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Published byConner Dennett Modified over 9 years ago
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RADIATION & PREGNANCY
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Diagnostic & Therapeutic procedures causing exposure of the abdomen of women likely to be pregnant should be avoided unless there is a strong clinical indications
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STOCHASTIC EFFECTS STOCHASTIC EFFECTS
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Stochastic Effects are caused by mutations in a cell or in small group of cells
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STOCHASTIC EFFECTS STOCHASTIC EFFECTS The absorbed dose is not important for severity of the effect, but for probability of the effect depend on the absorbed dose
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STOCHASTIC EFFECTS STOCHASTIC EFFECTS Examples of stochastic effect malignancies and hereditary effects. No threshold dose.
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DETERMINISTIC EFFECTS
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Result from killing of cells. There is a threshold dose. e.g.: Fetal death, gross malformation
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DETERMINISTIC EFFECTS Pre-Implantation: 0 – 8 days post- conception Death of embryo 5 cGy rats 0.9 cGy mice Threshold dose: 10 cGy
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DETERMINISTIC EFFECTS Embryonic = 9 – 60 days Risk of embryonic death remain. higher threshold dose. Risk of malformation is in the order of 0.5% per cGy Threshold dose = 10 cGy Small head size 1% per cGy Threshold dose = 10 – 20 cGy Growth retardation threshold dose = 5 – 25 cGy
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DETERMINISTIC EFFECTS Early fetal = 61 – 104 days Threshold dose for lethality = 0.5 Gy Mental retardation 0.4% per cGy Threshold dose = 12 cGy 0.3 IQ points per cGy Unprovoked seizures 4 – 8 cGy threshold dose All seizure 11 – 15 cGy threshold dose
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DETERMINISTIC EFFECTS Mid fetal = 105 – 175 days post-conception Risk of fetal death remain in this period, but seems to be lower than in the earlier period Threshold doses 0.65Gy for mental retardation 0.5 Gy for small head size 0.5 Gy for growth retardation
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DETERMINISTIC & EFFECTS Late fetal = more than 175 days post-conception Risk of fetal death seem to be low Risk of malformation & mental retardation are negligible
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STOCHASTIC EFFECTS
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Excess Fatal Cancer Natural prevalence of fatal childhood cancer up to the age of 15-year (1:1300) 0.03% per cGy 0.04% - 0.05% cGy Higher risk for those irradiated in the second trimester than those in third trimester
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TUMOURS
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TUMOURS Leukemia, tumours of CNS
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RISK OF GENETIC DISEASE
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NATURAL PREVALENCE IS 1.6%
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Maternal age > 35 Total chromosal abnormality is 2.26% & 9.6% age above 45 1 cGy 0.012% It is clear that risk of radiation effects is smaller than risk effect by age
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Normal risk that a child will have congenital defect is 3% – 6%
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When dose exceed 10 cGy probability increase to 10%
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A dose of 10 cGy – 20 cGy is radiologically not accepted as an indication for an abortion
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Dose to the embryo of 20 cGy at 3-Weeks could be accepted as a reason for “Therapeutic Abortion” Whalen & Batter
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Dose from Nuclear Medicine Diagnostic test is at’s highest estimate 1 cGy
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Threshold dose for deterministic effect is in the order of 10 cGy – 60 cGy
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The risk of cancer induction is 0.03% - 0.06% per cGy If patient received 0.5 cGy (1.5 – 2.5) out of 10,000 Risk of genetic defect (0.5 – 5) out of 10,000
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ProjectionExamination Estimated Fetal Dose per Examination (mGy) Mean (this work) Reported Mean Range (this work) Reported Range APAbdomen a 2.91.90.26 – 15.00.16 – 9.2 PAAbdomen a 1.30.530.64 – 3.00.35 – 0.82 Abdomen b 2.62.5 [1.4]0.26 – 15.00.25 – 19.0 {4.2} APChest a < 0.01 PAChest a < 0.01 Chest b < 0.010.01 [< 0.01]0.002 – 0.43< 0.01 APLumbar Spine a 7.51.90.31 – 40.00.20 – 15.0 LATLumbar Spine a 0.910.410.09 – 3.50.09 – 3.1 Lumbar Spine b 4.24.0 [1.7]0.09 – 40.00.27 – 40.0 {10.0} LATLumbosacral Joint a 1.10.560.10 – 2.030.09 – 2.4 APPelvis b 3.42.0 [1.1]1.4 – 15.00.55 – 22.0 {4.0} APThoracic Spine a < 0.01 < 0.01 – 0.03 PAThoracic Spine a < 0.01 < 0.01 – 0.01 Thoracic Spine b < 0.01< 0.1 [< 0.01]< 0.01< 0.1-0.55 {<0.01} COMPARISON OF THE ESTIMATED MEAN & RANGE OF FETAL DOSE a – Reported mean & range are adapted from Shrimpton et al b – Reported mean & range are adapted from Wagner et al Mean values in square brackets & values curly brackets (representing only maximum values) are adapted from Sharp et al
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ProjectionExamination Estimated Fetal Dose per Examination (mGy) Mean (this work) Reported Mean Range (this work) Reported Range IVU4.86.0 [1.7]2.9 – 6.80.7 – 55.0 {10.0} Barium Enema6.110.0 [6.8]0.3 – 10.40.28 – 130.0 {24.0} Barium Meal1.5- [1.1]0.1 – 2.3- {5.8} Cholecystography0.61.00.08 – 1.10.05 – 16.0 APUrinary Bladder3.90.56 – 11.0 COMPARISON OF THE ESTIMATED MEAN & RANGE OF FETAL DOSE a – Reported mean & range are adapted from Shrimpton et al b – Reported mean & range are adapted from Wagner et al Mean values in square brackets & values curly brackets (representing only maximum values) are adapted from Sharp et al
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ProjectionExamination Fetal dose per examination (mGy) RangeMean APAbdomen0.26 – 15.02.9 PAAbdomen0.64 – 3.01.3 Abdomen a 0.26 – 15.02.6 APChest< 0.01 – 0.01< 0.01 PAChest< 0.01 Chest b > 0.01 – 0.01< 0.01 a – Average for the various projections b – For only one examination MEAN FETAL ABSORBED DOSE PER EXAMINATION (GXR) Contd…
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ProjectionExamination Fetal dose per examination (mGy) RangeMean APHip joint0.11 – 2.10.9 APLumbar Spine0.31 – 40.07.5 LATLumbar Spine0.09 – 3.50.91 OBLLumbar Spine0.61 – 2.01.3 Lumbar Spine a 0.09 – 40.04.2 LATLumbosacral Joint0.10 – 2.01.1 APPelvis1.4 – 15.03.4 APThoracic Spine< 0.01 LATThoracic Spine< 0.01 b Thoracic Spine b < 0.01 a – Average for the various projections b – For only one examination MEAN FETAL ABSORBED DOSE PER EXAMINATION (GXR)
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Examination No. of Cases Fetal dose per examination (mGy) RangeMean Liver42.0 – 4.43.6 Lumbar Spine12.8 Lung21.0 – 1.41.2 Pelvis265.0 – 114.089.0 MEAN FETAL ABSORBED DOSE PER EXAMINATION (CT)
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COMPARISON OF THE ESTIMATED MEAN & RANGE OF FETAL DOSE Radiopharmaceutical Conversion factor (cGy/MBq) [1,3] Activity (MBq] Route of Administration Dose to the Uterus (cGy) 123 I-Sodiumiodide1.4x10 -3 20i.v.2.8x10 -2 123 I-MIBG1.1x10 -3 30i.v.3.3x10 -2 131 I-MIBG8.0x10 -3 300i.v.2.4 67 Ga-citrate7.9X10 -3 150i.v.1.18 201 Tl-chloride5.0x10 -3 100-150i.v.5-7x10 -1 99m Tc-tetrofosmin (1-day protocol, rest) 8.4x10 -4 150i.v.1.3x10 -1 99m Tc-tetrofosmin (1-day protocol, effort) 7.3x10 -4 450i.v.3.3x10 -1 MIBG, Metaiodobenzylguanidine; MDP, methylene diphosphonate; HDP, hydroxydiphosphonate; MAA, macroaggregated albumin; MAG3, mercaptoacetyltriglycine
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COMPARISON OF THE ESTIMATED MEAN & RANGE OF FETAL DOSE Radiopharmaceutical Conversion factor (cGy/MBq) [1,3] Activity (MBq] Route of Administration Dose to the Uterus (cGy) 99m Tc-sestamibi (1-day protocol, rest) 7.8x10 -4 150i.v.1.2x10 -1 99m Tc-sestamibi (1-day protocol, effort) 7.2x10 -4 450i.v.3.2x10 -1 99m Tc-MDP6.1x10 -4 400i.v.2.4x10 -1 99m Tc-HDP6.1x10 -4 400i.v.2.4x10 -1 99m Tc-MAA2.4x10 -4 100i.v.2.4x10 -2 81m Kr-gas 6.0x10 -8 (per minute) Generator: 450-750 MBq/minute Inhalation< 10 -3 99m Tc-MAG31.2x10 -3 40i.v.4.8x10 -2 MIBG, Metaiodobenzylguanidine; MDP, methylene diphosphonate; HDP, hydroxydiphosphonate; MAA, macroaggregated albumin; MAG3, mercaptoacetyltriglycine
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131 I-Therapy & Pregnancy
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10 – 12 Weeks thyroid gland of fetus start to function. For every 10mCi the mother receive, the fetus will receive 1 cGy..
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Radiation Worker’s & Pregnancy Radiation worker who is pregnant should not receive more than 1 mSv during the whole pregnancy.
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CONCLUSION
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CONCLUSION For diagnostic examination whether radiological or Nuclear Medicine, the risks for the fetus are Extremely low For therapeutic dose The doses may be high enough to cause unacceptable tissue damage.
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