Connect with us

Technology

Research Solutions Reports Fiscal Second Quarter 2025 Results

Published

on

Reports 23 Percent Increase in ARR to $19.1 Million and 61 Net New Platform Deployments

HENDERSON, Nev., Feb. 13, 2025 /PRNewswire/ — Research Solutions, Inc. (NASDAQ: RSSS), the leading AI-powered research workflow platform, reported financial results for its fiscal second quarter ended December 31, 2024.

Fiscal Second Quarter 2025 Summary

Total revenue of $11.9 million, a 15.5% increase from the prior-year quarter.Platform revenue up 47% to $4.6 million. Platform revenue accounted for 39% of total revenue as compared to 30% in the prior-year quarter.Annual Recurring Revenue (“ARR”) up 23% to $19.1 million, which includes approximately $12.7 million of B2B recurring revenue and $6.4 million of B2C recurring revenue.Gross profit up 30% from the prior-year quarter. Total gross margin improved 540 basis points to 48.9%.Net loss of $2.0 million or ($0.07) per share, compared to a net loss of ($54,000) or nil per share in the prior-year quarter. The quarter’s results include a charge of approximately $2.4 million related to increasing the projected contingent earnout liability for Scite.Adjusted EBITDA of $963,000 compared to $318,000 in the prior-year quarter.   The result is inclusive of $112,000 in commission fees related to the sale of stock by the Company’s former Chairman.  On a trailing twelve-months (“TTM”) basis, the Company has now generated Adjusted EBITDA of $4.6 million, which represents a 9.5% margin.Cash flow from operations of over $1 million in the quarter, compared to $0.3 million in the prior-year quarter.

“Our second quarter results benefited from the continued recognition of the advantages and savings our products offer within the research process and the conclusion of the election cycle, which removed some near-term economic uncertainty. We experienced strong growth in both B2B and B2C ARR.  The 61 net new B2B platform deployments represent our best organic performance ever recorded in a quarter, and we also recorded a nearly $1 million sequential increase in B2C recurring revenue. The reported net loss in the quarter is related to the continued outperformance of Scite, which experienced strong academic B2B sales in the quarter in addition to B2C growth,” said Roy W. Olivier, President and CEO of Research Solutions. “Lastly, I am delighted that during the quarter our former Chairman largely exited his ownership position, eliminating an overhang that had weighed down the stock price for some time, enabling that stock to be diversified across multiple new shareholders.” 

Fiscal Second Quarter 2025 Results

Total revenue was $11.9 million, a 15.5% increase from $10.3 million in the year-ago quarter as both platform and transaction revenue increased from the prior period.

Platform subscription revenue increased 47% to $4.6 million compared to $3.1 million in the year-ago quarter. The increase was primarily due to an increase in the total number of paid Platform deployments and B2C subscribers, as well as upsells to existing customers. The quarter ended with annual recurring revenue of $19.1 million, up 23% year-over-year (see the company’s definition of annual recurring revenue below).

Transaction revenue was $7.3 million, compared to $7.2 million in the second quarter of fiscal 2024. The increase was primarily due to increased copyright revenues. The transaction customer count for the quarter was 1,384, compared to 1,398 customers in the prior-year quarter (see the Company’s definition of active customer accounts and transactions below).

Total gross margin improved 540 basis points from the prior-year quarter to 48.9%. The increase was primarily driven by a continued revenue mix shift to the higher-margin Platforms business as well as increased margins in that business.

Total operating expenses were $5.7 million, compared to $4.9 million in the second quarter of 2024. The increases were related to additional costs in Sales and Marketing and Technology and Product Development, which include having a full quarter of Scite expenses in the period, compared to one month in the prior-year quarter.  There was also an increase in non-cash depreciation and amortization expense associated with the acquisitions completed in fiscal year 2024.

Net loss for the second quarter was $2.0 million, or ($0.07) per share, compared to net loss of ($54,000), or nil per share, in the prior-year quarter. The quarter’s results include a provision of approximately $2.4 million related to increasing the projected contingent earnout liability for Scite. Adjusted EBITDA was $963,0000, compared to $318,000 in the year-ago quarter (see definition and further discussion about the presentation of Adjusted EBITDA, a non-GAAP term, below).

Conference Call
Research Solutions President and CEO Roy W. Olivier and CFO Bill Nurthen will host the conference call, followed by a question and answer period.

Date: Thursday, February 13, 2025
Time: 5:00 p.m. ET (2:00 p.m. PT)
Dial-in number: 1-203-518-9848
Conference ID: RESEARCH

The conference call will be broadcast live and available for replay until March 13, 2025 by dialing  1-412-317-6671 and using the replay ID 11157678, and via the investor relations section of the company’s website at http://researchsolutions.investorroom.com/.

Fiscal Second Quarter Financial and Operational Summary Tables vs. Prior-Year Quarter

Quarter Ended December 31,

Six Months Ended December 31,

2024

2023

Change

% Change

2024

2023

Change

% Change

Revenue:

Platforms

$     4,601,257

$     3,125,584

$    1,475,673

47.2 %

$     8,930,902

$     5,725,776

$    3,205,126

56.0 %

Transactions

$     7,312,962

$     7,188,158

124,804

1.7 %

$   15,027,799

$   14,648,937

378,862

2.6 %

Total Revenue

11,914,219

10,313,742

1,600,477

15.5 %

23,958,701

20,374,713

3,583,988

17.6 %

Gross Profit:

Platforms

3,981,415

2,639,399

1,342,016

50.8 %

7,763,893

4,856,977

2,906,916

59.9 %

Transactions

1,839,678

1,844,403

(4,725)

-0.3 %

3,823,076

3,658,391

164,685

4.5 %

Total Gross Profit

5,821,093

4,483,802

1,337,291

29.8 %

11,586,969

8,515,368

3,071,601

36.1 %

Gross profit as a % of revenue:

Platforms

86.5 %

84.4 %

2.1 %

86.9 %

84.8 %

2.1 %

Transactions

25.2 %

25.7 %

-0.5 %

25.4 %

25.0 %

0.5 %

Total Gross Profit

48.9 %

43.5 %

5.4 %

48.4 %

41.8 %

6.6 %

Operating Expenses:

Sales and marketing

1,343,087

804,927

538,160

66.9 %

2,533,494

1,489,943

1,043,551

70.0 %

Technology and product development

1,506,849

1,336,558

170,291

12.7 %

2,879,607

2,581,137

298,470

11.6 %

General and administrative

2,008,201

2,023,848

(15,648)

-0.8 %

3,938,377

4,566,717

(628,340)

-13.8 %

Depreciation and amortization

306,233

155,749

150,484

96.6 %

618,328

215,369

402,959

187.1 %

Stock-based compensation

534,322

596,455

(62,133)

-10.4 %

952,311

1,188,269

(235,958)

-19.9 %

Foreign currency translation loss

29,554

(13,738)

43,292

NM

(74,686)

(7,118)

(67,568)

949.3 %

Total Operating Expenses

5,728,246

4,903,799

824,446

16.8 %

10,847,431

10,034,317

813,114

8.1 %

Income (loss) from operations

92,847

(419,997)

512,844

122.1 %

739,538

(1,518,949)

2,258,487

148.7 %

Other Income (Expenses):

Other income

(2,057,887)

376,426

(2,434,313)

NM

(1,989,362)

516,737

(2,506,099)

NM

Provision for income taxes

(15,194)

(10,057)

(5,137)

51.1 %

(61,406)

(39,459)

(21,947)

55.6 %

Total Other Income (Expenses):

(2,073,081)

366,369

(2,439,450)

NM

(2,050,768)

477,278

(2,528,046)

NM

Net income (loss)

$    (1,980,234)

$        (53,628)

(1,926,606)

NM

$   (1,311,230)

$   (1,041,671)

(269,559)

NM

NM

Adjusted EBITDA

$        962,956

$        318,469

$       644,487

202.4 %

$     2,235,491

$      (122,429)

$    2,357,920

-1926.0 %

Quarter Ended December 31,

Six Months Ended December 31,

2024

2023

Change

% Change

2024

2023

Change

% Change

Platforms:

B2B ARR (Annual recurring revenue*):

  Beginning of Period

$   12,187,834

$   11,020,241

$    1,167,593

10.6 %

$   12,060,201

$     9,444,130

$    2,616,071

27.7 %

   Incremental ARR

550,422

594,507

(44,085)

-7.4 %

678,055

2,170,618

(1,492,563)

-68.8 %

  End of Period

$   12,738,256

$   11,614,748

$    1,123,508

9.7 %

$   12,738,256

$   11,614,748

$    1,123,508

9.7 %

Deployments:

  Beginning of Period

1,029

880

149

16.9 %

1,021

835

186

22.3 %

   Incremental Deployments

61

62

(1)

-1.6 %

69

107

(38)

-35.5 %

  End of Period

1,090

942

148

15.7 %

1,090

942

148

15.7 %

ASP (Average sales price):

  Beginning of Period

$          11,844

$          12,523

$             (679)

-5.4 %

$          11,812

$          11,310

$              502

4.4 %

  End of Period

$          11,686

$          12,330

$             (643)

-5.2 %

$          11,686

$          12,330

$            (643)

-5.2 %

B2C ARR (Annual recurring revenue*):

  Beginning of Period

$     5,430,795

$                 –

$    5,430,795

NM

$     5,363,129

$                 –

$    5,363,129

NM

   Incremental ARR

940,586

3,954,090

(3,013,504)

NM

1,008,252

3,954,090

(2,945,838)

NM

  End of Period

$     6,371,381

$     3,954,090

$    2,417,291

61.1 %

$     6,371,381

$     3,954,090

$    2,417,291

61.1 %

Total ARR (Annualized recurring revenue):

$   19,109,637

$   15,568,838

$    3,540,799

22.7 %

$   19,109,637

$   15,568,838

$    3,540,799

22.7 %

Transaction Customers:

Corporate customers

1,051

1,065

(14)

-1.3 %

1,063

1,078

(15)

-1.3 %

Academic customers

333

333

–

0.0 %

325

319

6

1.9 %

Total customers

1,384

1,398

(14)

-1.0 %

1,388

1,397

(9)

-0.6 %

 

Active Customer Accounts, Transactions and Annual Recurring Revenue

The Company defines active customer accounts as the sum of the total quantity of customers per month for each month in the period divided by the respective number of months in the period. The quantity of customers per month is defined as customers with at least one transaction during the month.

A transaction is an order for a unit of copyrighted content fulfilled or managed in the Platform.

The Company defines annual recurring revenue (“ARR”) as the value of contracted Platform subscription recurring revenue normalized to a one-year period.  For B2C ARR, this includes the annualized value of monthly subscriptions, meaning their monthly value multiplied by twelve.

Use of Non-GAAP Measure – Adjusted EBITDA

Research Solutions’ management evaluates and makes operating decisions using various financial metrics. In addition to the Company’s GAAP results, management also considers the non-GAAP measure of Adjusted EBITDA. Management believes that this non-GAAP measure provides useful information about the Company’s operating results.

The tables below provide a reconciliation of this non-GAAP financial measure with the most directly comparable GAAP financial measure. Adjusted EBITDA is defined as net income (loss), plus interest expense, other income (expense) including any change in fair value of contingent earnout liability, foreign currency transaction loss, provision for income taxes, depreciation and amortization, stock-based compensation, and other potential adjustments that may arise. Set forth below is a reconciliation of Adjusted EBITDA to net income (loss):

Quarter Ended December 31,

Six Months Ended December 31,

2024

2023

Change

% Change

2024

2023

Change

% Change

Net Income (loss)

$    (1,980,234)

$        (53,628)

$   (1,926,606)

NM

$   (1,311,230)

$   (1,041,671)

$     (269,559)

NM

 Add (deduct):

–

Other (income) expense

2,057,887

(376,426)

2,434,313

NM

1,989,362

(516,737)

2,506,099

NM

Foreign currency translation loss (gain)

29,554

(13,738)

43,292

NM

(74,686)

(7,118)

(67,568)

949.3 %

Provision for income taxes

15,194

10,057

5,137

51.1 %

61,406

39,459

21,947

55.6 %

Depreciation and amortization

306,233

155,749

150,484

96.6 %

618,328

215,369

402,959

187.1 %

Stock-based compensation

534,322

596,455

(62,133)

-10.4 %

952,311

1,188,269

(235,958)

-19.9 %

 Adjusted EBITDA

$        962,956

$        318,469

$       644,487

202.4 %

$     2,235,491

$      (122,429)

$    2,357,920

1926.0 %

 

About Research Solutions
Research Solutions, Inc. (NASDAQ: RSSS) provides cloud-based technologies to streamline the process of obtaining, managing, and creating intellectual property. Founded in 2006 as Reprints Desk, the Company was a pioneer in developing solutions to serve researchers. Today, more than 70 percent of the top pharmaceutical companies, prestigious universities, and emerging businesses rely on Article Galaxy, the Company’s SaaS research platform, to streamline access to the latest scientific research and data with 24/7 customer support. For more information and details, please visit www.researchsolutions.com 

Important Cautions Regarding Forward-Looking Statements
Certain statements in this press release may contain “forward-looking statements” regarding future events and our future results. All statements other than statements of historical facts are statements that could be deemed to be forward-looking statements. These statements are based on current expectations, estimates, forecasts, and projections about the markets in which we operate and the beliefs and assumptions of our management. Words such as “expects,” “anticipates,” “targets,” “goals,” “projects”, “intends,” “plans,” “believes,” “seeks,” “estimates,” “endeavors,” “strives,” “may,” or variations of such words, and similar expressions are intended to identify such forward-looking statements. Readers are cautioned that these forward-looking statements are subject to a number of risks, uncertainties and assumptions that are difficult to predict, estimate or verify. Therefore, actual results may differ materially and adversely from those expressed in any forward-looking statements. Such risks and uncertainties include those factors described in the Company’s most recent annual report on Form 10-K, as such may be amended or supplemented by subsequent quarterly reports on Form 10-Q, or other reports filed with the Securities and Exchange Commission. Examples of forward-looking statements in this release include statements regarding enhanced product offerings, additional customers, and the Company’s prospects for growth. Readers are cautioned not to place undue reliance on these forward-looking statements. The forward-looking statements are made only as of the date hereof, and the Company undertakes no obligation to publicly release the result of any revisions to these forward-looking statements. For more information, please refer to the Company’s filings with the Securities and Exchange Commission. 

Research Solutions, Inc. and Subsidiaries

Consolidated Balance Sheets

December 31, 

2024

June 30, 

(unaudited)

2024

Assets

Current assets:

Cash and cash equivalents

$

7,701,155

$

6,100,031

Accounts receivable, net of allowance of $129,895 and $68,579, respectively

7,116,055

6,879,800

Prepaid expenses and other current assets

742,166

643,553

Prepaid royalties

589,068

1,067,237

Total current assets

16,148,444

14,690,621

Non-current assets:

Property and equipment, net of accumulated depreciation of $932,773 and $922,558, respectively

63,355

88,011

Intangible assets, net of accumulated amortization of $2,129,868 and $1,535,310, respectively

10,230,439

10,764,261

Goodwill

16,345,888

16,315,888

Deposits and other assets

867

981

Total assets

$

42,788,993

$

41,859,762

Liabilities and Stockholders’ Equity

Current liabilities:

Accounts payable and accrued expenses

$

8,104,118

$

8,843,612

Deferred revenue

8,853,415

9,023,848

Contingent earnout liability, current portion

3,963,956

—

Total current liabilities

20,921,489

17,867,460

Non-current liabilities:

Contingent earnout liability, long-term portion

10,741,044

12,298,114

Total liabilities

31,662,533

30,165,574

Commitments and contingencies

Stockholders’ equity:

Preferred stock; $0.001 par value; 20,000,000 shares authorized; no shares issued and outstanding

—

—

Common stock; $0.001 par value; 100,000,000 shares authorized; 32,640,407 and 32,295,373 shares
issued and outstanding, respectively

32,640

32,295

Additional paid-in capital

38,836,646

38,089,958

Accumulated deficit

(27,620,476)

(26,309,246)

Accumulated other comprehensive loss

(122,350)

(118,819)

Total stockholders’ equity

11,126,460

11,694,188

Total liabilities and stockholders’ equity

$

42,788,993

$

41,859,762

 

Research Solutions, Inc. and Subsidiaries

Consolidated Statements of Operations and Other Comprehensive Loss

(Unaudited)

Three Months Ended

Six Months Ended

December 31, 

December 31, 

2024

2023

2024

2023

Revenue:

Platforms

$

4,601,257

$

3,125,584

$

8,930,902

$

5,725,776

Transactions

7,312,962

7,188,158

15,027,799

14,648,937

Total revenue

11,914,219

10,313,742

23,958,701

20,374,713

Cost of revenue:

Platforms

619,842

486,185

1,167,009

868,799

Transactions

5,473,284

5,343,755

11,204,723

10,990,546

Total cost of revenue

6,093,126

5,829,940

12,371,732

11,859,345

Gross profit

5,821,093

4,483,802

11,586,969

8,515,368

Operating expenses:

Selling, general and administrative

5,422,013

4,748,050

10,229,103

9,818,948

Depreciation and amortization

306,233

155,749

618,328

215,369

Total operating expenses

5,728,246

4,903,799

10,847,431

10,034,317

Income (loss) from operations

92,847

(419,997)

739,538

(1,518,949)

Other income

348,999

108,194

417,524

248,505

Change in fair value of contingent earnout liability

(2,406,886)

268,232

(2,406,886)

268,232

Loss before provision for income taxes

(1,965,040)

(43,571)

(1,249,824)

(1,002,212)

Provision for income taxes

(15,194)

(10,057)

(61,406)

(39,459)

Net loss

(1,980,234)

(53,628)

(1,311,230)

(1,041,671)

Other comprehensive income (loss):

Foreign currency translation

2,637

6,349

(3,531)

5,403

Comprehensive loss

$

(1,977,597)

$

(47,279)

$

(1,314,761)

$

(1,036,268)

Loss per common share:

Net loss per share, basic and diluted

$

(0.07)

$

–

$

(0.04)

$

(0.04)

Weighted average common shares outstanding, basic and diluted

30,421,808

28,092,945

30,384,339

27,564,404

 

Research Solutions, Inc. and Subsidiaries

Consolidated Statements of Cash Flows

(Unaudited)

Six Months Ended

December 31, 

2024

2023

Cash flow from operating activities:

Net loss

$

(1,311,230)

$

(1,041,671)

Adjustment to reconcile net loss to net cash provided by (used in) operating activities:

Depreciation and amortization

618,328

215,369

Stock options expense

88,045

61,714

Restricted common stock expense

864,266

1,105,606

Modification cost of accelerated vesting of restricted common stock

—

20,949

Adjustment to contingent earnout liability

2,406,886

(268,232)

Changes in operating assets and liabilities:

Accounts receivable

(266,255)

(681,502)

Prepaid expenses and other current assets

(98,613)

(67,986)

Prepaid royalties

478,169

121,100

Accounts payable and accrued expenses

(737,670)

349,310

Deferred revenue

(170,433)

(241,545)

Net cash provided by (used in) operating activities

1,871,493

(426,888)

Cash flow from investing activities:

Purchase of property and equipment

(5,404)

(55,763)

Payment for acquisition of Resolute, net of cash acquired

—

(2,718,253)

Payment for acquisition of Scite, net of cash acquired

—

(7,305,493)

Net cash used in investing activities

(5,404)

(10,079,509)

Cash flow from financing activities:

Common stock repurchase

(205,278)

(68,748)

Payment of contingent acquisition consideration

(62,560)

(278,195)

Net cash used in financing activities

(267,838)

(346,943)

Effect of exchange rate changes

2,873

5,666

Net increase (decrease) in cash and cash equivalents

1,601,124

(10,847,674)

Cash and cash equivalents, beginning of period

6,100,031

13,545,333

Cash and cash equivalents, end of period

$

7,701,155

$

2,697,659

Supplemental disclosures of cash flow information:

Cash paid for income taxes

$

61,406

$

39,459

Non-cash investing and financing activities:

Contingent consideration accrual on asset acquisition

$

30,198

$

36,364

 

View original content to download multimedia:https://www.prnewswire.com/news-releases/research-solutions-reports-fiscal-second-quarter-2025-results-302376348.html

SOURCE Research Solutions, Inc.

Continue Reading

Technology

CHIME and ScaleHealth Announce Joint Venture to Expand Healthcare’s Innovation Ecosystem

Published

on

By

ScaleHealth, powered by CHIME, creates new pathways connecting healthcare leaders, innovators, technology partners, and investors to accelerate the future of digital health.

ANN ARBOR, Mich., Oct. 27, 2026 /PRNewswire/ — The College of Healthcare Information Management Executives (CHIME) today announced a strategic joint venture with ScaleHealth, Inc. to create ScaleHealth, powered by CHIME, LLC, a new innovation ecosystem designed to connect healthcare’s most pressing challenges with the innovators, leaders, organizations, and partners capable of solving them. By combining CHIME’s trusted digital health community with ScaleHealth’s expansive innovation ecosystem, the venture creates a unique environment where healthcare organizations, entrepreneurs, established technology companies, and investors can discover, connect, validate, and advance the ideas shaping the future of healthcare.

For 35 years, CHIME has evolved alongside the digital health leaders it serves. What began as a community centered on healthcare CIOs has grown into a global network of digital health leaders supported through education, events, research, policy initiatives, media platforms, executive collaboration, and professional communities. The creation of ScaleHealth, powered by CHIME represents the next chapter in that evolution, expanding CHIME’s ecosystem to include the innovators, entrepreneurs, and emerging technology companies helping define what comes next in healthcare.

As healthcare organizations face increasing pressure to improve outcomes, strengthen operations, address workforce challenges, improve cybersecurity, and realize the promise of emerging technologies including artificial intelligence, the need for stronger connections across the innovation ecosystem has never been greater. ScaleHealth, powered by CHIME was created to help build those connections.

“CHIME has spent 35 years bringing together the leaders responsible for solving healthcare’s most important technology and transformation challenges,” said Russ Branzell, President and CEO of CHIME. “As the pace of innovation continues to accelerate, we have an opportunity to expand that trusted community even further. ScaleHealth, powered by CHIME, extends our ecosystem to include entrepreneurs, innovators, investors, and emerging technology companies so that healthcare leaders can engage earlier, collaborate more effectively, and help shape the innovations that will define the future of healthcare.”

The opportunity emerged through CHIME’s growing innovation programming, particularly its Innovation Summit series, where healthcare leaders and technology companies increasingly expressed a desire to engage more directly with innovators and entrepreneurial organizations. At the same time, startups and growth-stage companies were seeking trusted pathways into healthcare and stronger connections to leaders who understand the industry’s real-world operational challenges.

“Healthcare has no shortage of innovation. The challenge is creating trusted pathways that connect innovators with the healthcare leaders who understand the industry’s most urgent problems,” said Taylor McPartland, CEO of ScaleHealth and leader of the new venture. “By combining ScaleHealth’s innovation ecosystem with CHIME’s trusted community of digital health leaders, we’re creating an environment where meaningful connections can lead to validation, partnership, and real-world impact. This is about bringing together everyone who has a role to play in the future of healthcare innovation and helping them move great ideas forward.”

Unlike traditional accelerators, startup showcases, or innovation marketplaces, ScaleHealth, powered by CHIME is designed as a trusted innovation ecosystem. Healthcare organizations bring forward meaningful challenges. Innovators and startups contribute cutting-edge ideas and technologies. Established technology organizations bring expertise, infrastructure, and scale. Investors provide capital and growth pathways. Together, these stakeholders create an environment where innovation can move from discovery and connection to validation, partnership, and measurable impact.

“Throughout its history, CHIME has grown by bringing the right people together around the challenges that matter most,” said Tressa Springmann, Senior Vice President and Chief Information and Digital Officer at LifeBridge Health and Chair of the CHIME Foundation Board of Directors. “Today, innovation is essential to every aspect of healthcare transformation. ScaleHealth, powered by CHIME extends that trusted community into a broader innovation ecosystem, creating new opportunities for healthcare leaders, entrepreneurs, technology partners, and investors to collaborate, learn from one another, and accelerate meaningful progress across healthcare.”

The venture reflects CHIME’s belief that the next era of digital health will be co-created by healthcare leaders, technology partners, entrepreneurs, investors, and innovators working together to solve the challenges that matter most. By creating a trusted environment for discovery, collaboration, validation, and advancement, ScaleHealth, powered by CHIME aims to become the connective layer between healthcare’s needs and the innovation being built to address them.

Read the full release here.

About CHIME
The College of Healthcare Information Management Executives (CHIME) is the leading professional organization for digital health executives and leaders. CHIME provides a trusted, collaborative environment where members and partners connect, share best practices, advance professional development, and advocate for the effective use of information and technology to improve health and care in the communities they serve. For more information, please visit chimecentral.org.

For media inquiries, please contact:

Contact

Calli Dretke
Executive Vice President & Chief Digital and Marketing Officer
CHIME                                                                                                           
734.412.6255
cdretke@dhinsights.org

View original content to download multimedia:https://www.prnewswire.com/news-releases/chime-and-scalehealth-announce-joint-venture-to-expand-healthcares-innovation-ecosystem-302921260.html

SOURCE College of Healthcare Information Management Executives (CHIME)

Continue Reading

Technology

In HelloNation, Prenatal Imaging Expert Erika Lambright Explains Ultrasound Differences Between 2D, 3D, And 4D Imaging

Published

on

By

The article outlines how each type of pregnancy ultrasound supports fetal development and family understanding.

DENISON, Texas, Oct. 27, 2026 /PRNewswire/ — What is the difference between 2D, 3D, and 4D ultrasound imaging during pregnancy? HelloNation has published an article that clearly explains the differences between ultrasound and other prenatal imaging modalities and how each supports fetal development.

The HelloNation article explains that a 2d ultrasound is the most common form of prenatal imaging used during routine pregnancy ultrasound appointments. It produces flat, black-and-white images that allow medical providers to assess fetal development, monitor growth, and evaluate vital structures. The article notes that 2D ultrasound plays a central role in identifying potential concerns early and remains the foundation of prenatal diagnostic imaging.

According to the article, a 3d ultrasound builds on the same technology but creates a more detailed still image with depth. This form of prenatal imaging allows families to see clearer views of the baby’s face, hands, and feet. While 3d ultrasound can support certain medical evaluations, the article describes its primary value as helping parents better visualize fetal development in a more lifelike way.

The article further describes how a 4D ultrasound adds motion to the 3d ultrasound image. This allows families to view real-time video of the baby moving, stretching, or making facial expressions. The article explains that this type of pregnancy ultrasound creates a more engaging experience and helps strengthen the emotional connection, while still using the same safe, noninvasive prenatal imaging technology.

The HelloNation article emphasizes that understanding ultrasound differences helps families set clear expectations before imaging sessions. Each type of pregnancy ultrasound serves a distinct purpose. 2D ultrasound focuses on medical accuracy and fetal development monitoring, while 3D and 4D ultrasound provide enhanced visualization and connection. The article highlights that medical professionals typically rely on 2D ultrasound for diagnostic purposes, while 3D and 4D ultrasound are often optional.

The article also notes that several factors can affect the quality of prenatal imaging results. Baby position, gestational age, and fluid levels all play a role in how clearly images appear, especially during 3D and 4D ultrasound sessions. The article explains that providers often guide families on the best timing for ultrasound visits during pregnancy to improve image clarity and achieve better results.

Prenatal Imaging Experts emphasize through the article that learning about ultrasound differences can reduce uncertainty and help families feel more prepared. By understanding how each type of prenatal imaging contributes to monitoring fetal development, expectant parents can approach each pregnancy ultrasound appointment with clearer expectations.

The article concludes that while 2D ultrasound remains essential for medical care, the added perspectives of 3D and 4D ultrasound offer families a broader, more personal understanding of fetal development. Together, these forms of prenatal imaging provide both clinical insight and meaningful connection throughout pregnancy.

What Is the Difference Between 2D, 3D, and 4D Ultrasounds Explained Simply features insights from Erika Lambright, Prenatal Imaging Experts of Denison, Texas, in HelloNation.

About HelloNation
HelloNation is America’s Good News Network, a premier media platform built on the idea that good news travels faster when real people tell real stories. Through its community-focused digital publications and innovative “edvertising” approach, HelloNation delivers expert-driven, good-news content that informs, inspires, and spotlights the leaders making a meaningful impact in their communities. HelloNation maintains partnerships with the U.S. Conference of Mayors and the United States First Responders Association.

View original content to download multimedia:https://www.prnewswire.com/news-releases/in-hellonation-prenatal-imaging-expert-erika-lambright-explains-ultrasound-differences-between-2d-3d-and-4d-imaging-302792440.html

SOURCE HelloNation

Continue Reading

Technology

Grünenthal presents Phase III results for Qutenza® in post-surgical neuropathic pain at IASP 2026 World Congress on Pain

Published

on

By

Late-breaking data from the Phase III RISE trial further strengthen the well-established efficacy and safety profile of Qutenza®. Post-surgical neuropathic pain is a debilitating complication of surgery affecting millions of patients every year.1 

AACHEN, Germany, Oct. 27, 2026 /PRNewswire/ — Grünenthal, a global leader in pain management and research, today announced new data from the Phase III RISE trial (NCT04967664), evaluating Qutenza® versus control in people with post-surgical neuropathic pain. These data were shared today as late-breaking poster presentations at the 2026 International Association for the Study of Pain (IASP) World Congress on Pain in Bangkok, Thailand.

The trial (n=409) showed that Qutenza® achieved a statistically significantly greater reduction in average pain intensity (API) than the control treatment over weeks 2-12, meeting one of its pre-specified primary endpoints. When evaluating API at week 12 specifically, at the point when patients would typically return for retreatment, the numerical difference favoured Qutenza® but did not reach statistical significance. In the extension phase of the trial, in which up to 4 retreatments were allowed, Qutenza® achieved a statistically significantly greater reduction in API than the control treatment over weeks 2-42. Safety findings were consistent with previous Qutenza® trials and no new safety signals were observed. These data support the well-established efficacy and safety profile of Qutenza®.2,3

“Post-surgical neuropathic pain can be difficult to manage with current treatment options, and there is an urgent need for patient-centred, effective solutions. The RISE trial provides encouraging evidence that Qutenza® can deliver clinically meaningful and sustained pain reduction for up to 42 weeks, having shown a greater reduction in average pain intensity than the control,” said Prof. Patrice Forget, MD, PhD, FFPMRCA, Clinical Chair (full professor) in Anaesthesia, University of Aberdeen, and Honorary Consultant, NHS Grampian, Aberdeen, UK. “As IASP shines a global spotlight on neuropathic pain at this year’s congress, findings such as these are important to help improve outcomes for patients and reduce the burden of pain on families and healthcare systems.”

“Post-surgical neuropathic pain has been relatively understudied and continues to go under-recognised in clinical practice,” said Uli Brödl, Chief Scientific Officer, Grünenthal. “These results build on the robust body of evidence for Qutenza® and reinforce its potential to provide meaningful, long-lasting pain relief for people living with pain.”

Post-surgical neuropathic pain is a poorly recognised potential complication of surgery that can result in devastating outcomes. It affects millions of patients every year, with pain lasting for months or years post-procedure.1 It can also have a significant mental health impact, with patients reporting feeling extremely depressed or anxious, and having problems with daily activities.4

Qutenza® is already approved in Europe for the treatment of peripheral neuropathic pain in adults, either alone or in combination with other medicinal products for the treatment of pain.5 It is also approved in the US for the treatment of neuropathic pain associated with postherpetic neuralgia and for the treatment of neuropathic pain associated with diabetic peripheral neuropathy (DPN) of the feet in adults.6

About the RISE trial2,3
The RISE (AV-001) trial is a Phase III multi-centre, randomised, double-blind, parallel-group trial to confirm the efficacy and safety of Qutenza 179mg cutaneous patch versus a low-dose capsaicin control patch in people with moderate to severe post-surgical neuropathic pain.

It included eligible adults with a 24-hour average pain intensity (API) score of 4 or more, a pain duration of 6 to 60 months after index surgery and a DN4 (Douleur Neuropathique 4) Interview score of 3 or more.

Participants were randomly assigned to receive treatment with either a 60-minute Qutenza patch (8%) or a low-dose capsaicin control patch (0.04%).

The trial had two primary endpoints:

Change in 24-hour API from baseline to the average score of the entire period between Week 2 and Week 12.Change in 24-hour API from baseline to the average score at Week 12.

The primary sponsor of the trial is Averitas Pharma, Inc., Grünenthal’s U.S. subsidiary.

About post-surgical neuropathic pain
Post-surgical neuropathic pain (PSNP) is defined as chronic pain with neuropathic characteristics that develops or increases after surgery and persists beyond the normal healing process. It is thought to arise, at least in part, from nerve injury and pain sensitisation associated with surgery.7

The signs and symptoms of peri- and post-surgical pain can vary based on the person and the severity of the injury caused in surgery. Reported symptoms include pain caused by stimuli that are normally painless (allodynia), abnormally increased sensitivity to pain (hyperalgesia), tingling, numbness, phantom pain and scar pain.8,9,10 

About Qutenza®
In Europe, Qutenza® (capsaicin) is indicated for the treatment of peripheral neuropathic pain in adults, either alone or in combination with other medicinal products for the treatment of pain.5

Qutenza® (capsaicin) 8% topical system is approved in the US for the treatment of neuropathic pain associated with postherpetic neuralgia and for the treatment of neuropathic pain associated with diabetic peripheral neuropathy (DPN) of the feet in adults. Important US safety information is available at www.qutenza.com.6

Qutenza® is a topical TRPV1 agonist, designed to provide neuropathic pain relief for up to three months through defunctionalisation of nociceptors and nerve fibre regeneration.

About Grünenthal
Grünenthal is a global leader in pain management and related diseases. As a science-based, fully integrated pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to patients worldwide. Our purpose is to change lives for the better – and innovation is our passion. We focus all our activities and efforts on working towards our vision of a World Free of Pain.

Grünenthal is headquartered in Aachen, Germany, and has affiliates in 28 countries across Europe, Latin America, and the U.S. Our products are available in approx. 100 countries. In 2025, Grünenthal employed around 4,100 people and achieved revenues of €1.8 billion.

More information: www.grunenthal.com

Follow us on LinkedIn & Instagram

For further information, please contact:

Matt Crabb, Head of Global Communications (Interim) at Grünenthal

matt.crabb@grunenthal.com 

References

1 Gregory P & Settles K. Pract Pain Manag. 2013;13(9):1–6.
2 Wallace M et al. Efficacy of high-concentration capsaicin patch in post-surgical neuropathic pain (RISE). Presented at the International Association for the Study of Pain World Congress 2026.
3 Wallace M et al. Safety and tolerability of high-concentration capsaicin patch in post-surgical neuropathic pain (RISE). Presented at the International Association for the Study of Pain World Congress 2026.
4 Santos MP, Lemos F, Gomes J, Romao JM, Veiga D. Br J Pain 2024;18(1):42–56.
5 European Medicines Agency. Qutenza 179 mg cutaneous patch SmPC. Available at: https://www.medicines.org.uk/emc/product/573/smpc
6 US Food and Drug Administration. Qutenza® Prescribing Information. Available at: https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/022395s019lbl.pdf
7 Correl D. F1000Res. 2017;6:1054.
8 Werner MU & Kongsgaard UE. Br J Anaesth. 2014;113(1):1–4.
9 Macrae WA. Br J Anaesth. 2008;101:77–86.
10 Searle RD & Simpson KH. Contin Educ Anaesth Crit Care Pain. 2010;10:12–14.

View original content:https://www.prnewswire.com/news-releases/grunenthal-presents-phase-iii-results-for-qutenza-in-post-surgical-neuropathic-pain-at-iasp-2026-world-congress-on-pain-302921015.html

SOURCE Grünenthal Group

Continue Reading

Trending