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1.
Stud Health Technol Inform ; 184: 377-9, 2013.
Article in English | MEDLINE | ID: mdl-23400187

ABSTRACT

We introduce a novel platform for medical device training: hybrid physical-virtual simulators of medical devices, combining touchscreen-enabled virtual emulations of real devices with sensorized physical peripherals to enable tactile, hands-on interaction between the trainee, simulated device and standardized patients or mannequins. The system enables objective measurement and recording of trainee performance, including interactions with both the virtual device elements and the physical components, and can include metrics and feedback not available in the real device. The system also includes an integrated wireless signaling device for use with standardized patients. We present the implementation of an example system, a virtual defibrillator with sensorized paddles and wireless signaling of successful defibrillator operation.


Subject(s)
Biomedical Engineering/education , Biomedical Engineering/instrumentation , Computer-Assisted Instruction/methods , Equipment and Supplies , Models, Theoretical , User-Computer Interface , Computer Simulation , Computer-Assisted Instruction/instrumentation
2.
Stud Health Technol Inform ; 173: 257-9, 2012.
Article in English | MEDLINE | ID: mdl-22356997

ABSTRACT

We have enhanced a common medical device, the chest tube drainage container, with electronic sensing of fluid volume, automated detection of critical alarm conditions and the ability to automatically send alert text messages to a nurse's cell phone. The PleurAlert system provides a simple touch-screen interface and can graphically display chest tube output over time. Our design augments a device whose basic function dates back 50 years by adding technology to automate and optimize a monitoring process that can be time consuming and inconvenient for nurses. The system may also enhance detection of emergency conditions and speed response time.


Subject(s)
Clinical Alarms , Drainage , Internet , Thorax , Safety Management , Telecommunications , Transducers
3.
Stud Health Technol Inform ; 173: 433-9, 2012.
Article in English | MEDLINE | ID: mdl-22357032

ABSTRACT

Augmented reality offers the potential to radically extend and enhance the capabilities of physical medical simulators such as full-body mannequin trainers. We have developed a system that transforms the surface of a mannequin simulator into both a display screen and an input device. The BodyWindows system enables a user to open, size, and reposition multiple viewports onto the simulator body. We demonstrate a dynamic viewport that displays a beating heart. Similar viewports could be used to display real-time physiological responses to interventions the user applies to the mannequin, such as injection of a simulated drug. Viewport windows can be overlapping and show anatomy at different depths, creating the illusion of "cutting" multiple windows into the body to reveal structures at different depths from the surface. The developed low-cost interface employees an IR light pen and the Nintendo Wiimote. We also report experiments using the Microsoft Kinect computer vision sensor to provide a completely hand-gesture based interface.


Subject(s)
Computer Simulation , Manikins , Models, Anatomic , Data Display , Imaging, Three-Dimensional , Physiological Phenomena , User-Computer Interface
4.
Stud Health Technol Inform ; 163: 549-51, 2011.
Article in English | MEDLINE | ID: mdl-21335854

ABSTRACT

We have developed a prototype of a real-time, interactive projective overlay (IPO) system that creates augmented reality display of a medical procedure directly on the surface of a full-body mannequin human simulator. These images approximate the appearance of both anatomic structures and instrument activity occurring within the body. The key innovation of the current work is sensing the position and motion of an actual device (such as an endotracheal tube) inserted into the mannequin and using the sensed position to control projected video images portraying the internal appearance of the same devices and relevant anatomic structures. The images are projected in correct registration onto the surface of the simulated body. As an initial practical prototype to test this technique we have developed a system permitting real-time visualization of the intra-airway position of an endotracheal tube during simulated intubation training.


Subject(s)
Computer-Assisted Instruction/methods , Imaging, Three-Dimensional/methods , Intubation, Intratracheal/methods , Manikins , Models, Biological , Surgery, Computer-Assisted/methods , User-Computer Interface , Computer Simulation , Computer Systems , Humans , Teaching/methods
5.
Stud Health Technol Inform ; 163: 552-4, 2011.
Article in English | MEDLINE | ID: mdl-21335855

ABSTRACT

We are developing a simulator of peripheral nerve block utilizing a mixed-reality approach: the combination of a physical model, an MRI-derived virtual model, mechatronics and spatial tracking. Our design uses tangible (physical) interfaces to simulate surface anatomy, haptic feedback during needle insertion, mechatronic display of muscle twitch corresponding to the specific nerve stimulated, and visual and haptic feedback for the injection syringe. The twitch response is calculated incorporating the sensed output of a real neurostimulator. The virtual model is isomorphic with the physical model and is derived from segmented MRI data. This model provides the subsurface anatomy and, combined with electromagnetic tracking of a sham ultrasound probe and a standard nerve block needle, supports simulated ultrasound display and measurement of needle location and proximity to nerves and vessels. The needle tracking and virtual model also support objective performance metrics of needle targeting technique.


Subject(s)
Electric Stimulation/methods , Models, Biological , Nerve Block/instrumentation , Nerve Block/methods , Surgery, Computer-Assisted/methods , Ultrasonography, Interventional/methods , User-Computer Interface , Computer Simulation , Electric Stimulation/instrumentation , Equipment Design , Equipment Failure Analysis , Humans , Manikins , Surgery, Computer-Assisted/instrumentation , Systems Integration , Ultrasonography, Interventional/instrumentation
6.
Integr Cancer Ther ; 5(1): 40-7, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16484713

ABSTRACT

BACKGROUND: Brainstem glioma carries the worst prognosis of all malignancies of the brain. Most patients with brainstem glioma fail standard radiation therapy and chemotherapy and do not survive longer than 2 years. Treatment is even more challenging when an inoperable tumor is of high-grade pathology (HBSG). The objective of this report is to summarize the outcome of patients with HBSG treated with antineoplastons in 4 phase 2 trials. PATIENTS: The following group of 18 patients was evaluable: 4 patients with glioblastomas and 14 patients with anaplastic HBSG. Fourteen patients had diffuse intrinsic tumors. Twelve patients suffered from recurrence, and 6 patients did not have radiation therapy or chemotherapy. METHODS: Antineoplastons, which consist of antineoplaston A10 (A10I) and AS2-1 injections, were given in escalating doses by intravenous injections. The median duration of antineoplaston administration was 5 months, and the average dosage of A10I was 9.22 g/kg/d and of AS2-1 was 0.31 g/kg/d. Responses were assessed by gadolinium-enhanced magnetic resonance imaging and positron emission tomography. RESULTS: The overall survival at 2 and 5 years was 39% and 22%, respectively, and maximum survival was more than 17 years for a patient with anaplastic astrocytoma and more than 5 years for a patient with glioblastoma. Progression-free survival at 6 months was 39%. Complete response was achieved in 11%, partial response in 11%, stable disease in 39%, and progressive disease in 39% of patients. Antineoplastons were tolerated very well with 1 case of grade 4 toxicity (reversible anemia). CONCLUSION: Antineoplastons contributed to more than a 5-year survival in recurrent diffuse intrinsic glioblastomas and anaplastic astrocytomas of the brainstem in a small group of patients.


Subject(s)
Benzeneacetamides/administration & dosage , Brain Stem Neoplasms/drug therapy , Glioma/drug therapy , Glutamine/analogs & derivatives , Neoplasm Recurrence, Local/drug therapy , Phenylacetates/administration & dosage , Piperidones/administration & dosage , Adolescent , Adult , Benzeneacetamides/adverse effects , Brain Stem Neoplasms/mortality , Brain Stem Neoplasms/pathology , Child , Child, Preschool , Dose-Response Relationship, Drug , Drug Administration Schedule , Drug Combinations , Female , Follow-Up Studies , Glioma/mortality , Glioma/pathology , Glutamine/administration & dosage , Glutamine/adverse effects , Humans , Injections, Intravenous , Magnetic Resonance Imaging , Male , Maximum Tolerated Dose , Neoplasm Recurrence, Local/mortality , Neoplasm Recurrence, Local/pathology , Neoplasm Staging , Phenylacetates/adverse effects , Piperidones/adverse effects , Risk Assessment , Survival Analysis , Treatment Outcome
7.
Integr Cancer Ther ; 4(2): 168-77, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15911929

ABSTRACT

Primitive neuroectodermal tumors (PNETs) are usually successfully treated with craniospinal radiation and chemotherapy; however, difficulties with standard treatment can be encountered in very young children, in adult patients at high risk of complication from standard treatment, and in patients with recurrent tumors. Thirteen children, either with recurrent disease or high risk, were treated in phase II studies with antineoplastons (ANP). The median age of patients was 5 years, 7 months (range, 1-11). Medulloblastoma was diagnosed in 8 patients, pineoblastoma in 3 patients, and other PNET in 2 patients. Previous treatments included surgery in 12 patients (1 had biopsy only, suboccipital craniotomy), chemotherapy in 6 patients, and radiation therapy in 6 patients. Six patients had not received prior chemotherapy or radiation. The treatment consisted of intravenous infusions of 2 formulations of ANP, A10 and AS2-1, and was administered for an average of 20 months. The average dosage of A10 was 10.3 g/kg/d and of AS2-1 was 0.38 g/kg/d. Complete response was accomplished in 23%, partial response in 8%, stable disease in 31%, and progressive disease in 38% of cases. Six patients (46%) survived more than 5 years from initiation of ANP; 5 were not treated earlier with radiation therapy or chemotherapy. The serious side effects included single occurrences of fever, granulocytopenia, and anemia. The study is ongoing and accruing additional patients. The percentage of patients' response is lower than for standard treatment of favorable PNET, but long-term survival in poor-risk cases and reduced toxicity makes ANP promising for very young children, patients at high risk of complication of standard therapy, and patients with recurrent tumors.


Subject(s)
Antineoplastic Agents/administration & dosage , Benzeneacetamides/administration & dosage , Brain Neoplasms/drug therapy , Glutamine/analogs & derivatives , Neuroectodermal Tumors, Primitive/drug therapy , Phenylacetates/administration & dosage , Piperidones/administration & dosage , Antineoplastic Agents/adverse effects , Benzeneacetamides/adverse effects , Child, Preschool , Disease Progression , Drug Combinations , Drug Therapy, Combination , Female , Glutamine/administration & dosage , Glutamine/adverse effects , Humans , Infant , Male , Neoplasm Recurrence, Local/prevention & control , Phenylacetates/adverse effects , Piperidones/adverse effects , Survival Analysis , Treatment Outcome
8.
Drugs R D ; 5(6): 315-26, 2004.
Article in English | MEDLINE | ID: mdl-15563234

ABSTRACT

OBJECTIVE: To evaluate the response rates, survival and toxicity of treatment with antineoplaston A10 and AS2-1 (ANP) in the first 12 children enrolled in our studies diagnosed with incurable recurrent and progressive multicentric glioma. PATIENTS AND METHODS: The patients' median age was 9 years. Six patients were diagnosed with pilocytic astrocytoma, four with low-grade astrocytoma and one with astrocytoma grade 2. In one case of visual pathway glioma, a biopsy was not performed due to a dangerous location. Patients received ANP intravenously initially and subsequently orally. The average duration of intravenous ANP therapy was 16 months and the average dosage of A10 was 7.95 g/kg/day and of AS2-1 was 0.33 g/kg/day. The average duration of oral ANP was 19 months and the average dosage of A10 and AS2-1 was 0.28 g/kg/day. Responses were assessed by MRI according to the National Cancer Institute's criteria and confirmed by PET scans in some cases. RESULTS: Complete response was accomplished in 33%, partial response in 25%, and stable disease in 33% of patients, and there was no progressive disease. One patient was non-evaluable due to only 4 weeks of ANP and lack of follow-up scans. One patient who had stable disease discontinued ANP against medical advice and died 4.5 years later. Ten patients are alive and well from 2 to >14 years post-diagnosis. Only one case of serious toxicity of reversible tinnitus, of one day's duration, was described. The study continues with accrual of additional patients. CONCLUSION: The results of the present study are favourable in comparison with radiation therapy and chemotherapy. We believe that confirmation of these results through further studies may introduce a new promising treatment for incurable paediatric brain tumours.


Subject(s)
Antineoplastic Agents/therapeutic use , Benzeneacetamides/therapeutic use , Brain Neoplasms/drug therapy , Glioma/drug therapy , Glutamine/analogs & derivatives , Glutamine/therapeutic use , Phenylacetates/therapeutic use , Piperidones/therapeutic use , Adolescent , Antineoplastic Agents/adverse effects , Astrocytoma/drug therapy , Astrocytoma/pathology , Benzeneacetamides/adverse effects , Child , Child, Preschool , Disease Progression , Drug Combinations , Drug Therapy, Combination , Female , Glutamine/adverse effects , Humans , Infant , Magnetic Resonance Imaging , Male , Neoplasm Recurrence, Local/prevention & control , Phenylacetates/adverse effects , Piperidones/adverse effects , Survival Analysis , Treatment Outcome
9.
Drugs R D ; 4(2): 91-101, 2003.
Article in English | MEDLINE | ID: mdl-12718563

ABSTRACT

OBJECTIVE: A phase II study of antineoplaston A10 and AS2-1 was conducted to evaluate the antineoplastic activity in patients with recurrent diffuse intrinsic brain stem glioma. PATIENTS AND METHODS: This report describes the results of treatment of the first 12 patients admitted to the study. Patients received escalating doses of antineoplaston A10 and AS2-1 by intravenous bolus injections. The median duration of treatment was 6 months and the average dosage of antineoplaston A10 was 11.3 g/kg/day and of antineoplaston AS2-1 0.4 g/kg/day. Responses were assessed by gadolinium-enhanced magnetic resonance imaging of the head. RESULTS: Of ten evaluable patients, complete response was determined in two cases (20%), partial response in three (30%), stable disease in three (30%) and progressive disease in two (20%). Survival at 2 years was 33.3%. Currently, of all 12 patients, two (17%) were alive and tumour free for over 5 years since initial diagnosis; one was alive for more than 5 years, and another for more than 4 years from the start of treatment. Only mild and moderate toxicities were observed, which included three cases of skin allergy, two cases of anaemia, fever and hypernatraemia, and single cases of agranulocytosis, hypoglycaemia, numbness, tiredness, myalgia and vomiting. CONCLUSION: The results of this study compared favourably with the responses of patients treated with radiation therapy and chemotherapy. The study continues with accrual of additional patients.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Benzeneacetamides/adverse effects , Benzeneacetamides/therapeutic use , Brain Stem Neoplasms/drug therapy , Glioma/drug therapy , Glutamine/analogs & derivatives , Glutamine/adverse effects , Glutamine/therapeutic use , Phenylacetates/adverse effects , Phenylacetates/therapeutic use , Piperidones/adverse effects , Piperidones/therapeutic use , Adolescent , Adult , Brain Stem Neoplasms/mortality , Cerebral Angiography , Child , Drug Combinations , Glioma/mortality , Humans , Karnofsky Performance Status , Risk Assessment/methods , Time Factors
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