Craig K. Tagawa
Analyst · Eastwood Partners
Thank you, John, and thank you, all, for joining us for AMS' Fourth Quarter and 2012 Financial Results Conference Call and Webcast. Please note that various remarks that we may make on this conference call about future expectations, plans and prospects for the company constitute forward-looking statements for the purposes of Safe Harbor provisions under the Private Securities Litigation Reform Act of 1995. Actual results may vary materially from those indicated by these forward-looking statements as a result of various important factors, including those discussed in the company's filings with the Securities and Exchange Commission, including the company's annual report on Form 10-K for the year ended December 31, 2012 and the definitive proxy statement for the annual meeting of shareholders held on June 7, 2012. The company assumes no obligation to update the information contained in this conference call. As you know, the recently enacted American Taxpayer Relief Act of 2012 or ATRA included a provision, Provision 634, that reduces Medicare reimbursement for Gamma Knife services by approximately $4,000 per treatment compared to 2012 Medicare reimbursement levels. Provision 634 is effective beginning today. In the 3 months since ATRA's enactment, AMS and other affected parties have engaged lobbyists and attorneys and have worked vigorously to have this provision rescinded or modified. While we have not yet been successful, we will continue to fight for rescission or modification of Provision 634. This provision was enacted under the assumption that Gamma Knife and linear accelerator-based radiosurgery treatments are clinically equal, and therefore should be reimbursed by Medicare at like amounts. This is contrary to the decision made by the Centers for Medicare and Medicaid in November 2012, just a few months ago, and prior to Provision 634, that the different reimbursement rates assigned to the Gamma Knife and linear accelerator-based radiosurgery devices were appropriate. But just as important, we strongly disagree that the 2 technologies are clinically equal. There have been no randomized studies that demonstrate that Gamma Knife and linear accelerator-based radiosurgery are clinically equivalent. Additionally, there is a significant difference in how these technologies are reimbursed by Medicare. Unlike the Gamma Knife, linear accelerator-based radiosurgery devices are reimbursed for every treatment session, up to 5 treatment sessions. And this is the key point. Since we believe a majority of linear accelerator-based radiosurgery devices treat patients in multiple sessions, the majority of linear accelerator-based radiosurgery treatments are more costly than Gamma Knife treatment, even prior to ATRA. This is why we continue to believe that once all of the facts are thoroughly analyzed, the Gamma Knife's unequaled, clinically documented patient results and cost effectiveness will result in the rescission or modification of Provision 634. We believe our arguments are compelling, and we'll fight for what we believe is the proper outcome. But that is not all we are doing. We also are implementing an aggressive program to lower our costs. Among other steps, this program includes the subleasing of our office space, payroll reductions and the refinancing of existing equipment loans and leases. We expect the reimbursement rate cut to reduce revenues at AMS' 5 U.S. retail Gamma Knife sites, where the company receives a percentage of the hospital's Medicare reimbursement. We do not know what, if any, impact the change in reimbursement might have on our remaining 12 U.S. centers, where AMS' revenue per procedure is contractually fixed with the hospital. As a result of this uncertainty, we are unable to accurately predict the effect that reduced Medicare reimbursement will have on our financial results. To try to put things in perspective, if AMS' business mix in the last 9 months of 2012 -- or 2013 is identical to that in the last 9 months of 2012, we estimate that revenues would be reduced by approximately $500,000 to $650,000 and pretax income by approximately $300,000 to $400,000 during the period. Please note, however, that actual results could vary materially based on many factors, including payer mix volumes, the impact, if any, from the company's other contracts, increases in treatment volume, our continuing mitigation efforts and the results of our cost reduction program. Even as we work to mitigate ATRA's effects and reduce costs, we are moving forward in our Gamma Knife business. We continue to see opportunities to place systems at new and existing AMS sites both in the U.S. and internationally. This past January, the government of Turkey approved reimbursement under the country's health insurance program for treatment with the Perfexion system at Florence Nightingale Hospital Group in Istanbul supplied by AMS through our EWRS Turkey subsidiary. Our newest Perfexion site, Sacred Heart Health System in Pensacola, Florida began treating patients last week. The installation of our 14th Perfexion system at Northern Westchester Hospital in Mt. Kisco, New York is scheduled for the second quarter of 2013. These recent additions to our Perfexion portfolio demonstrate that neurosurgeons and radiation oncologists who know the competing technologies best continue to demand this unequal stereotactic radiosurgery system for treating cancers and other diseases of the brain. Turning briefly to our proton therapy business, construction at MD Anderson Orlando's dedicated proton center is underway. We continue to expect this facility to begin treating patients next year. As we announced previously, AMS has received a firm financing commitment for the MEVION S250 Proton Therapy System we will supply for this $25 million facility. FDA approval of the Mevion device was received last year. The MD Anderson Cancer Center Orlando will be the model for additional proton centers we are developing. AMS owns approximately 1% of Mevion Medical Systems, the developer of the MEVION S250. In addition to the Orlando center, we are developing proton therapy centers in Boston and Long Beach, California, which are expected to employ the Mevion device. We believe our equity investment in Mevion will turn out to be a valuable asset for AMS and our shareholders. AMS is also developing a 1-room proton therapy center in Dayton, Ohio. Now I will turn the call over to Norm Houck to review our financial results. Norm?