FMT for Feeding Intolerance Due to Gastrointestinal Dysfunction in Critically Ill Patients (FMT-FIT)
Fecal Microbiota Transplantation for Feeding Intolerance Due to Gastrointestinal Dysfunction in Critically Ill Patients: A Single-Center, Single-Blind, Randomized Controlled Trial
Critically ill patients admitted to the intensive care unit (ICU) frequently present with gastrointestinal dysfunction and are at elevated risk of malnutrition. Gastrointestinal dysfunction is correlated with adverse clinical outcomes, including prolonged mechanical ventilation duration, extended ICU length of stay, and increased 90-day mortality.
In critically ill ICU patients, severe gut microbiota dysbiosis and intestinal barrier impairment may occur due to the burden of primary critical illnesses, as well as the administration of proton pump inhibitors and antibiotics. This cascade contributes to a high prevalence of gastrointestinal dysfunction, alongside profound gut-derived systemic inflammatory responses and organ damage. Given the pivotal role of gut microbiota in maintaining intestinal homeostasis, fecal microbiota transplantation (FMT) holds promise as a novel therapeutic strategy for enteral feeding intolerance secondary to gastrointestinal dysfunction in critically ill ICU patients.
This study intends to deliver FMT via a nasojejunal tube to critically ill patients with gastrointestinal dysfunction admitted to the ICU. Its objectives are to evaluate the intervention's effects on gastrointestinal function recovery and the alleviation of enteral feeding intolerance, while also assessing its impacts on intestinal barrier function, gut microbiota composition and metabolic profiles, serum metabolite signatures, immune-inflammatory responses (including lymphocyte subsets, cytokines, C-reactive protein, and procalcitonin), ICU delirium, ICU sleep quality, and clinical outcomes (encompassing ICU mortality, in-hospital mortality, 28-day all-cause mortality, 90-day all-cause mortality, 90-day readmission rate, and 90-day incidence of secondary infections).
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Jiancheng Zhang
- 電話番号:+86-13554105815
- メール:zhjcheng1@126.com
研究場所
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Hubei
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Wuhan、Hubei、中国、460022
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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コンタクト:
- Jiancheng Zhang
- 電話番号:+86-13554105815
- メール:zhjcheng1@126.com
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Aged 18 to 70 years inclusive, regardless of ethnicity or gender;
- Female participants are either non-fertile (i.e., physiologically incapable of pregnancy, including women with ≥2 years of menopause) or have no pregnancy plans;
- Have been admitted to the ICU for ≥24 hours;
- Expected ICU stay ≥7 days after study enrollment;
- Screened positive for ≥1 manifestation of gastrointestinal dysfunction (intra-abdominal hypertension [IAH], massive gastric retention, diarrhea, lower gastrointestinal paralysis, bowel dilatation); enteral nutrition is then implemented under the guidance of the enteral feeding intolerance (FI) score, and participants with persistent FI after a 3-day trial are formally enrolled;
- Participants can actively cooperate or passively complete relevant examinations and follow-up procedures;
- Have signed a written informed consent form.
Exclusion Criteria:
- Severe systemic infection in the early resuscitation phase, with hemodynamic instability, insufficient tissue perfusion, or severe fluid-electrolyte and acid-base imbalances;
- Patients assessed by clinicians as having a high risk of death within 5 days, or those with restricted treatment decisions;
- Active gastrointestinal bleeding, perforation, or other conditions with severe intestinal barrier impairment;
- Patients unable to tolerate enteral nutrition meeting 50% of caloric requirements due to severe diarrhea, significant fibrotic intestinal stenosis, massive gastrointestinal bleeding, or high-output enterocutaneous fistula;
- Planned or recent abdominal surgery (within 14 days prior to enrollment);
- Current diagnosis of fulminant colitis or toxic megacolon;
- Neutropenia (neutrophil count < 1500 cells/µL);
- Patients with congenital or acquired immunodeficiency disorders;
- Recent receipt of high-risk immunosuppressive or cytotoxic agents, e.g., rituximab, doxorubicin, or medium-to-high-dose corticosteroids (≥ 20 mg/day prednisone equivalent) for a duration of > 4 weeks;
- Pregnant or lactating women;
- Participation in another clinical trial as a subject at the time of enrollment or within 3 months prior to enrollment;
- Doubtful validity of informed consent: subjects with mental illness, intellectual disability, poor motivation, or other factors that restrict the validity of informed consent for participation in this study.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
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介入なし:Control group
Patients received standard ICU care.
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実験的:FMT intervention group
Patients received FMT via a nasojejunal tube in addition to standard ICU care.
Specifically, 50-100 mL of intestinal microbiota suspension was administered daily via the nasojejunal tube between 11:00 and 13:00 for three consecutive days.
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Patients received FMT via a nasojejunal tube in addition to standard ICU care.
Specifically, 50-100 mL of intestinal microbiota suspension was administered daily via the nasojejunal tube between 11:00 and 13:00 for three consecutive days.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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Enteral nutrition FI improvement rate
時間枠:24, 48, 72, 96, and 120 hours after study enrollment
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24, 48, 72, 96, and 120 hours after study enrollment
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Gut microbiota composition as well as α and β diversity measured from rectal swabs by 16S rRNA gene sequencing
時間枠:24-0 hours and 120 hours after study enrollment
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24-0 hours and 120 hours after study enrollment
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Fecal metabolite profile (by untargeted LC-MS) from rectal swabs
時間枠:24-0 hours and 120 hours after study enrollment
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24-0 hours and 120 hours after study enrollment
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Serum metabolite profile (by untargeted LC-MS)
時間枠:24-0 hours and 120 hours after study enrollment
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24-0 hours and 120 hours after study enrollment
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Serum level of citrulline
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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APACHE II score
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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SOFA score
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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Cumulative intravenous dose of vasopressor agents (including norepinephrine, epinephrine, dobutamine, etc.)
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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Serum level of C-reactive protein
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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Serum level of procalcitonin
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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Peripheral blood level of cytokines (including IL-6, IL-17, TNF-α, IL-10, IL-1β, etc.)
時間枠:0 and 120 hours after study enrollment
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0 and 120 hours after study enrollment
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Peripheral blood lymphocyte subsets (including CD4+ T, CD8+ T, B lymphocytes, NK cells, etc.)
時間枠:0, 24, 48, 72, 96, and 120 hours after study enrollment
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0, 24, 48, 72, 96, and 120 hours after study enrollment
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ICU mortality
時間枠:Within 28 days after study enrollment
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Within 28 days after study enrollment
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In-hospital mortality
時間枠:Within 60 days after study enrollment
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Within 60 days after study enrollment
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28-day all-cause mortality
時間枠:Within 28 days after study enrollment
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Within 28 days after study enrollment
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90-day all-cause mortality
時間枠:Within 90 days after study enrollment
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Within 90 days after study enrollment
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90-day readmission rate
時間枠:Within 90 days after study enrollment
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Within 90 days after study enrollment
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90-day secondary infection rate
時間枠:Within 90 days after study enrollment
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Within 90 days after study enrollment
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協力者と研究者
出版物と役立つリンク
一般刊行物
- Piton G, Manzon C, Cypriani B, Carbonnel F, Capellier G. Acute intestinal failure in critically ill patients: is plasma citrulline the right marker? Intensive Care Med. 2011 Jun;37(6):911-7. doi: 10.1007/s00134-011-2172-x. Epub 2011 Mar 12.
- Uhde M, Ajamian M, Caio G, De Giorgio R, Indart A, Green PH, Verna EC, Volta U, Alaedini A. Intestinal cell damage and systemic immune activation in individuals reporting sensitivity to wheat in the absence of coeliac disease. Gut. 2016 Dec;65(12):1930-1937. doi: 10.1136/gutjnl-2016-311964. Epub 2016 Jul 25.
- Schluter J, Peled JU, Taylor BP, Markey KA, Smith M, Taur Y, Niehus R, Staffas A, Dai A, Fontana E, Amoretti LA, Wright RJ, Morjaria S, Fenelus M, Pessin MS, Chao NJ, Lew M, Bohannon L, Bush A, Sung AD, Hohl TM, Perales MA, van den Brink MRM, Xavier JB. The gut microbiota is associated with immune cell dynamics in humans. Nature. 2020 Dec;588(7837):303-307. doi: 10.1038/s41586-020-2971-8. Epub 2020 Nov 25.
- McClave SA, Patel J, Bhutiani N. Should fecal microbial transplantation be used in the ICU? Curr Opin Crit Care. 2018 Apr;24(2):105-111. doi: 10.1097/MCC.0000000000000489.
- Heming N, Carlier R, Prigent H, Mekki A, Jousset C, Lofaso F, Ambrosi X, Bounab R, Maxime V, Mansart A, Crenn P, Moine P, Foltzer F, Cuenoud B, Konz T, Corthesy J, Beaumont M, Hartweg M, Roessle C, Preiser JC, Breuille D, Annane D. Effect of an enteral amino acid blend on muscle and gut functionality in critically ill patients: a proof-of-concept randomized controlled trial. Crit Care. 2022 Nov 17;26(1):358. doi: 10.1186/s13054-022-04232-5.
- Yadegar A, Bar-Yoseph H, Monaghan TM, Pakpour S, Severino A, Kuijper EJ, Smits WK, Terveer EM, Neupane S, Nabavi-Rad A, Sadeghi J, Cammarota G, Ianiro G, Nap-Hill E, Leung D, Wong K, Kao D. Fecal microbiota transplantation: current challenges and future landscapes. Clin Microbiol Rev. 2024 Jun 13;37(2):e0006022. doi: 10.1128/cmr.00060-22. Epub 2024 May 8.
- Beyi AF, Wannemuehler M, Plummer PJ. Impacts of Gut Microbiota on the Immune System and Fecal Microbiota Transplantation as a Re-Emerging Therapy for Autoimmune Diseases. Antibiotics (Basel). 2022 Aug 12;11(8):1093. doi: 10.3390/antibiotics11081093.
- Arunachala Murthy T, Chapple LS, Lange K, Marathe CS, Horowitz M, Peake SL, Chapman MJ. Gastrointestinal dysfunction during enteral nutrition delivery in intensive care unit (ICU) patients: Risk factors, natural history, and clinical implications. A post-hoc analysis of The Augmented versus Routine approach to Giving Energy Trial (TARGET). Am J Clin Nutr. 2022 Aug 4;116(2):589-598. doi: 10.1093/ajcn/nqac113.
- Deane A, Chapman MJ, Fraser RJ, Bryant LK, Burgstad C, Nguyen NQ. Mechanisms underlying feed intolerance in the critically ill: implications for treatment. World J Gastroenterol. 2007 Aug 7;13(29):3909-17. doi: 10.3748/wjg.v13.i29.3909.
- Nguyen NQ, Fraser RJ, Chapman MJ, Bryant LK, Holloway RH, Vozzo R, Wishart J, Feinle-Bisset C, Horowitz M. Feed intolerance in critical illness is associated with increased basal and nutrient-stimulated plasma cholecystokinin concentrations. Crit Care Med. 2007 Jan;35(1):82-8. doi: 10.1097/01.CCM.0000250317.10791.6C.
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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最終確認日
詳しくは
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