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100 D. Maulik<br />

on average 0.23 8C above the temperature of the uterine<br />

wall [32] and fetal core temperature is 0.75 8C<br />

above its skin temperature [33].<br />

Miller and Ziskin [23] suggested that the probability<br />

of any measurable bioeffects from diagnostic insonation<br />

is minimal or nonexistent if the maximum<br />

temperature rise remains 28C or less in an afebrile<br />

subject. Temperature elevations not exceeding 398C<br />

are most unlikely to induce any fetal abnormalities.<br />

However, at higher temperatures, the duration of ultrasound<br />

exposure becomes a significant factor. Indeed,<br />

as shown in Fig. 8.2, these authors have defined<br />

a boundary line based on the temperature rise and<br />

exposure duration; below this line, risks of thermal<br />

bioeffects are virtually nonexistent. The authors recommended<br />

that an ultrasound examination need not<br />

be restricted if the combination of temperature elevation<br />

and exposure duration remains below this<br />

boundary line.<br />

In obstetrical ultrasonography, fetal developmental<br />

issues require additional considerations. Fetal vulnerability<br />

in the worst case scenario demands prudent<br />

practice while not depriving the patient of the benefits<br />

of diagnostic ultrasonography. This issue has been discussed<br />

extensively by the various international societies<br />

who have issued official statements on thermal effects<br />

and the safe use of diagnostic insonation.<br />

The WFSUMB endorsed the following recommendations<br />

regarding Doppler in 1997:<br />

ªIt has been demonstrated in experiments with unperfused<br />

tissue that some Doppler diagnostic<br />

equipment has the potential to produce biologically<br />

significant temperature rises, specifically at<br />

bone/soft tissue interfaces. The effects of elevated<br />

temperatures may be minimised by keeping the<br />

time for which the beam passes through any one<br />

point in tissue as short as possible. Where output<br />

power can be controlled, the lowest available<br />

power level consistent with obtaining the desired<br />

diagnostic information should be used. Although<br />

the data on humans are sparse, it is clear from animal<br />

studies that exposures resulting in temperatures<br />

less than 38.5 8C can be used without reservation<br />

on thermal grounds. This includes obstetric<br />

applicationsº [10].<br />

The 1997 AIUM position on temperature elevation<br />

and exposure duration is as follows [7]:<br />

n ªFor exposure duration up to 50 hours, there have<br />

been no significant biological effects observed due<br />

to temperature increases less than or equal to 28C<br />

above normal.<br />

n For temperature increases greater than 28C above<br />

normal, there have been no significant biological<br />

effects observed due to temperature increases less<br />

than or equal to 6±(log 10 t/0.6), where t is the exposure<br />

duration ranging from 1 to 250 min. For<br />

example, for temperature increases of 4 8C and<br />

6 8C, the corresponding limits for the exposure<br />

duration t are 16 min and 1 min respectively.<br />

n In general, adult tissues are more tolerant of temperature<br />

increases than fetal and neonatal tissues.<br />

Fig. 8.2. Thermal bioeffects. A plot of thermally produced<br />

biological effects that have been reported in the literature<br />

in which the temperature elevation and exposure durations<br />

are provided. Each data point represents either the lowest<br />

temperature reported for any duration or the shortest<br />

duration for any temperature reported for a given effect.<br />

The solid lines link multiple data points relating to the<br />

same bioeffect. The dashed line represents a lower boundary<br />

(t43 = 1) for observed, thermally induced biological effects.<br />

(With permission from [23])

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