Suppr超能文献

成人烧伤的病理生理反应。

Pathophysiological Response to Burn Injury in Adults.

机构信息

Department of Surgery, Division of Plastic Surgery, University of Toronto, Toronto, Ontario, Canada; Department of Immunology, University of Toronto, Toronto, Ontario, Canada; Ross Tilley Burn Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; and Sunnybrook Research Institute, Toronto, Ontario, Canada.

出版信息

Ann Surg. 2018 Mar;267(3):576-584. doi: 10.1097/SLA.0000000000002097.

Abstract

OBJECTIVE

The aim of this study was to compare the hypermetabolic, and inflammatory trajectories in burned adults to gain insight into the pathophysiological alterations and outcomes after injury.

SUMMARY OF BACKGROUND DATA

Burn injury leads to a complex response that is associated with hypermetabolism, morbidity, and mortality. The underlying pathophysiology and the correlations between humoral changes and organ function have not been well delineated in adult burn patients.

METHODS

Burned adult patients (n = 1288) admitted to our center from 2006 to 2016 were enrolled in this prospective study. Demographics, clinical data, metabolic and inflammatory markers, hypermetabolism, organ function, and clinical outcomes were obtained throughout acute hospitalization. We then stratified patients according to burn size (<20%, 20% to 40%, and >40% total body surface area [TBSA]) and compared biomedical profiles and clinical outcomes for these patients.

RESULTS

Burn patients were hypermetabolic with elevated resting energy expenditure (REE) associated with increased browning of white adipose tissue from weeks 2 to 4. Hyperglycemia and hyperinsulinemia peaked 7 to 14 days after injury. Oral glucose tolerance and insulin resistance (QUICKI, HOMA2) tests further confirmed these findings with similar areas under the curve for moderate (20% to 40% TBSA) and severe burn (>40% TBSA). Lipid metabolism in sera revealed elevated pro-inflammatory stearic and linoleic acid, with complementary increases in anti-inflammatory free fatty acids. Similar increases were observed for inflammatory cytokines, chemokines, and metabolic hormones. White adipose tissue from the site of injury had increased ER stress, mitochondrial damage, and inflammasome activity, which was exacerbated with increasing burn severity.

CONCLUSIONS

In this large prospective trial, we delineated the complexity of the pathophysiologic responses postburn in adults and concluded that these profound responses are time and burn size dependent. Patients with medium-size (20% to 40% TBSA) burn demonstrated a very robust response that is similar to large burns.

摘要

目的

本研究旨在比较烧伤成年人的高代谢和炎症轨迹,以深入了解损伤后的病理生理改变和结局。

摘要背景数据

烧伤导致的复杂反应与高代谢、发病率和死亡率有关。尚未在成人烧伤患者中充分描述潜在的病理生理学以及体液变化与器官功能之间的相关性。

方法

本前瞻性研究纳入了 2006 年至 2016 年期间我院收治的 1288 例烧伤成年患者。在急性住院期间获得了患者的人口统计学、临床数据、代谢和炎症标志物、高代谢、器官功能和临床结局。然后,我们根据烧伤面积(<20%、20%至 40%和>40%总体表面积[TBSA])对患者进行分层,并比较这些患者的生物医学特征和临床结局。

结果

烧伤患者存在高代谢,静息能量消耗(REE)增加,与伤后第 2 至 4 周白色脂肪组织的褐色化有关。伤后 7 至 14 天出现高血糖和高胰岛素血症。口服葡萄糖耐量和胰岛素抵抗(QUICKI、HOMA2)检测进一步证实了这些发现,中等程度(20%至 40% TBSA)和严重烧伤(>40% TBSA)的曲线下面积相似。血清中的脂质代谢显示促炎的硬脂酸和亚油酸升高,同时抗炎的游离脂肪酸也相应增加。炎症细胞因子、趋化因子和代谢激素也观察到类似的增加。损伤部位的白色脂肪组织出现内质网应激、线粒体损伤和炎症小体活性增加,且随着烧伤严重程度的增加而加剧。

结论

在这项大型前瞻性试验中,我们描述了成年患者烧伤后病理生理反应的复杂性,并得出结论,这些深刻的反应是时间和烧伤面积依赖性的。中等大小(20%至 40% TBSA)烧伤患者表现出非常强烈的反应,与大面积烧伤相似。

相似文献

1
Pathophysiological Response to Burn Injury in Adults.
Ann Surg. 2018 Mar;267(3):576-584. doi: 10.1097/SLA.0000000000002097.
2
Burn size determines the inflammatory and hypermetabolic response.
Crit Care. 2007;11(4):R90. doi: 10.1186/cc6102.
3
Pathophysiologic response to severe burn injury.
Ann Surg. 2008 Sep;248(3):387-401. doi: 10.1097/SLA.0b013e3181856241.
6
Is there a difference in clinical outcomes, inflammation, and hypermetabolism between scald and flame burn?
Pediatr Crit Care Med. 2011 Nov;12(6):e275-81. doi: 10.1097/PCC.0b013e31820ac2c5.
7
Mouse models in burns research: Characterisation of the hypermetabolic response to burn injury.
Burns. 2020 May;46(3):663-674. doi: 10.1016/j.burns.2019.09.014. Epub 2019 Oct 10.
8
Long-term persistance of the pathophysiologic response to severe burn injury.
PLoS One. 2011;6(7):e21245. doi: 10.1371/journal.pone.0021245. Epub 2011 Jul 18.
9
Burn Induces Browning of the Subcutaneous White Adipose Tissue in Mice and Humans.
Cell Rep. 2015 Nov 24;13(8):1538-44. doi: 10.1016/j.celrep.2015.10.028. Epub 2015 Nov 12.
10
Temporal cytokine profiles in severely burned patients: a comparison of adults and children.
Mol Med. 2008 Sep-Oct;14(9-10):553-60. doi: 10.2119/2007-00132.Finnerty.

引用本文的文献

1
Review of the 100 Most Cited Articles in from 2014 to 2024: A Bibliometric Analysis.
Eur Burn J. 2025 Jun 10;6(2):33. doi: 10.3390/ebj6020033.
4
Metabolic response to burn injury: a comprehensive bibliometric study.
Front Med (Lausanne). 2025 Jan 3;11:1451371. doi: 10.3389/fmed.2024.1451371. eCollection 2024.
5
Factors influencing vancomycin trough concentration in burn patients: a single center retrospective study.
Front Pharmacol. 2024 Dec 12;15:1377930. doi: 10.3389/fphar.2024.1377930. eCollection 2024.
6
Decoding burn trauma: biomarkers for early diagnosis of burn-induced pathologies.
Biomark Res. 2024 Dec 23;12(1):160. doi: 10.1186/s40364-024-00707-5.
7
Longitudinal analysis of ARDS variability and biomarker predictive power in burn patients.
Sci Rep. 2024 Nov 2;14(1):26376. doi: 10.1038/s41598-024-77188-x.
8
New-onset autoantibodies to selenoprotein P following severe burn injury.
Front Immunol. 2024 Aug 8;15:1422781. doi: 10.3389/fimmu.2024.1422781. eCollection 2024.
10
Systemic immune response of burns from the acute to chronic phase.
Acute Med Surg. 2024 Jun 18;11(1):e976. doi: 10.1002/ams2.976. eCollection 2024 Jan-Dec.

本文引用的文献

1
Burned Adults Develop Profound Glucose Intolerance.
Crit Care Med. 2016 Jun;44(6):1059-66. doi: 10.1097/CCM.0000000000001605.
2
Impaired Immune Response in Elderly Burn Patients: New Insights Into the Immune-senescence Phenotype.
Ann Surg. 2016 Jul;264(1):195-202. doi: 10.1097/SLA.0000000000001408.
3
Pathophysiologic Response to Burns in the Elderly.
EBioMedicine. 2015 Jul 31;2(10):1536-48. doi: 10.1016/j.ebiom.2015.07.040. eCollection 2015 Oct.
4
Burn Induces Browning of the Subcutaneous White Adipose Tissue in Mice and Humans.
Cell Rep. 2015 Nov 24;13(8):1538-44. doi: 10.1016/j.celrep.2015.10.028. Epub 2015 Nov 12.
5
Browning of Subcutaneous White Adipose Tissue in Humans after Severe Adrenergic Stress.
Cell Metab. 2015 Aug 4;22(2):219-27. doi: 10.1016/j.cmet.2015.06.022.
6
The systemic immune response to trauma: an overview of pathophysiology and treatment.
Lancet. 2014 Oct 18;384(9952):1455-65. doi: 10.1016/S0140-6736(14)60687-5. Epub 2014 Oct 17.
8
Hypoglycemia is associated with increased postburn morbidity and mortality in pediatric patients.
Crit Care Med. 2014 May;42(5):1221-31. doi: 10.1097/CCM.0000000000000138.
9
Mitochondrial cardiolipin is required for Nlrp3 inflammasome activation.
Immunity. 2013 Aug 22;39(2):311-323. doi: 10.1016/j.immuni.2013.08.001. Epub 2013 Aug 15.
10
Mild obesity is protective after severe burn injury.
Ann Surg. 2013 Dec;258(6):1119-29. doi: 10.1097/SLA.0b013e3182984d19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验