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PERSPECTIVE article

Front. Med., 26 January 2026

Sec. Translational Medicine

Volume 13 - 2026 | https://doi.org/10.3389/fmed.2026.1737301

Evidence-based nursing strategies for the prevention and management of oral mucositis in hematopoietic stem cell transplantation patients

  • Department of Hematology, The First Affiliated Hospital of Harbin Medical University, Harbin, China

Hematopoietic stem cell transplantation (HSCT) is a cornerstone therapy for hematological malignancies, frequently complicated by treatment-related oral mucositis (OM). This complication leads to severe pain, nutritional compromise, heightened infection risk, and may result in treatment delays, prolonged hospitalization, and diminished long-term health-related quality of life. While clinical guidelines exist, a significant gap persists between evidence and practice, especially in the systematic and individualized application of preventive strategies. From an evidence-based nursing perspective, this perspective article proposes a comprehensive management framework. This framework integrates evidence synthesis, patient-specific risk assessment, dynamic monitoring, and multidisciplinary collaboration to align standardized interventions with personalized patient needs across all phases of HSCT. By synthesizing current evidence, analyzing practical challenges, and proposing a structured management pathway, this perspective article aims to guide clinical practice, inform future research, and ultimately improve care standards for OM in HSCT patients.

1 Introduction

1.1 Severity of the problem

Hematopoietic stem cell transplantation (HSCT) is a critical and potentially curative intervention for malignant hematological disorders, certain solid tumors, and genetic immunodeficiencies (1, 2). However, the necessary pre-transplant conditioning regimens—involving high-dose chemotherapy and/or radiotherapy—directly damage the rapidly dividing basal epithelial cells of the oral mucosa (3). Consequently, oral mucositis (OM) is an exceedingly common complication, with a reported incidence of 70 to 100% following HSCT (3, 4). Approximately one-third to one-half of these cases are severe [World Health Organization (WHO) Grades III-IV], representing a major clinical management challenge (5).

The pathogenesis of HSCT-associated OM is now recognized not as a simple inflammatory response, but as a dynamic and complex biological process (6). It is initiated by direct cytotoxic injury, which triggers a cascade of molecular and cellular events (7). The upregulation and release of pro-inflammatory cytokines (e.g., tumor necrosis factor-alpha, interleukins-1β and interleukins-6) amplify tissue damage and mediate significant pain (6, 8). Subsequent loss of mucosal barrier integrity permits the translocation of oral commensal microorganisms into the bloodstream, substantially increasing the risk of life-threatening systemic infections (7, 8). Therefore, OM is best characterized as a multifaceted biological injury, driven by a dysregulated cytokine network and shaped by interactions between the epithelium, submucosa, and local microbiome (6, 9).

The risk and severity of OM differ substantially between autologous and allogeneic HSCT. Autologous transplantation primarily involves acute, chemotherapy-induced mucosal toxicity, which is often self-limiting (10). In contrast, allogeneic HSCT entails more intensive conditioning, prolonged immune dysregulation, immunosuppressive therapy, and the potential for graft-versus-host disease, all of which contribute to more severe, persistent, and complex mucosal damage (11). This distinction necessitates differentiated nursing assessment strategies, with allogeneic recipients requiring closer monitoring for prolonged ulceration, secondary infection, and chronic oral sequelae (12).

The impact of OM on patients is profound and multidimensional. Acutely, severe pain frequently impedes oral intake, leading to malnutrition, dehydration, and a common reliance on opioid analgesia and total parenteral nutrition (13). The ulcerated mucosa provides a portal for pathogenic entry, increasing the risk of bacteremia and sepsis, which may increase transplant-related mortality (14, 15). Furthermore, severe OM can delay hematopoietic engraftment, prolong hospitalization, increase treatment costs, and potentially compromise therapeutic efficacy by necessitating treatment modifications (5, 14). Beyond the physical sequelae, the associated pain and functional impairment contribute to significant psychological distress, including anxiety and depression, adversely affecting health-related quality of life (HR-QOL) long after clinical recovery (16, 17).

1.2 Rationale for evidence-based nursing

The complexity of OM makes reliance on anecdotal experience or routine care insufficient for optimal management. Consequently, integrating an evidence-based nursing (EBN) framework is essential. EBN is a systematic, problem-solving approach to clinical decision-making that combines the best available research evidence, clinician expertise, and individual patient values and preferences (18, 19).

For OM management, the value of EBN is threefold. First, it grounds nursing interventions in robust scientific evidence—such as data from high-quality randomized controlled trials and systematic reviews—ensuring strategies are scientifically sound and effective (20, 21). Second, clinician expertise contextualizes this evidence, as skilled nurses adapt generalized recommendations to a patient’s specific clinical status, comorbidities, and treatment plan (21, 22). Finally, and pivotally, care plans should incorporate patient values and preferences, such as choices regarding mouthwash use, pain management, or nutritional support (18, 23). This integrated approach is fundamental to developing personalized, effective, and humane OM management strategies that promote patient adherence and improve outcomes.

1.3 Aim and framework

This perspective article aims to examine the prevention and management of OM in HSCT patients through an EBN lens. It synthesizes established evidence to propose a structured, actionable, and forward-looking strategic framework. The discussion will first establish the evidence base for OM risk assessment and evaluation. It will then construct a comprehensive management framework integrating primary prevention, secondary intervention, and supportive care throughout the HSCT continuum. Finally, the perspective article will explore the process of translating evidence into practice by addressing implementation barriers and proposing integrative pathways. Ultimately, this perspective study seeks to provide a clear conceptual and practical guide for clinicians and to highlight promising research directions to improve care quality and outcomes.

This perspective article does not seek to reproduce or substitute for established evidence-based guidelines, such as those from the Multinational Association of Supportive Care in Cancer and the European Society for Medical Oncology. Instead, it focuses on the application of guideline evidence within routine nursing practice across the HSCT trajectory. We define a care pathway as a practical framework that details the timing, methodology, and responsible personnel for implementing evidence-based interventions at each clinical stage, thereby extending beyond the general recommendations of clinical guidelines. Consequently, this article addresses the practical gap between evidence and bedside care from a nursing-led implementation perspective.

2 Accurate assessment of OM risk and standardization of evaluation criteria

An effective OM prevention and management strategy relies on two key elements: accurately identifying high-risk patients before transplantation and reliably evaluating intervention outcomes afterward. Together, these form the foundation for personalized and precise clinical decision-making.

2.1 Application of risk prediction pathways

Precise identification of high-risk patients enables the proactive allocation of resources and targeted preventive strategies (24). While tools like the Oral Mucositis Assessment Scale (OMAS) are valued for objectively quantifying erythema and ulceration, they are of limited pre-transplant value as mucosal damage has not yet occurred (25). An evidence-based approach therefore emphasizes integrating objective tools with patient-specific clinical factors to build a comprehensive predictive pathway (25, 26). Critical risk factors include transplant type (allogeneic carries higher risk than autologous), the mucotoxicity of the conditioning regimen (e.g., containing high-dose melphalan), patient age, and pre-transplant oral health (24, 26). We recommend that this comprehensive risk assessment be adopted as a routine, standardized pre-HSCT procedure. By systematically analyzing these data, clinicians can prioritize patients for intensified prevention, shifting the clinical paradigm from reactive response to proactive prevention.

2.2 Standardization of efficacy evaluation criteria

A standardized and reliable method for assessing OM is essential to accurately evaluate intervention outcomes and advance evidence-based practice. Currently, multiple validated grading scales are available, each with distinct characteristics. For example, the WHO scale combines clinical signs with functional impact, such as the patient’s ability to eat (27, 28). The National Cancer Institute’s Common Terminology Criteria for Adverse Events provides detailed, graded symptom descriptions to support clinical documentation and decision-making (27). The OMAS improves sensitivity to changes in severity by quantifying the area of erythema and ulceration at specific oral sites (2729). However, the variety of tools presents a methodological challenge, hindering direct comparison of results across studies and potentially introducing inconsistency in clinical practice. This variability may compromise continuity of care and weaken the overall evidence base (30, 31). Therefore, we strongly recommend consistently using a single validated assessment instrument within individual institutions and in multicenter research. Such standardization is fundamental to ensuring reliable evaluation, enabling meaningful cross-study comparisons, and supporting the implementation of robust evidence-based care pathways.

3 An evidence-based, comprehensive management system

Effective prevention and management of OM in HSCT patients require an evidence-based strategy spanning the entire transplant process. This section outlines a structured management pathway organized around a Prevention-Intervention-Support framework. While oncology nurses have traditionally been central to OM care, their responsibilities have focused primarily on symptom monitoring and supportive care. This pathway expands that role by positioning nurses as key implementers of evidence-based pathways, responsible for conducting dynamic risk assessments, delivering stage-specific interventions, and ensuring continuity of care from pre-transplant preparation through to post-discharge follow-up.

3.1 Primary prevention: a proactive approach

Prevention is the cornerstone of OM management, aiming to reduce its severity and delay its onset (32). A fundamental component is standardized basic oral care, which all preventive strategies incorporate (33). Strong evidence supports the implementation of a standardized oral care protocol before transplantation and its continuation throughout the treatment course (34). This protocol should emphasize gentle yet thorough cleansing. Key components include using a soft-bristled toothbrush to minimize trauma and frequent rinsing with non-irritating solutions, such as saline or sodium bicarbonate, to maintain mucosal hydration and clear debris (35, 36). This necessitates collaboration with dentists for pre-transplant oral evaluation and management of any existing dental issues to establish an optimal baseline oral health status. The goal is to preserve the physiological balance of the oral cavity.

For patients receiving specific high-dose chemotherapy (e.g., melphalan) or total body irradiation, palifermin is strongly supported by evidence for significantly reducing the incidence and duration of severe OM (37). It acts as a form of “biological prevention” by stimulating epithelial cell growth and repair. Low-level laser therapy (LLLT) has also demonstrated efficacy in clinical trials for OM prevention, attributed to its anti-inflammatory and tissue-healing properties (38). However, its application is limited by cost, the lack of standardized protocols, and the need for specialized training (39). Cryotherapy (ice chips) is effective for specific agents like 5-fluorouracil or melphalan by cooling the oral mucosa, thereby reducing local blood flow and the delivery of cytotoxic drugs (39, 40). Its use is restricted to the infusion period, and patient tolerance varies (39, 40). Agents such as granulocyte-colony stimulating factor mouthwashes or glutamine supplements are not routinely recommended due to insufficient or inconsistent evidence, despite a theoretical rationale (41).

3.2 Secondary prevention and intervention: early recognition and targeted management

When primary prevention is unsuccessful, the focus shifts to early detection and precise intervention to control OM progression and alleviate symptoms. A nurse-led, daily oral assessment using validated tools (e.g., WHO scale or OMAS) is critical for this process (38). Nurses are optimally positioned to detect early signs, such as erythema or patient-reported discomfort, enabling timely intervention before severe ulceration develops (38, 42).

Pain management for OM should be proactive and systematic, typically guided by the principles of the WHO analgesic ladder (43, 44). A key strategy is preemptive analgesia with scheduled dosing rather than “as-needed” administration to prevent the onset of severe pain (45). For mild pain, non-opioids such as acetaminophen may suffice. Moderate to severe pain requires the timely administration of systemic opioids (e.g., morphine, fentanyl), and patient-controlled analgesia can provide effective relief (45, 46). Topical anesthetics (e.g., lidocaine mouthwash) may be used adjunctively before meals to facilitate oral intake, but their use should be limited to avoid side effects such as impaired taste and aspiration risk (38).

In addition to ongoing pain and nutritional management, the therapeutic goals for established ulcers encompass promoting healing and preventing secondary infection. Topical growth factors may accelerate mucosal regeneration (37). Protective barrier films (e.g., sucralfate) can coat ulcers to shield them from further irritation (47). If a secondary fungal or viral infection is suspected, targeted antifungal or antiviral therapy should be initiated, preferably guided by microbiological data.

3.3 Supportive care: sustaining vital functions and HR-QOL

Supportive care is essential for maintaining physiological stability and psychological well-being throughout treatment. Nutritional support should adapt as needed, ensuring a transition from an oral diet to enteral and, if required, parenteral nutrition (48, 49). The early involvement of a dietitian is crucial for comprehensive assessment and the development of an individualized plan (49).

Infection control requires careful consideration of risks and benefits. The routine prophylactic use of broad-spectrum antimicrobial or antifungal mouthwashes is not recommended, as it can disrupt the oral microbiome, promote resistance, and lacks strong supporting evidence (38). These agents should be reserved for patients with clear signs of localized infection and, whenever feasible, guided by microbiological identification.

Patients and their families should be engaged as active partners in care (50). Providing structured education on the causes, symptoms, and self-management of OM is fundamental (49). Training in self-management techniques (e.g., pain logging, dietary modifications) enhances patient empowerment and adherence (51). Furthermore, consistent psychological support to address anxiety and depression is vital for improving long-term adherence and HR-QOL.

4 From evidence to practice: challenges and integrative pathways

Successfully translating research evidence into routine care is essential for improving patient outcomes, yet this process often encounters significant barriers that require targeted strategies to overcome.

4.1 Bridging the evidence-to-practice gap

A persistent gap often separates published guidelines from their application in clinical settings. This disconnect stems from several key factors. First, clinical guidelines can become outdated, failing to incorporate emerging research and leaving clinical nurses at the bedside nurses without current recommendations (52). Second, high workloads and staffing shortages limit the time available for nurses to search for, appraise, and integrate new evidence (53). Third, cost constraints can preclude the adoption of effective but expensive interventions, such as palifermin or LLLT (54). Finally, a lack of awareness of current evidence and deeply ingrained practice habits among staff presents a significant barrier (52). Proactively identifying these challenges is a prerequisite for effective implementation.

Despite these barriers, implementation research confirms that integrating evidence-based OM guidelines into nursing practice yields measurable benefits (45). The adoption of structured oral care protocols has been shown to improve assessment consistency, facilitate earlier symptom recognition, reduce mucositis severity, and enhance patient-reported outcomes (45, 5557). These findings underscore that the efficacy of guidelines depends fundamentally on their systematic integration into clinical workflows, highlighting the central role of nursing-led strategies—including standardized assessments, structured documentation, and patient education—in translating evidence into tangible patient benefits (57, 58).

For clarity and comparative purposes, Table 1 summarizes key evidence-based OM guidelines and the available evidence concerning their integration into routine clinical practice. This synthesis reveals that while evidence-based guidelines exist, published research on their systematic implementation within standard HSCT nursing care and the assessment of related outcomes remains limited. This evidence gap substantiates the need for the structured, nurse-led clinical care pathway proposed in this perspective article.

Table 1
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Table 1. Comparison of major evidence-based guidelines and the proposed nursing-led integrative care pathway for OM in HSCT patients.

4.2 Developing structured care pathways

A principal strategy for translating evidence into practice is the adoption of structured care pathways. In this context, a “care pathway” is explicitly distinguished from a clinical guideline. While guidelines provide evidence-based recommendations for what should be done, pathways operationalize these by specifying how, when, and by whom care should be delivered within a specific clinical setting. Consequently, care pathways focus on workflow integration, clear role delineation, and intervention timing—elements fundamental for ensuring consistent implementation in nursing practice.

This approach involves integrating the best available evidence on risk assessment, basic care, pain management, and nutrition into standardized clinical pathways for HSCT patients (59, 60). These pathways provide a timeline, detailing essential assessments and interventions for each transplant phase (60). By establishing a clear protocol, they reduce practice variation, ensure consistent delivery of evidence-based care to all patients, and thereby improve overall care quality (59, 61).

4.3 Strengthening the multidisciplinary team framework

Effective OM management requires robust collaboration within a multidisciplinary team (38, 50). In this framework, nurses serve as central coordinators, continuously monitoring patient status, administering interventions, and facilitating communication among all team members. This necessitates close collaboration with physicians on treatment plans, pharmacists on medication management, dietitians on nutritional support, dentists on oral health, and psychologists on addressing patient distress (38, 45). Only through such integrated teamwork can evidence-based guidelines be woven into a seamless, patient-centered care plan, ensuring translation into improved patient outcomes.

5 Future perspectives

Although current evidence-based strategies have improved OM management, significant opportunities remain to optimize patient outcomes. Future efforts should focus on addressing critical research gaps and strengthening nursing leadership in this field.

5.1 Critical research directions

Several key areas warrant focused research to advance the field. First, effectiveness and implementation research is foundational. Priorities should include pragmatic clinical trials comparing nurse-led OM management pathways to usual care, measuring outcomes such as OM incidence, opioid use, hospital length of stay, and patient-reported HR-QOL (62, 63). Concurrently, implementation science studies are needed to evaluate strategies for integrating evidence-based OM protocols into clinical workflows, for example through electronic health record integration with clinical decision support and automated documentation (64, 65). These studies should systematically assess feasibility and patient-centered outcomes, including nursing workload, protocol adherence, and patient satisfaction, to evaluate a pathway’s real-world effectiveness and sustainability (65, 66). Second, personalized prediction is crucial. Research should investigate biomarkers from genomics, transcriptomics, and the oral microbiome to identify signatures predictive of severe OM, enabling precise risk stratification and preemptive care intensification (67). Third, regarding novel interventions, the potential of mesenchymal stem cell therapy for mucosal regeneration should be explored, alongside the development of advanced biomaterial-based dressings to protect ulcerated surfaces and enhance therapeutic delivery (68). Fourth, digital health technologies hold promise. The development and validation of mobile health applications for remote symptom monitoring and management could improve patient self-efficacy, engagement, and adherence (69). Finally, advancing health economics research is essential (70). Rigorous cost-effectiveness analyses of advanced interventions are required to inform their rational allocation and adoption within healthcare systems (70).

5.2 The evolving role of nursing leadership

To meet future challenges in OM management, nurses should proactively expand their leadership roles. While historically serving as clinical nurses at the bedside caregivers, their professional scope is evolving to encompass evidence translation, quality improvement leadership, and digital health integration (7174). This progression firmly establishes nurses as pivotal agents in bridging the evidence-to-practice gap. Specifically, we advocate for nursing professionals to transcend traditional boundaries by becoming active knowledge translators who systematically disseminate and implement best practices within their institutions (75); clinical change agents who lead initiatives to integrate new evidence and technologies into standardized care pathways (76); and engaged research partners who contribute essential clinical insights to shape research agendas and participate in scientific studies (77). Through demonstrated leadership in these domains, the nursing profession will solidify its indispensable role in advancing OM management and enhancing HR-QOL for HSCT patients (78).

6 Summary

In summary, the EBN management of oral mucositis in HSCT patients necessitates a proactive, dynamic, systematic, and individualized strategy. This strategy integrates three essential elements: the application of best available evidence, the implementation of optimized clinical pathways, and effective multidisciplinary collaboration. This integrated approach transforms OM care from a series of isolated interventions into a coordinated, patient-centered continuum. Its consistent application can reduce the clinical burden of OM, alleviate patient suffering, and improve overall outcomes. Ultimately, this represents high-quality nursing care that synthesizes scientific rigor with compassionate practice to enhance the patient experience throughout the HSCT journey.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Author contributions

MC: Conceptualization, Data curation, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing.

Funding

The author(s) declared that financial support was not received for this work and/or its publication.

Conflict of interest

The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declared that Generative AI was not used in the creation of this manuscript.

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References

1. Snowden, JA, Sánchez-Ortega, I, Corbacioglu, S, Basak, GW, Chabannon, C, de la Camara, R, et al. Indications for haematopoietic cell transplantation for haematological diseases, solid tumours and immune disorders: current practice in Europe, 2022. Bone Marrow Transplant. (2022) 57:1217–39. doi: 10.1038/s41409-022-01691-w,

PubMed Abstract | Crossref Full Text | Google Scholar

2. Mora, J. Autologous stem-cell transplantation for high-risk neuroblastoma: historical and critical review. Cancers (Basel). (2022) 14:2572. doi: 10.3390/cancers14112572,

PubMed Abstract | Crossref Full Text | Google Scholar

3. Kara, H, Arıkan, F, Çil Kazan, S, Atay Turan, S, and Ören, R. Evaluation of the incidence and stage of oral mucositis in patients undergoing hematopoietic stem cell transplantation: a retrospective study. Florence Nightingale J Nurs. (2024) 32:261–8. doi: 10.5152/FNJN.2024.23049,

PubMed Abstract | Crossref Full Text | Google Scholar

4. Nakagaki, M, Kennedy, GA, Gavin, NC, Clavarino, A, and Whitfield, K. The incidence of severe oral mucositis in patients undergoing different conditioning regimens in haematopoietic stem cell transplantation. Support Care Cancer. (2022) 30:9141–9. doi: 10.1007/s00520-022-07328-4,

PubMed Abstract | Crossref Full Text | Google Scholar

5. Agholme, MB, Dahllöf, G, Törlén, JK, Majorana, A, Brennan, MT, von Bültzingslöwen, I, et al. Incidence, severity, and temporal development of oral complications in pediatric allogeneic hematopoietic stem cell transplant patients-a multicenter study. Support Care Cancer. (2023) 31:702. doi: 10.1007/s00520-023-08151-1,

PubMed Abstract | Crossref Full Text | Google Scholar

6. Singh, V, and Singh, AK. Oral mucositis. Natl J Maxillofac Surg. (2020) 11:159–68. doi: 10.4103/njms.NJMS_10_20,

PubMed Abstract | Crossref Full Text | Google Scholar

7. Haverman, TM, Raber-Durlacher, JE, Rademacher, WM, Vokurka, S, Epstein, JB, Huisman, C, et al. Oral complications in hematopoietic stem cell recipients: the role of inflammation. Mediat Inflamm. (2014) 2014:378281. doi: 10.1155/2014/378281,

PubMed Abstract | Crossref Full Text | Google Scholar

8. Bowen, J, and Cross, C. The role of the innate immune response in oral mucositis pathogenesis. Int J Mol Sci. (2023) 24:16314. doi: 10.3390/ijms242216314,

PubMed Abstract | Crossref Full Text | Google Scholar

9. Lionel, D, Christophe, L, Marc, A, and Jean-Luc, C. Oral mucositis induced by anticancer treatments: physiopathology and treatments. Ther Clin Risk Manag. (2006) 2:159–68. doi: 10.2147/tcrm.2006.2.2.159,

PubMed Abstract | Crossref Full Text | Google Scholar

10. Rubenstein, EB, Peterson, DE, Schubert, M, Keefe, D, McGuire, D, Epstein, J, et al. Clinical practice guidelines for the prevention and treatment of cancer therapy-induced oral and gastrointestinal mucositis. Cancer. (2004) 100:2026–46. doi: 10.1002/cncr.20163,

PubMed Abstract | Crossref Full Text | Google Scholar

11. Chaudhry, HM, Bruce, AJ, Wolf, RC, Litzow, MR, Hogan, WJ, Patnaik, MS, et al. The incidence and severity of oral mucositis among allogeneic hematopoietic stem cell transplantation patients: a systematic review. Biol Blood Marrow Transplant. (2016) 22:605–16. doi: 10.1016/j.bbmt.2015.09.014,

PubMed Abstract | Crossref Full Text | Google Scholar

12. Fall-Dickson, JM, Pavletic, SZ, Mays, JW, and Schubert, MM. Oral complications of chronic graft-versus-host disease. J Natl Cancer Inst Monogr. (2019) 2019:lgz007. doi: 10.1093/jncimonographs/lgz007,

PubMed Abstract | Crossref Full Text | Google Scholar

13. Eglseer, D, Seymann, C, Lohrmann, C, and Hoedl, M. Nutritional problems and their non-pharmacological treatment in adults undergoing haematopoietic stem cell transplantation-a systematic review. Eur J Cancer Care. (2020) 29:e13298. doi: 10.1111/ecc.13298,

PubMed Abstract | Crossref Full Text | Google Scholar

14. Sonis, ST, Oster, G, Fuchs, H, Bellm, L, Bradford, WZ, Edelsberg, J, et al. Oral mucositis and the clinical and economic outcomes of hematopoietic stem-cell transplantation. J Clin Oncol. (2001) 19:2201–5. doi: 10.1200/JCO.2001.19.8.

Crossref Full Text | Google Scholar

15. Messina, JA, Jiang, D, Selvan, B, Hill, L, Bush, A, Bokman, J, et al. The impact of Mucositis on the Oral microbiome and clinical outcomes in allogenic hematopoietic stem cell transplantation. Open Forum Infect Dis. (2023) 10:ofad500-366. doi: 10.1093/ofid/ofad500.366

Crossref Full Text | Google Scholar

16. Chaitanya, NC, Garlapati, K, Priyanka, DR, Soma, S, Suskandla, U, and Boinepally, NH. Assessment of anxiety and depression in oral mucositis patients undergoing cancer chemoradiotherapy: a randomized cross-sectional study. Indian J Palliat Care. (2016) 22:446–54. doi: 10.4103/0973-1075.191797,

PubMed Abstract | Crossref Full Text | Google Scholar

17. Bezinelli, LM, Eduardo, FP, Neves, VD, Correa, L, Lopes, RM, Michel-Crosato, E, et al. Quality of life related to oral mucositis of patients undergoing haematopoietic stem cell transplantation and receiving specialised oral care with low-level laser therapy: a prospective observational study. Eur J Cancer Care. (2016) 25:668–74. doi: 10.1111/ecc.12344,

PubMed Abstract | Crossref Full Text | Google Scholar

18. Melnyk, BM, Fineout-Overholt, E, Stillwell, SB, and Williamson, KM. Evidence-based practice: step by step: the seven steps of evidence-based practice. Am J Nurs. (2010) 110:51–3. doi: 10.1097/01.NAJ.0000366056.06605.d2.,

PubMed Abstract | Crossref Full Text | Google Scholar

19. Ominyi, J, Nwedu, A, Agom, D, and Eze, U. Leading evidence-based practice: nurse managers' strategies for knowledge utilisation in acute care settings. BMC Nurs. (2025) 24:252. doi: 10.1186/s12912-025-02912-5,

PubMed Abstract | Crossref Full Text | Google Scholar

20. Brunt, B. A., and Morris, M. M. Nursing professional development evidence-based practice. 2023. In: M. M. Morris editor, StatPearls. Treasure Island (FL): StatPearls Publishing; 2025.

Google Scholar

21. Connor, L, Dean, J, McNett, M, Tydings, DM, Shrout, A, Gorsuch, PF, et al. Evidence-based practice improves patient outcomes and healthcare system return on investment: findings from a scoping review. Worldviews Evid-Based Nurs. (2023) 20:6–15. doi: 10.1111/wvn.12621,

PubMed Abstract | Crossref Full Text | Google Scholar

22. McHugh, MD, and Lake, ET. Understanding clinical expertise: nurse education, experience, and the hospital context. Res Nurs Health. (2010) 33:276–87. doi: 10.1002/nur.20388,

PubMed Abstract | Crossref Full Text | Google Scholar

23. Stacey, D, Légaré, F, Lewis, K, Barry, MJ, Bennett, CL, Eden, KB, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. (2017) 4:CD001431. doi: 10.1002/14651858.CD001431.pub5,

PubMed Abstract | Crossref Full Text | Google Scholar

24. Wong, SP, Tan, SM, Lee, CS, Law, KB, Lim, YAL, and Rajasuriar, R. Prospective longitudinal analysis of clinical and immunological risk factors associated with oral and gastrointestinal mucositis following autologous stem cell transplant in adults. Support Care Cancer. (2023) 31:494. doi: 10.1007/s00520-023-07947-5,

PubMed Abstract | Crossref Full Text | Google Scholar

25. Wardill, HR, Sonis, ST, Blijlevens, NMA, van Sebille, YZA, Ciorba, MA, Loeffen, EAH, et al. Prediction of mucositis risk secondary to cancer therapy: a systematic review of current evidence and call to action. Support Care Cancer. (2020) 28:5059–73. doi: 10.1007/s00520-020-05579-7,

PubMed Abstract | Crossref Full Text | Google Scholar

26. Rezende, SB, Campos, L, de Souza, MC, Schoenmann, M, Macedo, MCMA, da Silva, RL, et al. Determinants of severe oral mucositis development despite photobiomodulation therapy in stem cell transplant patients. Dent J. (2025) 13:411. doi: 10.3390/dj13090411,

PubMed Abstract | Crossref Full Text | Google Scholar

27. Villa, A, Vollemans, M, De Moraes, A, and Sonis, S. Concordance of the WHO, RTOG, and CTCAE v4.0 grading scales for the evaluation of oral mucositis associated with chemoradiation therapy for the treatment of oral and oropharyngeal cancers. Support Care Cancer. (2021) 29:6061–8. doi: 10.1007/s00520-021-06177-x.,

PubMed Abstract | Crossref Full Text | Google Scholar

28. Minhas, S, Sajjad, A, Chaudhry, RM, Zahid, H, Shahid, A, and Kashif, M. Assessment and prevalence of concomitant chemo-radiotherapy-induced oral mucositis in patients with oral squamous cell carcinoma. Turk J Med Sci. (2021) 51:675–84. doi: 10.3906/sag-2007-131,

PubMed Abstract | Crossref Full Text | Google Scholar

29. Sung, L, Tomlinson, GA, Greenberg, ML, Koren, G, Judd, P, Ota, S, et al. Validation of the oral mucositis assessment scale in pediatric cancer. Pediatr Blood Cancer. (2007) 49:149–53. doi: 10.1002/pbc.20863,

PubMed Abstract | Crossref Full Text | Google Scholar

30. Abdalla-Aslan, R, Bonomo, P, Keefe, D, Blijlevens, N, Cao, K, Cheung, YT, et al. Guidance on mucositis assessment from the MASCC Mucositis study group and ISOO: an international Delphi study. EClinicalMedicine. (2024) 73:102675. doi: 10.1016/j.eclinm.2024.102675,

PubMed Abstract | Crossref Full Text | Google Scholar

31. Peterson, DE, Boers-Doets, CB, Bensadoun, RJ, and Herrstedt, JESMO Guidelines Committee. Management of oral and gastrointestinal mucosal injury: ESMO clinical practice guidelines for diagnosis, treatment, and follow-up. Ann Oncol. (2015) 26 Suppl 5:v139–51. doi: 10.1093/annonc/mdv202,

PubMed Abstract | Crossref Full Text | Google Scholar

32. Cheng, KK, Molassiotis, A, Chang, AM, Wai, WC, and Cheung, SS. Evaluation of an oral care protocol intervention in the prevention of chemotherapy-induced oral mucositis in paediatric cancer patients. Eur J Cancer. (2001) 37:2056–63. doi: 10.1016/s0959-8049(01)00098-3,

PubMed Abstract | Crossref Full Text | Google Scholar

33. Elad, S, Raber-Durlacher, JE, Brennan, MT, Saunders, DP, Mank, AP, Zadik, Y, et al. Basic oral care for hematology-oncology patients and hematopoietic stem cell transplantation recipients: a position paper from the joint task force of the multinational Association of Supportive Care in Cancer/International Society of Oral Oncology (MASCC/ISOO) and the European Society for Blood and Marrow Transplantation (EBMT). Support Care Cancer. (2015) 23:223–36. doi: 10.1007/s00520-014-2378-x,

PubMed Abstract | Crossref Full Text | Google Scholar

34. Hong, CHL, Gueiros, LA, Fulton, JS, Cheng, KKF, Kandwal, A, Galiti, D, et al. Systematic review of basic oral care for the management of oral mucositis in cancer patients and clinical practice guidelines. Support Care Cancer. (2019) 27:3949–67. doi: 10.1007/s00520-019-04848-4,

PubMed Abstract | Crossref Full Text | Google Scholar

35. Di Fede, O, Canepa, F, Maniscalco, L, Tozzo, P, Matranga, D, and Giuliana, G. Prevention and the treatment of oral mucositis: the efficacy of sodium bicarbonate vs other agents: a systematic review. BMC Oral Health. (2023) 23:4. doi: 10.1186/s12903-022-02586-4,

PubMed Abstract | Crossref Full Text | Google Scholar

36. Colella, G, Boschetti, CE, Vitagliano, R, Colella, C, Jiao, L, King-Smith, N, et al. Interventions for the prevention of oral mucositis in patients receiving cancer treatment: evidence from randomised controlled trials. Curr Oncol. (2023) 30:967–80. doi: 10.3390/curroncol30010074,

PubMed Abstract | Crossref Full Text | Google Scholar

37. Spielberger, R, Stiff, P, Bensinger, W, Gentile, T, Weisdorf, D, Kewalramani, T, et al. Palifermin for oral mucositis after intensive therapy for hematologic cancers. N Engl J Med. (2004) 351:2590–8. doi: 10.1056/NEJMoa040125,

PubMed Abstract | Crossref Full Text | Google Scholar

38. Lalla, RV, Bowen, J, Barasch, A, Elting, L, Epstein, J, Keefe, DM, et al. MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy. Cancer. (2014) 120:1453–61. doi: 10.1002/cncr.28592,

PubMed Abstract | Crossref Full Text | Google Scholar

39. Cascinu, S, Fedeli, A, Fedeli, SL, and Catalano, G. Oral cooling (cryotherapy), an effective treatment for the prevention of 5-fluorouracil-induced stomatitis. Eur J Cancer B Oral Oncol. (1994) 30B:234–6. doi: 10.1016/0964-1955(94)90003-5,

PubMed Abstract | Crossref Full Text | Google Scholar

40. Gupta, A, Meena, JP, Gupta, AK, Khan, MA, and Seth, R. Oral cryotherapy for the prevention of oral mucositis in children with hematolymphoid malignancies receiving IV methotrexate-based chemotherapy: a randomized controlled trial. Pediatr Blood Cancer. (2025) 72:e31842. doi: 10.1002/pbc.31842,

PubMed Abstract | Crossref Full Text | Google Scholar

41. Worthington, HV, Clarkson, JE, Bryan, G, Furness, S, Glenny, AM, Littlewood, A, et al. Interventions for preventing oral mucositis for patients with cancer receiving treatment. Cochrane Database Syst Rev. (2010) 12:CD000978. doi: 10.1002/14651858.CD000978.pub3

Crossref Full Text | Google Scholar

42. Chaudhry, S, and Ehtesham, Z. Treatment options for cancer patients suffering from oral mucositis. Asian Pac J Cancer Care. (2023) 8:181–4. doi: 10.31557/APJCC.2023.8.1.181

Crossref Full Text | Google Scholar

43. Borowski, GW, Zasadzińska, M, Bakuła, P, and Jałocha, K. Oral mucositis pain management-an overview of current guidelines and clinical approaches. Oncol Clin Pract. (2025). doi: 10.5603/ocp.105698

Crossref Full Text | Google Scholar

44. Suhaimi, N, Abdul Razak, NAH, and Ramli, R. Pain control in oral mucositis according to the severity scale: a narrative literature review. J Clin Med. (2025) 14:4478. doi: 10.3390/jcm14134478,

PubMed Abstract | Crossref Full Text | Google Scholar

45. Peterson, DE, Bensadoun, RJ, and Roila, FESMO Guidelines Working Group. Management of oral and gastrointestinal mucositis: ESMO clinical practice guidelines. Ann Oncol. (2011) 22:vi78–84. doi: 10.1093/annonc/mdr391,

PubMed Abstract | Crossref Full Text | Google Scholar

46. Villa, JF, Strang, A, Owolabi, A, and Ramirez, MF. Addressing pain in oral mucositis: narrative review of current practices and emerging treatments. J Pain Res. (2025) 18:3723–41. doi: 10.2147/JPR.S533351,

PubMed Abstract | Crossref Full Text | Google Scholar

47. McCullough, RW. Barrier therapies supporting the biology of the mucosal barrier-medical devices for common clinical mucosal disorders. Transl Gastroenterol Hepatol. (2021) 6:15. doi: 10.21037/tgh.2020.02.02,

PubMed Abstract | Crossref Full Text | Google Scholar

48. McClave, SA, Martindale, RG, Vanek, VW, McCarthy, M, Roberts, P, Taylor, B, et al. Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.). JPEN J Parenter Enteral Nutr. (2009) 33:277–316. doi: 10.1177/0148607109335234,

PubMed Abstract | Crossref Full Text | Google Scholar

49. Arends, J, Bachmann, P, Baracos, V, Barthelemy, N, Bertz, H, Bozzetti, F, et al. ESPEN guidelines on nutrition in cancer patients. Clin Nutr. (2017) 36:11–48. doi: 10.1016/j.clnu.2016.07.015,

PubMed Abstract | Crossref Full Text | Google Scholar

50. Elad, S, Cheng, KKF, Lalla, RV, Yarom, N, Hong, C, Logan, RM, et al. MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy. Cancer. (2020) 126:4423–31. doi: 10.1002/cncr.33100,

PubMed Abstract | Crossref Full Text | Google Scholar

51. Elsehrawy, MG, Ibrahim, NM, Eltahry, SI, and Elgazzar, SE. Impact of educational guidelines on oral mucositis severity and quality of life in oncology patients receiving chemotherapy: a quasi-experimental study. Asian Pac J Cancer Prev. (2024) 25:2427–38. doi: 10.31557/APJCP.2024.25.7.2427,

PubMed Abstract | Crossref Full Text | Google Scholar

52. Alsadaan, N, and Ramadan, OME. Barriers and facilitators in implementing evidence-based practice: a parallel cross-sectional mixed methods study among nursing administrators. BMC Nurs. (2025) 24:403. doi: 10.1186/s12912-025-03059-z,

PubMed Abstract | Crossref Full Text | Google Scholar

53. Wang, T, Tan, JY, Liu, XL, and Zhao, I. Barriers and enablers to implementing clinical practice guidelines in primary care: an overview of systematic reviews. BMJ Open. (2023) 13:e062158. doi: 10.1136/bmjopen-2022-062158,

PubMed Abstract | Crossref Full Text | Google Scholar

54. McArthur, C, Bai, Y, Hewston, P, Giangregorio, L, Straus, S, and Papaioannou, A. Barriers and facilitators to implementing evidence-based guidelines in long-term care: a qualitative evidence synthesis. Implement Sci. (2021) 16:70. doi: 10.1186/s13012-021-01140-0,

PubMed Abstract | Crossref Full Text | Google Scholar

55. Zhang, L, Luo, Y, Long, J, Yin, Y, Fu, Q, Wang, L, et al. Enhancing standardized practices for oral mucositis prevention in pediatric hematopoietic stem cell transplantation: a best practice implementation project. Risk Manag Healthc Policy. (2024) 17:1909–20. doi: 10.2147/RMHP.S471877,

PubMed Abstract | Crossref Full Text | Google Scholar

56. Agussalim,. The effect of oral care intervention in mucositis management among pediatric cancer patients: an updated systematic review. J Multidiscip Healthc. (2024) 17:4071–2. doi: 10.2147/JMDH.S488007,

PubMed Abstract | Crossref Full Text | Google Scholar

57. Hogan, R. Implementation of an oral care protocol and its effects on oral mucositis. J Pediatr Oncol Nurs. (2009) 26:125–35. doi: 10.1177/1043454209334356,

PubMed Abstract | Crossref Full Text | Google Scholar

58. Farrington, M, Cullen, L, and Dawson, C. Evidence-based oral care for oral mucositis. ORL Head Neck Nurs. (2013) 31:6–15.

Google Scholar

59. Majhail, NS, Giralt, S, Bonagura, A, Crawford, S, Farnia, S, Omel, JL, et al. Guidelines for defining and implementing standard episode of care for hematopoietic stem cell transplantation within the context of clinical trials. Biol Blood Marrow Transplant. (2015) 21:583–8. doi: 10.1016/j.bbmt.2014.12.030

Crossref Full Text | Google Scholar

60. Kazak, AE, Swain, AM, Canter, K, Vega, G, Joffe, N, Deatrick, JA, et al. A psychosocial clinical care pathway for pediatric hematopoietic stem cell transplantation. Pediatr Blood Cancer. (2019) 66:e27889. doi: 10.1002/pbc.27889,

PubMed Abstract | Crossref Full Text | Google Scholar

61. Fang, Y, Liu, MJ, Zhang, WW, Xie, C, and Liu, ZZ. Nutrition support practices of hematopoietic stem cell transplantation centers in mainland China. Curr Med Sci. (2020) 40:691–8. doi: 10.1007/s11596-020-2231-z,

PubMed Abstract | Crossref Full Text | Google Scholar

62. Nurhidayah, I, Rustina, Y, Hastono, SP, and Mediani, HS. The effect of honey in oral care intervention against chemotherapy-induced mucositis in pediatric cancer patients: a pilot study. BMC Complement Med Ther. (2024) 24:415. doi: 10.1186/s12906-024-04710-z

Crossref Full Text | Google Scholar

63. Kaisha, P, Li, X, Tang, Y, and Zheng, Y. Clinical pharmacists and nurses in the management of oral mucositis in head and neck cancer patients during antineoplastic therapy: a scoping review. SAGE Open Med. (2025) 13:20503121251339581. doi: 10.1177/20503121251339581

Crossref Full Text | Google Scholar

64. Tao, Y, Zeng, X, and Mao, H. Predictive models for chemotherapy-induced oral mucositis: a systematic review. Front Oncol. (2025) 15:1608505. doi: 10.3389/fonc.2025.1608505,

PubMed Abstract | Crossref Full Text | Google Scholar

65. Amiri Khosroshahi, R, Talebi, S, Zeraattalab-Motlagh, S, Imani, H, Rashidi, A, Travica, N, et al. Nutritional interventions for the prevention and treatment of cancer therapy-induced oral mucositis: an umbrella review of systematic reviews and meta-analysis. Nutr Rev. (2023) 81:1200–12. doi: 10.1093/nutrit/nuac105,

PubMed Abstract | Crossref Full Text | Google Scholar

66. Guberti, M, Botti, S, Fusco, A, Caffarri, C, Cavuto, S, Savoldi, L, et al. Stem cell transplantation patients receiving a novel oral care protocol for oral mucositis prevention and treatment: patient-reported outcomes and quality of life. Support Care Cancer. (2022) 30:6317–25. doi: 10.1007/s00520-022-07073-8,

PubMed Abstract | Crossref Full Text | Google Scholar

67. Bruno, JS, Al-Qadami, GH, Laheij, AMGA, Bossi, P, Fregnani, ER, and Wardill, HR. From pathogenesis to intervention: the importance of the microbiome in oral mucositis. Int J Mol Sci. (2023) 24:8274. doi: 10.3390/ijms24098274,

PubMed Abstract | Crossref Full Text | Google Scholar

68. Guan, Z, Zhang, J, Jiang, N, Tian, M, Wang, H, and Liang, B. Efficacy of mesenchymal stem cell therapy in rodent models of radiation-induced xerostomia and oral mucositis: a systematic review. Stem Cell Res Ther. (2023) 14:82. doi: 10.1186/s13287-023-03301-y

Crossref Full Text | Google Scholar

69. Lin, TH, Wang, YM, and Huang, CY. Effects of a mobile oral care app on oral mucositis, pain, nutritional status, and quality of life in patients with head and neck cancer: a quasi-experimental study. Int J Nurs Pract. (2022) 28:e13042. doi: 10.1111/ijn.13042,

PubMed Abstract | Crossref Full Text | Google Scholar

70. Parra-Rojas, S, Cassol Spanemberg, J, Del Mar Díaz-Robayna, N, Peralta-Mamani, M, and Velázquez Cayón, RT. Assessing the cost-effectiveness of photobiomodulation for oral mucositis prevention and treatment: a systematic review. Biomedicine. (2024) 12:2366. doi: 10.3390/biomedicines12102366,

PubMed Abstract | Crossref Full Text | Google Scholar

71. Cummings, GG, Lee, SD, and Tate, KC. The evolution of oncology nursing: leading the path to change. Can Oncol Nurs J. (2018) 28:314–7.

Google Scholar

72. Emfield Rowett, K, and Christensen, D. Oncology nurse navigation: expansion of the navigator role through telehealth. Clin J Oncol Nurs. (2020) 24:24–31. doi: 10.1188/20.CJON.S1.24-31,

PubMed Abstract | Crossref Full Text | Google Scholar

73. Eilers, J, and Million, R. Clinical update: prevention and management of oral mucositis in patients with cancer. Semin Oncol Nurs. (2011) 27:e1–e16. doi: 10.1016/j.soncn.2011.08.001,

PubMed Abstract | Crossref Full Text | Google Scholar

74. Stone, R, Fliedner, MC, and Smiet, AC. Management of oral mucositis in patients with cancer. Eur J Oncol Nurs. (2005) 9:S24–32. doi: 10.1016/j.ejon.2005.08.004,

PubMed Abstract | Crossref Full Text | Google Scholar

75. Chan, RJ, Knowles, R, Hunter, S, Conroy, T, Tieu, M, and Kitson, A. From evidence-based practice to knowledge translation: what is the difference? What are the roles of nurse leaders? Semin Oncol Nurs. (2023) 39:151363. doi: 10.1016/j.soncn.2022.151363,

PubMed Abstract | Crossref Full Text | Google Scholar

76. Välimäki, M, Hu, S, Lantta, T, Hipp, K, Varpula, J, Chen, J, et al. The impact of evidence-based nursing leadership in healthcare settings: a mixed methods systematic review. BMC Nurs. (2024) 23:452. doi: 10.1186/s12912-024-02096-4,

PubMed Abstract | Crossref Full Text | Google Scholar

77. Kenyon, M, and Murray, J. The roles of the HCT nurse. In: Sureda, A., Corbacioglu, S., Greco, R., Kröger, N., and Carreras, E. editors. The EBMT handbook: hematopoietic cell transplantation and cellular therapies. 8th. Cham (CH): Springer; 2024. Chapter 32.

Google Scholar

78. Yates, P. Oncology nursing leadership around the world. Ann Palliat Med. (2023) 12:999–1003. doi: 10.21037/apm-22-1145,

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: clinical pathway, evidence-based nursing, hematopoietic stem cell transplantation, management strategy, multidisciplinary collaboration, oral mucositis, patient-centered care, supportive care

Citation: Cui M (2026) Evidence-based nursing strategies for the prevention and management of oral mucositis in hematopoietic stem cell transplantation patients. Front. Med. 13:1737301. doi: 10.3389/fmed.2026.1737301

Received: 01 November 2025; Revised: 25 December 2025; Accepted: 12 January 2026;
Published: 26 January 2026.

Edited by:

Jacqueline W. Mays, National Institutes of Health (NIH), United States

Reviewed by:

Jane Fall-Dickson, Uniformed Services University, United States

Copyright © 2026 Cui. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Min Cui, TWluQ3VpMDJAaG90bWFpbC5jb20=

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