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Diagnosing pulmonary embolism in pregnancy: rationalizing fetal radiation exposure in radiological procedures
Author(s) -
Nijkeuter M.,
Geleijns J.,
De Roos A.,
Meinders A. E.,
Huisman M. V.
Publication year - 2004
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/j.1538-7836.2004.00929.x
Subject(s) - radiological weapon , medicine , pulmonary embolism , pregnancy , radiation exposure , obstetrics , radiology , fetus , cardiology , nuclear medicine , genetics , biology
In pregnancy, the diagnosis of pulmonary embolism (PE) is problematic. There is doubt as to whether objective diagnostic tests are needed and confusion as to what objective test is the safest with respect to fetal radiation exposure. A recent study has reported a very low (1.8%) prevalence of high-probability ventilation-perfusion (VQ) lung scans in pregnant women suspected of PE [1]. From this study it is apparent that the clinical diagnosis of PE is inaccurate and therefore objective diagnostic tests are mandatory, in order to avoid treatment of women that do not have PE. Currently, helical computerized tomography (CT) and VQ scintigraphy are themost common diagnostic tests used in nonpregnant patients with suspected PE. Physicians are reluctant to perform helical CT in pregnant women because of potential adverse effects of radiation exposure to the fetus. VQ scintigraphy has been assumed to be associated with less radiation exposure than helical CT. To compare the relative amounts of radiation exposure to the fetus, we calculated fetal radiation exposure when singleand multidetector row helical CT and VQ scintigraphy were performed using our local hospital protocols. Further, we compared our data with data of the literature. Since there are no established methods for calculating fetal radiation exposure in diagnostic radiological procedures, we used a pragmatic approach. The amount of radiation absorbed by the fetus was assumed to be equal to that absorbed by the uterus of a non-pregnant woman. Assessment of the uterus dose was achieved by measurement of the computed tomography dose index and the application of organ dose conversion factors [2]. The following CT protocols were used for fetal dose assessment: 120 kV, 250 mAs, slice thickness 3 mm and pitch factor 1.7 for single-detector row helical CT (Philips AVE, Best, the Netherlands) 2 and 120 kV, 85 mAs, slice thickness 16 · 0.5 mm and pitch factor 1.4 for multidetector row helical CT (Toshiba Aquilion 16, Shimoishigami, Otawara-shi, Tochigi, Japan) 3 . The scanned range extends from the dorsal lung sinus to the top of the lung. Since fetal radiation exposure was calculated, physical measures (e.g. abdominal shielding with lead) to reduce radiation exposure were not taken into account. For the perfusion scintigraphy protocol we used 40 MBq of Technetium-labeled albumin aggregates. In our institution, ventilation scintigraphy is performed with Krypton-81 m, which is inhaled for two minutes per image. The RubidiumKrypton generator generates 450–750 MBq per min. Our calculated data of CT radiation exposure were compared with doses in nuclear medicine and doses calculated by the International Commission on Radiological Protection (ICRP) and the National Radiological Protection Board (NRPB) of the UK [3,4]. The calculated dose of radiation absorbed by the fetus for a single-detector row helical CT was 0.026 mSv. An even lower dose (0.013 mSv) was calculated for the multidetector row helical CT. In comparison, the calculated dose of fetal radiation with perfusion scintigraphy was 0.11–0.20 mSv. In comparison with doses given by the ICRP and NRPB (Table 1), our calculated doses of helical CT were low. Our study suggests that performing a helical CT according to our local protocol, whether singleor multidetector row, exposes the fetus to less radiation than perfusion scintigraphy. Our findings are clearly contradictive to the general idea that helical CT is more hazardous to the fetus than perfusion scintigraphy. Regarding the generalizability of our data, it is apparent that our calculated fetal radiation dose for CT is well within the range of that found by others. It has been documented that radiation exposure to the patient for a given radiological procedure can vary considerably between different institutions and even within the same institution. There are several factors that affect radiation dose from CT, e.g. (beam energy, tubecurrent time product, pitch, collimation, patient size and dose reduction options). Each institution should therefore carefully scrutinize its protocol for performing helical CT and define the optimal balance between minimal patient radiation exposure and maximal diagnostic CT image quality. Correspondence: Dr M.V. Huisman, Department of General Internal Medicine, Room C1 R 43, Leiden University Medical Center, PO Box 960

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