Prevalence and risk factors of postoperative delirium after spinal surgery: a meta-analysis

Hua Gao, Hui-Juan Ma, Ying-Jia Li, Ci Yin, Zheng Li, Hua Gao, Hui-Juan Ma, Ying-Jia Li, Ci Yin, Zheng Li

Abstract

Objective: Postoperative delirium (POD) was common after spinal surgery, but the main findings in previous studies remained conflicting. This current meta-analysis was aimed at exploring the prevalence and risk factors of POD after spinal surgery.

Methods: PubMed and Embase were searched from inception to June 2019. Studies which reported the prevalence and risk factors of POD after spinal surgery were included. STATA version 12.0 was employed to analyze the pooled data. Statistical heterogeneity across included studies was identified using the I2 statistics.

Results: A total of 28 studies with 588,732 patients were included in the meta-analysis. The pooled prevalence of POD after spinal surgery was 0.85% (95%CI, 0.83-0.88%) with substantial heterogeneity (I2 = 97.3%). The central nervous system disorder (OR 4.73; 95%CI, 4.30-5.19) was a strong predictor for POD, whereas age (OR 1.16; 95%CI, 1.05-2.47; I2 = 99.2%) and blood loss (OR 1.10; 95%CI, 1.01-1.20; I2 = 93.3%) were weaker predictors. The funnel plot and statistical tests suggested that there existed potential publication bias, but the trim and fill method indicated that the pooled prevalence basically kept stable after adding two "missing" studies.

Conclusions: The pooled POD after spinal surgery ranges from 0.83 to 0.88%. The central nervous system disorder, age, and blood loss were potential risk factors for POD.

Keywords: Delirium; Meta-analysis; Prevalence, Risk factor; Spinal surgery.

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Flow diagram of the selection of reports for this meta-analysis
Fig. 2
Fig. 2
Forest plot for incidence of postoperative delirium after spinal surgery. a Fixed-effect model. b Random-effects model
Fig. 3
Fig. 3
Funnel plot of postoperative delirium after spinal surgery (Egger’s test, p = 0.797 and Begg’s test, p = 0.008). a Adjusted funnel plot of postoperative delirium after spinal surgery after adding two “missing” studies from the “trim and fill” analysis (b)

References

    1. Inouye SK, Westendorp RG, Saczynski JS. Delirium in elderly people. Lancet. 2014;383:911–922. doi: 10.1016/S0140-6736(13)60688-1.
    1. Bryczkowski SB, Lopreiato MC, Yonclas PP, et al. Delirium prevention program in the surgical intensive care unit improved the outcomes of older adults. J Surg Res. 2014;190:280–288. doi: 10.1016/j.jss.2014.02.044.
    1. Oh ES, Fong TG, Hshieh TT, et al. Delirium in older persons: advances in diagnosis and treatment. JAMA. 2017;318:1161–1174. doi: 10.1001/jama.2017.12067.
    1. Bhattacharya B, Maung A, Barre K, et al. Postoperative delirium is associated with increased intensive care unit and hospital length of stays after liver transplantation. J Surg Res. 2017;207:223–228. doi: 10.1016/j.jss.2016.08.084.
    1. Ashley KE, Hillegass WB. Costs of postoperative delirium with transcatheter aortic valve replacement: improved yet still present. Catheter Cardiovasc Interv. 2019;93:1137. doi: 10.1002/ccd.28276.
    1. Daiello LA, Racine AM, Yun Gou R, et al. Postoperative delirium and postoperative cognitive dysfunction: overlap and divergence. Anesthesiology. 2019.
    1. Vlisides P, and Avidan M. Recent advances in preventing and managing postoperative delirium. F1000Res. 2019; 8.
    1. Shi C, Yang C, Gao R. et al. Risk factors for delirium after spinal surgery: a meta-analysis. .
    1. Liao Y, Flaherty JH, Yue J, et al. The incidence of delirium after cardiac surgery in the elderly: protocol for a systematic review and meta-analysis. BMJ Open. 2017;7:e014726. doi: 10.1136/bmjopen-2016-014726.
    1. Texakalidis P, Tzoumas A, Giannopoulos S, et al. Risk factors for restenosis following carotid revascularization: a meta-analysis of hazard ratios. World Neurosurg. 2019.
    1. Gul W, Fuller HR, Wright H, et al. A systematic review and meta-analysis of the effectiveness of surgical decompression in treating patients with malignant middle cerebral artery infarction. World Neurosurg. 2018;120:e902–e920. doi: 10.1016/j.wneu.2018.08.189.
    1. Hong EP, Kim BJ, Jeon JP, et al. Association of endothelin receptor type A with intracranial aneurysm in 20,609 East Asians: an updated meta-analysis. World Neurosurg. 2019.
    1. Kim BS, Kim KH, Lee MH, et al. Stereotactic radiosurgery for brainstem cavernous malformations: an updated systematic review and meta-analysis. World Neurosurg. 2019.
    1. Lu VM, Wahood W, Akinduro OO, et al. Four independent predictors of postoperative seizures after meningioma surgery: a meta-analysis. World Neurosurg. 2019.
    1. Begg CB, Mazumdar M. Operating characteristics of a rank correlation test for publication bias. Biometrics. 1994;50:1088–1101. doi: 10.2307/2533446.
    1. Weng S, Wang W, Wei Q, et al. Effect of tranexamic acid in patients with traumatic brain injury: a systematic review and meta-analysis. World Neurosurg. 2019;123:128–135. doi: 10.1016/j.wneu.2018.11.214.
    1. Zhang Y, Liu W, Xu J. Prognostic utility and clinical significance of lysyl oxidase-like 2 protein expression in digestive system cancers. J Cell Physiol. 2019.
    1. Adogwa O, Elsamadicy AA, Vuong VD, et al. Association between baseline cognitive impairment and postoperative delirium in elderly patients undergoing surgery for adult spinal deformity. Journal of neurosurgery. Spine. 2018;28:103–108. doi: 10.3171/2017.5.SPINE161244.
    1. Bollen L, de Ruiter Gc Fau - Pondaag W, Pondaag W Fau - Arts MP, et al. Risk factors for survival of 106 surgically treated patients with symptomatic spinal epidural metastases.
    1. Brown CH, LaFlam A, Max L, et al. Delirium after spine surgery in older adults: incidence, risk factors, and outcomes. Journal of the American Geriatrics Society. 2016;64:2101–2108. doi: 10.1111/jgs.14434.
    1. Cho KJ, Suk SI, Park SR, et al. Complications in posterior fusion and instrumentation for degenerative lumbar scoliosis. Spine. 2007;32:2232–2237. doi: 10.1097/BRS.0b013e31814b2d3c.
    1. Cui XP, Jing ZZ, Song JF, et al. A retrospective study on risk factors associated with postoperative delirium in elderly patients with spinal operation. Zhongguo gu shang = China journal of orthopaedics and traumatology. 2019; 32: 549-554.
    1. Dea N, Versteeg A, Fisher C, et al. Adverse events in emergency oncological spine surgery: a prospective analysis. Journal of neurosurgery. Spine. 2014;21:698–703. doi: 10.3171/2014.7.SPINE131007.
    1. Elsamadicy AA, Adogwa O, Lydon E, et al. Depression as an independent predictor of postoperative delirium in spine deformity patients undergoing elective spine surgery. Journal of neurosurgery. Spine. 2017;27:209–214. doi: 10.3171/2017.4.SPINE161012.
    1. Elsamadicy AA, Charalambous LT, Sergesketter AR, et al. Intraoperative ketamine may increase risk of post-operative delirium after complex spinal fusion for adult deformity correction. Journal of spine surgery (Hong Kong). 2019; 5: 79-87.
    1. Fineberg SJ. Nandyala Sv Fau - Marquez-Lara A, Marquez-Lara A Fau - Oglesby M, et al. Incidence and risk factors for postoperative delirium after lumbar spine surgery. .
    1. Gao R, Yang ZZ, Li M, et al. Probable risk factors for postoperative delirium in patients undergoing spinal surgery. European Spine Journal. 2008;17:1531–1537. doi: 10.1007/s00586-008-0771-1.
    1. Glennie RA, Ailon T, Yang K, et al. Incidence, impact, and risk factors of adverse events in thoracic and lumbar spine fractures: an ambispective cohort analysis of 390 patients. The spine journal : official journal of the North American Spine Society. 2015;15:629–637. doi: 10.1016/j.spinee.2014.11.016.
    1. Jiang X, Chen D, Lou Y, et al. Risk factors for postoperative delirium after spine surgery in middle- and old-aged patients. Aging clinical and experimental research. 2017;29:1039–1044. doi: 10.1007/s40520-016-0640-4.
    1. Kawaguchi Y, Kanamori M, Ishihara H, et al. Postoperative delirium in spine surgery. The spine journal : official journal of the North American Spine Society. 2006;6:164–169. doi: 10.1016/j.spinee.2005.06.010.
    1. Kelly A, Batke JN, Boyd M, et al. Prospective analysis of adverse events in surgical treatment of degenerative spondylolisthesis. Spine Journal. 2012;12:108S–109S. doi: 10.1016/j.spinee.2012.08.296.
    1. Kim KH, Kang SY, Shin DA, et al. Parkinson’s disease-related non-motor features as risk factors for post-operative delirium in spinal surgery. PLoS ONE. 2018;13.
    1. Kin K, Yasuhara T, Tomita Y, et al. SF-36 scores predict postoperative delirium after surgery for cervical spondylotic myelopathy. Journal of neurosurgery. Spine. 2019:1–6.
    1. Kobayashi K, Imagama S, Ando K, et al. Risk factors for delirium after spine surgery in extremely elderly patients aged 80 years or older and review of the literature: Japan Association of Spine Surgeons with ambition multicenter study. Global Spine Journal. 2017;7:560–566. doi: 10.1177/2192568217700115.
    1. Kobayashi K, Imagama S, Sato K, et al. Postoperative complications associated with spine surgery in patients older than 90 years: a multicenter retrospective study. Global Spine J. 2018;8:887–891. doi: 10.1177/2192568218767430.
    1. Lee JK, Park YS. Delirium after spinal surgery in Korean population. Spine. 2010;35:1729–1732. doi: 10.1097/BRS.0b013e3181c423fc.
    1. Li H, Li CD, Yi XD, et al. Analysis of risk factors for delirium in the elderly patients after spinal operation. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 2012; 44: 847-850.
    1. Morino T, Hino M, Yamaoka S, et al. Risk factors for delirium after spine surgery: an age-matched analysis. Asian spine journal. 2018;12:703–709. doi: 10.31616/asj.2018.12.4.703.
    1. Oe S, Togawa D, Yamato Y, et al. Preoperative age and prognostic nutritional index are useful factors for evaluating postoperative delirium among patients with adult spinal deformity. Spine. 2019;44:472–478. doi: 10.1097/BRS.0000000000002872.
    1. Pan Z, Huang K, Huang W, et al. The risk factors associated with delirium after lumbar spine surgery in elderly patients. Quantitative imaging in medicine and surgery. 2019;9:700–710. doi: 10.21037/qims.2019.04.09.
    1. Radcliff K, Ong KL, Lovald S, et al. Cervical spine surgery complications and risks in the elderly. Spine. 2017;42:E347–e354. doi: 10.1097/BRS.0000000000001799.
    1. Seo JS, Park SW, Lee YS, et al. Risk factors for delirium after spine surgery in elderly patients. Journal of Korean Neurosurgical Society. 2014;56:28–33. doi: 10.3340/jkns.2014.56.1.28.
    1. Soh S, Shim JK, Song JW, et al. Postoperative delirium in elderly patients undergoing major spinal surgery: role of cerebral oximetry. J Neurosurg Anesthesiol. 2017;29:426–432. doi: 10.1097/ANA.0000000000000363.
    1. Susano MJ, Scheetz SD, Grasfield RH, et al. Retrospective analysis of perioperative variables associated with postoperative delirium and other adverse outcomes in older patients after spine surgery. J Neurosurg Anesthesiol. 2018.
    1. Ushida T, Yokoyama T, Kishida Y, et al. Incidence and risk factors of postoperative delirium in cervical spine surgery. Spine. 2009;34:2500–2504. doi: 10.1097/BRS.0b013e3181b321e6.
    1. Tanaka M, Tani N, Maruo T, et al. Risk factors for postoperative delirium after deep brain stimulation surgery for parkinson disease. World Neurosurg. 2018;114:e518–e523. doi: 10.1016/j.wneu.2018.03.021.
    1. Wang XQ, Zhuang HX. Zhang LX, et al. World Neurosurg: Nomogram for predicting postoperative delirium after deep brain stimulation surgery for Parkinson’s disease; 2019.
    1. Fukuoka H, Afshari NA. The impact of age-related cataract on measures of frailty in an aging global population. Curr Opin Ophthalmol. 2017;28:93–97. doi: 10.1097/ICU.0000000000000338.
    1. Fong TG, Davis D, Growdon ME, et al. The interface between delirium and dementia in elderly adults. Lancet Neurol. 2015;14:823–832. doi: 10.1016/S1474-4422(15)00101-5.
    1. FitzGerald JM, Perera G, Chang-Tave A, et al. The incidence of recorded delirium episodes before and after dementia diagnosis: differences between dementia with lewy bodies and Alzheimer’s disease. J Am Med Dir Assoc. 2019;20:604–609. doi: 10.1016/j.jamda.2018.09.021.
    1. Hov KR, Bolstad N, Idland AV, et al. Cerebrospinal fluid S100B and Alzheimer’s disease biomarkers in hip fracture patients with delirium. Dement Geriatr Cogn Dis Extra. 2017;7:374–385. doi: 10.1159/000481853.
    1. Racine AM, Fong TG, Travison TG, et al. Alzheimer’s-related cortical atrophy is associated with postoperative delirium severity in persons without dementia. Neurobiol Aging. 2017;59:55–63. doi: 10.1016/j.neurobiolaging.2017.07.010.
    1. de Havenon A, Meyer C, McNally JS, et al. Subclinical cerebrovascular disease: epidemiology and treatment. Curr Atheroscler Rep. 2019;21:39. doi: 10.1007/s11883-019-0799-1.
    1. McKetton L, Cohn M, Tang-Wai DF, et al. Cerebrovascular resistance in healthy aging and mild cognitive impairment. Front Aging Neurosci. 2019;11:79. doi: 10.3389/fnagi.2019.00079.
    1. Tong X, Yang Q, Ritchey MD, et al. The burden of cerebrovascular disease in the United States. Prev Chronic Dis. 2019;16:E52. doi: 10.5888/pcd16.180411.
    1. Raats JW, Steunenberg SL, de Lange DC, et al. Risk factors of post-operative delirium after elective vascular surgery in the elderly: a systematic review. Int J Surg. 2016;35:1–6. doi: 10.1016/j.ijsu.2016.09.001.
    1. Raats JW, van Eijsden WA, Crolla RM, et al. Risk factors and outcomes for postoperative delirium after major surgery in elderly patients. PLoS One. 2015;10:e0136071. doi: 10.1371/journal.pone.0136071.
    1. Tei M, Ikeda M, Haraguchi N, et al. Risk factors for postoperative delirium in elderly patients with colorectal cancer. Surg Endosc. 2010;24:2135–2139. doi: 10.1007/s00464-010-0911-7.
    1. Tei M, Wakasugi M, Kishi K, et al. Incidence and risk factors of postoperative delirium in elderly patients who underwent laparoscopic surgery for colorectal cancer. Int J Colorectal Dis. 2016;31:67–73. doi: 10.1007/s00384-015-2335-2.

Source: PubMed

3
Suscribir