Edwards Lifesciences Reports First Quarter Results
- Q1 sales grew by 10% to $1.6 billion.
- TAVR sales grew by 6%, with a 8% increase on a constant currency basis adjusted for billing days.
- TMTT sales grew by 75%.
- EPS for Q1 was $0.58, with adjusted EPS of $0.66.
- Raised 2024 sales guidance to the high end of the previous 8 to 10% range.
- Raised full-year 2024 sales guidance for TMTT and Surgical segments.
- Confident in TAVR sales guidance.
- Critical Care spin-off on track with raised 2024 sales guidance.
- Expecting healthy and sustainable TAVR growth in the future.
- Company remains committed to addressing the significant unmet needs of structural heart disease patients.
- Adjusted gross profit margin decreased to 76.0% from 77.5% in the same period last year.
- Increase in selling, general, and administrative expenses to $490 million or 30.6% of sales.
- Research and development expenses increased to $285 million or 17.8% of sales.
- Total debt was approximately $600 million.
- Negative impact on gross profit margin due to foreign exchange.
- Investments in transcatheter field-based personnel driving up expenses.
Insights
Edwards Lifesciences' Q1 report highlights a robust performance, with sales growing 10%. Most notably, the TAVR segment continues as a stalwart, contributing $1.0 billion in sales. The company has adeptly adjusted for currency fluctuations, showing methodical planning in an international context.
Investors should note the substantial 75% growth in TMTT sales. This indicates the company's strategic push into the mitral and tricuspid disease space is gaining traction, likely bolstered by the recent FDA approval of the EVOQUE system. Edwards' forward-looking investments in clinical trials, like EARLY TAVR and PROGRESS, are set to potentially redefine treatment protocols.
Adjusted profit margins have seen a marginal decrease likely due to transient forex pressures. Yet, the company's commitment to R&D investments suggests a confident approach to sustaining innovation and market competitiveness. Edwards has a healthy balance sheet with $1.7 billion in cash and equivalents, versus a manageable debt of $600 million. The revised full-year guidance implies strong underlying business fundamentals and an expected continuation of growth trends.
The Q1 results signify Edwards Lifesciences' deepening footprint in the structural heart disease market. The 13% growth in Critical Care sales reflects not just product demand but also the successful penetration of Smart Recovery technologies. This product suite, including the Acumen IQ sensor, is becoming increasingly vital in the ICU setting, underscoring the importance of continuous patient monitoring.
With a keen eye on the competitive landscape, Edwards maintains a stable global position with surgical products like INSPIRIS, MITRIS and KONECT. The anticipated completion of the MOMENTIS clinical study can significantly bolster this segment by providing clinical substantiation of its offerings one year ahead of schedule.
The strategic move to spin off the Critical Care business could sharpen the company's focus and potentially unlock shareholder value. This restructuring suggests that Edwards is streamlining operations to accentuate core growth areas, particularly in the transcatheter space. The impact on the stock may be closely tied to the execution efficiency of this corporate strategy.
The progression of clinical studies such as EARLY TAVR and PROGRESS by Edwards is pivotal. These trials have the potential to redefine the treatment landscape for aortic stenosis patients, which may translate to a broader market reach and extended patent lifespans for TAVR technologies. This research momentum complements the revenue growth, indicating a synergy between Edwards' scientific endeavors and commercial success.
Furthermore, the EVOQUE system's FDA approval for tricuspid regurgitation treatment presents a significant milestone. It not only validates the company's innovation but also opens up new therapeutic frontiers, possibly leading to a paradigm shift in cardiac care. The emphasis on the treatment of tricuspid regurgitation, historically an undertreated condition, underscores Edwards' commitment to addressing unmet medical needs, likely to resonate positively within the investing community.
Highlights and Outlook
-
Q1 sales grew
10% on a reported and constant currency1 basis to$1.6 billion -
Q1 TAVR sales grew
6% ; constant currency sales grew8% adjusted for billing days -
Q1 TMTT sales grew
75% -
Q1 EPS of
; adjusted1 EPS of$0.58 $0.66 -
Raising 2024 sales guidance to the high end of previous 8 to
10% 1 range - Raising full-year 2024 sales guidance for TMTT and Surgical; confident in TAVR guidance
- Critical Care spin-off on track; raising 2024 sales guidance
“Edwards is positioned to extend our leadership and deliver sustainable growth as a result of the strategic investments we have made across our transcatheter platforms to address the large and growing needs of patients impacted by aortic, mitral and tricuspid disease. We are pleased with our total company performance with first quarter sales growth of
Transcatheter Aortic Valve Replacement (TAVR)
For the quarter, the company reported TAVR sales of
Edwards remains pleased with the performance of its SAPIEN 3 Ultra RESILIA platform, which is the leading platform in the
Edwards is positioned for healthy and sustainable TAVR growth well into the future driven by the company’s development of differentiated TAVR technologies, a deep commitment to advancing patient care through high-quality clinical evidence, and its investment in patient activation initiatives. Importantly, Edwards’ groundbreaking research into the treatment of aortic stenosis through its EARLY TAVR and PROGRESS trials could fundamentally change how AS patients are treated.
Transcatheter Mitral and Tricuspid Therapies (TMTT)
In the first quarter, the company drove positive momentum around its unique and broad portfolio strategy of both repair and replacement technologies for mitral and tricuspid patients. The company made significant progress advancing important therapies, including the PASCAL repair system, EVOQUE tricuspid replacement system, and SAPIEN M3 mitral replacement system.
First quarter sales were
In February, EVOQUE became the first transcatheter therapy to receive
Surgical Structural Heart and Critical Care
Surgical Structural Heart sales for the quarter were
Critical Care sales were
Additional Financial Results
For the quarter, the adjusted gross profit margin was
Selling, general and administrative expenses in the first quarter were
Research and development expenses in the first quarter were
Cash, cash equivalents and short-term investments totaled
Outlook
Overall, given the strong first quarter performance, the company now expects full-year 2024 sales growth to be at the high end of the prior guidance of 8 to
The company is maintaining its full-year 2024 adjusted earnings per share guidance of
For the second quarter of 2024, the company projects total sales to be between
About Edwards Lifesciences
Edwards Lifesciences is the global leader of patient-focused innovations for structural heart disease and critical care monitoring. We are driven by a passion for patients, dedicated to improving and enhancing lives through partnerships with clinicians and stakeholders across the global healthcare landscape. For more information, visit www.edwards.com and follow us on Facebook, Instagram, LinkedIn, X and YouTube.
Conference Call and Webcast Information
The company will be hosting a conference call today at 2:00 p.m. PT to discuss its first quarter results. To participate in the conference call, dial (877) 704-2848 or (201) 389-0893. The call will also be available live and archived on the “Investor Relations” section of the Edwards website at ir.edwards.com or www.edwards.com.
This news release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. These forward-looking statements can sometimes be identified by the use of words such as “may,” “will,” “should,” “anticipate,” “believe,” “plan,” “project,” “estimate,” “forecast,” “potential,” “predict,” "early clinician feedback," “expect,” “intend,” “guidance,” “outlook,” “optimistic,” “aspire,” “confident” or other forms of these words or similar expressions and include, but are not limited to, statements made by Mr. Zovighian, second quarter and full year 2024 financial guidance, statements regarding the international adoption of TAVR, statements regarding transforming patient treatment, investments, expansion of evidence, approvals, clinical outcomes, adoption, and the information in the Outlook section. No inferences or assumptions should be made from statements of past performance, efforts, or results which may not be indicative of future performance or results. Forward-looking statements are based on estimates and assumptions made by management of the company and are believed to be reasonable, though they are inherently uncertain, difficult to predict, and may be outside of the company’s control. The company's forward-looking statements speak only as of the date on which they are made and the company does not undertake any obligation to update any forward-looking statement to reflect events or circumstances after the date of the statement. If the company does update or correct one or more of these statements, investors and others should not conclude that the company will make additional updates or corrections.
Forward-looking statements involve risks and uncertainties that could cause actual results or experience to differ materially from that expressed or implied by the forward-looking statements. Factors that could cause actual results or experience to differ materially from that expressed or implied by the forward-looking statements include risk and uncertainties associated with the spin-off of our Critical Care product group; our ability to develop new products and avoid manufacturing and quality issues; challenges related to clinical trial or commercial results or new product approvals and therapy adoption; the impact of domestic and global economic conditions; competitive dynamics; our reliance on vendors, suppliers, and other third parties; damage, failure, or interruption of our information technology systems; the impact of public health crises; consolidation in the healthcare industry; our ability to protect our intellectual property; our compliance with applicable regulations; our exposure to product liability claims; use of our products in unapproved circumstances; changes to reimbursement for the company's products; the impact of currency exchange rates; unanticipated actions by the
Edwards, Edwards Lifesciences, the stylized E logo, EVOQUE, MOMENTIS, PASCAL, PASCAL Precision, RESILIA, SAPIEN, SAPIEN 3, SAPIEN 3 Ultra, and SAPIEN 3 Ultra RESILIA are trademarks of Edwards Lifesciences Corporation or its affiliates. All other trademarks are the property of their respective owners.
___________________ | ||
[1] |
"Constant currency” growth rates exclude foreign exchange fluctuations. Sales growth guidance refers to constant currency. “Adjusted” amounts are non-GAAP items. "Constant currency” growth rates in this press release exclude foreign exchange fluctuations. Sales growth guidance refers to constant currency. Adjusted earnings per share is a non-GAAP item computed on a diluted basis and in this press release also excludes an intellectual property agreement and certain litigation expenses, amortization of intangible assets, fair value adjustments to contingent consideration liabilities arising from acquisitions, and one-time separation costs related to the planned spin-off of Critical Care. See “Non-GAAP Financial Information” and reconciliation tables below. |
EDWARDS LIFESCIENCES CORPORATION Unaudited Consolidated Statements of Operations (in millions, except per share data) |
|||||||
|
Three Months Ended
|
||||||
|
|
2024 |
|
|
|
2023 |
|
Net sales |
$ |
1,598.2 |
|
|
$ |
1,459.6 |
|
Cost of sales |
|
385.6 |
|
|
|
329.5 |
|
|
|
|
|
||||
Gross profit |
|
1,212.6 |
|
|
|
1,130.1 |
|
|
|
|
|
||||
Selling, general, and administrative expenses |
|
489.7 |
|
|
|
436.3 |
|
Research and development expenses |
|
285.2 |
|
|
|
261.2 |
|
Intellectual property agreement and certain litigation expenses |
|
8.9 |
|
|
|
43.5 |
|
Change in fair value of contingent consideration liabilities |
|
— |
|
|
|
0.7 |
|
Separation costs |
|
41.3 |
|
|
|
— |
|
|
|
|
|
||||
Operating income |
|
387.5 |
|
|
|
388.4 |
|
|
|
|
|
||||
Interest income, net |
|
(16.5 |
) |
|
|
(8.6 |
) |
Other income, net |
|
(5.4 |
) |
|
|
(1.6 |
) |
|
|
|
|
||||
Income before provision for income taxes |
|
409.4 |
|
|
|
398.6 |
|
|
|
|
|
||||
Provision for income taxes |
|
58.4 |
|
|
|
58.1 |
|
|
|
|
|
||||
Net income |
$ |
351.0 |
|
|
$ |
340.5 |
|
|
|
|
|
||||
Net loss attributable to noncontrolling interest |
|
(0.9 |
) |
|
|
— |
|
|
|
|
|
||||
Net income attributable to Edwards Lifesciences Corporation |
$ |
351.9 |
|
|
$ |
340.5 |
|
|
|
|
|
||||
Earnings per share: |
|
|
|
||||
Basic |
$ |
0.58 |
|
|
$ |
0.56 |
|
Diluted |
$ |
0.58 |
|
|
$ |
0.56 |
|
|
|
|
|
||||
Weighted-average common shares outstanding: |
|
|
|
||||
Basic |
|
601.6 |
|
|
|
607.5 |
|
Diluted |
|
604.1 |
|
|
|
610.9 |
|
|
|
|
|
||||
Operating statistics |
|
|
|
||||
As a percentage of net sales: |
|
|
|
||||
Gross profit |
|
75.9 |
% |
|
|
77.4 |
% |
Selling, general, and administrative expenses |
|
30.6 |
% |
|
|
29.9 |
% |
Research and development expenses |
|
17.8 |
% |
|
|
17.9 |
% |
Operating income |
|
24.2 |
% |
|
|
26.6 |
% |
Income before provision for income taxes |
|
25.6 |
% |
|
|
27.3 |
% |
Net income |
|
22.0 |
% |
|
|
23.3 |
% |
|
|
|
|
||||
Effective tax rate |
|
14.3 |
% |
|
|
14.6 |
% |
___________________ |
Note: Numbers may not calculate due to rounding. |
EDWARDS LIFESCIENCES CORPORATION Unaudited Balance Sheets (in millions) |
|||||||
|
March 31, 2024 |
|
December 31, 2023 |
||||
ASSETS |
|
|
|
||||
Current assets |
|
|
|
||||
Cash and cash equivalents |
$ |
1,224.6 |
|
|
$ |
1,144.0 |
|
Short-term investments |
|
473.0 |
|
|
|
500.5 |
|
Accounts receivables, net |
|
817.6 |
|
|
|
775.1 |
|
Other receivables |
|
59.3 |
|
|
|
61.8 |
|
Inventories |
|
1,207.3 |
|
|
|
1,168.2 |
|
Prepaid expenses |
|
138.1 |
|
|
|
146.8 |
|
Other current assets |
|
250.6 |
|
|
|
239.3 |
|
Total current assets |
|
4,170.5 |
|
|
|
4,035.7 |
|
Long-term investments |
|
455.6 |
|
|
|
583.9 |
|
Property, plant, and equipment, net |
|
1,767.9 |
|
|
|
1,749.4 |
|
Operating lease right-of-use assets |
|
98.4 |
|
|
|
94.0 |
|
Goodwill |
|
1,252.8 |
|
|
|
1,253.5 |
|
Other intangible assets, net |
|
446.8 |
|
|
|
428.4 |
|
Deferred income taxes |
|
776.7 |
|
|
|
754.6 |
|
Other assets |
|
767.6 |
|
|
|
463.7 |
|
Total assets |
$ |
9,736.3 |
|
|
$ |
9,363.2 |
|
LIABILITIES AND STOCKHOLDERS’ EQUITY |
|
|
|
||||
Current liabilities |
|
|
|
||||
Accounts payable and accrued liabilities |
$ |
1,086.0 |
|
|
$ |
1,170.5 |
|
Operating lease liabilities |
|
24.8 |
|
|
|
24.9 |
|
Total current liabilities |
|
1,110.8 |
|
|
|
1,195.4 |
|
Long-term debt |
|
597.2 |
|
|
|
597.0 |
|
Taxes payable |
|
79.6 |
|
|
|
80.6 |
|
Operating lease liabilities |
|
77.2 |
|
|
|
73.0 |
|
Uncertain tax positions |
|
336.6 |
|
|
|
339.3 |
|
Litigation agreement accrual |
|
82.0 |
|
|
|
94.2 |
|
Other liabilities |
|
266.5 |
|
|
|
264.3 |
|
Total liabilities |
|
2,549.9 |
|
|
|
2,643.8 |
|
Stockholders’ equity |
|
|
|
||||
Common stock |
|
651.8 |
|
|
|
650.5 |
|
Additional paid-in capital |
|
2,379.8 |
|
|
|
2,274.4 |
|
Retained earnings |
|
9,344.3 |
|
|
|
8,992.4 |
|
Accumulated other comprehensive loss |
|
(233.3 |
) |
|
|
(242.8 |
) |
Treasury stock, at cost |
|
(5,024.7 |
) |
|
|
(5,024.5 |
) |
Total Edwards Lifesciences Corporation stockholders’ equity |
|
7,117.9 |
|
|
|
6,650.0 |
|
Noncontrolling interest |
|
68.5 |
|
|
|
69.4 |
|
Total equity |
|
7,186.4 |
|
|
|
6,719.4 |
|
Total liabilities and equity |
$ |
9,736.3 |
|
|
$ |
9,363.2 |
|
EDWARDS LIFESCIENCES CORPORATION
Non-GAAP Financial Information
To supplement the consolidated financial results prepared in accordance with Generally Accepted Accounting Principles (“GAAP”), the Company uses non-GAAP historical financial measures. Management makes adjustments to the GAAP measures for items (both charges and gains) that (a) do not reflect the core operational activities of the Company, (b) are commonly adjusted within the Company’s industry to enhance comparability of the Company’s financial results with those of its peer group, or (c) are inconsistent in amount or frequency between periods (albeit such items are monitored and controlled with equal diligence relative to core operations). The Company uses the terms "adjusted" and “constant currency" when referring to non-GAAP sales and sales growth information, respectively, which excludes currency exchange rate fluctuations. The Company uses the term "billing days adjusted growth rate" when also excluding the impact of billing days. The Company uses the term “adjusted” to also exclude certain litigation expenses, intellectual property agreements, amortization of intangible assets, fair value adjustments to contingent consideration liabilities arising from acquisitions, and one-time separation costs related to the planned spin-off of Critical Care.
Management uses non-GAAP financial measures internally for strategic decision making, forecasting future results, and evaluating current performance. These non-GAAP financial measures are used in addition to, and in conjunction with, results presented in accordance with GAAP and reflect an additional way of viewing aspects of the Company's operations by investors that, when viewed with its GAAP results, provide a more complete understanding of factors and trends affecting the Company's business and facilitate comparability to historical periods.
Non-GAAP financial measures are not prepared in accordance with GAAP; therefore, the information is not necessarily comparable to other companies and should be considered as a supplement to, and not as a substitute for, or superior to, the corresponding measures calculated in accordance with GAAP. A reconciliation of non-GAAP historical financial measures to the most comparable GAAP measure is provided in the tables below.
Fluctuations in currency exchange rates impact the comparative results and sales growth rates of the Company's underlying business. Management believes that excluding the impact of currency exchange rate fluctuations from its sales growth provides investors a more useful comparison to historical financial results. The impact of the fluctuations has been detailed in the "Reconciliation of Sales by Product Group and Region."
Guidance for sales and sales growth rates is provided on a "constant currency basis," and projections for diluted earnings per share, net income and growth, gross profit margin, taxes, and free cash flow are also provided on a non-GAAP basis, as adjusted, for the items identified above due to the inherent difficulty in forecasting such items without unreasonable efforts. The Company is not able to provide a reconciliation of the non-GAAP guidance to comparable GAAP measures due to the unknown effect, timing, and potential significance of special charges or gains, and management's inability to forecast charges associated with future transactions and initiatives.
Management considers free cash flow to be a liquidity measure which provides useful information to management and investors about the amount of cash generated by business operations, after deducting payments for capital expenditures, which can then be used for strategic opportunities or other business purposes including, among others, investing in the Company's business, making strategic acquisitions, strengthening the balance sheet, and repurchasing stock.
The items described below are adjustments to the GAAP financial results in the reconciliations that follow:
Certain Litigation Expenses - The Company incurred certain litigation expenses of
Change in Fair Value of Contingent Consideration Liabilities - The Company recorded expense of
Amortization of Intangible Assets - The Company recorded amortization expense related to developed technology and patents in the amount of
Separation Costs - The Company incurred separation costs of
Intellectual Property Agreement - The Company recorded a
Provision for Income Taxes - The income tax impacts of the expenses and gains discussed above are based upon the items' forecasted effect upon the Company's full year effective tax rate. Adjustments to forecasted items unrelated to the expenses and gains above, as well as impacts related to interim reporting, will have an effect on the income tax impact of these items in subsequent periods.
Adjusted Free Cash Flow - The Company defines free cash flow as cash flows from operating activities less capital expenditures. During 2024, the Company excluded from its calculation payments for separation costs associated with the planned spin-off of Critical Care and a material tax deposit made to mitigate interest on potential tax liabilities that the Company is contesting through the judicial process.
EDWARDS LIFESCIENCES CORPORATION Unaudited Reconciliation of GAAP to Non-GAAP Financial Information (in millions, except per share and percentage data) |
||||||||||||||||||
|
|
Three Months Ended March 31, 2024 |
||||||||||||||||
|
|
Net Sales |
|
Gross
|
|
Operating
|
|
Net Income
|
|
Diluted
|
|
Effective
|
||||||
GAAP |
|
$ |
1,598.2 |
|
75.9 |
% |
|
$ |
387.5 |
|
$ |
351.9 |
|
$ |
0.58 |
|
14.3 |
% |
Non-GAAP adjustments: (A) (B) |
|
|
|
|
|
|
|
|
|
|
|
|
||||||
Certain litigation expenses |
|
|
— |
|
— |
|
|
|
8.9 |
|
|
7.4 |
|
|
0.01 |
|
— |
|
Amortization of intangible assets |
|
|
— |
|
0.1 |
|
|
|
1.4 |
|
|
1.2 |
|
|
— |
|
(0.1 |
) |
Separation costs |
|
|
— |
|
— |
|
|
|
41.3 |
|
|
36.8 |
|
|
0.07 |
|
(0.2 |
) |
Adjusted |
|
$ |
1,598.2 |
|
76.0 |
% |
|
$ |
439.1 |
|
$ |
397.3 |
|
$ |
0.66 |
|
14.0 |
% |
|
|
Three Months Ended March 31, 2023 |
||||||||||||||||
|
|
Net Sales |
|
Gross
|
|
Operating
|
|
Net Income
|
|
Diluted
|
|
Effective
|
||||||
GAAP |
|
$ |
1,459.6 |
|
77.4 |
% |
|
$ |
388.4 |
|
$ |
340.5 |
|
$ |
0.56 |
|
14.6 |
% |
Non-GAAP adjustments: (A) (B) |
|
|
|
|
|
|
|
|
|
|
|
|
||||||
Certain litigation expenses |
|
|
— |
|
— |
|
|
|
6.5 |
|
|
5.3 |
|
|
0.01 |
|
0.1 |
|
Change in fair value of contingent consideration liabilities |
|
|
— |
|
— |
|
|
|
0.7 |
|
|
0.6 |
|
|
— |
|
— |
|
Amortization of intangible assets |
|
|
— |
|
0.1 |
|
|
|
1.5 |
|
|
1.3 |
|
|
— |
|
— |
|
Intellectual property agreement |
|
|
— |
|
— |
|
|
|
37.0 |
|
|
30.5 |
|
|
0.05 |
|
0.2 |
|
Adjusted |
|
$ |
1,459.6 |
|
77.5 |
% |
|
$ |
434.1 |
|
$ |
378.2 |
|
$ |
0.62 |
|
14.9 |
% |
___________________ | ||
(A) |
See description of non-GAAP adjustments under "Non-GAAP Financial Information." | |
(B) |
The tax effect on non-GAAP adjustments is calculated based upon the impact of the relevant tax jurisdictions’ statutory tax rates on the Company’s estimated annual effective tax rate, or discrete rate in the quarter, as applicable. The impact on the effective tax rate is reflected on each individual non-GAAP adjustment line item. |
RECONCILIATION OF GAAP OPERATING CASH FLOW TO ADJUSTED FREE CASH FLOW |
|||||||
|
Three Months Ended March 31, |
||||||
|
|
2024 |
|
|
|
2023 |
|
Net cash (used in) provided by operating activities |
$ |
(53.5 |
) |
|
$ |
314.1 |
|
Capital expenditures |
|
(65.3 |
) |
|
|
(61.5 |
) |
Tax deposit |
|
305.1 |
|
|
|
— |
|
Separation cost payments |
|
19.9 |
|
|
|
— |
|
Adjusted Free Cash Flow (A) |
|
206.2 |
|
|
|
252.6 |
|
___________________ | ||
(A) |
See description of "Adjusted Free Cash Flow" under "Non-GAAP Financial Information." |
RECONCILIATION OF SALES BY PRODUCT GROUP AND REGION |
||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
2023 Adjusted |
|
|
||||||||||
Sales by Product Group (QTD) |
|
|
1Q 2024 |
|
|
1Q 2023 |
|
Change |
|
GAAP
|
|
FX
|
|
1Q 2023
|
|
Constant
|
||||||
Transcatheter Aortic Valve Replacement |
|
$ |
1,007.9 |
|
$ |
947.9 |
|
$ |
60.0 |
|
6.3 |
% |
|
$ |
(2.1 |
) |
|
$ |
945.8 |
|
6.6 |
% |
Transcatheter Mitral and Tricuspid Therapies |
|
|
72.9 |
|
|
41.6 |
|
|
31.3 |
|
75.2 |
% |
|
|
0.7 |
|
|
|
42.3 |
|
72.2 |
% |
Surgical Structural Heart |
|
|
266.1 |
|
|
248.2 |
|
|
17.9 |
|
7.2 |
% |
|
|
(1.4 |
) |
|
|
246.8 |
|
7.9 |
% |
Critical Care |
|
|
251.3 |
|
|
221.9 |
|
|
29.4 |
|
13.3 |
% |
|
|
(2.3 |
) |
|
|
219.6 |
|
14.4 |
% |
Total |
|
$ |
1,598.2 |
|
$ |
1,459.6 |
|
$ |
138.6 |
|
9.5 |
% |
|
$ |
(5.1 |
) |
|
$ |
1,454.5 |
|
9.9 |
% |
|
|
|
|
|
|
|
|
|
2023 Adjusted |
|
|
||||||||||||
Sales by Region (QTD) |
|
|
1Q 2024 |
|
|
1Q 2023 |
|
Change |
|
GAAP
|
|
FX
|
|
1Q 2023
|
|
Constant
Rate * |
|||||||
|
|
$ |
940.7 |
|
$ |
849.1 |
|
$ |
91.6 |
|
|
10.8 |
% |
|
$ |
— |
|
|
$ |
849.1 |
|
10.8 |
% |
|
|
|
367.8 |
|
|
331.1 |
|
|
36.7 |
|
|
11.1 |
% |
|
|
8.3 |
|
|
|
339.4 |
|
8.4 |
% |
|
|
|
110.8 |
|
|
114.1 |
|
|
(3.3 |
) |
|
(2.8 |
)% |
|
|
(11.7 |
) |
|
|
102.4 |
|
8.2 |
% |
Rest of World |
|
|
178.9 |
|
|
165.3 |
|
|
13.6 |
|
|
8.2 |
% |
|
|
(1.7 |
) |
|
|
163.6 |
|
9.4 |
% |
Outside of |
|
|
657.5 |
|
|
610.5 |
|
|
47.0 |
|
|
7.7 |
% |
|
|
(5.1 |
) |
|
|
605.4 |
|
8.6 |
% |
Total |
|
$ |
1,598.2 |
|
$ |
1,459.6 |
|
$ |
138.6 |
|
|
9.5 |
% |
|
$ |
(5.1 |
) |
|
$ |
1,454.5 |
|
9.9 |
% |
___________________ |
* Numbers may not calculate due to rounding. |
RECONCILIATION OF TAVR BILLING DAYS ADJUSTED GROWTH RATE |
||
|
Three Months
|
|
|
2024 |
|
TAVR constant currency growth rate |
6.6 |
% |
Impact of billing days |
1.1 |
% |
TAVR billing days adjusted growth rate |
7.7 |
% |
View source version on businesswire.com: https://www.businesswire.com/news/home/20240425889009/en/
Media Contact: Amy Hytowitz, 949-250-4009
Investor Contact: Mark Wilterding, 949-250-6826
Source: Edwards Lifesciences Corporation
FAQ
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