MEDICAL EMC
Mapping
EMI in the Modern Hospital
Basile
Spyropoulos, Dimitris Glotsos, Dimitris Batistatos, and Ioannis
Marneris
An on-line
EMI distribution mapping system pinpoints potential EMI threats
and provides information for determining preventive action.
The electromagnetic environment
of hospitals has changed dramatically over the past 20 years, and
such change is ongoing. New, sophisticated electronic medical systems
are being introduced continually to modern hospitals to facilitate
healthcare services in the forms of diagnosis and therapy.
But without proper precautions,
such benefits can be counterbalanced by potential electromagnetic
interference (EMI) to the normal operations of these systems. Electromagnetic
compatibility, or EMC, refers to the capability of
all electronic equipment to function properly within its electromagnetic
environment.1 Medical systems, like all electronic
equipment, produce electromagnetic fields around them, the characteristics
of which determine the type of potential interference with their
electromagnetic environment. EMI-related issues can manifest not
only in the form of visually recognizable disturbances, but also
in the most complex and dangerous forms of "obscure opaque
influence" that can create life-threatening conditions for
patients.2
Consequently, considerable
research has centered on gathering representative data for the determination
of hospital EMI levels.3-5 Research groups
have also focused their attention on EMI-critical equipment, including
defibrillators, electrosurgical units, and wireless telecommunications.6-8
Their work has shown that potentially hazardous EMI can be analog
or digital. Analog signals can be affected by time-varying electromagnetic
fields in the surrounding environment, and digital packets of data
can be disturbed by unwanted signals entering the transportation
media (e.g., cables) and embedding themselves within the packets,
as "physiological" parts.
To prevent this type of
interaction, equipment manufacturers have begun to consider issues
of electromagnetic immunity during design and production. They have
also published several directives, of which the most common and
most widely accepted is international standard IEC 60601-1-2, which
has been adopted as harmonized European standard EN 60601-1-2.9,10
The standard refers to
two causes of EMC-related problems: the existence of source equipment
whose emissions must be limited, and the existence of susceptible
equipment that must be adequately shielded in order to be protected
from the disturbances in its environment. IEC 60601-1-2 addresses
issues relating to tests, measurement techniques, and safety levels
of emissions and susceptibility for medical equipment. It also proposes
installation and mitigation guidelines to achieve controllable emissions
and immunity of equipment.
 |
| Figure 1. On-line navigation
maps linked with relevant information. |
It is important to identify
critical EMI situations, particularly in healthcare where patient
safety is a factor. The research outlined in this article addresses
EMI concerns in a hospital environment.11,12
The study centers on an integrated on-line electromagnetic distribution
mapping system created and used to research the sources, types,
and levels of EMI in the departments of the General Distinct Anti-Cancer
Hospital (Piraeus, Metaxa, Greece) and the magnetic resonance imaging
(MRI) facility of a private clinic in Patras, Asklipios (see Figure
1). The goals were to recognize and understand potential EMI threats
and to facilitate problem solving within the hospital environment.
Following is a discussion of the mapping system and its implementation
and results.
 |
| Figure 2. ECG self-interfering
problem (left); measuring equipment (right). |
Materials and
Methods
Using specialized equipment,
the researchers carried out magnetic-field measurements in the General
Distinct Anti-Cancer Hospital and in the clinic's MRI facility.
A Metron Norway QA5 measuring device yielded the magnetic-field
intensity measurements. In addition, an appropriate home-developed
device measured the root-mean-square (rms) value of the induced
electromotive force (EMF) by the presence of a time-varying electromagnetic
field on a coil of one turn, enclosing an area of about 0.1 m2
(see Figure 2).
The researchers documented
this information in the form of electromagnetic distribution layouts
that were superimposed on plots of the buildings' structures, providing
a visual representation of the magnetic-field distribution covering
all departments within the hospital. The abbreviation OR that appears
in the electromagnetic distribution layouts and in Tables I-IV stands
for over range, meaning that the reading was higher than
the useful range of the instrument.
| Device Type |
Bmax
10–8
Telsa |
E (V/m) |
| Mixer |
OR |
OR |
| Photometer |
1000 |
3.00 |
| Microcentrifuge |
OR |
OR |
| Hematological analyzer |
1100 |
3.30 |
| Table centrifuge |
OR |
OR |
| Abbot wash |
1640 |
4.92 |
| Abbot analyzer |
OR |
OR |
| Hematological centrifuge |
500 |
1.50 |
| Electrophoresis |
1600 |
4.80 |
| Incubator |
630 |
1.89 |
|
| Table I. In vitro laboratory
and blood bank: typical devices checked. |
The information database
identified magnetic-field distribution areas, including the contribution
of each specific medical-equipment source of electromagnetic radiation
to the formation of the surrounding distribution. Equipment was
tested in all modes of operation, from standby to the various frequency
ranges of electrosurgical units (ESU). These navigation maps were
capable of isolating risk areas; that is, areas that presented an
increasing probability of EMI events according to IEC 60601-1-2,
and thus indicated susceptible equipment and potentially questionable
installations. Additional device-specific information accompanied
the maps. These data, in layouts and charts, indicated the magnetic-field
profiles around the devices and their frequency from several distances
and directions.
| Device Type |
Bmax
10–8
Telsa |
E (V/m) |
| Anesthesia |
1600 |
4.80 |
| ES unit 1 |
1800 |
5.40 |
| Oximeter |
160 |
0.48 |
| Central ICU unit |
OR |
OR |
| Suction pump |
1700 |
5.10 |
| ES unit 2 |
OR |
OR |
| Monitor |
OR |
OR |
| Cranial pressure |
OR |
OR |
|
| Table IIa. Intensive care
unit and surgery. |
Results
The researchers developed
magnetic-field distribution layouts for all departments in the hospital,
including the intensive care unit (ICU), operating theater, and
hospital wards, and for the private clinic's MRI facility. A virtual
tour consisting of HTML distribution maps is presented on a controlled-access
Web site, http://www.bmtl.bme.teiath.gr/
Electromagnetic%20Compatibility/index.htm. A restricted area
of the site includes digitized layouts based on all of the data
that were acquired, documented, and superimposed to the buildings'
structural plots. These layouts reconstruct the exact mobile and
nonmobile medical equipment installation, indicating susceptible
areas—areas that present increasing probability of EMI events—via
hot-spot links. Accompanying information consists of charts and
spreadsheets citing all measurements obtained from each device.
The readings documented in Tables I-IV are given in telsa (T)
and converted to volt/meter (V/m), assuming a far-field relationship
of E (V/m) = 377 W X H (A/m), and 1 T = 795,000 A/m. The measurements
were categorized according to their direction and mode of operation.
In the following study, only the maximum magnetic-field intensity
(Bmax) values were presented at a distance of 10 cm.
| Department |
EMI Source |
Receptor |
Observation |
| ICU (nursing room) |
ESU |
Vital-signs monitor |
Disturbance |
| ICU (machine storage area) |
Defibrillator |
Vital-signs monitor |
Disturbance |
| ICU (nursing room) |
ESU |
Dosimetric pump |
Disturbance |
| Operating theater |
ESU |
Vital-signs monitor |
Disturbance |
| Operating theater |
ESU |
Anesthesia |
Negative |
|
| Table IIb. High-risk EMI
conditions. |
In Vitro Diagnostic
Laboratories. The in vitro diagnostic laboratory environment
is comprised of a variety of different sources, including sensitive
computerized analyzers and such electrical motor components as centrifuges
and stirring devices (see Table I). Although no disturbances were
observed, electrical motors showed significant spreading of magnetic-field
profiles capable of interfering with sensitive microprocessor-based
components.
ICU and Surgery.
The equipment used in these areas (ESUs and defibrillators, for
example), exhibited strong magnetic- and electric field intensity
characteristics (see Table II). The units' electric-field extended
a few centimeters and exceeded 20 V/m—an intensity value capable
of causing EMI problems in the near vicinity. An outmoded electrocardiograph's
(ECG's) self-interfering power supply and a gamma-counter software
malfunction were among the EMI disturbances detected.
 |
| Figure 3. Layout of radiotherapy
department. |
But these were not the
only issues. To support a patient hospitalized in the ICU, many
of these medical systems had to be in operation mode and installed
near the patient. It is not uncommon for multiple instruments such
as ventilators, suction pumps, dosimetric pumps, vital-signs monitors,
and external pacemakers to be connected to just one patient. In
this hospital, the close proximity of all these devices in a limited
space around the nursing bed complicated the electromagnetic environment
in this area.
| Device Type |
Bmax
10–8
Telsa |
E (V/m) |
| Ultrasound |
1200 |
3.60 |
| Ultrasound |
1000 |
3.00 |
| CT Philips |
930 |
2.79 |
| Mobile Practix |
1280 |
3.84 |
| Film processor |
500 |
1.50 |
| Beta counter |
830 |
2.49 |
| Gamma counter |
1980 |
5.94 |
| Printer GT |
1600 |
4.80 |
| PC Hyuandai |
OR |
OR |
| PC Philips |
OR |
OR |
| Water bath |
50 |
0.15 |
| Survey XETEX |
OR |
OR |
| Gamma camera 1 |
300 |
0.90 |
| Gamma camera 2 |
OR |
OR |
|
| Table IIIa. Medical imaging:
typical devices checked. |
Radiotherapy.
During this study, no interference was observed in this department.
It should be noted, however, that mobile dosimetric systems (e.g.,
rate meters, calibration chambers, etc.) must be carefully checked
for EMI problems because the electronics embedded within them may
record noise and alter their output (see Figure 3).
Medical Imaging.
A gamma-counter unit demonstrated susceptibility symptoms (see Table
III). When strong electromagnetic emitters (e.g., ordinary centrifuges,
mixers, etc.) approached the unit, several software errors were
recorded. These errors disappeared when the emitters were drawn
away. Also, mobile x-ray units were found to interfere with outmoded
ECG units, altering output.
| Department |
EMI Source |
Receptor |
Observation |
| Nuclear medicine |
PC |
Gamma camera |
Negative |
| Nuclear medicine in vitro lab |
Mixer |
Gamma counter |
Disturbance |
| Radiology (x-ray) |
Mammography power
supply |
Mammography |
Negative |
| Radiology (x-ray) |
Digital x-ray
unit display monitor |
Digital x-ray
unit |
Negative |
| Radiology (US-CT) |
PC workstation |
PC |
Negative |
| Radiology (US-CT) |
Air conitioner |
CT |
Negative |
|
| Table IIIb. High-risk
EMI conditions. |
Wards.
Medical systems in the hospital wards were mostly mobile devices
assisting in-bed examination of patients. Among the most common
were mobile resorptions, mobile x-ray units, and ECGs, the latter
of which were found to be the most sensitive within their respective
electromagnetic environment (see Figure 2). The complexity of these
specialized areas increased when visitors brought in external mobile
sources such as cell phones. Such devices were measured in order
to determine whether their usage could influence in-bed hospital
examination equipment (see Table IV).
Outpatient Departments.
As in other areas of the hospital, some of the old-fashioned ECG
units showed susceptibility symptoms. When strong electromagnetic
emitters, such as electrosurgical devices, approached the unit,
the output was altered by noise contamination. In some cases, the
useful signal was totally overlapped and could not be distinguished
from the interference. When the ESUs were drawn away, these errors
disappeared.
| Device Type |
Bmax
10–8
Telsa |
E (V/m) |
| Total 400 |
110 |
0.33 |
| Siemens |
500 |
1.50 |
| Nokia 5110 |
930 |
2.79 |
| Panasonic G 600 |
1280 |
3.84 |
| Panasonic G 520 |
980 |
2.94 |
| Ericsson GF788 |
1800 |
5.4 |
| Ericsson GA628 |
OR |
OR |
| Ericsson 388 |
OR |
OR |
| Ericsson GSM 900 |
1300 |
3.90 |
| Philips Twist |
1240 |
3.72 |
|
Table
IV. Wards: typical mobile phones checked.
|
Auxiliary Facilities.
Several specialized facilities within the hospital environment were
studied. Facilities included areas such as the nutrition department,
the medicine storage area, the medical physics laboratory, the well-hole
area, the washing machines area, and the administration offices.
In contrast to other auxiliary facilities examined, the intercommunication
center and the power supply substation were of particular interest.
These two areas were heavily equipped with transformers that produced
significant levels of electromagnetic radiation. However, although
these high-emission areas were adjacent to the in vitro diagnostic
laboratories, the equipment in the labs was unaffected.
MRI Facility.
The private clinic's MRI installation was also tested.
The unit used a 0.5-T magnet, which was continuously in operation
mode due to the magnet's superconductive type. Cooling facilities
were located in the vicinity, within an adjacent and isolated room
containing the liquid nitrogen and helium installations. The superconductive
facility was shielded by a Faraday cage constructed with high-specification
RF enclosures. Therefore, no significant spread of the magnetic
field was recorded.
Discussion
Magnetic-field measurements
carried out both in the hospital and in the MRI facility covered
all medical equipment from a variety of angles, directions, and
distances. An information system created to administer the acquired
information was ultimately translated into electromagnetic distribution
layouts superimposed to structural plots of the buildings. The electromagnetic
distribution layouts were designed using maximum intensity values
with the distance from the source. An accessible Web site made the
data available to the various hospital departments. The information
facilitated recognition, understanding, and handling of potential
EMI events, which could cause inconvenience and even life-threatening
situations. Digitized layouts indicated high-risk areas in the form
of hot-spot link points and were accompanied by additional technical
information, including the initial raw measurements for each piece
of equipment during several modes of its operation.
Conclusion
Although the researchers
detected EMI in the hospital environment, it proved of minor significance
under real-world conditions in this particular hospital. The most
considerable disturbance was the self-interfering power supply of
an old-fashioned ECG device. The on-line EMI distribution mapping
system was tested successfully under real-world conditions, assisting
the interested parties in identifying the three elements that contributed
to the creation of EMI events to enable elimination of at least
one of them.
It has been shown, therefore,
that the system offered a cost-effective digital alternative for
assessing EMI-related threats. Hospitals and other environments
where EMI events pose a threat are advised to note such information
concerning potential EMI events and take appropriate precautions
when selecting and installing equipment.13-15
Acknowledgments
The authors would like
to express their appreciation to Kostas Panagiotopoulos, PhD, head
of the biomedical engineering department of the Regional General
Distinct Anti-Cancer Hospital of Piraeus, Metaxa, Greece, who enabled,
encouraged, and supported our measurements in all hospital units.
References
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Basile Spyropoulos,
PhD, Dimitris Glotsos, MSc, and Dimitris Batistatos, BSc, are with
the department of medical instrumentation at the Technological Institute
of Athens (Athens, Greece). Ioannis Marneris, PhD, is at the Brookhaven
National Laboratory (Upton, NY). Please direct queries to Spyropoulos.
He can be reached via e-mail at basile@teiath.gr.
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