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Rethinking GI Prophylaxis for the Critically Ill

Rethinking GI Prophylaxis for the Critically Ill

Medscape3 days ago
Prevention doesn't come easy. The bar is high. The decision to act medically because an untoward outcome could occur means creating intervention side-effect risk that's otherwise absent. Large patient numbers must be subjected to that side-effect risk to obtain net benefit. Last, your bedside modeling must be tight, and in medicine it never is.
The story of gastrointestinal (GI) prophylaxis in ICU highlights these challenges. It is best told by Deborah Cook, the godmother of ICU research. It's told through her work. She's randomized more patients than a sequence generator. Her name is the most critical MeSH term for your systematic review. If Churg, Strauss, and Wegener hadn't ruined the disease eponym practice, she'd have several to her name. Just as well; we're all transgressing some currently unidentified but soon-to-be-coined "-ism."
Cook's work has dominated the GI prophylaxis space since the early 1990s. If you're new to it, start with her New England Journal of Medicine (NEJM) review from 2018. It was published on the heels of the latest randomized control trial on GI prophylaxis in the ICU. The SUP-ICU trial, which randomized patients to pantoprazole vs placebo and was also published in NEJM, had equivocal results. The accompanying editorial provided a tepid endorsement of continued prophylaxis with proton pump inhibitors (PPI), but only for those at high risk for bleeding.
Two years later, a systematic review and another randomized trial (PEPTIC) found a mortality signal with PPIs, but in the wrong direction. This drove some back to H2 blockers even though they are less effective than PPI for preventing bleeding. Where I practice I see an equal number of ICU patients on PPI or H2 blockers. There seems to be no clear preference or consensus.
The indomitable Dr Cook just investigated the mortality difference in the REVISE trial, published last year. She and her colleagues also produced an updated systematic review. REVISE made me feel better. I've been a PPI-for-prophylaxis guy for anyone on mechanical ventilation. I held on after PEPTIC and SUP-ICU created doubt, and REVISE seemed to vindicate my practice. REVISE found that PPI decreased bleeding without increasing mortality. PPI didn't increase pneumonia or Clostridioides difficile infections either.
Unfortunately, it's never that simple. The mortality signal was still present in the updated systematic review. The mortality "noise" is dependent on severity of illness. It's the sicker patients who have a higher mortality when given PPI for prophylaxis. Why? I'm not sure. The pneumonia and C diff associations were absent in SUP-ICU, REVISE, and the updated systematic review. The systematic review authors list multiple possible explanations, given that PPI are associated with an altered microbiome, endothelial changes, and delirium. If there is a causal mechanism affecting mortality, it's not clear why the direction is discordant across levels of illness severity.
Conclusions drawn by the editorials accompanying SUP-ICU and REVISE are also discordant. Seven years ago, the idea was that PPIs were most beneficial in those who are 'seriously ill with a high risk of complications.' Fast-forward and the REVISE editorial suggests PPI for those on mechanical ventilation and an APACHE II score of less than 25. Figure 2 in Dr Cook's 2018 review lists risk factors for bleeding— lots of overlap with the APACHE and other illness severity scores. Can a patient be at high bleeding risk but have an APACHE II score less than 25? I'm sure they can, but that needle won't be easy to thread at the bedside.
Can Dr Cook snatch clarity from the jaws of this data quagmire? Perhaps. Her group just published another paper on GI bleeding in the ICU. The focus was on bleeding events that are considered important by ICU survivors and family members. This was a preplanned analysis of data from the REVISE trial. PPI shined again, reducing patient-important events regardless of illness severity. They used a proportional hazards model, that accounts for the competing risk for death, to analyze their primary outcome. Not sure if this provides clarity per se but it does make me feel better about continuing to use prophylactic PPI for my mechanically ventilated patients.
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Why People Leave Medicare Advantage Plans And Why It Matters To You
Why People Leave Medicare Advantage Plans And Why It Matters To You

Forbes

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Why People Leave Medicare Advantage Plans And Why It Matters To You

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Pharma Contract Research Organization (CRO) Services Market to Cross USD 36.66 Billion in 2025, Expanding at a CAGR of 10.04%
Pharma Contract Research Organization (CRO) Services Market to Cross USD 36.66 Billion in 2025, Expanding at a CAGR of 10.04%

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Pharma Contract Research Organization (CRO) Services Market to Cross USD 36.66 Billion in 2025, Expanding at a CAGR of 10.04%

The global pharma contract research organization (CRO) services market size is calculated at USD 36.66 billion in 2025 and is expected to reach around USD 87.03 billion by 2034, growing at a CAGR of 10.04% for the forecasted period. Ottawa, July 18, 2025 (GLOBE NEWSWIRE) -- The global pharma contract research organization (CRO) services market size was valued at USD 33.31 billion in 2024 and is predicted to hit around USD 87.03 billion by 2034, a study published by Towards Healthcare a sister firm of Precedence Research. The growth of the market is driven by the growing factors like increased research and development spending, a growing number of clinical trials, and the rising prevalence of chronic diseases, which drives the growth of the market. Get a quick preview of key market insights and trends shaping the Pharma CRO Services landscape: Key Takeaways North America dominated the global pharma contract research organization (CRO) services market in 2024. Asia-Pacific is anticipated to grow at the fastest rate in the market during the forecast period. By scale of operation, the discovery services segment held a dominant presence in the market in 2024. By scale of operation, the preclinical services segment is anticipated to grow at the fastest rate in the market during the studied years. By target therapeutic area, the oncological disorder segment held the largest share of the pharma contract research organization (CRO) services market in 2024. By target therapeutic area, the cardiovascular disorder segment is estimated to grow at a significant rate during the predicted timeframe. Market Overview & Potential A pharmaceutical Contract Research Organization (CRO) provides a range of research services to biotech, pharmaceutical, and medical device companies. These include preclinical studies, clinical trial management, regulatory support, and more, helping clients develop and get approval for new drugs and medical devices. CROs bring specialized expertise and resources that support the entire drug development process, from initial research to post-market monitoring. They offer benefits such as saving costs and time, access to expert knowledge, allowing clients to focus on their core activities, and increasing efficiency and speed, making them an attractive choice for consumers. Access detailed data tables, segment analysis, and regional breakdowns in our comprehensive market databook: What is the Growth Potential Responsible for The Growth of The Pharma Contract Research Organization (CRO) Services Market? The market growth is primarily fueled by the rising number of clinical trials, increased outsourcing of R&D activities, and the demand for cost-effective drug development solutions. Technological innovations, especially in AI and machine learning, along with the growing complexity of clinical trials, further drive the market. Additional growth factors include more clinical trials by pharma and biotech firms, cost efficiency, advanced technologies, complex trial designs, regulatory pressures, an expanding pipeline of new therapies, the rise of personalized medicine, and the broader scope of CRO services. What Are the Growing Trends Associated with the Pharma Contract Research Organization (CRO) Services Market? Outsourcing Of Clinical Trials The factors such as cost efficiency, specialised expertise, and advanced technology demand for outsourcing of clinical trial services. Technological Advancement The integration of AI and ML for electronic data capture and electronic master files, and automating the processes, is a growing trend that drives the growth. Focus On Personalized Medicine and Biologics The growing demand for personalized medicines and biologics catering to the needs of the patient and consumers drives the growth of the market. Increased Research and Development Spending The growing pharmaceutical sector demand for research and development of new and innovative formulations, which demands CRO services, fuels market growth. You can place an order or ask any questions, please feel free to contact us at sales@ What Is the Growing Challenge in the Pharma Contract Research Organization (CRO) Services Market? The key challenge that limits the growth of the market is the regulatory complexity, as different landscapes and regions demand significant expertise and resources, which is a challenge in the growth of the market. The high operational costs are also a challenge, like technological advancements, skilled labor, and regulatory compliance, con contribute to the high operational costs, which limit the growth of the market. Regional Analysis How Did North America Dominate the Pharma Contract Research Organization (CRO) Services Market in 2024? North America dominated the global pharma market in 2024. The growth of the market is driven by technological advancements in the market to improve efficiency and speed of drug development through data analytics and AI fuels the growth of the market. The key players in the region also play a major role in the growth due to the offering and innovation in product development, which drives the growth like IQVIA, Laboratory Corporation of America Holding, Syneos Health, Parexel International Corporation, and ICON plc are some of the major players in the region. The growth is also seen as driven by research and development spending, focus on chronic diseases, and growing demand for outsourcing of research; these factors boost the growth of the market in the region. Contract Research Organization (CRO) services in the U.S. are growing through increased outsourcing of clinical trials, rising biotech startups, and FDA support for faster approvals. Technological integration, decentralized trials, and access to diverse patient populations also drive expansion, making the U.S. a global hub for clinical research innovation. Canada's pharma contract research organization (CRO) services are expanding steadily through increasing biotech-pharma collaborations, government innovation funding, and adoption of virtual and AI-enabled clinical trials. Regulatory reliance on CROs for compliance, combined with growing oncology and rare-disease studies, is driving wider use across provinces. What Made Asia Pacific Significantly Grow in The Pharma Contract Research Organization (CRO) Services Market In 2024? Asia-Pacific is anticipated to grow at the fastest rate in the market during the forecast period. The growth of the market is driven by the increasing R&D spending, growing clinical trials, outsourcing trends, technological advancements, and cost effectiveness, which fuels the growth of the market in the region. The technological advancements and stringent regulatory standards attract companies that focus on the development of innovative drugs, which boosts the growth of the market. The expanding pharmaceutical companies, biotechnology firms, and medical devices companies in the region also promotes the growth of the market. The pricing and growing pool of skilled professionals in the region also contribute to the growth of the market. CRO services in China are growing through supportive regulatory reforms, such as faster clinical trial approvals and acceptance of foreign trial data. The government encourages innovation, prompting CROs to expand capabilities across drug discovery, toxicology, and clinical operations. Collaborations between academic institutions and CROs are increasing, and the growing pool of trained clinical researchers is enhancing service quality. Additionally, many CROs are integrating digital tools and AI to streamline trial processes. India's CRO growth is driven by a skilled, English-speaking workforce, a large and diverse patient population, and improvements in regulatory efficiency. Academic partnerships and government-backed innovation hubs foster research collaboration. CROs are adopting advanced technologies like remote monitoring, e-clinical platforms, and AI-based data analysis. Training programs enhance GCP compliance and clinical staff proficiency. Get the latest insights on life science industry segmentation with our Annual Membership: Segmental Insights By Scale Of Operation The discovery services segment held a dominant presence in the market in 2024. Discovery services represent a foundational segment in the pharma contract research organization (CRO) services market, focusing on early-stage research to identify promising drug candidates. These services include target identification, hit discovery, lead optimization, and assay development, providing critical scientific insights before preclinical studies begin. By outsourcing discovery work, pharmaceutical companies can accelerate timelines, reduce costs, and access specialized expertise. The growing demand for innovative therapies and rapid pipeline expansion strongly supports the growth of discovery services within the CRO market. The preclinical services segment is anticipated to grow at the fastest rate in the market during the studied period. Preclinical services are a crucial segment of the pharma contract research organization (CRO) services market, focusing on evaluating drug candidates' safety and efficacy before human trials. These services include toxicology studies, pharmacokinetics, pharmacodynamics, and bioanalytical testing, providing essential data for regulatory submissions. By outsourcing preclinical work, pharmaceutical companies reduce development costs, access advanced technologies, and accelerate timelines. The increasing complexity of drug molecules and stricter regulatory standards drive demand for preclinical services, fueling the growth of the CRO market globally. By Target Therapeutic Area The oncological disorder segment held the largest share of the pharma contract research organization (CRO) services market in 2024. Oncological disorders represent a major target therapeutic area in the pharma market, driven by the urgent need for effective cancer treatments. CROs support pharmaceutical and biotech companies by providing specialized services across the drug development spectrum, including discovery, preclinical, and clinical studies focused on oncology. The complexity of cancer research, demand for targeted and personalized therapies, and rising global cancer incidence fuel this segment's growth, making oncology one of the most heavily invested areas in CRO services worldwide. The cardiovascular disorder segment is estimated to grow at a significant rate during the predicted timeframe. Cardiovascular disorders are a significant target therapeutic area in the pharma contract research organization (CRO) services market, driven by the high global prevalence of heart-related diseases. CROs support drug development for cardiovascular therapies through specialized discovery, preclinical, and clinical services, including safety assessments, efficacy studies, and biomarker analysis. The need for innovative treatments to address heart failure, hypertension, and related conditions fuels demand for CRO expertise. This strong focus supports market growth and advances the development of life-saving cardiovascular drugs worldwide. Elevate your healthcare strategy with Towards Healthcare. Enhance efficiency and drive better outcomes schedule a call today: Recent Developments in the Pharma Contract Research Organization (CRO) Services Market In March 2025, LSK Global Pharma Services selected Oracle Argus to manage and expand its global pharmacovigilance operations, for the management of the databases of pharmaceutical companies, ensuring safety. In November 2024, Thermo Fisher Scientific launched a suite of expanded CRO and CDMO services under its brand. The company has introduced to the market its Accelerator™ Drug Development, which Thermo Fisher is marketing as '360°' CDMO and CRO drug development solutions. Top Companies and Their Contributions to the Pharma Contract Research Organization (CRO) Services Market Company Contributions & Offerings IQVIA A leader in data-driven CRO services, IQVIA offers clinical development, real-world evidence, and technology-enabled solutions globally. Parexel International Specializes in regulatory consulting, Phase I-IV clinical trials, and biotech partnerships, with a focus on patient-centric trials. Medpace Provides full-service clinical trial management, emphasizing therapeutic expertise and in-house services like labs and imaging. Charles River Laboratories Offers preclinical and early-phase clinical services, with expertise in drug discovery, safety assessment, and lab sciences. CTI Clinical Trial & Consulting Focuses on rare diseases and regenerative medicine, offering personalized CRO services from preclinical to commercialization. WuXi AppTec Delivers comprehensive R&D solutions, including lab testing, manufacturing, and clinical services, mainly serving pharma and biotech. Veeda Clinical Research India-based CRO offering cost-effective early and late-phase clinical trials, bioavailability and bioequivalence studies. ICON plc A global CRO with expertise across all phases, providing clinical development and commercialization support using advanced analytics. LabCorp (Covance) Integrates diagnostics and drug development, offering end-to-end clinical trial services through its Covance division. Syneos Health Blends clinical development with commercialization, offering biopharma integrated solutions and a strong site-network model. Top Companies in the Pharma Contract Research Organization (CRO) Services Market IQVIA Parexel International (MA) Corporation Medpace Charles River Laboratories CTI Clinical Trial & Consulting WuXi AppTec Veeda Clinical Research ICON plc Laboratory Corporation of America Holdings Syneos Health Browse More Insights of Towards Healthcare: Medical Device CRO Market:The medical device contract research organization (CRO) market is valued at USD 8.49 billion in 2024, grows to USD 9.25 billion in 2025, and is expected to reach USD 19.9 billion by 2034, with a strong annual growth rate (CAGR) of 8.98%. Biopharmaceuticals CRO Market:The biopharmaceuticals contract research organization market is expected to grow steadily from 2025 to 2034, potentially reaching hundreds of millions of dollars in revenue during the forecast period. Healthcare CRO Market:The healthcare contract research organization (CRO) market is estimated at USD 53.87 billion in 2024, rises to USD 57.66 billion in 2025, and could reach USD 106.25 billion by 2034, growing at a CAGR of 7.04%. Preclinical CRO Market:The preclinical contract research organization (CRO) market is expected to grow from USD 6.8 billion in 2025 to USD 14.34 billion by 2034, at a CAGR of 8.73%. Biologics CRO Market:The biologics contract research organization market is valued at USD 31.15 billion in 2024, will grow to USD 35.22 billion in 2025, and is projected to reach USD 106.28 billion by 2034. Biotechnology & Pharmaceutical Services Market:The biotechnology and pharmaceutical services market stands at USD 76.51 billion in 2024, increases to USD 80.7 billion in 2025, and is expected to reach USD 130.56 billion by 2034, growing at a CAGR of 5.48%. 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Regions Covered North America U.S. Canada Asia Pacific China Japan India South Korea Thailand Europe Germany UK France Italy Spain Sweden Denmark Norway Latin America Brazil Mexico Argentina Middle East and Africa (MEA) South Africa UAE Saudi Arabia Kuwait Download the complete strategic report with deep analysis, forecast and competitive intelligence tailored for decision-makers: You can place an order or ask any questions, please feel free to contact us at sales@ Gain access to the latest insights and statistics in the healthcare industry by subscribing to our Annual Membership. Stay updated on healthcare industry segmentation with detailed reports, market trends, and expert analysis tailored to your needs. Stay ahead of the curve with valuable resources and strategic recommendations. 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Healthcare Dispensing Systems Market worth $6.27 billion by 2030 with 6.3% CAGR
Healthcare Dispensing Systems Market worth $6.27 billion by 2030 with 6.3% CAGR

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Healthcare Dispensing Systems Market worth $6.27 billion by 2030 with 6.3% CAGR

DELRAY BEACH, Fla., July 18, 2025 /PRNewswire/ -- The global Healthcare Dispensing Systems Market, valued at US$4.36 billion in 2024, stood at US$4.61 billion in 2025 and is projected to advance at a resilient CAGR of 6.3% from 2025 to 2030, culminating in a forecasted valuation of US$6.27 billion by the end of the period. The market's accelerated growth trajectory is primarily driven by increasing demand for precision dispensing in pharmaceutical manufacturing, diagnostics, and medical device production. As the industry moves toward automation and miniaturization, advanced dispensing systems are streamlining workflows, improving dosing accuracy, and reducing contamination risks. Key trends such as the rise of lab-on-chip devices, personalized medicine, and point-of-care testing are expanding adoption across end-user segments. Additionally, technological innovations in microfluidics, robotics, and sensor integration are enhancing system performance. Regulatory support for digital health infrastructure and growing investment in life sciences R&D is further accelerating market expansion. Download PDF Brochure: Browse in-depth TOC on "Healthcare Dispensing Systems Market" 400 - Tables50 - Figures400 - Pages By type, the market is divided into automatic dispensing systems, semi-automated dispensing systems, stand-alone/manual dispensing instruments, and OEM/dispensing components. Automatic dispensing systems accounted for the largest share of the healthcare dispensing systems market in 2024. Their dominance is attributed to the increasing demand for high-throughput, precise, and contamination-free dispensing in diagnostic labs, pharmaceutical production, and medical device assembly. These systems are widely adopted due to their integration capabilities with automated workflows, improved operational efficiency, and reduced error rates. Advancements in tipless and non-contact dispensing, real-time data feedback, and motion control have further enhanced their appeal. Growing R&D activities, rising diagnostic volumes, and a global push for lab automation are expected to sustain the segment's leadership during the forecast period. By end user, the healthcare dispensing systems market is segmented into healthcare providers, pharma & biotech companies, MedTech companies, and other end users based on the end user. Among these, healthcare providers represent the largest segment, driven by the widespread use of dispensing systems across hospitals, diagnostic labs, outpatient centers, pharmacies, and long-term care facilities. These systems support accurate and safe medication administration, fluid handling in diagnostic workflows, and real-time inventory management. Hospitals and labs require automated dispensing to meet high patient volumes and ensure safety and quality standards compliance. The growing demand for efficient resource utilization, staff workload reduction, and integrated data systems further accelerates adoption among healthcare providers. For instance, over 90% of US acute care hospitals use Automated Dispensing Cabinets (ADCs), saving up to 35 hours of labor weekly and $64,300 annually, highlighting the strong impact of automation on hospital efficiency, cost reduction, and patient safety. As care delivery models shift toward decentralized and patient-centric approaches, healthcare providers continue to invest in dispensing systems to support scalable, connected, and efficient operations. By geography, in 2024, North America held the largest market share for healthcare dispensing systems. This dominance is due to a well-established diagnostic infrastructure, advanced pharmaceutical manufacturing capabilities, and a high concentration of biotech and medtech firms. The region benefits from substantial R&D investments, early adoption of automation, and strong support from both the government and private sector for digital transformation in healthcare. Additionally, the increasing demand for decentralized testing, the presence of major dispensing technology providers, and an emphasis on quality and regulatory compliance have all contributed to market leadership. The integration of smart dispensing solutions in diagnostics and medical device production further supports continued growth. Request Sample Pages : The prominent healthcare dispensing systems market players include Nordson Corporation (US), DH Life Sciences, LLC (US), and BRAND GMBH+Co. KG (Germany), Fisnar (US), PARKER HANNIFIN CORP (US), BioDot (US), Thermo Fisher Scientific Inc. (US), bdtronic (Germany), Agilent Technologies, Inc. (US), Hamilton Company (US), Graco Inc. (US), Imagene Technology Inc (US), Harro Höfliger Verpackungsmaschinen GmbH (Germany), Tecan Trading AG (Switzerland), IVEK Corporation (US), Revvity, Inc. (US), QIAGEN (Germany), Gilson Incorporated (US), Ascential Technologies (US), and LGC?Biosearch Technologies (UK). Nordson Corporation (US): Nordson Corporation is a key healthcare dispensing systems sector leader, leveraging its robust engineering expertise and extensive product portfolio to maintain a dominant market position. The company's global manufacturing footprint and enduring partnerships with pharmaceutical, biotech, and medical device companies reinforce its strategic advantage. Nordson delivers diverse precision dispensing solutions, specifically engineered for critical applications such as drug formulation, diagnostics production, and medical device assembly. The integration of automation, rigorous quality control measures, and strict compliance adherence into its systems solidifies its reputation as a preferred collaborator within regulated healthcare environments. Significant investment in research and development enables Nordson to continuously innovate, optimizing system precision, throughput speed, and reliability. Operating in over 35 countries across North America, Europe, Asia, and Latin America, the company provides localized support and expert technical services to its global clientele. Its deep-rooted experience in fluid management and microdispensing technologies cements Nordson's role as a pivotal enabler of high-throughput manufacturing processes within the healthcare industry. BioDot Inc. (US): BioDot Inc. is a pivotal entity in the healthcare dispensing systems sector. It is particularly recognized for its innovative ultra-low volume dispensing technologies for life sciences, diagnostics, and high-throughput manufacturing arenas. The company's expertise lies in precision fluid deposition systems, essential for applications such as point-of-care diagnostics, lateral flow assays, and biosensor development. BioDot's portfolio includes advanced solutions like the BioJet and the newly launched MODULIS platform. These systems are characterized by their integration of modular automation, intelligent conveyance mechanisms, and robust vision systems, facilitating scalable and high-volume production processes. With a footprint extending across over 50 countries, BioDot emphasizes system adaptability and manufacturing efficiency, enabling end-to-end dispensing solutions that empower manufacturers to expedite product development and shorten commercialization timelines. For more information, Inquire Now! Related Reports: Healthcare IT Market Drug Discovery Services Market Healthcare Analytics Market Healthcare IT Integration Market Microfluidics Market Get access to the latest updates on Healthcare Dispensing Systems IT Companies and Healthcare Dispensing Systems Market Size About MarketsandMarkets™: MarketsandMarkets™ has been recognized as one of America's Best Management Consulting Firms by Forbes, as per their recent report. MarketsandMarkets™ is a blue ocean alternative in growth consulting and program management, leveraging a man-machine offering to drive supernormal growth for progressive organizations in the B2B space. With the widest lens on emerging technologies, we are proficient in co-creating supernormal growth for clients across the globe. Today, 80% of Fortune 2000 companies rely on MarketsandMarkets, and 90 of the top 100 companies in each sector trust us to accelerate their revenue growth. 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