AUTHOR AND EDITOR INFORMATION

Section 1 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

INTRODUCTION

Section 2 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

The plastic bag (AngioFlush III fluid collection bag; AngioDynamics, Queensbury, NY) is filled with carbon dioxide through a 0.2-mm filter on the US Pharmacopeia grade cylinder (Custom Medical Devices).



Plastic bag and delivery system (AngioFlush III fluid collection system; AngioDynamics, Queensbury, NY). The carbon dioxide–filled bag is connected to the connecting tube by the check valves where the injection syringe is located. The second check valve, where a smaller syringe is located, prevents reflux of blood into the tube. The 3-way stopcock just distal to the check valve permits flushing and the injection of contrast material into the catheter.



Background

Carbon dioxide (CO₂) gas was used as a contrast agent in the venous circulation in the 1950s for the diagnosis of pericardial effusion. Studies in animals and patients demonstrated that a bolus intravenous injection of CO₂ in quantities of 100 to 200 cc caused no significant changes in vital signs.

In the 1970s, CO₂ was used as an intra-arterial contrast agent. With the advent of digital subtraction angiography (DSA) in 1980, CO₂ angiography became a useful diagnostic tool, particularly in patients who were hypersensitive to iodinated contrast material or whose renal function was compromised. Currently, CO₂ is used for imaging both arterial and venous circulations and to assist in a variety of endovascular interventions, even in patients without renal failure or contrast allergy (see Images 3-24).

Because the use of CO₂ is not associated with nephrotoxicity or allergic reactions, it is increasingly being used as a contrast agent for aortography, as well as for outflow assessment, renal arteriography, and visceral angiography. The gas is the preferred contrast agent for central venography of the upper extremity; for wedged hepatic venography, in order to visualize the portal venous system before transjugular intrahepatic portosystemic shunt (TIPS); and for fine-needle TIPS procedures.

CO₂ is used to guide various vascular interventions, including angioplasty and stent placement, transcatheter embolization, and endovascular abdominal aortic aneurysm (AAA) repair. The gas is also used as a contrast agent for cholangiography, nephrostomy, gastrostomy, and abscess or cyst injections. 

CO₂ should not be used as an arterial contrast agent in sites above the diaphragm because of the risk of gas embolism of the spinal, coronary, and cerebral arteries. CO₂ may be delivered by the hand-held syringe method or by the plastic bag system. Both the delivery systems are safe if used correctly. Because air is poorly soluble, air contamination must be prevented during the delivery of CO₂. Thorough understanding of the physical properties of CO₂ and facile catheterization technique are essential in obtaining optimal CO₂ imaging for both diagnosis and intervention.^{1, 2, 3, 4, 5, 6, 7, 8}

Chemical and physical properties of CO₂

When CO₂ is injected into the blood, it is combined with water to produce carbonic acid. It becomes bicarbonate (HCO₃^-) in the blood stream; bicarbonate reverts to CO₂ before being expelled out of capillaries into the lung. Carbonic anhydrase catalyzes the conversion of CO₂ to bicarbonate and protons. CO₂ is eliminated by the lungs in a single pass. However, CO₂ bubbles that were injected into the venous system may enter the systemic circulation via the patent foramen ovale or intracardiac septal defects.

CO₂ is a colorless and odorless gas, and it cannot be visually distinguished from air. The incorrect application of technique may result in air contamination, which may cause serious complications. A thorough understanding of the unique physical properties of CO₂ is necessary for the safe and effective performance of CO₂ angiography.

CO₂ is approximately 20 times more soluble than oxygen. When injected into a vessel, CO₂ bubbles completely dissolve within 2-3 minutes; however, if the gas is trapped in a large abdominal aneurysm, it may persist, allowing gas exchange between the CO₂ and nitrogen in the blood. This exchange may result in colonic ischemia, as a result of occlusion of the inferior mesenteric artery. Two to 3 minutes should elapse between injections of CO₂ to prevent the localized accumulation of gas bubbles, which may produce a significant gas embolism, particularly in the pulmonary artery.

CO₂ is compressible during injection; it expands in the vessel as it exits the catheter. Clearing the fluid of the catheter by using 3-5 cc of CO₂ before injection reduces the explosive delivery. The explosive delivery is unlikely to cause vascular damage, but it may contribute to discomfort during the injection. The low viscosity and compressibility of the gas accounts for the greater sensitivity of CO₂ as a contrast agent in detecting the source of bleeding (gastrointestinal tract and traumatic bleeding), as compared with iodinated contrast material.

CO₂ is lighter than blood plasma; therefore, it floats above the blood. When injected into a large vessel such as the aorta or inferior vena cava, CO₂ bubbles flow along the anterior part of the vessel, with incomplete blood displacement along the posterior portion. Because of their anterior point of origin, the celiac and superior mesenteric arteries fill well with small volumes (<30 cc) of CO₂. If gas fills the renal artery, the patient must be rotated so that the side of the renal artery is elevated above the level of the table. If the renal artery remains unfilled, catheterization of the artery and selective injection is indicated.

The buoyancy of the gas is not a problem when the vessel to be imaged is smaller than 10 mm in diameter because the gas bubbles tend to displace the blood in greater than 80% of the lumen. Elevation of the lower extremity to 15-20° in conjunction with the intra-arterial injection of 100-200 µg of nitroglycerin enhances gas flow and filling of the distal arteries in the lower extremity.

CO₂ is approximately 400 times less viscous than iodinated contrast medium. The low viscosity permits manual gas injection with small-bore catheters between the catheter and guide wire. Doses of CO₂ required for aortic imaging may be manually injected by using a 4-Fr or 5-Fr end-hole diagnostic catheter. The low viscosity accounts for better filling of collateral vessels for both arterial and venous occlusive diseases and for portal vein visualization after wedged hepatic injection with CO₂.

Iodinated contrast medium mixes with blood when injected into a vessel and becomes diluted, making it less dense as it travels through collateral vessels. By contrast, CO₂ does not mix with blood, and so it does not become diluted by collateral flow.

Advantages of CO₂ as a contrast agent
 
CO₂ is less dense than iodinated contrast medium, and the overall quality of CO₂ vascular images is slightly less than that obtained with contrast medium. Usually, multiple hand injections are required, and the radiation exposure to the operator and patient may be increased. However, CO₂ has several notable advantages, as compared with iodinated contrast medium.

CO₂ causes no allergic reaction. Because CO₂ is a natural byproduct, it cannot cause a hypersensitivity reaction. Therefore, CO₂ is an ideal alternative to iodinated contrast medium for patients who have a history of allergic reactions. No steroid preparation is needed when CO₂ is used.

CO₂ causes no renal toxicity. Experimental and clinical findings indicate that the selective injection of CO₂ into the aorta or into the renal artery is safe and causes no renal injury, even in patients with diabetes or compromised renal function. Therefore, the gas is the preferred contrast agent for renal artery angioplasty and stent placement.

CO₂ causes no hepatic toxicity. The authors have personally used CO₂ as a contrast agent for celiac, splenic, superior mesenteric, and hepatic arteriograms for patients with a variety of disorders. No injuries to the hepatic parenchyma have occurred after the injection of CO₂.

Unlimited amounts of CO₂ may be used for vascular imaging because the gas is effectively eliminated by means of respiration. However, the operator should allow sufficient time for its clearance. A minimum of 2 minutes is needed for the first CO₂ dose to completely dissolve before another dose is injected. CO₂ is particularly useful for patients with compromised cardiac and renal function who are undergoing complex vascular interventions.

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TECHNIQUES

Section 3 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

Patient preparation

No specific patient preparation is required for CO₂ angiography. The standard preparation for catheter angiography is used. Patients with a history of allergy to contrast material do not require steroid preparation. CO₂ may be used as a contrast agent for outpatient angiography.

Contraindications

There are no absolute contraindications to the use of CO₂. CO₂ should not be used in the thoracic aorta and in arteries above the diaphragm because of the risk of spinal, coronary, and carotid artery gas embolism. CO₂ should be used with caution in patients with pulmonary insufficiency or pulmonary hypertension because a diagnostic dose of CO₂ may cause an increase in pulmonary arterial pressure. CO₂ should not be used in patients with an intracardiac septal defect or a pulmonary arteriovenous malformation because of the possibility of paradoxical gas embolism.

Sedation and analgesia

Heavy sedation should be avoided during CO₂ angiography. Respiratory depression and hypotension caused by air contamination may be mistaken for adverse effects of the sedatives and/or analgesics.

Patient monitoring

All patients undergoing CO₂ angiography should be monitored with ECG and pulse oximetry; blood pressure, respiratory rate, and heart rate should also be monitored. Capnograms should be obtained if the patient is intubated. The blood pressure should be checked before the initial injection of CO₂, as well as 1, 2, and 3 minutes after the initial injection. 

A significant change in any monitoring parameter suggests either that the doses of CO₂ were excessive or that air contamination has occurred. Capnography (ETCO₂) is very useful during CO₂ angiography because it allows the monitoring of both ventilatory and hemodynamic functions in real time. Micro-cap (Oridion Medical, Ltd., Jerusalem, Israel) is a handheld capnometer that is currently available. It uses microstream infrared spectroscopy to measure the respiratory rate and ETCO₂ during exhalation.

CO₂ cylinder

The CO₂ delivery system should be filled with 99.99% laboratory-grade CO₂ from a disposable cylinder (CMD, Gainesville, FL). The cylinder is supplied with highly pure gas, a valve, a regulator, a gas gauge, and a metal diaphragm with the regulator set at 18 psi.
 
CO₂ delivery methods

CO₂ may be delivered into a vessel by use of a handheld syringe or by the plastic bag system (see Images 1-2). When a syringe is used, it should be filled directly from a CO₂ cylinder. CO₂ should not be aspirated into the syringe because this may cause air contamination. When the syringe has been filled with CO₂, its pressure should be reduced to the atmospheric level by quickly opening and closing the stopcock. The CO₂-filled syringe should not be left on the table with the stopcock open before injection because the CO₂ in the syringe (which has a CO₂ concentration of >99%) is rapidly replaced with air (which has a CO₂ concentration of 0.03%). The syringe method is inconvenient when multiple injections are necessary.

The plastic bag delivery system (AngioDynamics, Queensbury, NY) is particularly useful when multiple injections are needed. An AngioFlush 111 fluid collection bag is filled with CO₂ and is connected to the reservoir port of the AngioFlush 111 Fluid Management System. This system has airtight connections with the check valves, the injection port, the bleed-back port, and the catheter port.

The check valves reduce the need for stopcock manipulation, which in turn reduces the risk of air contamination. The bag must be tightly connected to the reservoir port of the delivery system to prevent air contamination. The bleed-back port near the catheter port allows sodium chloride solution, contrast medium, or CO₂ injections. If CO₂ is to be injected with a guide wire in the catheter, a Y-connector (Touy-Borst) is connected to the injection port; alternatively, a 30-mL syringe is connected to the bleed-back port. The bleed-back portis filledwithCO₂ from the injection syringe before the guide wire is introduced. The bag should be filled and emptied with CO₂ three times before the final filling to remove air from the bag.

CO₂ injection factors

The injection rate depends on the diameter, length, and flow of the vessels being imaged. For an abdominal aortogram or an inferior vena cavogram, 30-50 cc of CO₂ is injected. When imaging aortic branches (celiac, superior mesenteric, renal arteries) or arteries of the lower extremity, 20-30 cc is used. Because of the low viscosity of the gas, CO₂ may be injected through a 3F microcatheter for selective and superselective angiography and for vascular interventions.

CO₂ imaging

Digital subtraction angiography (DSA) should be used for CO₂ imaging. If available, a 1024 X 1024 digital subtraction angiographic system and magnification technique should be used. Stacking software for integrating a series of images has solved problems associated with the breakup of CO₂ bubbles after injection.

Respiratory motion and peristalsis become significant problems in mesenteric CO₂ angiography. Motion occurring between the time that the baseline image is made and the time that the CO₂ image is made causes marked degradation in the quality of the imaging. Additional mask images should be obtained to decrease motion artifacts by replacing later mask images for subtraction.

Rapid exposures (4 to 6 frames per second) should be obtained, and superselective injection of CO₂ as close to the target vessel as possible should be performed to optimize CO₂ imaging. Elevation of target vessels 15-20° above the level of the angiographic table, as well as the intra-arterial administration of 100-150 µg of nitroglycerin, may improve filling of the peripheral arteries in the lower extremities.^{9, 10, 11}

CLINICAL APPLICATIONS

Section 4 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

This frontal carbon dioxide digital subtraction aortogram shows a single right renal artery with a mild stenosis at the origin and 2 left renal arteries. The celiac and superior mesenteric arteries fill nicely because of their anterior origin.



This carbon dioxide digital subtraction angiogram shows patency of the external iliac and transplanted renal arteries.



This mesenteric carbon dioxide digital subtraction angiogram in a patient with small-bowel bleeding shows extravasation of carbon dioxide gas bubbles. Embolization with coils stopped the bleeding.



Carbon dioxide guided stent placement of right renal artery stenosis. A. CO2 DSA demonstrates orificeal stenosis of right renal artery (arrow). B. DSA with the injection of CO2 through the sheath demonstrates the stent in good position (arrow). C. After stent deployment, the renal artery is widely patent.



CO2 aortogram demonstrates celicomesenteric trunk, common origin of the celiac axis (CA) and superior mesenteric arteries. Common hepatic (HA) and splenic (SA) arteries are visualized.



This carbon dioxide aortogram obtained with the injection of CO2 through the sheath during endovascular aortic repair demonstrates the right (RRA) and left (LRA) renal arteries. AAA=abdominal aortic aneurysm


CO₂ is used widely as an intravascular contrast agent for imaging both the arterial and venous circulations, particularly for patients with renal insufficiency and for patients who have a history of hypersensitivity to iodinated contrast medium. CO₂ may be used as a contrast agent for various vascular interventions. A summary of the clinical applications of CO₂ as a contrast agent for vascular diagnosis and interventions follows. ^{12, 13, 14, 15, 16, 17, 18, 19, 20, 21}

CO₂ aortogram and runoff

CO₂ is frequently used as an alternative contrast agent for aortography and runoff in patients with contrast allergy and renal insufficiency. In most patients, all outflow studies may be done with CO₂. Small amounts of iodinated contrast medium are used if needed for additional vascular information. 

The technique involves the percutaneous retrograde catheterization of the femoral artery and introduction of a 4-Fr end-hole catheter, such as a shepherd hook or a Cobra-shaped catheter. An abdominal aortogram is performed with the injection of 30-50 cc of CO₂ and DSA imaging at 4 frames per second. Then CO₂ is injected into the distal aorta or the iliac artery to image the iliac and femoral arteries. The catheter is then advanced into the contralateral superficial femoral artery for a runoff study.

If the infrapopliteal arteries are poorly visualized, a 3-Fr microcatheter is advanced coaxially into the popliteal artery to image the tibial and peroneal arteries. The retrograde approach is then converted to the antegrade approach; CO₂ angiography is performed in the same fashion as on the contralateral side. For imaging of the iliac, femoral, and popliteal arteries, 20 cc of CO₂ is selectively injected.

Elevation of the legs and the intra-arterial injection of nitroglycerin (100-150 µg) allow improved visualization of the tibial and plantar branches. Because of its buoyancy and low viscosity, CO₂ may provide better filling of collateral arteries and distal branches than iodinated contrast medium provides. In 92% of cases, the vascular information provided by CO₂ angiography is adequate for a surgical or endovascular intervention. 

CO₂ renal digital subtraction angiography

CO₂ is most frequently used as a contrast agent for renal DSA in patients who are allergic to contrast magnets or who have renal failure. CO₂ allows visualization of the proximal renal arteries and renal artery stenoses. Because of the posterior position of the kidney relative to the aorta, the distal renal arteries do not fill well, owing to the buoyancy of the gas.

After percutaneous femoral artery catheterization, a 4-Fr or 5-Fr catheter such as the shepherd hook catheter is advanced into the abdominal aorta; 30 to 40 cc of CO₂ is then injected into the aorta with the plastic bag delivery system in the anteroposterior projection. If filling of the renal artery is suboptimal, the patient may be rotated so as to orient the renal artery above the aorta.

Cross-table lateral imaging with the patient in the lateral decubitus position usually provides excellent filling of the renal artery. Selective renal DSA is performed with the injection of CO₂ (20 cc) into the main renal artery. For visualization of the segmental renal artery branches, a more distal injection is needed.

Following renal angioplasty and stent placement, CO₂ injection distal to the stent allows visualization of the main renal artery by reflux. CO₂ angiography may allow visualization of vascular renal cell carcinoma, as well as tumor invasion of the renal vein or inferior vena cava. CO₂ may also allow visualization of the intrarenal arteriovenous fistula, stenosis, and aneurysm.

CO₂ visceral angiography

Carbon dioxide angiography has value in selected situations requiring visceral angiography. CO₂ aortography and visceral arteriography have been found to be useful in the evaluation of the arterial anatomy, as well as in the evaluation of chronic mesenteric ischemia, aneurysms, arteriovenous fistula, and bleeding.

From the femoral artery approach, 30-40 cc of CO₂ is injected 1 to 2 cm above the celiac axis using an end-hole catheter with the plastic bag delivery system; imaging is acquired in the anteroposterior and lateral projections. Lateral aortography is obtained during both full inspiration and expiration to evaluate median arcuate ligament compression on the celiac artery. Median arcuate ligament compression produces an extrinsic, concave impression on the cranial aspect of the celiac axis just distal to its origin at the expiratory aortogram.
 
Because of its low viscosity, CO₂ DSA is more sensitive than iodinated contrast medium in detecting bleeding from the GI tract, liver, spleen, and retroperitoneal space. If extravasation is seen on the CO₂ aortogram, selective arteriography is performed with CO₂. Repeat arteriography is usually needed with iodinated contrast medium to provide a vascular road map before superselective catheterization of the bleeding artery. Use of CO₂ allows visualization of the visceral arterial stenoses and collaterals. CO₂ is useful in visualizing hepatocellular carcinoma and transcatheter embolization.

CO₂ angiography of tumors

CO₂ angiography is useful in various oncologic interventions. The low viscosity of CO₂ allows the injection of the gas through a 3-Fr microcatheter for superselective angiography. CO₂ may be used to assist selective embolization of hepatic, renal, and bone tumors. It is also useful in placing hepatic arterial infusion catheters; for embolization of the gastroduodenal artery, to minimize gastrointestinal toxicity; for evaluation of a malfunctioning hepatic artery pump; and in hepatic arterial redistribution procedures.

CO₂ for iliac and femoral angioplasty and stent placement

Because of the low viscosity, CO₂ may be injected between the guide wire and catheter, allowing imaging before, during, and after angioplasty. CO₂ may also be injected through the sheath to guide angioplasty and stent placement. The plastic bag system provides multiple rapid injections with the guide wire in place. CO₂ has definitive advantages over iodinated contrast medium, in that its use is not associated with risks of renal toxicity or allergic reactions.

CO₂-guided renal angioplasty and stent placement

CO₂ is very useful for renal angioplasty and stent placement. The plastic bag system allows multiple injections in various oblique projections so as to accurately position the stent. When CO₂ is injected into the renal artery, the gas always fills the renal artery with reflux of the gas into the aorta. This allows visualization of the orifice of the renal artery, which is helpful for accurately deploying the stent.

After an aortogram is obtained, the renal artery is catheterized with a 4-Fr or 5-Fr shepherd hook or a Cobra catheter, and a dual pressure recording is obtained in the renal artery distal to the stenosis and the aorta. If a significant pressure gradient is present, a 6-Fr sheath is advanced into the abdominal aorta over a 0.035-in Rosen wire. An expanding balloon stent of appropriate diameter and length is then advanced into the renal artery stenosis. CO₂ is injected through the sheath and is imaged in multiple projections to precisely place the stent.

After stent deployment, a 4-Fr catheter is advanced into the renal artery, and the pressure gradient between the renal artery and the aorta is measured. If no significant gradient is present, CO₂ is injected through the Cobra catheter into the renal artery to visualize the stented renal artery.

CO₂-guided endovascular aneurysm repair (EVAR)

EVAR is a well-accepted treatment modality for AAA. The use of CO₂ as an alternative contrast agent during EVAR may reduce the risk of renal failure. Because of its low viscosity, CO₂ may be injected through the introducer, which is preloaded with a stent graft, so as to demonstrate the renal and hypogastric artery before deployment of the stent graft. After deployment, a completion aortogram is performed with CO₂, using the Cobra catheter, to demonstrate the patency of the renal and hypogastric arteries and to identify any endoleak.

CO₂  upper-extremity venography

CO₂ digital subtraction venography is safe and useful in the evaluation of the central veins of the upper extremities. Because of its low viscosity and its buoyancy, CO₂ may be injected through a 21-gauge peripheral IV access device for diagnostic central venography. The injection of CO₂ into a vein of small diameter may cause pain at the injection site. It is preferable to obtain IV access via the antecubital vein. 

When 20-30 cc of CO₂ is injected into the antecubital vein, the subclavian vein becomes well filled within 5 seconds of the injection. Occasionally, CO₂ reflux occurs into the contralateral innominate vein. CO₂ is also used for upper-extremity venography before surgical placement of an arteriovenous fistula, before transvenous pacer insertion, and before placement of a central venous catheter in selected patients.

There are no absolute contraindications to the use of CO₂ in upper-extremity venography. Relative contraindications include severe emphysema, pulmonary hypertension, and known intracardiac septal defects or pulmonary arteriovenous malformations. Initially, small amounts of CO₂ (20 cc) should be used, so as to evaluate the effect of CO₂ on the vital signs.

The injection of CO₂ with the patient in the left lateral decubitus position facilitates the trapping of gas in the right atrium, thus preventing passage of the gas into the pulmonary arteries. Once CO₂ is injected into a vein, the gas rapidly passes through the central veins and right cardiac chambers into the pulmonary arteries. The gas trapped in the pulmonary artery is absorbed within 15 to 30 seconds in the absence of air contamination. 

The intravenous injection of CO₂ in diagnostic doses (20 to 50 cc) has no effect on vital signs. If the systolic blood pressure drops from the baseline value by 10 to 20 mm Hg, air contamination should be suspected, and the delivery system should be checked for a potential source of air contamination. CO₂ injections should be administered at intervals of 2 to 3 minutes to allow complete absorption of the gas.

CO₂  wedged hepatic venography

CO₂ wedged hepatic venography and manometry are important in the workup of patients with cirrhosis and portal hypertension, ascites of unknown etiology, hepatic venous outflow obstruction, suspected portal vein occlusion, and TIPS; it is also important for patients who require transjugular liver biopsy.

A 5-Fr diagnostic catheter is wedged into a peripheral hepatic vein, using either the jugular vein or femoral vein approach. An occlusion balloon catheter may also be used to occlude the hepatic vein. CO₂ is injected at a dose of 30 to 50 cc into a wedged hepatic vein to allow visualization of the intra- and extra-hepatic portal veins. In the absence of presinusoidal obstruction, the portal vein will also be visualized, regardless of the direction of the intrahepatic portal blood flow.

Wedged hepatic venography with iodinated contrast medium is used to determine the intrahepatic portal hemodynamics and to assess the morphology of the liver. The success rate of portal vein visualization with CO₂wedged hepatic venography is approximately 90%. For a TIPS procedure, more than 1 injection may be required to fill the central portal vein before portal vein puncture. 

If CO₂ wedged hepatic injections fail to show the portal vein, CO₂ is injected into the parenchyma using a 21-gauge needle, available in the Fine-needle portal access set (AngioDynamics, Queensbury, NY). We have performed wedged hepatic venography with CO₂ and contrast medium in hundreds of patients. On several occasions, extravasation of CO₂ into the subcapsular space and peritoneal cavity has occurred. In one of these cases, transfusion was required because of bleeding. The combination of CO₂ wedged hepatic venography, hepatic manometry, and transjugular liver biopsy may provide the diagnostic information necessary for instituting appropriate therapy for patients with hepatic dysfunction.

CO₂  inferior vena cavography

CO₂ is a safe and effective contrast agent for inferior vena cavography in patients with contrast allergy and renal failure. CO₂ angiography may provide accurate measurement of vena caval diameter and vascular road mapping before filter placement and vena caval interventions.

We use the plastic bag delivery system for the CO₂ injection for vena cavography. The technique used for CO₂ venography before filter placement is as follows: a 5-Fr Cobra catheter is introduced from the right femoral vein and is advanced into the contralateral iliac vein for CO₂ vena cavography to exclude the presence of a left-sided inferior vena cava. If reflux of CO₂ into the left renal vein has not occurred, the catheter is advanced into the left renal vein for a CO₂ renal venogram.

The catheter is also used to catheterize a retroaortic left renal vein. A filter is then deployed in the inferior vena cava below the lowest renal vein. If caval duplication is present, the filter is placed above the renal veins. CO₂ may demonstrate nonocclusive caval thrombus, stenosis, and occlusion. CO₂ may also be used as a contrast agent in the recanalization procedure of the occluded vena cava. Vital signs should remain stable following a bolus injection of CO₂ in amounts of 30 to 50 cc. CO₂ should be used with caution in patients with pulmonary insufficiency, pulmonary hypertension, and known intracardiac septal defects.

CO₂  splenoportography

Splenoportography with contrast medium has been largely replaced by noninvasive imaging modalities (CTA and MRV) and arterial portography (also called indirect portography). Because of the low viscosity of CO₂, diagnostic quantities (15 to 30 cc of CO₂) of the gas may be injected into the splenic parenchyma, using a 22- to 25-gauge needle. Both in experimental animals and in patients, the intrasplenic injections of CO₂ cause no splenic laceration or hematoma. The splenic and portal veins are well visualized with CO₂. This technique is particularly useful in pediatric patients for whom imaging studies of portal vein patency are inconclusive; it eliminates the need for femoral artery catheterization for arterial portography.

CO₂-guided TIPS

TIPS is a well accepted means of treating patients with variceal bleeding that is unresponsive to sclerotherapy; it is also used in cases of intractable ascites and cirrhotic hydrothorax. After the right or left internal jugular vein is accessed, a 10-Fr sheath is introduced. Pressure is measured in the right atrium and the inferior vena cava. A 5-Fr Cobra catheter or a curved-tipped catheter is advanced into the right hepatic vein to measure the free hepatic vein pressure. 

A CO₂ hepatic venogram is then performed with the injection of 20 cc of CO₂ using DSA imaging of the hepatic vein and pulmonary artery. The CO₂ trapped in the central pulmonary artery dissolves within 30 seconds after the injection. Persistence of the gas bubble over 30 seconds suggests air contamination; in such cases, the procedure should be aborted and the plastic bag system should be checked for any source of air contamination. Vital signs should be monitored, and the blood pressure should be checked 1 minute after the initial CO₂ injection. 

The catheter is then advanced until it becomes wedged. Once the catheter is wedged, the injection of 1 to 2 cc of contrast medium produces a sinusoidal blush; the wedged hepatic vein pressure is then measured. A CO₂ wedged hepatic venogram is performed with the injection of 30 to 40 cc of CO₂ and is imaged using the DSA technique.

The three commonly used TIPS sets are the Ring transjugular liver access set (Cook, Inc. Bloomington, IN), the Rosch-Uchida transjugular liver access set (Cook, Inc.), and the fine-needle transjugular access set (AngioDynamics, Queensbury, NY). Once the portal vein has been punctured using the Ring or Rosch-Uchida access needle, a 5-Fr pigtail catheter is advanced to the proximal splenic vein.

After measuring portal vein pressure, a CO₂ splenoportogram is performed with the injection of 30 to 40 cc of CO₂. At this time, 20 cc of CO₂ or 10 cc of contrast medium is injected into the hepatic parenchymal tract and imaged with the DSA technique to rule out transgression of the hepatic artery or bile duct. CO₂ may be injected through the sheath to accurately deploy the stent from the portal vein through the parenchyma to the central hepatic vein.

If repeat pressure measurement reveals a gradient of less than 12 mm Hg between the right atrium and the portal vein, a completion digital subtraction portogram is obtained with the injection of 30 cc of CO₂.

In the CO₂ fine-needle TIPS procedure, the right or middle hepatic vein is catheterized with a 5-Fr Cobra catheter; 20 cc of CO₂ is then injected using the plastic bag system. The hepatic vein and the pulmonary artery are then imaged with DSA. The CO₂ trapped in the pulmonary artery usually dissolves within 30 seconds in the absence of air contamination.

The 21-gauge needle is then advanced from the central hepatic vein toward the portal vein, and 20 cc of CO₂ is injected through the 21-gauge needle, using the plastic bag system in the anteroposterior projection. A repeat injection is made in the left anterior oblique projection to demonstrate the position of the needle in relation to the target portal vein.

Once the 0.018-inch guidewire is advanced toward the portal vein, CO₂ is injected between the guidewire and the needle to confirm the position of the wire in the portal vein. Once the portal vein has been catheterized, the subsequent procedural steps for CO₂ administration are the same as with the large-needle TIPS procedure.

ADVERSE EFFECTS AND MANAGEMENT

Section 5 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

The occurrence and severity of the adverse effects of angiography may be related to the dose or to air contamination.

CO₂ aortography and celiac arteriography may cause nausea and pain lasting 2-3 minutes. No specific treatment is required. Placing the patient in a left- or right-side-up position may relieve the pain. A decrease in the doses of CO₂ usually reduces the frequency and severity of pain.

The injection of CO₂ for runoff of the lower extremities may cause pain. Decreasing the amount of CO₂ with selective injection and stacking technique helps in reducing the pain.

The injection of CO₂ into a peripheral vein for upper-extremity venography may cause pain at the injection site. The mechanism of pain is probably the explosive delivery secondary to gas compression. Purging the injection tube with 3 cc of CO₂ and administering 20-40 mg of lidocaine immediately before the injection of CO₂ for venous imaging helps in reducing the pain.

When CO₂ is trapped in an aortic aneurysm, the gas bubbles may occlude the inferior mesenteric artery, resulting in colonic ischemia.

Inadvertent injection of excessive volumes of CO₂ or air contamination may cause a vapor lock in the pulmonary artery, which results in severe hypotension. When air contamination occurs, fluoroscopy of the chest shows gas bubbles in the pulmonary artery that persists for longer than 30 seconds. If hypotension develops, the patient should be placed in the Trendelenburg and left lateral decubitus positions. If possible, air should be aspirated from the pulmonary artery using a catheter.^{22, 23}

FURTHER READING

Section 6 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

Guidelines on the diagnosis and treatment of acute heart failure.
European Society of Cardiology.  2005.  36 pages.  NGC:004184
 

MULTIMEDIA

Section 7 of 8  

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

Media file 1:  The plastic bag (AngioFlush III fluid collection bag; AngioDynamics, Queensbury, NY) is filled with carbon dioxide through a 0.2-mm filter on the US Pharmacopeia grade cylinder (Custom Medical Devices).
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Media file 2:  Plastic bag and delivery system (AngioFlush III fluid collection system; AngioDynamics, Queensbury, NY). The carbon dioxide–filled bag is connected to the connecting tube by the check valves where the injection syringe is located. The second check valve, where a smaller syringe is located, prevents reflux of blood into the tube. The 3-way stopcock just distal to the check valve permits flushing and the injection of contrast material into the catheter.
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Media file 3:  This frontal carbon dioxide digital subtraction aortogram shows a single right renal artery with a mild stenosis at the origin and 2 left renal arteries. The celiac and superior mesenteric arteries fill nicely because of their anterior origin.
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Media file 4:  This carbon dioxide digital subtraction angiogram shows patency of the external iliac and transplanted renal arteries.
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Media file 5:  This carbon dioxide digital subtraction angiogram (stacked image) of the left lower extremity shows the popliteal, anterior tibial, peroneal, and posterior tibial arteries.
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Media file 6:  This mesenteric carbon dioxide digital subtraction angiogram in a patient with small-bowel bleeding shows extravasation of carbon dioxide gas bubbles. Embolization with coils stopped the bleeding.
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Media file 7:  This carbon dioxide digital subtraction venogram shows stenosis of the right subclavian vein.
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Media file 8:  This carbon dioxide digital subtraction angiogram was obtained with an injection of carbon dioxide into the wedged hepatic venous catheter. Both the intrahepatic and extrahepatic portal veins fill nicely.
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Media file 9:  This carbon dioxide digital subtraction arteriogram in a patient with occlusion of the aorta (longer arrow) and both common iliac arteries (shorter arrows) was obtained with the injection of 30 cc of CO2 in the left external iliac artery using a 3F dilator. Because of the low viscosity, the gas flows well through the collaterals to the aorta and contralateral iliac arteries.
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Media file 10:  Carbon dioxide guided stent placement of right renal artery stenosis. A. CO2 DSA demonstrates orificeal stenosis of right renal artery (arrow). B. DSA with the injection of CO2 through the sheath demonstrates the stent in good position (arrow). C. After stent deployment, the renal artery is widely patent.
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Media file 11:  CO2 aortogram (cross-table lateral DSA) demonstrates narrowing of the celiac axis with concave impression (arrow) secondary to median arcuate ligament compression.
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Media file 12:  Celiac stenosis caused by median arcuate ligament compression. CO2 superior mesenteric DSA demonstrates filling of the gastroduodenal (GDA), common hepatic (CHA), and splenic (SA) arteries from the superior mesenteric artery (arrow).
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Media file 13:  CO2 celiac DSA. CO2 refluxes from the celiac axis back into the aorta, filling the superior mesenteric and bilateral renal arteries (RRA and LRA). The gastroduodenal (GDA), common hepatic (HA), splenic (SA), left gastric (LGA) and replaced left hepatic (LHA) arteries are visualized.
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Media file 14:  CO2 aortogram demonstrates celicomesenteric trunk, common origin of the celiac axis (CA) and superior mesenteric arteries. Common hepatic (HA) and splenic (SA) arteries are visualized.
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Media file 15:  This carbon dioxide aortogram obtained with the injection of CO2 through the sheath during endovascular aortic repair demonstrates the right (RRA) and left (LRA) renal arteries. AAA=abdominal aortic aneurysm
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Media file 16:  CO2 celiac angiogram in a patient with gastrointestinal bleeding following hepatic tumor resection shows a large pseudoaneurysm (arrow) arising from the distal celiac axis. Embolization controlled the bleeding
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Media file 17:  Right hepatic DSA with CO2 demonstrates a vascular tumor in the right hepatic lobe (arrow). The shorter arrow points at the tip of the microcatheter passed coaxially through the 5-Fr catheter positioned in the celiac axis. CO2 refluxed, filling the left hepatic and common hepatic arteries.
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Media file 18:  Carbon dioxide trapped in the pulmonary artery (arrow) following the intravenous injection (A). The trapped gas has dissolved within 30 seconds (B)
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Media file 19:  This carbon dioxide venogram of the left jugular vein (LIJ) was taken during parathyroid venous sampling for the localization of the source of parathyroid hormone excess. Left innominate (LI) and right innominate veins are visualized.
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Media file 20:  Carbon dioxide wedged hepatic venogram demonstrates stenosis of the portal vein (arrow).
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Media file 21:  Carbon dioxide guided filter placement. A. CO2 inferior vena cavogram. B. Left renal venogram with CO2 (LRV). C. Inferior vena cavogram after deployment of a G2 filter (arrow).
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Media file 22:  Left upper extremity venogram with CO2 nicely fills the subclavian (SV), innominate (IV), and superior vena cava (SVC). CO2 bubbles are seen in the right atrium (RA) and right ventricle (LV).
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Media file 23:  Splenoportogram with the injection of CO2 into the spleen (S) using a 22 gauge needle shows patent splenic (SV) and diminutive portal vein (PV). There is retrograde filling of the inferior mesenteric (IMV) and superior mesenteric (SMV) veins. L = liver
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Media file 24:  Carbon dioxide celiac angiogram in a patient with splenic injury demonstrates multiple small areas of gas collection in the spleen (arrow) and filling of the splenic (SV) and portal (PV) veins through intrasplenic arteriovenous fistula.
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REFERENCES

Section 8 of 8

• Authors and Editors
• Introduction
• Techniques
• Clinical Applications
• Adverse Effects and Management
• Further Reading
• Multimedia
• References

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13. Hahn ST, Pfammatter T, Cho KJ. Carbon dioxide gas as a venous contrast agent to guide upper-arm insertion of central venous catheters. Cardiovasc Intervent Radiol. May-Jun 1995;18(3):146-9. [Medline].
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15. Kerns SR, Hawkins IF. Carbon dioxide digital subtraction angiography: expanding applications and technical evolution. AJR Am J Roentgenol. Mar 1995;164(3):735-41. [Medline].
16. Vlachogiannakos J, Patch D, Watkinson A, et al. Carbon-dioxide portography: an expanding role?. Lancet. Mar 18 2000;355(9208):987-8. [Medline].
17. Weaver FA, Pentecost MJ, Yellin AE, et al. Clinical applications of carbon dioxide/digital subtraction arteriography. J Vasc Surg. Feb 1991;13(2):266-72; discussion 272-3. [Medline].
18. Criado E, Kabbani L, Cho K. Catheter-less angiography for endovascular aortic aneurysm repair: A new application of carbon dioxide as a contrast agent. J Vasc Surg. Jul 14 2008;[Medline].
19. Mahnken AH, Bruners P, Mommertz G, Mühlenbruch G, Jacobs MJ, Günther RW, et al. Carbon dioxide contrast agent for CT arteriography: results in a porcine model. J Vasc Interv Radiol. Jul 2008;19(7):1055-64. [Medline].
20. Schatlo B, Gläsker S, Zauner A, Thompson GB, Oldfield EH, Pluta RM. Correlation of end-tidal CO2 with transcranial Doppler flow velocity is decreased during chemoregulation in delayed cerebral vasospasm after subarachnoid haemorrhage--results of a pilot study. Acta Neurochir Suppl. 2008;104:249-50. [Medline].
21. Giday SA, Ko CW, Clarke JO, Shin EJ, Magno P, Jagannath SB, et al. EUS-guided portal vein carbon dioxide angiography: a pilot study in a porcine model. Gastrointest Endosc. Oct 2007;66(4):814-9. [Medline].
22. Caridi JG, Hawkins IF. CO2 digital subtraction angiography: potential complications and their prevention. J Vasc Interv Radiol. May-Jun 1997;8(3):383-91. [Medline].
23. Matsuo T, Fujiwara H, Gobara H, Mimura H, Kanazawa S. Central Retinal and Posterior Ciliary Artery Occlusion After Intralesional Injection of Sclerosant to Glabellar Subcutaneous Hemangioma. Cardiovasc Intervent Radiol. Jun 20 2008;[Medline].

Article Last Updated: Oct 21, 2008