Doug Coltharp
Analyst · Mizuho
Thanks, Mark, and good morning, again, everyone. I will take a few moments to walk through the details of the quarter and elaborate on a number of the concepts that Mark alluded to in his discussion. As Mark just summarized Q1 was a solid start to the year characterized by solid operating performance in both segments. During Q1, consolidated net operating revenues increased by 7.1% and consolidated adjusted EBITDA rose by 4.5%. Diluted earnings per share of $0.70 for Q1 increased by 14.8% over the prior year period benefit from lower interest expense, a lower effective tax rate and reduced share count. As Mark mentioned, we continue to generate high levels of free cash flow. As can be seen on Slide 13 of the supplemental materials, Q1 adjusted free cash of $147.5 million increased by 5.8% over Q1 2016. We extended our track record of utilizing free cash flow to expand the capacity of our two business segments via high quality growth opportunities and complementing these investments and growth with shareholder distributions. As depicted on Slide 17, during Q1 approximately $39 million of free cash flow was deployed to core growth opportunities and approximately $40 million was returned to our shareholders in the form of common stock dividends and share repurchases. As we think about cash flow for the final three quarters of the year, please note that we have revised our estimate for 2017 cash taxes to a range of $95 million to $115 million from the previous estimate of $120 million to $175 million. This revision stems from the approval we received from the IRS for a tax accounting method change related to billings denied under prepayment claims reviews. This is good news and that we are no longer required to pay taxes on revenue that has not been received because of our prepayment claims denial. The immediate impact was to replenish our NOL by approximately $130 million creating a tax benefit of approximately $54 million. Please note that this results in a tax deferral as income taxes will be payable if and when the denied claims are paid. As maybe seen on Slide 16, we essentially consumed the replenished NOL in Q1 and thus we estimate that cash taxes for 2017 will be ratably spread over quarters two through four. Our funded debt was reduced by $63 million during Q1 resulting in a leverage ratio at the end of quarter of 3.7 times. We have no significant debt maturities prior to 2020 and ended Q1 with approximately $479 million of unfunded availability under our revolving credit facility. We continue to enjoy one of the strongest balance sheets in the post-acute sector and given our real estate ownership position, this advantage will be further highlighted with the adoption of the new lease accounting standard beginning in 2019. Turning to our business segment results. IRF revenues increased by 5.8% in Q4, driven by a combination of pricing and volume. Net revenue per discharge increased 3.6% owing to our patient mix as we made further progress on treating stroke and neurological patients. For Q1, neuro was approximately 22.1% of our patient mix and stroke was approximately 18.3% both representing year-over-year and sequential quarter increases. Discharge growth for Q1 was 2.8% including same-store discharge of 1.6%. I will again remind you that the 2.8% same-store discharge growth we posted in Q1 2016 benefited by an estimated 80 basis points to 100 basis points due to leap year. IRF segment adjusted EBITDA of $205.4 million for Q1 rose 4.3% over the prior year period. SWB for Q1 was 50.2% of revenues, an increase of approximately 80 basis points over the same period last year. As Mark discussed, the year-over-year increase in SWB was primarily attributable to an increase in FTEs arising from achieving target staffing levels in the former Reliant hospitals, our planned investments in additional clinical staff due to increased regulatory reporting requirements and also the ramp-up of new stores. Bad debt expense for Q1 was 1.9% of revenue, down from 2.1% in Q1 2016. The decrease was primarily attributable to the resolution of the administrative payment delays that impacted collections in 2016. As can be seen on Slide 20, the level of new prepayment claims denials during the quarter was relatively consistent with that experienced over the course of 2016. As may also be glean from Slide 20, we continue to see no evidence of progress on reducing the very substantial and growing backlog of claims awaiting adjudication. Moving to the home health and hospice segment, Q1 revenue increased by 13.5% and adjusted EBITDA rose 5.8%. The segment growth was driven by volume with admissions increasing 19.6% including 13.9% attributable to same-store growth. And similar to Q4, approximately 20% of the same-store admissions growth can be traced to the clinical collaboration with HealthSouth IRFs. The effects of higher volume were partially offset by a decrease in pricing as revenue per episode for Q1 declined by 1.4%. The pricing decline was a result of the Medicare reimbursement reductions partially offset by a higher therapy mix primarily related to clinical collaboration. While we are on the topic of clinical collaboration and as Mark mentioned in his remarks, we continue to make tangible progress on this important initiative, which is focused on improving patient outcomes over a longer episode of care and doing so in a cost effective manner. As is depicted on Slide 6, our clinical collaboration rate for Q1 was 28.9% an increase of 630 basis points over Q1 2016. As Mark also discussed, we launched our clinical collaboration TeamWorks initiative in February and our teams are actively engaged in identifying and quantifying best practices to be standardized across all overlap markets. It will take some time for these new practices to be fully implemented in all overlap markets but based on our previous success with TeamWorks initiatives and the enthusiastic commitment of our associates at HealthSouth and Encompass, we are confident this approach will help facilitate the achievement of our 35% to 40% collaboration rate target in the intermediate term. As I have mentioned in the past, the progression towards this objective is more likely to be step function than a smooth linear ascension. And I note specifically that as we move into the back half of this year, we will be comping against 2016 collaboration rates that already reflected substantial gains. Just to conclude my comments on the home health and hospice segment, Q1 adjusted EBITDA increased 5.8% over the prior year period to $23.9 million. Operating expenses rose as a percentage of revenue due to the reduction in Medicare reimbursement rates, a higher cost per visit, which was driven by an increase in therapy patients and salary and benefit increases. I will take a moment to elaborate on the therapy mix impact here. We have stated previously that more than 55% of the patients discharged from our IRFs require and qualify for home health services. Not surprisingly given the conditions we treat in our hospitals, there is a heavy component of therapy continuation embodied in the home treatment plan on patients discharge from our facilities. As compared to home nursing services, therapy services generally carry both a higher reimbursement and a higher cost per visit resulting in a lower gross margin percentage but higher gross margin dollars. Please also note that the home health pre-claims review demonstration which was schedule to expand into Florida has been postponed for a minimum of 30 days with a 30-day notice to be provided prior to reinstatement. We believe we are fully prepared for the PCRD expansion with the exception of hiring additional FTEs, which can be initiated when notice of reinstatement is received. I will close my remarks with a brief update on our risk sharing pilot strategies. As we have discussed on these calls beginning with Q3 of last year, our initial focus has been on developing a proposal to serve as a collaborator with certain acute care hospitals on fracture DRGs in certain CJR markets. We established the goal of approaching 20 to 25 acute care hospitals located within 18 to 20 CJR markets by the end of Q1 with the further objective of having 46 collaborator agreements in place by mid-year. As I updated you on our Q4 call, speculations at the new administration would convert CJR from mandatory to volunteer together with low degree of financial risk faced by acute care providers related to CJR in 2016, as a reminder, the risk corridor is at 5% for the current year, has significantly decreased the prioritization and sense of urgency on the acute care hospitals to engage in risk sharing on this program. The delayed implementation of the cardiac shift to bundled payment program until at least October 1 has only served to endorse this view. Nonetheless, we believe the data we have assimilated and the value proposition we have articulated in the preparation for the collaborator discussions are resonating with acute care hospitals and in a number of instance have lead to request a preferred provider agreement specific to the CRJ DRGs. As Mark stated, regardless of the timing or mandatory nature of these pilots, we continue to believe that the progression towards episodic and value based payment models will continue and eventually accelerate. We continue to focus on building the tools necessary to serve as a value added partner to payors and acute care hospitals for all of their post acute needs. This includes developing the analytical and clinical capabilities to effectively serve as a true post-acute care navigator, a role we expect to being piloting later this year. And now, operator, we will open the line for questions.