Good evening. My name is Michelle, and I will be your conference facilitator today. I would like to welcome everyone to the DaVita Second Quarter 2025 Earnings Call. Thank you, Mr. Eliason, you may begin your conference.

Thank you, and welcome to our second quarter conference call. We appreciate your continued interest in our company. I'm Nic Eliason, Group Vice President of Investor Relations, and joining me today are Javier Rodriguez, our CEO; and Joel Ackerman, our CFO. Please note that during this call, we may make forward-looking statements within the meaning of the federal securities laws. All of these statements are subject to known and unknown risks and uncertainties that could cause the actual results to differ materially from those described in the forward-looking statements. For further details concerning these risks and uncertainties, please refer to our second quarter earnings press release and our SEC filings, including our most recent annual report on Form 10-K, all subsequent quarterly reports on Form 10-Q and other subsequent filings that we may make with the SEC. Our forward-looking statements are based on information currently available to us, and we do not intend and undertake no duty to update these statements, except as may be required by law. Additionally, we'd like to remind you that during this call, we will discuss some non-GAAP financial measures. A reconciliation of these non-GAAP measures to the most comparable GAAP financial measures is included in our earnings press release furnished to the SEC and available on our website. I will now turn the call over to Javier Rodriguez.

Thank you, Nic, and thank you for joining the call today. We are pleased to report another solid quarter where our focus on providing exceptional care for our patients and fostering a positive experience for our caregivers continues to drive results. We delivered on our financial commitments, supported by strong clinical performance and disciplined execution across our businesses. Today, I will share the highlights of our second quarter results, offer insights on key policy developments, discuss the evolving landscape of device innovation, and finish by sharing our outlook for the rest of the year. But first, as always, let's begin with a clinical highlight. While I usually focus on a specific clinical achievement, today, I want to take a step back and reflect on the exciting opportunities ahead for DaVita and the kidney care community. To offer some historical perspective, in the 2 decades leading up to the COVID-19 pandemic, the kidney care community made remarkable clinical strides. Advances in technology and pharmaceuticals, combined with the adoption of more standardized care led to improved outcomes and significant reductions in mortality rates. Then came COVID, a disruption that impacted not only operations but also the health acuity of our patients. Yet from where we stand today, I am optimistic about what's ahead, and I believe we're entering a new wave of clinical innovation that holds exciting potential for the patients we serve. Breakthrough technologies from advanced IT systems to the transformative power of artificial intelligence are positioned to help us personalize care in unprecedented ways. Greater adoption of new drug classes like GLP-1s and SGLT2s, along with the next-generation devices that improve the clearance of middle-sized molecules, offer the potential to extend life and ease recovery from dialysis. Powered with these tools, the kidney care community is positioned to once again improve clinical outcomes. We have the opportunity to lower mortality, enhance the quality of life of our patients, and deliver better care. Of course, this evolution will take time and investment, but we're moving forward with conviction, grounded in our vision of an unwavering pursuit of a healthier tomorrow. Let me transition now to our second quarter performance. Adjusted operating income and adjusted earnings per share came in slightly ahead of our expectations. These results are indicative of two important themes that we highlighted last quarter and which continue to resonate strongly today. The first theme is our ability to deliver on our commitment of 3% to 7% adjusted OI growth despite not yet achieving our volume growth objectives. This was evident during the second quarter, where the strong performance in patient care costs more than offset cyber-related weakness in revenue per treatment and volume. That said, improving volume remains a primary focus, and we continue to believe we will return to 2% annual treatment growth over time. While the rebound takes shape, we're executing against other opportunities to achieve our long-term operating income and EPS targets. Our proven track record of managing costs across our operations, coupled with our significant investment in systems and IT in recent years, gives us the confidence that we can achieve cost savings that offset current volume weakness. The second theme I want to highlight is the resilience of our business to navigate environmental and unexpected challenges. We're now roughly three months out from the onset of the cyber incident we discussed last quarter. So let me provide more detail on our recovery and associated financial impact. Operationally, we continue to provide uninterrupted patient care. The financial impact incurred can be split into two high-level categories. The first is discrete costs associated with the incident, such as outside consultants, technology costs, legal costs, and so forth. In the second quarter, those costs were approximately $13 million and are excluded from second quarter adjusted operating income as non-GAAP expenses. The second and more significant category is the impact on treatment volume and revenue per treatment due to lower patient admissions, increased missed treatments, and lower expected yield on claims for treatment this quarter, among other things. Aside from the continued impact of the lower census from lost admit opportunities, we believe the impact of the cyber event is largely behind us, and there will be limited ongoing effect on adjusted results. Joel will provide more color on these dynamics. I'll now transition to providing a few policy updates. Last quarter, we provided an update on various policy changes, including tariffs, Medicaid cuts, and qualified health plans. Although Congress has passed further legislation and each of these topics remains fluid, our estimates of the impact of these items on DaVita remain unchanged from last quarter. Additionally, in late June, CMS published the 2026 ESRD proposed rule. The approximate 2% increase from dialysis rate was in line with our expectations, yet much like recent years, continues to fall short of actual inflation experienced by dialysis providers. As a reminder, the Medicare rate is subject to an incremental update in the final rule later this year. One final topic before I move on to guidance. There's a lot of discussion and energy in the industry regarding new technology in the United States to improve clinical outcomes through better clearance of middle-sized molecules during dialysis. High-volume hemodiafiltration or HDF is one example of this technology. We actively champion clinical innovation that can improve patient outcomes and quality of life, and these technologies offer promising potential. In terms of where we stand today, we are active with a number of work streams. This includes monitoring existing and future clinical studies to assess the efficacy of various solutions, including not only HDF machines, but advanced dialyzers, which may provide similar clinical outcomes. As more clinical evidence comes to light, we will listen to physicians' preferences. And finally, we're assessing the operational implications of each innovation with consideration of clinical outcomes and health economics. So there's a lot to be excited about, but still a lot to learn. We remain committed to staying at the forefront of clinical innovation, and we're energized by the opportunity to deliver even better care for the patients we serve. Looking ahead to the remainder of the year, we're reaffirming our guidance range for adjusted operating income of $2.01 billion to $2.16 billion and our adjusted earnings per share range of $10.20 to $11.30, despite the negative impact of the cyber incident. Furthermore, we continue to have confidence in our ability to deliver adjusted operating income and adjusted EPS growth consistent with our long-term guidance. I will now turn it over to Joel to discuss our financial performance and outlook in more detail.

Thank you, Javier. Second quarter adjusted operating income was $551 million. Adjusted earnings per share was $2.95, and free cash flow was $157 million. I'll provide detail on the individual components of our results, beginning with U.S. dialysis. Starting with treatment volume. U.S. treatments per day declined 1.1% versus the second quarter of 2024, which was approximately 50 basis points below our expectations for the quarter. The weakness was largely the result of a higher-than-expected missed treatment rate. We believe that the cyber outage was the primary driver, but it's difficult to differentiate between impacts from cyber and other underlying trends. In light of the higher-than-expected missed treatment rate in Q2, we've increased our expectations for missed treatment rate for the remainder of the year, thereby lowering our expectations for full-year treatment volume. We now anticipate a year-over-year decline of 75 to 100 basis points as compared to our previous guide of down 50 basis points. I will remind you that this forecast is for the absolute number of treatments and not treatments per day or non-acquired growth. Moving on to revenue per treatment. RPT increased approximately $4.50 versus the first quarter. This typical sequential step-up is due to higher patient responsibility for co-pays and deductibles in Q1. The overall increase was below our expectations, primarily related to the cyber incident in April. RPT for the quarter was also negatively impacted versus our expectations by lower dispensing volumes of binders. As a result of these two dynamics, we now expect full-year RPT growth near the lower end of our original range of 4.5% to 5.5%. Moving on to patient care costs. PCCs per treatment declined by approximately $3.50 sequentially. This was primarily the result of three factors: First is higher treatment count compared to Q1. Second is improved labor productivity in our centers; and third is binders. As I mentioned before, binder dispensing volume was below our expectations and down from Q1. We anticipate the outperformance in patient care costs to continue for the rest of the year, resulting in a full-year increase of 5% to 6% versus 2024, better than our original expectations. Focusing on binders for a moment. As I mentioned, both revenue and patient care costs associated with phosphate binders were lower in Q2 versus Q1 due to lower dispensing volumes. We expect no net impact from this and other small changes in our assumptions for the back half of the year. As a result, our full-year adjusted OI expectation from the addition of binders to the bundle remains unchanged at approximately $50 million. International adjusted operating income increased $6 million versus the first quarter primarily due to a one-time benefit. We are excited that the fourth and final of the Latin American acquisitions related to clinics in Brazil closed last week. Integrated Kidney Care, or IKC, our value-based care business, had adjusted operating income of $26 million in the second quarter. IKC benefited from approximately $40 million of revenue that we expected to recognize later this year. This reflects a timing benefit for the second quarter and has no impact on our full year expectations. Transitioning to capital structure. During the second quarter, we repurchased 3.1 million shares, and we repurchased an additional 2.7 million shares since the end of the quarter. We finished the quarter with a leverage ratio of 3.34x consolidated EBITDA, which is up from Q1, but still comfortably within our target range. In May, we raised $1 billion of senior unsecured debt. And in July, we repriced our Term Loan B, reducing the spread by 25 basis points and raised an additional $250 million, which we used to pay down a portion of our Term Loan A. These transactions represent our continuous efforts to optimize our interest rates, maturities, and liquidity, all within our existing capital allocation philosophy. Let me now turn to our expectations for full-year 2025. As Javier noted, we are reiterating our full-year adjusted operating income and adjusted earnings per share guidance ranges as reflected in our press release. We are confident that we can continue to deliver results consistent with our 2025 and long-term guidance while caring intensely for our patients and teammates and investing in our future. That concludes my prepared remarks for today. Operator, please open the call for Q&A.

Our first caller is Andrew Mok with Barclays.

I appreciate all the color on guidance. Can you give us a sense for how census and treatments track following the cyber attack and how you're thinking about volumes in the back half? Because on the one hand, you signaled there wouldn't be an ongoing impact, but then you assumed, I think, elevated missed treatments persist for the back half of the year and revised the treatment growth outlook. So maybe just help us understand how you're thinking about that.

Thanks, Andrew. This is Javier. Before Joel gets into explaining, that's very important because there's a lot of dynamics going on in treatment volume. I think on the simpler side, so we can start at 10,000 feet, the year is going as expected with the exception of two significant items, which are the severe flu season and the cyber incident. And that, of course, puts all those dynamics that you highlighted in play. But sometimes it's just easier to start with a high level before you get into the detail. So now, Joel, if you can bridge all those questions...

Sure. So Andrew, let me try and unpack this for you. So during the call last quarter, we anticipated challenges on the admit side associated with the cyberattack of a few hundred, 500, 600 admits. And that has played out largely as we expected. We saw the challenges for a few weeks, but everything has normalized since then. What we did not anticipate was a spike in missed treatment rates, which is a number that tends to follow a regular seasonal pattern, high in Q1, down in Q2 and Q3, and then back up in Q4. Q1 was higher than normal associated with the flu, and we expected it to come down along a typical curve in Q2, and that's not what we saw. It was elevated in April and actually even worse in May and then came back down in June, although not as far as we would normally expect. So we saw a big jump in missed treatment rates in Q2 year-over-year, which we attribute to the cyber incident. And as a result of that dynamic, we decided to change our view on missed treatment rate for the back half of the year where previously, we had thought it would come down a bit relative to 2024. Given the challenges we've seen in the first half of the year due to both flu and cyber, we updated our assumptions and assume missed treatment rate is roughly flat relative to last year for the back half of the year. So that's the math. I'll remind you, we're talking about 0.1% delta roughly. So we're really focusing in on numbers, and the tighter you get, the harder it is to really call out the precision. But that's the dynamic. So if you think about the change in guide on volume growth from negative 50 bps to negative 75 to negative 100, it's pretty much all about a higher missed treatment rate, partially in Q2, partially in the back half of the year.

Great. And maybe just a few follow-ups on phosphate binders. First, can you give us the phosphate binder contribution to RPT and CPT in the quarter? And why was the dispensing volumes lower in the quarter? Is that due to the lower treatments? Or did the mix of patients on binders go down?

Yes. So on the volume side, it's about a reduction in the number of scripts. It's not a mix issue. What we believe is happening is adherence is not what we expected. Some patients are getting their binders through other means outside of DaVita, and some are just relying on over-the-counter solutions. So volume is lower than expected. In terms of contribution to RPT and CPT, the RPT number was somewhere in the low 8s, and CPT was in the high 6s.

Andrew, one of the things that you might not be familiar with other people on the call is for these binders, the pill burden is pretty heavy. And so there's also some adherence issue around that because you have to take the pills with a meal. I think that there's some leakage in that dynamic.

I would like to discuss the operating income guidance and how you are managing to maintain it despite the worsening treatment growth due to missed treatments and a lower revenue per treatment. Can you explain how you are achieving this? Is it due to cost management in core kidney operations, improvements in international markets, or ITC? Please clarify how you are reconciling these two negative factors while sustaining your operating income guidance.

Yes. Generally, it's two components. By far, the biggest one is cost per treatment, and that's largely a labor dynamic in U.S. dialysis. The other is on international, which was roughly $10 million ahead of plan for the quarter, largely nonrecurring. So I wouldn't annualize that in the back half of the year.

Okay. With the updated treatment growth down 75 basis points to 100 basis points, the first half of the year was down 70. So, at the midpoint of the range, we're now down 1% to 1.1% in the second half of the year. Can you discuss incidents, mortality, and transplants? Also, regarding missed treatments, why would they be structural? I understand factors like the flu in the first quarter and cybersecurity in the second quarter, but generally, these patients need treatments; otherwise, they face serious consequences. How can missed treatments be regarded as a structural challenge?

Yes, let me begin with the missed treatment rate. This is a figure that fluctuates. It has been higher since COVID, peaking at about 1% worse than pre-COVID levels in 2022. We expected it to decline after that, and it did decrease in 2023 and 2024 but has risen again this year. Your observation is quite valid. However, we are only discussing maybe one-tenth or 15 basis points. Therefore, we are okay with keeping it flat compared to 2014. I wouldn’t categorize it as a structural issue, but based on our expectations for the upcoming quarters, we have slightly reduced it. Regarding other dynamics, admits in Q2 were negatively affected by cyber incidents, aligning with our expectations. Excluding that factor, it would have been a typical month for admits, showing year-over-year growth similar to what we have observed in most quarters over the last few years. As for mortality, it remains elevated, consistent with last year's Q2. The excess mortality from flu seen in Q1 has decreased, but overall mortality remains higher than pre-COVID levels, consistent with last year.

Peter, one of the things that's really important because sometimes in the interest of being simple, people talk about the CKD population and GLP-1s and the impact upstream. We are not seeing it in the admits. It's really important what you asked because it's this mortality and missed treatment dynamic that really needs to be rectified. As you mentioned, missed treatments are a little trickier. But mortality, we have a three-pronged plan to work on it. It will take some time to get there. But at the end of the day, you've heard it in the opening remarks, we need better clearance of middle molecules as the first step. Number two, on pharma, we need more patients on GLP-1s. There's barely any patients on them. And then number three is we're working on a whole bunch of protocols and IT to ensure that we can predict hospitalization and other things like that. But at the end of the day, we need to lower mortality.

Just maybe ask about the comment on IKC, $40 million more in Q2. And it sounds like you obviously believe that's a pull forward. I wonder, can you maybe give us a little more on what happened and why do you think that's a pull forward versus potentially a better trend in the underlying business that might carry over in the back half of the year?

Yes. So the reason we feel comfortable that it's a pull forward is it is all revenue associated with 2024 plan years. The dynamic is as the data comes in and our actuarial and accounting teams gain confidence that we have actually earned shared savings, then we will recognize revenue. Our expectation was that we would get that level of clarity in Q3 and Q4, but we were able to get some of the clarity earlier in the year. And as a result, we recognized the revenue early, but we didn't recognize more revenue than we had expected during the year, which is why it's a timing thing rather than a net positive for the year.

Okay. I’d also like to ask, in your prepared remarks, you mentioned that the cyberattack affected revenue per treatment. I’m not sure I fully understand why that happened. Can you explain the dynamic involved? Do you think this will also impact the second half of the year?

Yes. So you heard it right, A.J. We do think the cyber incident had an impact on RPT. We don't think it will impact the second half of the year. There are really two components to this. The larger one is the impact on revenue for treatments done in Q2. So think about it: as we're working our way through the cyber incident, some processes have gone manual. Some processes are either delayed or not being done. If I had to give you a couple of examples here, it would be something like prior authorizations or data gathering of certain elements that you'd want on a claim. As we're working either manually or in a delayed fashion, we expect some of the claims that would normally get approved will not get approved for Q2. So that's the bigger chunk. The smaller chunk relates to older claims that were in the queue that had been previously denied, and we're now working to get them reapproved, either gathering information that wasn't on the claim or updating coverage that had changed. And just as time moves on, it gets harder and harder to collect on those claims. We think the impact of the cyber incident on systems and other processes will lower our ultimate yield and basically increase bad debt on some of those older claims.

Appreciate it. Just a few numbers questions for me. Joel, I think you said last quarter, you expected revenue per treatment ex-binders at about 3% for the year. Just curious if you've got an updated assumption on that number.

Yes. We would peg the number now at around 2.25% for the year. The big difference really is the RPT impact of the cyber incident.

Even though that was you're saying you think is contained to the quarter, how much was that of an impact to the revenue per treatment in the quarter? Do you have a number there?

I'd call it $40 million to $50 million.

Great. Then you talked about the missed treatments in the first half of the year. And then I think you talked about the second half as being flat year-over-year, where before you had expected it to be down. Is that right?

That's right.

And what was the growth year-over-year in missed treatments in the first half? Trying to get a comparison.

It was a little worse in Q1 than in Q2, but it averaged about 50 basis points for the first half of the year.

Okay. Got it. Then the last question for me is that you're indicating a treatment growth number of down 75 to 100 basis points, and that's total treatment growth. What do you think that equates to?

That's total U.S. treatment.

Right. That's total U.S. treatment growth, right? But I think most people, including myself, focus on same-store non-acquired. What do you think that equates to there?

I would say the same-store non-acquired number would be roughly down 50 bps.

Okay. So on a non-acquired basis, you're expecting things to get a little bit better than the second quarter, looking more like the first quarter, and that's because you think the second quarter cyberattack kind of filters through and is done? Why do you expect it to get better than the first half?

Yes. I don't think MAG is a great number for modeling. So I'm a little reluctant to answer your question. Remember, year-over-year growth also depends on the shape of the census trend from the prior year. So you can't just rely on quarter-over-quarter numbers. But I would say volume growth in the back half of the year, you'd expect it to be worse in Q3 and then better in Q4.

I wanted to ask another question about the volumes, I guess, in particular, the increased mortality. I appreciate the comments about some of the things that you guys are planning to do to address it, but it's still not clear to me why we have a higher mortality issue to begin with because I guess higher mortality implies something that is above where it was pre-COVID. So the issues that you singled out kind of sound like newer options to potentially address the issue rather than something went backwards and we're going to get it back to where it was. It's more that it's elevated, and now you have new tools to potentially bring it down. So I'm just trying to figure out why mortality in your view is persistently elevated versus where it was historically.

Yes, thank you for the question, Kevin. The actuarial teams are noting that this issue is present nationwide, not only in kidney diseases but across all medical conditions. The prevailing theory is that COVID has contributed to this situation by delaying care and that individuals with comorbid conditions, particularly those who are more severely ill, are experiencing higher mortality rates. These are the two primary factors, but it's important to note that this is a hypothesis without definitive studies to validate it at this time. Joel, do you have anything else to add?

Well, first, welcome back, Kevin. Look, Javier said it right. This is, we believe, a holdover from COVID, and you see it nationally, the mortality rate for all-cause mortality in the U.S. is up roughly similar to what DaVita sees our mortality is up. So it's a national issue. It's not a kidney issue. I think the point we were trying to emphasize here is we're not passively waiting for the environment to improve, although obviously, that would help. But there are things that we and the rest of the industry can do to improve mortality. And this is not a new dynamic. This is really the underpinning of volume growth for the better part of 20 years pre-COVID was mortality improvement in the dialysis community as a result of things that dialysis providers were able to accomplish.

And that's helpful. I guess as we think about the three things you outlined as ways to try to mitigate this, I mean, how should we think about the timing of these and when they might expect to impact results?

Yes. The timing will be gradual. If you look at the better clearance of middle molecules, the HDF or the cutoff dialyzer, that will take some time to play out. If you look at pharma and GLP-1s, again, here we are x years into it, and the numbers are in the low teens of patients on the drug. So it's also low. And then on the protocols and systems, again, they're gradual and they're incremental. But it's a cumulative portfolio of things that over time has an impact, but you should think about it in years and not just a couple of quarters.

Okay. And then I guess maybe the last question. It sounds like the story for the quarter is you obviously had some headwinds from volume, headwinds from pricing, but you were able to offset it on the cost side of things. Are these cost initiatives, things that you can still pull even when volumes come back? I mean it's been impressive to see the cost control in the last few years. Does that mean when volumes do start to come back that you should be growing even faster than the 3% to 7% OI? Or like it seems like you can maintain this cost control; then there's a lot of opportunity once volumes normalize.

Well, we take a lot of pride in our operational excellence and discipline, and we're always looking for variables that can move the needle. So the short answer is, of course, who knows because it depends on what volume pickups, etc. But our hope and our strategy right now is that we will continue this efficiency. And of course, as technology advances, we think we can make it happen.

Maybe just to Kevin's question a little bit more, I guess, on the patient care cost. Any specifics on what's sort of driving that performance? And I guess, I think it sounds like you're expecting this to continue through the rest of the year. If that's true, is there really any reason why we shouldn't expect this to carry into next year?

The main driver, as Joel said, is productivity. And if you were going to double-click because, as you know, productivity has a lot of variables in there, you would say that our teammates are staying longer, so our retention is a bit better. Our training costs have come down a bit as we are more effective at putting people in their jobs effectively quicker.

Got it. And then just lastly, I guess on the cyber incident, does this have any sort of impact on longer-term spending sort of expectations in terms of hardware, software, anything you might need to invest in just to mitigate the chances of this happening again?

It's a marginal cost. Look, at the end of the day, these cyber criminals are quite sophisticated, and they keep reinventing themselves. The corporations and the industry have to continue to innovate ourselves. So we've made some investments that we believe to be appropriate and prudent, but I don't think I would call out anything material.

Just a question on the new technologies available in the market and this focus on removing larger molecules. Baxter's Theranova dialyzer has been in the market in the U.S. for several years. And obviously, FMC is ramping up their HDF rollout for next year. For Theranova, and I guess also for HDF because you run clinics in Europe, too, how much have you used these technologies in your clinics thus far? And I suppose, how are you going to go about really collecting the clinical data, running sort of effectively, I assume, clinical trials? And how long do you think it will really take to get an idea of how much of an impact these new technologies can make?

Yes. So let me unpack it and see if I get to all your questions. Number one, we are experienced on both the HDF and the middle molecule dialyzers. We are using different brands. So I won't get into what brand of dialyzer we are using. Different countries have different beliefs. And so in countries where HDF is there, sometimes you have almost the entire country there and sometimes you have literally only 20%. So it's got dynamics of clinical practices. It's got dynamics of reimbursement and other things. As you know, the CONVINCE study had some very encouraging results on mortality. Now there is a study in Spain called the mother study, and that is literally putting both technologies head-to-head. At the end of the day, what we want is what's best for the patients and what our physicians and patients want. But of course, we're watching the science because it's a lot easier to change a dialyzer than it is to change your fleet of machines and prescriptions and all the other things. But at the end of the day, if that's what the doctors want or that's where the science points us, we will do it. So we are watching like you are, and we're conducting a couple of studies ourselves, and we will be moving as appropriate.

Great. And just a follow-up on the phosphate binders. There's a lot of generics in the market, and then there's, I guess, two newer alternatives. Are the pill loads on that better because I know one of them should be going generic soon? Or do you see this as more of an adherence problem rather than a cost problem?

I would say probably more adherence. The mix that we saw hasn't changed much between Q1 and Q2. That said, look, we're only about six months into this. So we're still learning. That said, I think from an OI standpoint, we feel pretty good about where we are for the year, and the number of moving pieces are going down every quarter. So the $50 million of OI feels like a pretty reasonable estimate for the rest of the year.

Just free cash flow, I think it's tracking about $112 million for the first half of the year, but guidance was reiterated at $1 billion to $1.25 billion. I guess, can you bridge us how you get back to that level of free cash flow in the back half of the year?

Yes. Free cash flow is generally lighter in the first half of the year, and the cyber incident slowed us down a lot in Q2. So catching up on cyber will be the biggest component. I think cash taxes is probably the other thing I'd point to in the back half of the year that will be significantly better than the first half.

Okay. Great. And then on IKC, this big reversal of operating income in Q2, patients begin growing again. I guess what are you seeing there? And what do you assume in the back half of the year from IKC? Is this because you guys unloaded a bunch of patients in the first quarter? Or just kind of what should we expect for IKC in the back half of the year?

So look, IKC was roughly breakeven for the first half of the year. We haven't changed our guide for the year of, call it, negative $20 million-ish. So that's what you should expect: negative $20 million over the back half of the year. Typically, Q4 should be a better quarter than Q3, although the phasing of OI in IKC is very variable and tough to predict, as you can see based on what happened in Q2.

Okay. And then a few quickies here. What is your MA penetration at this point? Are you still getting positive pricing pressure or pricing tailwinds from growth in MA?

There's really not much to call out anymore on MA. We're roughly moving with the market. There's really very little of note there.

Okay. And then on fixed subsidies expiring for 2026, can those patients get enrolled via the American Kidney Fund before the drop into government reimbursement?

Certainly a possibility, yes.

Okay. And then last, what was the commercial mix this quarter? And were there any changes to home balances?

Immaterial, minor, minor variability on both. So nothing to call out.

Okay. And then my last one here, I promise. Was that Berkshire sale that came out today just part of the normal process to reach that 45% range?

That's exactly right, Pito. It was in a normal course. It was pursuant to the standstill agreement that we have with them.

At this time, we are showing no further questions. I'll turn the call back over to you.

Okay. Thank you, Michelle, and thank you all for your time this afternoon. As we highlighted today, we're first and foremost committed to providing exceptional care for our patients. As we achieve our clinical objectives, our financial performance will follow. Thank you all for joining the call and be well.

Thank you. This concludes today's conference call. You may go ahead and disconnect at this time.