Difference between revisions of "CT with IV contrast"

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'''Contrast CT''' is '''[[CT scan]]''' using [[radiocontrast]], and in Radlines it refers to a CT scan using IV contrast except otherwise noted.
+
'''[[CT scan|Computed tomography]] (CT) with intravenous (IV) [[contrast medium]]''':
  
 +
==Related terms==
 
'''Bolus tracking''' is where a specified location within the circulatory system is monitored during IV contrast infusion, and the timing of the main imaging is counted from when the contrast reaches this location (sufficiently to achieve a specified threshold).
 
'''Bolus tracking''' is where a specified location within the circulatory system is monitored during IV contrast infusion, and the timing of the main imaging is counted from when the contrast reaches this location (sufficiently to achieve a specified threshold).
  
 
'''Washout''' is where tissue loads radiocontrast during arterial phase, but then returns to a rather hypodense state in venous or later phases. This is a property of for example [[hepatocellular carcinoma]] as compared to the rest of the liver parenchyma.<ref name="ChoiLee2014">{{cite journal|last1=Choi|first1=Jin-Young|last2=Lee|first2=Jeong-Min|last3=Sirlin|first3=Claude B.|title=CT and MR Imaging Diagnosis and Staging of Hepatocellular Carcinoma: Part II. Extracellular Agents, Hepatobiliary Agents, and Ancillary Imaging Features|journal=Radiology|volume=273|issue=1|year=2014|pages=30–50|issn=0033-8419|doi=10.1148/radiol.14132362|pmc=4263770|pmid=25247563}}</ref>
 
'''Washout''' is where tissue loads radiocontrast during arterial phase, but then returns to a rather hypodense state in venous or later phases. This is a property of for example [[hepatocellular carcinoma]] as compared to the rest of the liver parenchyma.<ref name="ChoiLee2014">{{cite journal|last1=Choi|first1=Jin-Young|last2=Lee|first2=Jeong-Min|last3=Sirlin|first3=Claude B.|title=CT and MR Imaging Diagnosis and Staging of Hepatocellular Carcinoma: Part II. Extracellular Agents, Hepatobiliary Agents, and Ancillary Imaging Features|journal=Radiology|volume=273|issue=1|year=2014|pages=30–50|issn=0033-8419|doi=10.1148/radiol.14132362|pmc=4263770|pmid=25247563}}</ref>
  
==Contrast-induced nephropathy==
+
==Risk factors==
Decreased renal function and several other conditions increase the risk of contrast-induced nephropathy, which is a potentially lethal renal injury to the kidney following intravenous radiocontrast.<ref name="RudnickFeldman2008">{{cite journal|last1=Rudnick|first1=M.|last2=Feldman|first2=H.|title=Contrast-Induced Nephropathy: What Are the True Clinical Consequences?|journal=Clinical Journal of the American Society of Nephrology|volume=3|issue=1|year=2008|pages=263–272|issn=1555-9041|doi=10.2215/CJN.03690907}}</ref>  
+
In Swedish practice<ref>{{NU Hospital Group}}</ref> the standard risk factor questions include presence or absence of:
 +
*Renal or urinary disease
 +
*Thyroid disorders
 +
*Myasthenia gravis: Older forms of iodinated contrast have caused an increased risk of exacerbation of the disease, but modern forms have no immediate increased risk.<ref name="MehriziPascuzzi2014">{{cite journal|last1=Mehrizi|first1=Mehyar|last2=Pascuzzi|first2=Robert M.|title=Complications of radiologic contrast in patients with myasthenia gravis|journal=Muscle & Nerve|volume=50|issue=3|year=2014|pages=443–444|issn=0148639X|doi=10.1002/mus.24254|pmid=24677227}}</ref>
 +
*Diabetes and heart disease: These are aggravating factors in low renal function (see [[CT with IV contrast in low renal function]])
  
[[File:Contrast CT in low GFR.png|thumb|250px|In case of low GFR, the procedure depends on whether the dose that can be given is larger or less than the needed dose.]]
+
===Low renal function===
The main alternatives in people with a risk of contrast-induced nephropathy are:
+
{{Main|CT with IV contrast in low renal function}}
*'''Adjustment''' of the radiocontrast dose
+
Decreased renal function and several other conditions increase the risk of '''contrast-induced nephropathy''', which is a potentially lethal renal injury to the kidney following intravenous radiocontrast.<ref name="RudnickFeldman2008">{{cite journal|last1=Rudnick|first1=M.|last2=Feldman|first2=H.|title=Contrast-Induced Nephropathy: What Are the True Clinical Consequences?|journal=Clinical Journal of the American Society of Nephrology|volume=3|issue=1|year=2008|pages=263–272|issn=1555-9041|doi=10.2215/CJN.03690907}}</ref>
*'''Treating or mitigating risk factors'''
 
*Using '''no intravenous contrast''' for the investigation.
 
*Switching to '''another modality''' such as [[ultrasonography]] or [[MRI]]
 
  
===Risk factors===
+
;When it matters
The Roxana Mehran score predictor applies the following ten variables:<ref name=Modi2017>{{cite web|url=https://www.ncbi.nlm.nih.gov/books/NBK448066/|title=Contrast-Induced Nephropathy|website=StatPearls Publishing|year=2017|author=Kalgi Modi, Scott C. Dulebohn}} [http://creativecommons.org/licenses/by/4.0/ CC-BY-4.0]</ref>
+
According to European guidelines, the main risk factors of ''contrast-induced nephropathy'':<ref name="NymanAhlkvist2018">{{cite journal|last1=Nyman|first1=Ulf|last2=Ahlkvist|first2=Joanna|last3=Aspelin|first3=Peter|last4=Brismar|first4=Torkel|last5=Frid|first5=Anders|last6=Hellström|first6=Mikael|last7=Liss|first7=Per|last8=Sterner|first8=Gunnar|last9=Leander|first9=Peter|title=Preventing contrast medium-induced acute kidney injury|journal=European Radiology|year=2018|issn=0938-7994|doi=10.1007/s00330-018-5678-6}}</ref>
*Age (4 points if older than 75 years old)
+
*Estimated glomerular filtration rate (eGFR) of less than '''30 ml/min'''/1.73 m2 before intra-venous or intra-arterial radiocontrast administration with second-pass renal exposure (passing lungs or other tissues before the kidneys).
*Anemia (3 points)
+
*eGFR of less than 45 ml/min/1.73 m<sup>2</sup> before intra-arterial administration with first-pass renal exposure or in ICU patients
*Use of an intra-aortic balloon pump (5 points)
+
*Known or suspected acute renal failure
*Decreased real function. In terms of estimated glomerular filtration rate in ml/min:
+
*Large doses of radiocontrast given IA with first-pass renal exposure
:*eGFR 60 to 40 (2 points)
+
*Multiple radiocontrast injections within 48-72 h
:*eGFR 40 to 20 (4 points)
 
:*eGFR less than 20 (6 points)
 
*Hypotension (5 points, if systolic BP less than 80 mmHg for at least one hour requiring inotropic support)
 
*Contrast media volume (1 point per 100 ml)
 
*Congestive heart failure (5 points)
 
*Diabetes (3 points).
 
A risk score of less than 6 carries a risk of 7.5% to score more than 16 carries up to 57% risk.<ref name=Modi2017/>
 
  
===Adjustment of dose===
+
[[File:Contrast CT in low GFR.png|thumb|260px|center|In case of low GFR, other risk factors need to be checked. Subsequently, the procedure depends on whether the dose that can be given is larger or less than the needed dose.]]
If and how to adjust the dose depends on supply and demand:
 
  
====How much contrast can be given?====
+
''Further reading: [[CT with IV contrast in low renal function]]''
In some emergent conditions such as [[CT of aortic aneurysm]] with suspected rupture, the need for contrast is greater than the risk of contrast-induced nephropathy.
 
  
For the rest of the investigations, evidence suggests that contrast doses should be limited to a ratio of grams of iodine to glomerular filtration rate (I<sub>gram</sub> / GFR<sub>ml/min</sub>) of a maximum of 1 g/(ml/min).<ref name="KeaneyHannon2013">{{cite journal|last1=Keaney|first1=J. J.|last2=Hannon|first2=C. M.|last3=Murray|first3=P. T.|title=Contrast-induced acute kidney injury: how much contrast is safe?|journal=Nephrology Dialysis Transplantation|volume=28|issue=6|year=2013|pages=1376–1383|issn=0931-0509|doi=10.1093/ndt/gfs602}}</ref> According to European guidelines, the ratio should be less than 1.1 g/(ml/min) for intra-arterial contrast medium administration with first-pass renal exposure (not passing lungs or peripheral tissue before reaching the kidneys).<ref name="NymanAhlkvist2018">{{cite journal|last1=Nyman|first1=Ulf|last2=Ahlkvist|first2=Joanna|last3=Aspelin|first3=Peter|last4=Brismar|first4=Torkel|last5=Frid|first5=Anders|last6=Hellström|first6=Mikael|last7=Liss|first7=Per|last8=Sterner|first8=Gunnar|last9=Leander|first9=Peter|title=Preventing contrast medium-induced acute kidney injury|journal=European Radiology|year=2018|issn=0938-7994|doi=10.1007/s00330-018-5678-6}}</ref> Swedish guidelines are more restrictive, recommending a ratio of less than 0.5 g/(ml/min) in patients with risk factors and irrespective of route of administration, and even more caution in first-pass renal exposure.<ref name="NymanAhlkvist2018"/>
+
===Allergy===
 
+
[[File:Intramuscular site of adrenaline.jpg|150px|thumb]]
{|class="wikitable" align="center"
 
|+ Volume for various Iodine concentrations
 
! I<sub>gram</sub> / GFR<sub>ml/min</sub> <br>ratio !! 240 mg/ml !! 350 mg/ml !! 370 mg/ml
 
|-
 
| 0.5 || 2.1 ml *GFR<sub>ml/min</sub> || 1.4 ml *GFR<sub>ml/min</sub> || 1.4 ml *GFR<sub>ml/min</sub>
 
|-
 
| 1 || 4.2 ml *GFR<sub>ml/min</sub> || 2.9 ml *GFR<sub>ml/min</sub> || 2.7 ml *GFR<sub>ml/min</sub>
 
|-
 
| 1.1 || 4.6 ml *GFR<sub>ml/min</sub> || 3.1 ml *GFR<sub>ml/min</sub> || 3.0 ml *GFR<sub>ml/min</sub>
 
|}
 
 
 
====How much contrast is needed====
 
 
 
{|class="wikitable"
 
|+ Sufficient volume for normal weight adults
 
!colspan=2 rowspan=2| Exam !!colspan=3| Iodine concentration !!rowspan=2| Comments
 
|-
 
! 300 mg/ml !! 350 mg/ml !! 370 mg/ml
 
|-
 
|colspan=2| [[CT of the head|CT of brain]] || 95ml<ref name=NZ>{{cite web|url=http://www.medsafe.govt.nz/profs/Datasheet/o/Omnipaqueinj.pdf|title=New Zealand Datasheet|website=New Zealand Medicines and Medical Devices Safety Authority|accessdate=2018-10-16}}</ref> || 80 ml<ref name=NZ/> || 75 ml<ref name=NZ/> ||
 
|-
 
|rowspan=2| [[CT of the thorax|CT of thorax]] || Overall || 70 - 95 ml<ref name="IezziLarici2017" group="notes">0.3–0.4 gI/kg in a 70kg individual, according to:
 
*{{cite journal|last1=Iezzi|first1=Roberto|last2=Larici|first2=Anna Rita|last3=Franchi|first3=Paola|last4=Marano|first4=Riccardo|last5=Magarelli|first5=Nicola|last6=Posa|first6=Alessandro|last7=Merlino|first7=Biagio|last8=Manfredi|first8=Riccardo|last9=Colosimo|first9=Cesare|title=Tailoring protocols for chest CT applications: when and how?|journal=Diagnostic and Interventional Radiology|volume=23|issue=6|year=2017|pages=420–427|issn=13053825|doi=10.5152/dir.2017.16615}}</ref> || 60 - 80 ml<ref name="IezziLarici2017" group="notes"/> || 55 - 75 ml<ref name="IezziLarici2017" group="notes"/> || Parenchymal changes of the lung can often be evaluated adequately without the use of intravenous contrast.
 
|-
 
| [[CT pulmonary angiogram]] || 20 ml<ref name="LeroyerMeier2016" group="notes">Using dual energy CTA (such as 90/150SnkVp), according to:
 
*{{cite journal|last1=Leroyer|first1=Christophe|last2=Meier|first2=Andreas|last3=Higashigaito|first3=Kai|last4=Martini|first4=Katharina|last5=Wurnig|first5=Moritz|last6=Seifert|first6=Burkhardt|last7=Keller|first7=Dagmar|last8=Frauenfelder|first8=Thomas|last9=Alkadhi|first9=Hatem|title=Dual Energy CT Pulmonary Angiography with 6g Iodine—A Propensity Score-Matched Study|journal=PLOS ONE|volume=11|issue=12|year=2016|pages=e0167214|issn=1932-6203|doi=10.1371/journal.pone.0167214}}</ref> || 17 ml<ref name="LeroyerMeier2016" group="notes"/> || 15 ml<ref name="LeroyerMeier2016" group="notes"/> || Minimal amount when using specific low-contrast protocol.<ref name="LeroyerMeier2016" group="notes"/>
 
|-
 
|rowspan=2| [[CT of the abdomen and pelvis|CT of abdomen]] || Overall || 70 ml<ref name=NZ/> || 60 ml<ref name=NZ/> || 55 ml<ref name=NZ/> ||
 
|-
 
| Liver || 55 ml<ref name=Liver group="notes">The liver generally needs an enhancement of at least 30 HU for proper evaluation according to:
 
*{{cite book|title=Multislice CT|edition=3|year=2010|publisher=Springer-Verlag Berlin and Heidelberg GmbH & Co. KG|isbn=9783642069680}}
 
In males at 30 years of age, there is an estimated 0.027 HU of liver parenchymal enhancement per kilogram of body weight and per gram of iodine, when injected at 4 ml per second, according to:
 
*{{cite journal|last1=Bae|first1=Kyongtae T.|title=Intravenous Contrast Medium Administration and Scan Timing at CT: Considerations and Approaches|journal=Radiology|volume=256|issue=1|year=2010|pages=32–61|issn=0033-8419|doi=10.1148/radiol.10090908}}
 
This example takes the example of a man with a typical weight of 70 kg.</ref> || 45 ml<ref name=Liver group="notes"/> || 40-45 ml<ref name=Liver group="notes"/> || Minimal required amount.<ref name=Liver group="notes"/>
 
|-
 
|colspan=2| [[CT angiography]] || 25 ml<ref name=Angiography group="notes">CT-angiography in a 70kg person, with 100-150 mg I/kg by using 80 kVp, mAs-compensation for constant CNR, fixed injection duration adapted to scan time, automatic bolus tracking and a saline chaser, according to:
 
*{{cite journal|last1=Nyman|first1=Ulf|title=Contrast Medium-Induced Nephropathy (CIN) Gram-Iodine/GFR Ratio to Predict CIN and Strategies to Reduce Contrast Medium Doses|year=2012|doi=10.5772/29992}}</ref> ||colspan=2| 20 ml<ref name=Angiography group="notes"/> || When using specific low-contrast protocol.<ref name=Angiography group="notes"/>
 
|}
 
 
 
Departments often have formulas that give the amount of contrast needed for various investigations, using patient sex and weight as main parameters. These may include creatitine levels as well, and in such cases it can help to get a value of of much contrast would hypothetically have been given if the creatinine level was normal, such as for example 80 μmol/L or 0.9 mg/dL. This value can be compared to how much can actually be given in order to determine if it is worth doing the exam with contrast.
 
 
 
===Treating risk factors===
 
Risk factors can sometimes be treated or at least mitigated, especially if having suddenly appeared, such as a decreased renal function when it was previously normal. In such cases a common easily treated cause is dehydration.
 
 
 
'''Hydration''' by drinking or intravenous volume expander, either before or after contract administration, decreases the risk of contrast-induced nephropathy.<ref name="YangHiremath2013">{{cite journal|last1=Yang|first1=Xiaoming|last2=Hiremath|first2=Swapnil|last3=Akbari|first3=Ayub|last4=Shabana|first4=Wael|last5=Fergusson|first5=Dean A.|last6=Knoll|first6=Greg A.|title=Prevention of Contrast-Induced Acute Kidney Injury: Is Simple Oral Hydration Similar To Intravenous? A Systematic Review of the Evidence|journal=PLoS ONE|volume=8|issue=3|year=2013|pages=e60009|issn=1932-6203|doi=10.1371/journal.pone.0060009}}</ref>
 
 
 
==Allergy==
 
===Contrast medium reaction===
 
[[File:Injection Sites Intramuscular Thigh Adult.png|300px|right]]
 
 
{{Main|Contrast medium reaction}}
 
{{Main|Contrast medium reaction}}
 
In a more severe reaction:<ref name=SURF>Unless otherwise specified in lists and table: {{cite web|url=http://www.mastcellssjukdom.se/wp-content/uploads/2015/12/Nationella_rekommendationer_%C3%B6verk%C3%A4nslighetsreaktioner_kontrastmedel__PDF_2014-10-17.pdf|title=Hypersensitivity reactions against contrast media - Swedish Society of Uroradiology [Swedish: Överkänslighetsreaktioner mot kontrastmedel – SURFs kontrastmedelsgrupp] ], 2014-10-17}}</ref>
 
In a more severe reaction:<ref name=SURF>Unless otherwise specified in lists and table: {{cite web|url=http://www.mastcellssjukdom.se/wp-content/uploads/2015/12/Nationella_rekommendationer_%C3%B6verk%C3%A4nslighetsreaktioner_kontrastmedel__PDF_2014-10-17.pdf|title=Hypersensitivity reactions against contrast media - Swedish Society of Uroradiology [Swedish: Överkänslighetsreaktioner mot kontrastmedel – SURFs kontrastmedelsgrupp] ], 2014-10-17}}</ref>
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*Summon an '''anesthesiologist'''
 
*Summon an '''anesthesiologist'''
  
===Pre-medication===
+
;Prevention
Before a contrast CT of a patient with known allergic-like or unknown-type of contrast reaction to the same class of contrast medium (such as iodinated), the American College of of Radiology recommends premedication with a glucocorticoid, preferably starting 12 or 13 hours before contrast administration.<ref>{{cite web|url=https://www.acr.org/-/media/ACR/Files/Clinical-Resources/Contrast_Media.pdf#page=11|Page 9 in: Manual on Contrast Media|website=American College of Radiology, Committee on Drugs and Contrast Media|accessdate=2018-08-25}} Version 10.3. 2018. ACR </ref>  
+
{{Main|Prevention of contrast medium reaction}}
 +
Before a contrast CT of a patient with known allergic-like or unknown-type of contrast reaction to the same class of contrast medium (such as iodinated), the American College of of Radiology recommends premedication with a glucocorticoid, preferably starting 12 or 13 hours before contrast administration.<ref>{{cite web|url=https://www.acr.org/-/media/ACR/Files/Clinical-Resources/Contrast_Media.pdf#page=11|title=Page 9 in: ACR Manual On Contrast Media|website=American College of Radiology, Committee on Drugs and Contrast Media|accessdate=2018-08-25}} Version 10.3. 2018. ACR </ref>
 +
 
 +
===Hyperthyroidism===
 +
Patients at risk for contrast-induced hyperthyroidism are mainly those with diagnosed yet untreated hyperthyroidism, which may motivate contrast-free alternatives such as using a different modality.<ref name=UpToDate-thyr>{{cite web|url=https://www.uptodate.com/contents/iodine-induced-thyroid-dysfunction|title=Iodine-induced thyroid dysfunction|author=Martin I Surks, MD|website=UpToDate}} This topic last updated: Apr 02, 2019.</ref>
 +
 
 +
In older patients with multinodular goiter and borderline low or subnormal TSH concentrations, a suggested measure is measurement of thyroid function tests three to four weeks after contrast administration.<ref name=UpToDate-thyr/> Limited evidence suggests that antithyroid agents before the investigation may blunt or prevent hyperthyroidism.<ref name=UpToDate-thyr/>
 +
 
 +
===Pregnancy===
 +
Iodinated contrast in pregnancy, when orally administered, is harmless.<ref name=acog>{{cite web|url=https://www.acog.org/Resources-And-Publications/Committee-Opinions/Committee-on-Obstetric-Practice/Guidelines-for-Diagnostic-Imaging-During-Pregnancy-and-Lactation|title=Guidelines for Diagnostic Imaging During Pregnancy and Lactation|website=[[American Congress of Obstetricians and Gynecologists]]}} February 2016</ref> Intravenous administration of iodinated radiocontrast agents can cross the placenta and enter the fetal circulation, but animal studies have reported no teratogenic or mutagenic effects from its use. There have been theoretical concerns about potential harm of free iodide on the fetal thyroid gland,<ref name=acog/> but multiple studies have shown that a single dose of intravenously administered iodinated contrast medium to a pregnant mother has no effect on neonatal thyroid function.<ref>{{cite web|url=https://www.acr.org/~/media/37D84428BF1D4E1B9A3A2918DA9E27A3.pdf|title=ACR Manual on Contrast Media. Version 10.3|year=2017|website=American College of Radiology|publisher=American College of Radiology Committee on Drugs and Contrast Media|accessdate=2017-07-30}}</ref> Nevertheless, it generally is recommended that radiocontrast only be used if absolutely required to obtain additional diagnostic information that will improve the care of the fetus or mother.<ref name=acog/>
  
Asthma, atopy, and drug or food allergy have been regarded as generally not conferring enough risk to motivate glucocorticiod premedication.<ref>{{cite web|url=https://www.cdha.nshealth.ca/|website=Nova Scotia Department of Health and Wellness|accessdate=2018-08-25|title=Guidelines for contrast media pre-medication}} October 2014</ref>
+
===Breastfeeding===
 +
American College of Radiology guidelines state that iodinated contrast administration to a breastfeeding mother is considered safe for both the mother and child.<ref name=yale>{{cite web|url=https://medicine.yale.edu/diagnosticradiology/patientcare/policies/breastfeeding.aspx|title=Diagnostic Radiology Procedures on Breastfeeding Patients|website=[[Yale School of Medicine]]|accessdate=2019-07-08}}</ref> Still, mothers who remain concerned about any potential adverse effects to the child are recommended to have the option of abstaining from breastfeeding for 24 hours, with continued milk extraction such as by a breast pump during that period.<ref name=yale/> Mothers that opt for this for non-emergent exams may also use a breast pump to obtain milk before the exam in order to feed the child during the 24-hour abstinence period.<ref name=yale/>
  
 
==Phases==
 
==Phases==
Depending on the purpose of the investigation, there are standardized protocols for time intervals between intravenous radiocontrast administration and image acquisition, in order to visualize the dynamics of contrast enhancements in different organs and tissues.<ref name="Bae2010">{{cite journal|last1=Bae|first1=Kyongtae T.|title=Intravenous Contrast Medium Administration and Scan Timing at CT: Considerations and Approaches|journal=Radiology|volume=256|issue=1|year=2010|pages=32–61|issn=0033-8419|doi=10.1148/radiol.10090908}}</ref> The main phases thereof are as follows:<ref name=radiologyassistant>{{cite web|url=http://www.radiologyassistant.nl/en/p52c04470dbd5c/ct-contrast-injection-and-protocols.html|title=CT contrast injection and protocols|author=Robin Smithuis|website=Radiology Assistant|accessdate=2017-12-13}}</ref>
+
Depending on the purpose of the investigation, there are standardized protocols for time intervals between intravenous radiocontrast administration and image acquisition, in order to visualize the dynamics of contrast enhancements in different organs and tissues.<ref name="Bae2010">{{cite journal|last1=Bae|first1=Kyongtae T.|title=Intravenous Contrast Medium Administration and Scan Timing at CT: Considerations and Approaches|journal=Radiology|volume=256|issue=1|year=2010|pages=32–61|issn=0033-8419|doi=10.1148/radiol.10090908}}</ref> The main phases thereof are as follows in table below.<ref name=radiologyassistant>{{cite web|url=http://www.radiologyassistant.nl/en/p52c04470dbd5c/ct-contrast-injection-and-protocols.html|title=CT contrast injection and protocols|author=Robin Smithuis|website=Radiology Assistant|accessdate=2017-12-13}}</ref>
 +
 
 +
'''CT angiography''' is a CT scan corresponding with contrast filling one or more blood vessels of interest.
  
 
{|class="wikitable"
 
{|class="wikitable"
Line 118: Line 74:
 
| 6-13 sec<ref name=IFMBE>[https://books.google.se/books?id=oVGjnOLXUgkC&pg=PA584 Page 584] in: {{cite book|title=5th European Conference of the International Federation for Medical and Biological Engineering 14 - 18 September 2011, Budapest, Hungary. Volume 37 of IFMBE Proceedings|author=Ákos Jobbágy|publisher=Springer Science & Business Media|year=2012|isbn=9783642235085}}</ref>  || -  
 
| 6-13 sec<ref name=IFMBE>[https://books.google.se/books?id=oVGjnOLXUgkC&pg=PA584 Page 584] in: {{cite book|title=5th European Conference of the International Federation for Medical and Biological Engineering 14 - 18 September 2011, Budapest, Hungary. Volume 37 of IFMBE Proceedings|author=Ákos Jobbágy|publisher=Springer Science & Business Media|year=2012|isbn=9783642235085}}</ref>  || -  
 
|
 
|
*[[Pulmonary embolism]]
+
*[[CT of pulmonary embolism]] (can use [[bolus tracking]] in [[pulmonary trunk]] + 6 seconds)<ref>{{cite web|url=https://posterng.netkey.at/esr/viewing/index.php?module=viewing_poster&doi=10.1594/ecr2018/C-1831|title=Introducing the use of Flash CTPA; how does it compare to standard CTPA?|website=Postering|author=Pavan Nandra|year=2018}}</ref>
 
|-
 
|-
 
! [[Pulmonary vein|Pulmonary venous]] phase
 
! [[Pulmonary vein|Pulmonary venous]] phase
Line 160: Line 116:
 
|}
 
|}
  
==Gastrointestinal contrast==
+
==Locations==
'''Rectally administered contrast''' is indicated in cases where a suspicion remains of penetrating trauma to the colon where an initial CT shows no reason for immediate surgery.<ref>{{cite web|url=http://www.radiologyassistant.nl/en/p466181ff61073/acute-abdomen-role-of-ct-in-trauma.html#i466184acd2fdb|title=Acute Abdomen - Role of CT in Trauma|author=Stephen Ledbetter and Robin Smithuis|website=Radiopaedia|date=2007-08-02}}</ref>
+
See '''[[CT#By location]]''' (CT with IV contrast, including CT angiography, is organized as other CT examinations).
 
 
 
{{Bottom}}
 
{{Bottom}}
  
 
[[Category:X-ray computed tomography]]
 
[[Category:X-ray computed tomography]]

Latest revision as of 12:43, 8 July 2019

A woman undergoing CT with IV contrast.

Author: Mikael Häggström [notes 1]
Computed tomography (CT) with intravenous (IV) contrast medium:

Related terms

Bolus tracking is where a specified location within the circulatory system is monitored during IV contrast infusion, and the timing of the main imaging is counted from when the contrast reaches this location (sufficiently to achieve a specified threshold).

Washout is where tissue loads radiocontrast during arterial phase, but then returns to a rather hypodense state in venous or later phases. This is a property of for example hepatocellular carcinoma as compared to the rest of the liver parenchyma.[1]

Risk factors

In Swedish practice[2] the standard risk factor questions include presence or absence of:

  • Renal or urinary disease
  • Thyroid disorders
  • Myasthenia gravis: Older forms of iodinated contrast have caused an increased risk of exacerbation of the disease, but modern forms have no immediate increased risk.[3]
  • Diabetes and heart disease: These are aggravating factors in low renal function (see CT with IV contrast in low renal function)

Low renal function

Main article: CT with IV contrast in low renal function

Decreased renal function and several other conditions increase the risk of contrast-induced nephropathy, which is a potentially lethal renal injury to the kidney following intravenous radiocontrast.[4]

When it matters

According to European guidelines, the main risk factors of contrast-induced nephropathy:[5]

  • Estimated glomerular filtration rate (eGFR) of less than 30 ml/min/1.73 m2 before intra-venous or intra-arterial radiocontrast administration with second-pass renal exposure (passing lungs or other tissues before the kidneys).
  • eGFR of less than 45 ml/min/1.73 m2 before intra-arterial administration with first-pass renal exposure or in ICU patients
  • Known or suspected acute renal failure
  • Large doses of radiocontrast given IA with first-pass renal exposure
  • Multiple radiocontrast injections within 48-72 h
In case of low GFR, other risk factors need to be checked. Subsequently, the procedure depends on whether the dose that can be given is larger or less than the needed dose.

Further reading: CT with IV contrast in low renal function

Allergy

Intramuscular site of adrenaline.jpg
Main article: Contrast medium reaction

In a more severe reaction:[6]

  • Adrenaline shot, 0.3-0.5mg in adults, given intramuscularly.
  • Summon an anesthesiologist
Prevention
Main article: Prevention of contrast medium reaction

Before a contrast CT of a patient with known allergic-like or unknown-type of contrast reaction to the same class of contrast medium (such as iodinated), the American College of of Radiology recommends premedication with a glucocorticoid, preferably starting 12 or 13 hours before contrast administration.[7]

Hyperthyroidism

Patients at risk for contrast-induced hyperthyroidism are mainly those with diagnosed yet untreated hyperthyroidism, which may motivate contrast-free alternatives such as using a different modality.[8]

In older patients with multinodular goiter and borderline low or subnormal TSH concentrations, a suggested measure is measurement of thyroid function tests three to four weeks after contrast administration.[8] Limited evidence suggests that antithyroid agents before the investigation may blunt or prevent hyperthyroidism.[8]

Pregnancy

Iodinated contrast in pregnancy, when orally administered, is harmless.[9] Intravenous administration of iodinated radiocontrast agents can cross the placenta and enter the fetal circulation, but animal studies have reported no teratogenic or mutagenic effects from its use. There have been theoretical concerns about potential harm of free iodide on the fetal thyroid gland,[9] but multiple studies have shown that a single dose of intravenously administered iodinated contrast medium to a pregnant mother has no effect on neonatal thyroid function.[10] Nevertheless, it generally is recommended that radiocontrast only be used if absolutely required to obtain additional diagnostic information that will improve the care of the fetus or mother.[9]

Breastfeeding

American College of Radiology guidelines state that iodinated contrast administration to a breastfeeding mother is considered safe for both the mother and child.[11] Still, mothers who remain concerned about any potential adverse effects to the child are recommended to have the option of abstaining from breastfeeding for 24 hours, with continued milk extraction such as by a breast pump during that period.[11] Mothers that opt for this for non-emergent exams may also use a breast pump to obtain milk before the exam in order to feed the child during the 24-hour abstinence period.[11]

Phases

Depending on the purpose of the investigation, there are standardized protocols for time intervals between intravenous radiocontrast administration and image acquisition, in order to visualize the dynamics of contrast enhancements in different organs and tissues.[12] The main phases thereof are as follows in table below.[13]

CT angiography is a CT scan corresponding with contrast filling one or more blood vessels of interest.

Phase Time from injection[13] Time from bolus tracking in proximal aorta[13] Targeted structures and findings[13]
Non-enhanced CT (NECT) - -
Pulmonary arterial phase 6-13 sec[14] -
Pulmonary venous phase 17-24 sec[14] -
Early systemic arterial phase 15-20 sec immediately
  • Arteries, without enhancement of organs and other soft tissues.
Late systemicarterial phase
Sometimes also called "arterial phase" or "early venous portal phase"
35-40 sec 15-20 sec
  • All structures that get their blood supply from the arteries have optimal enhancement.
  • Some enhancement of the portal vein
Pancreatic phase 30[16] or 40[17] - 50[17] sec 20-30 sec
Hepatic (most accurate) or late portal phase 70-80 sec 50-60 sec
  • Liver parenchyma enhances through portal vein supply, normally with some enhancement of the hepatic veins.
Nephrogenic phase 100 sec 80 sec
  • All of the renal parenchyma enhances, including the medulla, allowing detection of small renal cell carcinomas
Systemic venous phase 180 sec[18] 160 sec
Delayed phase
Sometimes called "wash out phase" or "equilibrium phase"
6[13]-15[18] minutes 6[13]-15[18] minutes
  • Disappearance of contrast in all abdominal structures except for tissue with fibrosis, which appears more radiodense.

Locations

See CT#By location (CT with IV contrast, including CT angiography, is organized as other CT examinations).

Notes

  1. For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Radlines:Authorship for details.

References

  1. Choi, Jin-Young; Lee, Jeong-Min; Sirlin, Claude B. (2014). "CT and MR Imaging Diagnosis and Staging of Hepatocellular Carcinoma: Part II. Extracellular Agents, Hepatobiliary Agents, and Ancillary Imaging Features ". Radiology 273 (1): 30–50. doi:10.1148/radiol.14132362. ISSN 0033-8419. PMID 25247563. 
  2. NU Hospital Group, Sweden
  3. Mehrizi, Mehyar; Pascuzzi, Robert M. (2014). "Complications of radiologic contrast in patients with myasthenia gravis ". Muscle & Nerve 50 (3): 443–444. doi:10.1002/mus.24254. ISSN 0148639X. PMID 24677227. 
  4. Rudnick, M.; Feldman, H. (2008). "Contrast-Induced Nephropathy: What Are the True Clinical Consequences? ". Clinical Journal of the American Society of Nephrology 3 (1): 263–272. doi:10.2215/CJN.03690907. ISSN 1555-9041. 
  5. Nyman, Ulf; Ahlkvist, Joanna; Aspelin, Peter; Brismar, Torkel; Frid, Anders; Hellström, Mikael; Liss, Per; Sterner, Gunnar; et al. (2018). "Preventing contrast medium-induced acute kidney injury ". European Radiology. doi:10.1007/s00330-018-5678-6. ISSN 0938-7994. 
  6. Unless otherwise specified in lists and table: . Hypersensitivity reactions against contrast media - Swedish Society of Uroradiology [Swedish: Överkänslighetsreaktioner mot kontrastmedel – SURFs kontrastmedelsgrupp ], 2014-10-17].
  7. . Page 9 in: ACR Manual On Contrast Media. American College of Radiology, Committee on Drugs and Contrast Media. Retrieved on 2018-08-25. Version 10.3. 2018. ACR
  8. 8.0 8.1 8.2 Martin I Surks, MD. Iodine-induced thyroid dysfunction. UpToDate. This topic last updated: Apr 02, 2019.
  9. 9.0 9.1 9.2 . Guidelines for Diagnostic Imaging During Pregnancy and Lactation. American Congress of Obstetricians and Gynecologists. February 2016
  10. . ACR Manual on Contrast Media. Version 10.3. American College of Radiology Committee on Drugs and Contrast Media (2017). Retrieved on 2017-07-30.
  11. 11.0 11.1 11.2 . Diagnostic Radiology Procedures on Breastfeeding Patients. Yale School of Medicine. Retrieved on 2019-07-08.
  12. Bae, Kyongtae T. (2010). "Intravenous Contrast Medium Administration and Scan Timing at CT: Considerations and Approaches ". Radiology 256 (1): 32–61. doi:10.1148/radiol.10090908. ISSN 0033-8419. 
  13. 13.0 13.1 13.2 13.3 13.4 13.5 Robin Smithuis. CT contrast injection and protocols. Radiology Assistant. Retrieved on 2017-12-13.
  14. 14.0 14.1 Page 584 in: Ákos Jobbágy (2012). 5th European Conference of the International Federation for Medical and Biological Engineering 14 - 18 September 2011, Budapest, Hungary. Volume 37 of IFMBE Proceedings . Springer Science & Business Media. ISBN 9783642235085. 
  15. Pavan Nandra (2018). Introducing the use of Flash CTPA; how does it compare to standard CTPA?. Postering.
  16. Raman SP, Fishman EK (2012). "Advances in CT Imaging of GI Malignancies. ". Gastrointest Cancer Res 5 (3 Suppl 1): S4-9. PMID 22876336. PMC: 3413036. Archived from the original. . 
  17. 17.0 17.1 17.2 Otto van Delden and Robin Smithuis. Pancreas - Carcinoma. Radiology Assistant. Retrieved on 2017-12-15.
  18. 18.0 18.1 18.2 18.3 Dongqing Wang (2013). Selected Topics on Computed Tomography . ISBN 9789535111023.  License: CC-BY-3.0. Chapter 1: "Computed Tomography in Abdominal Imaging: How to Gain Maximum Diagnostic Information at the Lowest Radiation Dose" by Kristie Guite, Louis Hinshaw and Fred Lee. DOI: 10.5772/55903