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Pulmonary embolism (PE) and deep venous thrombosis (DVT)<br />

are components of the same disease entity, accounting for<br />

300,000 to 600,000 hospitalizations and 50,000 to 100,000<br />

deaths a year in the United States. Since appropriate treatment is estimated<br />

to decrease the mortality by 30%, early and accurate diagnosis<br />

is essential. Until recently, many different imaging tests were used to<br />

evaluate pulmonary thromboembolic disease and thrombosis of the<br />

deep veins of the lower extremity. Ventilation perfusion scintigraphy<br />

(V/Q) has been the mainstay in the diagnosis of PE, with pulmonary<br />

angiography being the gold standard. However 40% to 70% of V/Q<br />

scans are nondiagnostic, thereby requiring additional testing for the<br />

diagnosis or exclusion of PE. Pulmonary angiography is an invasive<br />

test with a major complication rate of 1.3%. For the last 5 years, helical<br />

(spiral) CT has been used in the diagnostic evaluation of thromboembolic<br />

disease.<br />

The advent of faster helical scanners, particularly multislice scanners,<br />

has revolutionized the diagnosis of not only clinically significant<br />

central pulmonary emboli, but has also greatly improved the detection<br />

of subsegmental pulmonary emboli. 1-3 Faster scanning times, single<br />

breath-hold acquisitions, and thinner collimation has led to improved<br />

detection of both segmental and subsegmental pulmonary emboli with<br />

the diagnostic accuracy of CT pulmonary angiography (CTPA)<br />

approaching that of catheter angiography. 3 Therefore, CTPA is commonly<br />

used as a diagnostic modality of choice, especially in patients<br />

with an abnormal chest radiograph or underlying pulmonary disease,<br />

as both increase the frequency of a nondiagnostic V/Q scan. CTPA is<br />

also valuable as it yields an alternative diagnosis in 40% to 70% of<br />

patients with a negative PE scan, including bronchogenic carcinoma,<br />

metastatic disease, pericardial effusion, and aortic dissection. Recent<br />

studies demonstrate significantly improved visualization of segmental<br />

Paul M. Silverman, MD<br />

Editor-in-Chief<br />

Professor of <strong>Radiology</strong><br />

Gerald D. Dodd, Jr. Distinguished Chair Diagnostic Imaging<br />

Section of Body Imaging<br />

University of Texas M.D. Anderson Cancer Center<br />

Houston, TX<br />

Contributing Editors<br />

Smita Patel, MRCP, FRCR, Lecturer II<br />

University of Michigan Health System, Ann Arbor, MI<br />

Marc J. Fenstermacher, MD, Assistant Professor<br />

University of Texas M.D. Anderson Cancer Center, Houston, TX<br />

Farzin Eftekhari, MD, Professor<br />

University of Texas M.D. Anderson Cancer Center, Houston, TX<br />

Steve Venable, MBA, Senior Management Analyst<br />

University of Texas M.D. Anderson Cancer Center, Houston, TX<br />

V O L U M E 1 • I S S U E 1 • 2 0 0 1<br />

CT UPDATE<br />

Multislice CT: A New Comprehensive Tool for Evaluation<br />

of Pulmonary Embolism and Deep Venous Thrombosis<br />

Smita Patel, MD, MRCP, FRCR; Ella A. Kazerooni, MD; Paul M. Silverman, MD<br />

and subsegmental pulmonary arteries using thinner collimation.<br />

Remy-Jardin et al 1 reported improved visualization of the segmental<br />

pulmonary arteries from 85% to 93% and that of the subsegmental<br />

vessels from 37% to 61% using the 2-mm technique compared with<br />

the 3-mm technique with single-detector CT scanner (SDCT). 1 Patel<br />

et al 2 recently reported an incremental improvement in visualization of<br />

the segmental arteries from 74% to 79% to 89%, respectively, when<br />

comparing the 3-mm collimation technique using SDCT with the 2.5mm<br />

and 1.25-mm techniques using multidetector CT (MDCT). The<br />

incremental improvement was even better at the subsegmental levels,<br />

35% with the 3-mm technique and 44% and 68% with the 2.5-mm and<br />

1.25-mm techniques, respectively. 2 Not only were arteries seen more<br />

clearly, but reader agreement as to presence or absence of thrombus in<br />

segmental and subsegmental vessels was more consistent with the<br />

1.25-mm collimation technique. A recent large study compared the<br />

performance of dual-section helical CT with pulmonary angiography<br />

and concluded that the sensitivity, specificity, and positive- and negative-predictive<br />

values were 90%, 94%, 90%, and 94%, respectively. 3<br />

They concluded that helical CT may replace pulmonary angiography<br />

in the diagnosis of PE and that selective pulmonary angiography<br />

should be reserved for patients with an unresolved diagnosis. 3<br />

Ultrasonography (US), the most commonly used diagnostic tool for<br />

the evaluation of DVT, has a sensitivity of 95% and a specificity of 98%<br />

for the diagnosis of acute DVT. Currently, direct catheter venography,<br />

plethysmography, and isotope scanning are not often used. Recently,<br />

several investigators have compared US and helical CT in patients with<br />

suspected PE. Some authors advocate US to exclude a DVT in the event<br />

of a negative CTPA, thereby excluding clinically significant pulmonary<br />

embolism and the need for unnecessary anticoagulation, which has its<br />

own associated morbidity. However, this is at the expense of two different<br />

tests that take longer to perform, not to mention the additional costs.<br />

With the advent of newer and faster helical CT scanners, in particular<br />

multislice scanners, a single comprehensive exam can be performed to<br />

evaluate the pulmonary arterial bed and the deep veins of the pelvis and<br />

thighs. In a study of 71 patients, Loud et al 4 demonstrated that CT<br />

A B<br />

FIGURE 1. (A and B) Axial contrast-enhanced MDCT in a patient with<br />

metastatic breast cancer, demonstrating filling defects in the lobar (arrows),<br />

segmental (curved arrows), and subsegmental (arrowheads) pulmonary<br />

arteries, compatible with PE. Note the bilateral pleural effusions and a pericardial<br />

effusion. Mild enlargement of the subcarinal nodes is also noted.


FIGURE 2. Axial contrast-enhanced<br />

MDCT of the pelvis demonstrating<br />

normal optimal enhancement of the<br />

femoral veins (arrows).<br />

venography (CTV) is comparable<br />

with US in the evaluation of DVT<br />

with a sensitivity and specificity of<br />

100%. Garg et al 5 reported obtaining<br />

a good quality CTV examination<br />

in 97% of a total of 70<br />

patients. They demonstrated that<br />

CTV was more efficacious than<br />

US in 36% of cases, equivalent to<br />

US in 37%, and US was better<br />

than CTV in 27%. Duwe et al 6<br />

found an accuracy of 93% for<br />

CTV using US as the reference<br />

test in 74 patients, with a sensitivity of 89%, specificity of 94%, positive-predictive<br />

value of 67%, and negative-predictive value of 98%.<br />

The CTV techniques used by these authors differ, with the scan interval<br />

varying from 5 mm to 20 mm, collimation 5 mm to 10 mm, and the<br />

injection delay from 3 minutes to 3.5 minutes. All of these studies were<br />

performed on a single-detector helical scanner. CTV is particularly useful<br />

in postoperative patients or in obese and immobile patients in whom<br />

sonography can be challenging to perform.<br />

Multi-detector CT Scan Protocol: Part 1–Thorax<br />

For the thorax protocol, 150 cc of iohexol 300 mg/mL<br />

(Omnipaque ® [iohexol]; Amersham Health, Princeton, NJ) is injected<br />

via a 20-gauge angiocatheter in an antecubital vein at a rate of 4<br />

cc/sec. A scan delay of 25 seconds is used. Imaging is performed from<br />

the dome of the diaphragm to the aortic arch during a single breathhold,<br />

with the acquisition time varying between 15 to 19 seconds,<br />

depending on the size of the patient. Images are obtained at 1.25-mm<br />

collimation and reconstructed at 50% of the scan collimation (HS<br />

mode, pitch 6).<br />

Part 2–Leg/pelvic veins<br />

Three minutes following start of the contrast injection, acquisition<br />

of the pelvis and lower extremity veins is obtained from a caudad to<br />

cephalad direction from the level of the tibial plateaus to the iliac<br />

crests. Images are obtained at 7.5-mm collimation and reconstructed at<br />

50% of the scan collimation (HS mode, pitch 6). The entire study is<br />

then evaluated on a GE Advantage Windows Workstation (GE<br />

Medical Systems, Milwaukee, WI). Use of the HS mode in large<br />

patients may account for very noisy images, limiting evaluation of the<br />

pulmonary arteries. In these patients, the HQ mode can be used and<br />

thicker slices obtained. Acquisition of the pulmonary arteries and the<br />

deep veins of the pelvis and thighs is obtained with a single bolus of<br />

intravenous contrast.<br />

Study Interpretation<br />

The window level and width is altered for optimum evaluation of the<br />

pulmonary arteries. A wider window width and a higher level may be<br />

needed to evaluate for subtle emboli. Depending on the concentration<br />

of the contrast in the pulmonary arteries, this may need to be altered at<br />

different levels. Then, the main, lobar, segmental, and subsegmental<br />

arteries are examined systematically from their origins to the 5th or 6th<br />

order branches, using the scrolling mode device. Pulmonary emboli are<br />

diagnosed as partial or complete filling defects, enlargement of the<br />

pulmonary artery with a large occlusive clot, peripheral filling defect,<br />

or nonenhancement of a segment of the pulmonary artery (Figure 1).<br />

Evaluation for chronic pulmonary emboli is also possible, with the<br />

presence of webs or detection of small thick-walled pulmonary arteries<br />

with enhancing walls and filling defects. Systematic review of the<br />

entire pulmonary arterial circulation is performed bilaterally. Note is<br />

also made of additional findings such as pleural or pericardial effusions,<br />

nodules, tumors, nodal enlargement, consolidation, emphysema, and<br />

2<br />

aortic dissection or aneurysm. These aid clinicians in further management<br />

as the clinical presentation of the above diagnoses can be similar.<br />

Then, the veins of the pelvis and thighs are evaluated using the scroll<br />

mode device, after narrowing the window width and level, for optimum<br />

evaluation of the veins.<br />

DVT is diagnosed when there is a central filling defect, enlargement<br />

of the vein (pitfall, venous valves), segmental nonvisualization, wall<br />

enhancement, or perivenous subcutaneous edema (Figures 2 and 3).<br />

Prolonged arterial enhancement may represent extensive bilateral DVT.<br />

However this can also be found when the CT is performed too soon in<br />

the arterial phase or when there is severe bilateral arterial insufficiency.<br />

Observation of other pathology is also possible, such as pelvic tumor<br />

compressing the pelvic veins or a Baker’s cyst. Optimum venous<br />

enhancement is not uniform in all patients with an injection-to-scan<br />

delay of 3 minutes, as this varies according to the patient’s cardiac status<br />

and the state of the pelvic and lower limb arteries. Patients with<br />

altered inflow due to atherosclerotic disease may require a longer delay<br />

time.<br />

Multislice CT allows acquisition of 4 to 8 axial images with each<br />

revolution of the helical scanner, hence accounting for the short scan<br />

acquisition time, which is essential in sick, dyspneic intensive-care<br />

patients who cannot hold their breath. Not only has multislice CT<br />

improved evaluation of the segmental and subsegmental pulmonary<br />

arteries, but it has also allowed evaluation of the lower extremity veins,<br />

the source of PE, with a single injection of intravenous contrast. This<br />

translates into a single imaging modality for a quick, accurate, and efficient<br />

diagnosis of pulmonary thromboembolic disease. Recent studies<br />

have demonstrated


TECHNICAL ISSUES<br />

Abdominal CT Angiography<br />

in the Era of Multidetector CT<br />

Marc J. Fenstermacher, MD; Silvana Faria, MD;<br />

Paul M. Silverman, MD<br />

As new techniques have emerged over the last 15 years, the imaging<br />

evaluation of the vessels of the abdomen has undergone considerable<br />

evolution. Prior to the advent of multidetector CT (MDCT), much<br />

of the advancement has been in magnetic resonance angiography<br />

(MRA). A number of innovative MRA techniques have been utilized,<br />

including 2-dimensional (2D) and 3-dimensional (3D) time-of-flight<br />

(TOF), phase contrast, and, most recently, bolus contrast-enhanced 3D<br />

fast gradient echo techniques, with or without step-wise incremental<br />

couch movement. Currently, the latter approach is widely utilized in<br />

most practices, especially for the evaluation of the arterial and portal<br />

venous systems. The systemic venous system remains a challenge for<br />

accurate, high-contrast MRA, primarily because of the relatively low<br />

concentration of injected gadolinium once it reaches the iliac veins and<br />

inferior vena cava. All of the MRA techniques in the abdomen share a<br />

number of drawbacks, which have fueled the search for better noninvasive<br />

angiographic techniques. With MRA, it is not possible to<br />

demonstrate both the vasculature and the regional soft tissues in the<br />

same imaging sequence; the highest quality arterial MRA will demonstrate<br />

bright vessels and practically nothing else. This problem is particularly<br />

limiting in the oncologic setting, where noninvasive angiography<br />

is used primarily to stage tumors locally and in surgical planning.<br />

Even high-quality abdominal MRA techniques still suffer relatively<br />

low spatial resolution due to the requirement of imaging in the<br />

coronal plane for adequate coverage, with a large field-of-view, yet<br />

avoiding wrap-around aliasing artifacts. Tertiary or smaller branches<br />

are not visualized due to limitations in resolution and slice thickness.<br />

A B<br />

C<br />

D<br />

FIGURE 1. Comparison of magnetic<br />

resonance angiography (MRA) and<br />

computed tomography angiography<br />

(CTA) in a patient with testicular cancer<br />

and a left para-aortic nodal<br />

mass. This preoperative evaluation<br />

was performed prior to retroperitoneal<br />

lymph node dissection. (A)<br />

Coronal MIP projection from 3D<br />

bolus contrast-enhanced MRA in the<br />

arterial phase. (B) Double oblique<br />

coronal CTA reformation showing<br />

two right renal arteries and single left<br />

renal artery. (C and D) Two curved<br />

CTA reformations showing the (C)<br />

upper and (D) lower right renal arteries,<br />

and the left para-aortic nodal<br />

mass abutting the undersurface of<br />

the left renal artery.<br />

3<br />

Any patient motion during the 20- to 30-second breath-hold acquisition<br />

degrades the MRA images severely.<br />

With single-detector helical CT (SDCT), it first became possible to<br />

reconstruct the 3D helix retrospectively with the acquired slice thickness<br />

but with much smaller intervals, such as 50% of the collimation.<br />

This enabled the creation of high-quality multiplanar volume reformations<br />

and other angiographic images using a workstation, and we began<br />

using this technique in selected cases for visualizing the arterial and<br />

venous vasculature adjacent to tumors in the abdomen and pelvis. The<br />

limiting factors with SDCT have been the interrelated issues of slice<br />

thickness and coverage. All bolus-contrast-enhanced angiographic<br />

techniques depend on matching the timing of image acquisition to the<br />

transit of contrast through the vessels of interest. Since all acquisitions<br />

are in the axial plane, there is limited coverage with the 2- to 3-mm collimation<br />

and pitch of 2 usually used with SDCT. 1<br />

The advent of MDCT has allowed the acquisition of larger areas of<br />

coverage with thinner slice collimation and much faster imaging<br />

times per series. We routinely image the entire abdominal aorta and<br />

proximal common iliac arteries in


transit of the bolus of contrast through the aorta. An alternative to<br />

SmartPrep, which does incur a nominal though mandatory delay<br />

between contrast arrival in the abdomen and the initiation of scanning,<br />

is to perform a test injection in order to estimate the contrast travel<br />

time to the abdominal aorta. This step is time consuming and not used<br />

routinely in our department at this time.<br />

Data is transferred to a workstation, currently a Vital Images<br />

Vitrea2 (Vital Images, Inc., Minneapolis, MN) or an Advantage<br />

Windows workstation (GE Medical Systems), for creating and filming<br />

curved and multiple oblique reformations. Although this is a timeconsuming<br />

step for the radiologist, it is rewarding for the clinician.<br />

While a technologist with special interest and training in image processing<br />

can perform this step in many cases, optimizing reformatted<br />

imaging planes often requires a knowledge of anatomy and pathology<br />

that may be beyond their reach (Figure 2). At the current stage of<br />

development of these techniques, interested cross-sectional radiologists<br />

should be encouraged to perform the reformations and recon-<br />

PRACTICAL ISSUES<br />

Imaging Considerations in Pediatric<br />

Multislice CT: A Radiologist’s Perspective<br />

Farzin Eftekhari, MD and Paul M. Silverman, MD<br />

Multislice CT, occasionally referred to as multidetector or multidetector<br />

row CT, has made a significant impact on the imaging of<br />

pediatric patients by reducing the total study time in uncooperative or<br />

very ill patients. In many instances, this has virtually eliminated<br />

breathing or motion artifacts, and, even more importantly, the need for<br />

conscious sedation or general anesthesia. 1<br />

In those patients who require conscious sedation or general anesthesia,<br />

shorter examination time has minimized the sedation period,<br />

and, thus, the potential risks of sedation or anesthesia. This has<br />

increased patient throughput and the efficiency of the sedation team,<br />

enabling them to schedule additional pediatric CT, magnetic resonance<br />

(MR), or interventional radiology procedures.<br />

Table 1. Technical Considerations in Pediatric Multislice CT<br />

Approximate Approximate<br />

DFOV mA kV Age (y) Weight (kg)<br />


processes and to cover the smaller anatomy.<br />

It is also important to realize that the source-to-detector distance is<br />

decreased in the LightSpeed multislice scanner (94.9 cm) relative to<br />

the GE single-slice design (109.9 cm). This detector alone accounts for<br />

a 34% increase in radiation dose for the multislice system compared<br />

with the single-slice configuration using identical scan parameters.<br />

For pediatric abdominal/pelvic CT scanning, we use a slice thickness<br />

of 5 mm, high speed (HS), and a table speed of 22.5 mm/rotation.<br />

For pediatric chest CT, we use a slice thickness of 5 mm, HS,<br />

and 22.5 mm/rotation table speed.<br />

Pediatric patients receive iodinated contrast material when it is<br />

clinically indicated. To limit reactions or nausea and vomiting, we use<br />

low-osmolality contrast material (LOCM) at a dose of 1.5mL/kg<br />

body weight for the chest, and 2.0 mL/kg for abdominal and pelvic<br />

CT. We prefer to deliver all of the contrast before scanning and allow<br />

a 25-second delay for chest, and chest/abdomen/pelvis imaging<br />

(allowing a 12-second pause between chest and abdomen), and 50<br />

seconds for abdomen/pelvis imaging. Alternatively, when available,<br />

we use a computer automated scanning technology, such as<br />

SmartPrep, to ensure that scanning occurs during peak liver enhancement.<br />

This allows for consistency and optimal imaging to detect focal<br />

liver lesions.<br />

Injection rates for contrast material range from 0.3 to 3.0mL/sec,<br />

depending on the size of the IV access line (22- to 18-gauge angiocatheters,<br />

depending on the age of the child).<br />

Our pediatric technique (Table 1) is based on the child’s body size<br />

(depth of field of view), age, and weight. For children older than 6<br />

years of age, we use a slice thickness of 7.5 mm and 15 mm/rotation<br />

table speed. We use this table to select the appropriate mA setting for<br />

each case. The mA ranges from 140 to 230 with a kV of 120. This<br />

MEDICAL ECONOMICS<br />

Application of Six Sigma to Healthcare:<br />

Improving CT Efficiency<br />

Steve Venable, MBA and Paul M. Silverman, MD<br />

Six Sigma is a performance improvement methodology used to<br />

achieve significant change and improvement. The term Six Sigma<br />

refers to six standard deviations from the mean on a normal distribution<br />

model. This level of performance would seem impossible to attain at<br />

first, but the methodology leads to extraordinary improvement on<br />

processes and final results. Many large corporations, including Allied<br />

Signal, Honda, and GE, 1 have adopted Six Sigma to improve their<br />

financial performance and maintain a competitive advantage.<br />

Six Sigma represents a cultural shift to continuous, data-driven<br />

performance improvement. Though Six Sigma was originally used to<br />

decrease defects in manufacturing industries, it has moved to service<br />

industries, and is readily adapted to healthcare. The data-driven<br />

aspect of Six Sigma meshes well in the current hospital setting where<br />

dramatic efforts are being made to strive for marginal efficiency in a<br />

competitive environment. Physicians require a business methodology<br />

based on verifiable data and analysis. This focuses all groups on solutions<br />

to problems and quantitative measures of success.<br />

At the University of Texas M.D. Anderson Cancer Center<br />

(MDACC), we have used Six Sigma to provide a dramatic improvement<br />

in efficiency. In computed tomography (CT), a common reason<br />

given for patient delays was a lack of laboratory tests prior to the CT<br />

scan. More than 95% of our patients received IV contrast and labs<br />

were required prior to administering contrast. However, data analysis<br />

5<br />

table is designed for current GE multislice scanners in which the scan<br />

time is 0.8 seconds. However, since newer scanners offer shorter scan<br />

times, such as 0.5 seconds, we intend to update this table to adjust for<br />

mA values accordingly.<br />

Conclusion<br />

We feel that the use of multislice CT scanners has had a significant<br />

impact on imaging in pediatric patient population in terms of need for<br />

sedation and throughput, but we need to continue to look for ways to<br />

decrease the radiation dose to even lower levels.<br />

Acknowledgments<br />

The authors would like to thank Dianna D. Cody, PhD, and Donna<br />

M. Moxley, MS, from Diagnostic Physics for their valuable comments.<br />

REFERENCES<br />

1. Pappas JN, Donnelly LF, Frush DP. Reduced frequency of sedation of young children<br />

with multisection helical CT. <strong>Radiology</strong>. 2000;215:897-899.<br />

2. McCollough CH, Zink FE. Performance evaluation of a multislice CT system. Med<br />

Phys. 1999;26:2223-2230.<br />

3. Cody DD, Moxley DM, Eftekhari F, Silverman PM. Pediatric dose considerations<br />

in multislice helical CT. Helical CT Today. 2001;6(3):3-4.<br />

4. Motley DM, Hazle JD, Shepard JS, Zhou XJ. Dosimetry of a new multislice helical<br />

CT scanner: Calculated and measured patient doses [abstract]. <strong>Radiology</strong>.<br />

1999;213(P):284.<br />

5. Donnelly LF, Frush DP, Nelson RC. Multislice helical CT to facilitate combined CT<br />

of the neck, chest, abdomen, and pelvis in children. AJR Am J Roentgenol.<br />

2000;174:1620-1622.<br />

6. Brenner DJ, Elliston CD, Hall EJ, Berdon WE. Estimated risks of radiationinduced<br />

fatal cancer from pediatric CT. AJR Am J Roentgenol. 2001;176:289-296.<br />

7. Paterson A, Frush DP, Donnelly LF. Helical CT of the body: Are settings adjusted<br />

for pediatric patients? AJR Am J Roentgenol. 2001;176:297-301.<br />

found that


measured. We discovered that many long-held perceptions were inaccurate.<br />

Perception: “Many” patients reported without the requisite<br />

labs; Reality: 3 minutes, even for a combined chest, abdomen,<br />

and pelvis exam. We spent more time getting the patient onto and off<br />

the table, and the setup and cleaning of the room, 20 minutes total.<br />

The team concentrated on optimizing the patient-related activities and<br />

removed the excess idle time of the CT scanners.<br />

The Interpretive Process<br />

The teams also analyzed the activities in the reading rooms. The<br />

goal was to eliminate all nonvalue activities performed by the radiologists<br />

and shift those activities to others, allowing the radiologists to<br />

concentrate on film interpretation and reports. We began to print out<br />

the information needed by the radiologists for protocoling the patients<br />

putting pertinent information at their fingertips. We also began to hang<br />

the motorized viewers continuously throughout the day, relieving the<br />

radiologist of this tedious task. The results were a dramatic increase in<br />

throughput in the reading rooms and the radiologists were able to stay<br />

current with the growing patient activity.<br />

During the characterization process, several processes were determined<br />

not to need the full Six Sigma treatment, instead, a small group<br />

could work out a solution. An example was the 50% turnover in CT<br />

technologists. A working group interviewed the technologists and<br />

analyzed external market issues. It was determined that the techs were<br />

undercompensated compared with the local market and there were<br />

inconsistencies in the work environment. Work volumes between<br />

shifts and lack of communication between technologists on each shift<br />

were problematic. As soon as changes were implemented to correct<br />

these issues, turnover was reduced to 0% the following year.<br />

Conclusion<br />

When this Six Sigma project was initiated, we failed to realize its<br />

size and scope. We also underestimated the manpower resources<br />

required. Six Sigma touches the entire operation and the necessary<br />

resources must be dedicated to the project. Cultural changes and the<br />

fear of change must be overcome. Six Sigma is data rigorous and provides<br />

a framework for disciplined analysis and correction of processes<br />

not meeting the specification. The payoffs are tremendous for the<br />

corporate culture, for patient satisfaction, and in increased throughput<br />

(shortened patient wait times, faster exam times, decreased interpretation<br />

time resulting), with financial benefits in the increased capacity<br />

on the same resources. For the radiologist, we removed the nonvalue-added<br />

activities in the reading rooms and developed closer working<br />

relationships between the physician staff and technical and nursing<br />

staff. Weaknesses in our information systems were identified and<br />

detailed changes to the software were initiated. Our film printing system<br />

was woefully inadequate and a new system was designed, purchased,<br />

and installed to improve the film quality control function, add<br />

more capacity, and remove the film printing bottleneck. The financial<br />

returns for this project are projected at $15.8 million over 5 years. For<br />

every dollar invested in this project, MDACC expects $16 in return.<br />

The final lesson is that Six Sigma is never-ending; we monitor and<br />

improve our processes continuously. As new areas come into focus, we<br />

apply the tools and continue to reap the benefits of the program.<br />

REFERENCES<br />

1. Harry MJ, Schroeder R. Six Sigma: The Breakthrough Management Strategy Revolutionizing<br />

the World’s Top Corporations. pp. vii-viii: 112. New York: Random House,<br />

2000.<br />

2. Harry MJ, Lawson JR. Six Sigma Producibility Analysis and Process<br />

Characterization. pp. 4.2-4.4. Boston: Addison-Wesley Publishing Co., 1992.<br />

FUTURE MEETINGS AND CONVENTIONS<br />

Meeting date Meeting name Location Contact<br />

November 1-8, 2001 American Society for Therapeutic <strong>Radiology</strong> and Oncology San Francisco, CA 703-502-1550<br />

November 25-29, 2001 Radiological Society of North America Chicago, IL 630-571-2670<br />

CT Update is published by Anderson Publishing, Ltd., 1301 West Park Ave., Ocean, NJ 07712 • (732) 695-0600.<br />

O. Oliver Anderson, Publisher; Elizabeth A. McDonald, Managing Editor; Felice Ponger, Art Director.<br />

Sponsored by an educational grant from Amersham Health. The views and opinions expressed in this publication are those of the authors and do not necessarily<br />

reflectthose of the publisher or sponsor. Full and complete prescribing information should be reviewed regarding any product mentioned prior to use.<br />

6

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