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perimental treatment protocols and cannot therefore be recommended for

introduction into the A.S.P.

http://dx.doi.org/10.1016/j.ejmp.2016.01.470

F.462

ASSESSMENT OF WORKERS’ EXPOSURE DUE TO BLUE-LIGHT NEONATAL

PHOTOTHERAPY

C. Spadavecchia *

, a , b ,

C. Pasquali

b ,

R. Villa

a , b ,

C. Ghezzi

b ,

N. Paruccini

b ,

A. Crespi

b .

a

Scuola di Specializzazione in Fisica Medica, UNIMI, Milano, Italy;

b

A.O. San Gerardo, S.C. Fisica Sanitaria, Monza, Italy

Introduction:

Phototherapy is used for neonatal jaundice to decrease bili-

rubin level in blood: light converts bilirubin molecules into water soluble

isomers that can be excreted by the body.

The objective of this study was to assess workers’ exposure to Artificial

Optical Radiation, according to D.L.81/08.

Materials and Methods:

Spectral irradiances were acquired on 8 light-

emitting diodes (LEDs) neonatal systems with the HD2000

+

spectroradiometer, operating in the 200–1100 nm wavelength-band.

These measurements were performed both in high and low intensity

regimen, under the LEDs and in worker typical position (on the side of

infant’s bed) with the lamp covered and uncovered by a blanket attenu-

ating light.

Effective radiances were calculated using the spectral weighting func-

tions for retinal thermal and blue-light hazard then averaged on the 8

systems.

The direct spectra displayed a peak around 460 nm (blue region), corre-

sponding to the wavelength of maximum absorption of light by bilirubin

(458 nm).

Results:

In worker position using blanket, retinal thermal radiances Lr were

19.26 and 8.40 W/(m

2

sr) in the high and low intensity regimen respec-

tively, to be compared with the Lr recommended limit of 280,000 W/(m

2

sr).

Values of the blue-light radiances Lb were 1.90 (high) and 0.81 (low)

W/(m

2

sr) with a limit of 100 W/(m

2

sr).

Conclusions:

The results fully complied with the recommended limit levels.

The presence of a blanket covering the source reduced values of radiance

by almost 60%, confirming its use as a valid protective measure guaran-

teeing workers’ safety.

http://dx.doi.org/10.1016/j.ejmp.2016.01.471

F.463

ELECTROMAGNETIC FIELDS OF A NEW FERROMAGNETIC SURGICAL

SYSTEM

R. Villa

* , a , b ,

C. Spadavecchi

a a , b ,

C. Pasquali

b ,

G. Montanari

b ,

A. Crespi

b .

a

Scuola di Specializzazione in Fisica Medica, UNIMI, Milano, Italy;

b

A.O. San

Gerardo, S.C. Fisica Sanitaria, Monza, Italy

Introduction:

FMwand is a new ferromagnetic surgical system which con-

sists of a power generator and a handle: the energy is used to excite a

ferromagnetic coating at the tip of the handheld FMwand, producing rapid

heating to simultaneously cut and coagulate soft tissue.

Materials and methods:

The system operates at 40.68 MHz, a frequency

considerably higher than the typical ones of electrosurgical devices, and

has a closed loop energy circuit, that eliminates the need for a remote

grounding electrode and the passage of electric current through the patient’s

body.

Effective electric fields (ERMS) were measured with NARDA PMM 8053B

electrometer and EP330 field-probe. To have a comparison with a stan-

dard monopolar electrosurgery, ERMS were also acquired for Martin ME402.

ERMS were measured near the handheld and along the outspread cable every

75 cm, on contact and at a distance of 5 and 10 cm. The typical and the

highest power (30/60 W for FMwand, 100/360 W for Martin) were set on

the power generator.

Results:

Measurements confirmed that the cable is the main source of elec-

tric field, without correlation between the position along the cable and the

intensity of field.

ERMS decreased with the increasing of the distance from the cable.

Comparing the two systems, FMwand was characterized by an emitted ERMS

equal to 20% of the correspondent value acquired with the standard

monopolar electrosurgery Martin ME402.

Conclusions:

With the FMwand we obtained electric fields much lower than

a standard electrosurgical device, which is in agreement with some clin-

ical studies reporting that the system reduces electromagnetic interference

with cardiac implantable electronic devices (CIEDs), such as permanent pace-

makers and implantable cardioverter defibrillators.

http://dx.doi.org/10.1016/j.ejmp.2016.01.472

e137

Abstracts/Physica Medica 32 (2016) e135–e137