terms Button to search HSRD ® Inside VA Budget and Performance Inside the News Room National Observances Special Events » » » » » Management Briefs eBrief-no120 -- Health Services Research & Development Management eBrief no. 120 » Issue 120 December 2016 The report is a product of the VA/HSR&D Evidence Synthesis Program. The Effectiveness and Risks of Cranial Electrical Stimulation (...) : A Systematic Review Cranial electrical stimulation (CES) is a non-invasive method of applying low-intensity electrical current to the head. It is related to but distinct from other forms of transcranial electrical stimulation (i.e., electroconvulsive therapy and transcranial direct current stimulation), with different versions of stimulation varying in the placement of electrodes, intensity of the current, and waveform of the current. After an initial burst of research activity in the 1970s and early 1980s

2017 Veterans Affairs - R&D

37. Therapeutic Ultrasound Will Provide Better Management of Patients with Temporomandibular Myofascial Pain as Compared to Transcutaneous Electrical Nerve Stimulation

Therapeutic Ultrasound Will Provide Better Management of Patients with Temporomandibular Myofascial Pain as Compared to Transcutaneous Electrical Nerve Stimulation UTCAT3235, Found CAT view, CRITICALLY APPRAISED TOPICs University: | | ORAL HEALTH EVIDENCE-BASED PRACTICE PROGRAM View the CAT / Title Therapeutic Ultrasound Will Provide Better Management of Patients with Temporomandibular Myofascial Pain as Compared to Transcutaneous Electrical Nerve Stimulation Clinical Question For adult (...) patients with temporomandibular myofascial pain, will therapeutic ultrasound better reduce pain levels as compared to transcutaneous electrical nerve stimulation? Clinical Bottom Line Therapeutic ultrasound (Th US) will provide better management of patients with temporomandibular myofascial pain as compared to transcutaneous electrical nerve stimulation (TENS). This is supported by a randomized comparative study in which the effectiveness of Th US versus TENS was found to be statistically significant

2017 UTHSCSA Dental School CAT Library

38. Double-blind randomised controlled trial of percutaneous tibial nerve stimulation versus sham electrical stimulation in the treatment of faecal incontinence: CONtrol of Faecal Incontinence using Distal NeuromodulaTion (the CONFIDeNT trial)

Double-blind randomised controlled trial of percutaneous tibial nerve stimulation versus sham electrical stimulation in the treatment of faecal incontinence: CONtrol of Faecal Incontinence using Distal NeuromodulaTion (the CONFIDeNT trial) Double-blind randomised controlled trial of percutaneous tibial nerve stimulation versus sham electrical stimulation in the treatment of faecal incontinence: CONtrol of Faecal Incontinence using Distal NeuromodulaTion (the CONFIDeNT trial) Double-blind (...) randomised controlled trial of percutaneous tibial nerve stimulation versus sham electrical stimulation in the treatment of faecal incontinence: CONtrol of Faecal Incontinence using Distal NeuromodulaTion (the CONFIDeNT trial) Horrocks EJ, Bremner SA, Stevens N, Norton C, Gilbert D, O'Connell PR, Eldridge S, Knowles CH Record Status This is a bibliographic record of a published health technology assessment from a member of INAHTA. No evaluation of the quality of this assessment has been made for the HTA

2015 Health Technology Assessment (HTA) Database.

39. Rescue Leadless Pacemaker Implantation in a Pacemaker-Dependent Patient with Congenital Heart Disease and no Alternative Routes for Pacing Full Text available with Trip Pro

Rescue Leadless Pacemaker Implantation in a Pacemaker-Dependent Patient with Congenital Heart Disease and no Alternative Routes for Pacing Congenital heart disease patients are considered a unique group of patients regarding their high risk of conduction abnormalities , whether de novo or surgically induced , and the challenges in both implantation and management of device related complications. We present a case of a pacemaker-dependent patient with congenital heart disease who experienced (...) complications of both previous epicardial and transvenous pacing which rendered her a non-suitable candidate of both routes.

2017 Journal of atrial fibrillation

40. Schizophrenia TreAtment with electRic Transcranial Stimulation (STARTS): design, rationale and objectives of a randomized, double-blinded, sham-controlled trial. Full Text available with Trip Pro

Schizophrenia TreAtment with electRic Transcranial Stimulation (STARTS): design, rationale and objectives of a randomized, double-blinded, sham-controlled trial. Schizophrenia is a severe mental disorder. While some antipsychotic medications have demonstrated efficacy in treating positive symptoms, there is no widely recognized treatment for negative symptoms, which can cause significant distress and impairment for patients with schizophrenia. Here we describe the rationale and design (...) of the STARTS study (Schizophrenia TreAtment with electRic Transcranial Stimulation), a clinical trial aimed to test the efficacy of a non-pharmacological treatment known as transcranial direct current stimulation (tDCS) for treating the negative symptoms of schizophrenia.The STARTS study is designed as a randomized, sham-controlled, double-blinded trial evaluating tDCS for the treatment of the negative symptoms of schizophrenia. One-hundred patients will be enrolled and submitted to 10 tDCS sessions over

2019 Trends in psychiatry and psychotherapy Controlled trial quality: predicted high

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