Sage Journals: Discover world-class research

Abstract

Study design

Systematic review and meta-analysis.

Objective

This systematic review with meta-analysis is aimed at evaluating the impact of smoking (tobacco) on spinal fusion rates and the resulting PROMs.

Methods

Following the PRISMA guidelines, a systematic literature search was conducted in 4 databases. Studies focused on adult smokers vs non-smokers undergoing spinal fusion. Odds ratios (ORs) were calculated for dichotomous variables and mean differences or standardized mean differences for continuous variables. The primary outcomes assessed were non-union/pseudoarthrosis incidence and PROMs.

Results

A total of 29 studies were included in this analysis. The unadjusted incidence of pseudoarthrosis was significantly higher in smokers than in non-smokers (OR 1.97, 95% CI 1.55-2.52, P < 0.001). Subgroup analysis revealed significant differences in the cervical (OR 2.09, 95% CI 1.27-3.44, P < 0.05) and lumbar (OR 1.97, 95% CI 1.45-2.68, P < 0.001) regions. Adjusted analysis also showed a significantly higher incidence of pseudoarthrosis in smokers (OR 1.38, 95% CI 1.12-1.72, P < 0.05). Changes in ODI, VAS, EQ-5D, and SF-12 and SF-36, consistently favored nonsmoking patients. Smoking was associated with a lower rate of returning to work (OR 0.70, 95% CI 0.54-0.90, P < 0.05), and in the lumbar subgroup, reduced satisfaction (OR 0.24, 95% CI 0.12-0.49, P < 0.001). Former smokers (smoking cessation for at least 1 year prior to surgery) did not show significant differences compared to nonsmokers in terms of pseudarthrosis rate or pain scores.

Conclusion

Smoking is associated with an increased risk of pseudarthrosis and poorer PROMs after spinal fusion surgery. Healthcare providers should emphasize smoking cessation interventions to improve surgical outcomes and patient satisfaction.

Keywords

smoking spinal fusion non-union pseudoarthrosis patient-reported outcomes meta-analysis

Introduction

Pseudoarthrosis is a common complication in spinal surgery, significantly impacting both patients and the healthcare system.^1,2 Its incidence, especially at the cervical level, is approximately 2.6%.³ A key contributor to this complication is smoking, which negatively affects graft success due to the vasoconstrictive effects of nicotine.⁴ Studies in rabbits support this detrimental impact on spinal fusion.⁵ Smoking also worsens patient-reported outcomes (PROMs),^6,7 increasing the risk of complications and chronic pain after surgery.^6,8 With 19.7% of American adults using tobacco in 2018,⁹ understanding the full impact of smoking on surgical outcomes is vital. Evidence suggests that smoking interferes with spinal fusion and reduces patient satisfaction¹⁰ and that smoking cessation improves surgical outcomes.¹¹ Current smokers tend to have worse outcomes than non-smokers, with a clinically significant difference in pain relief,¹² while former smokers fare better but still worse than non-smokers.¹³ Despite associations with comorbidities, smoking independently raises surgical risks.¹⁴ However, some studies, like that of Phan et al, report no differences in clinical outcomes.¹⁵ Pseudoarthrosis and disability post-surgery also carry a considerable economic burden,¹⁶ and the role of bone substitutes and osteobiologics is crucial.¹⁷ Smoking is a modifiable risk factor, and previous systematic reviews indicate that cessation can improve surgical outcomes.¹⁸ This meta-analysis aims to assess smoking’s impact on spinal fusion, specifically its effect on pseudoarthrosis and PROMs, to enhance patient care and outcomes.

Methods

Eligibility Criteria

This study had a written protocol with review questions, search strategy, inclusion/exclusion criteria, and risk of bias assessment (PROSPERO: CRD42023482226). The current study followed the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) guidelines (Figure 1).¹⁹

Figure 1.

Study Selection Flow Diagram (Preferred Reporting Items for Systematic Reviews and Meta-Analyses)

The systematic review question was structured following the Population, Intervention, Comparison, Outcomes, Study design (PICOS) strategy. The study population (P) included patients undergoing spinal fusion surgery. The intervention (I) evaluated the current smoker status. These patients were compared (C) with non-smoker controls who underwent the same surgical procedure. The primary outcomes (O) examined included radiographic evidence of pseudarthrosis or pseudarthrosis observed on follow-up imaging, as well as patient-reported outcome measures (PROMs) assessing pain, function, and quality of life. Only comparative study (S) designs were considered eligible for inclusion, as they are typically used to investigate the impact of exposures, such as smoking.

Articles were excluded if they involved pediatric populations, case reports, or previous literature reviews to ensure that only primary studies contributing to new comparative results were incorporated. Duplicate publications, presenting data from the same patient cohort, were also excluded to avoid overlapping analyses and skewing findings. Studies lacking sufficient reporting of methods, participant characteristics, or outcome data useful for appraising risk of bias, and informed meta-analyses, were excluded due to incomplete reporting. Papers that did not present quantitative outcome data in a format that could be compiled across studies, such as those that only provided qualitative results or narratives, were omitted. Investigations focused on non-surgical interventions, including conservative treatment modalities alone, rather than spinal fusion surgical procedures, were also excluded to maintain relevance to the examined population. Lastly, studies specifying that the included patient groups did not undergo spinal fusion techniques, were excluded to ensure comparability with the population of interest undergoing surgical treatment.

Information Sources

A comprehensive search of multiple databases was conducted to identify the relevant literature. This included PubMed, EMBASE, Scopus, and Cochrane Library. No date or language restrictions were applied to capture all eligible publications. The reference lists of the included articles were also screened to uncover any potentially missed studies that met the inclusion criteria.

Search Methods for Identification of Studies

We used the following search terms to search all trials registers and databases: (“Spinal Fusion” OR “fusion rate” OR “spine failure”) AND (smoking OR tobacco OR cigarette) NOT meta-analysis NOT “systematic review” NOT “case report” (Supplementary File 1). Two reviewers independently agreed on the selection of eligible studies and reached a consensus on which studies to include. Two authors independently reviewed the studies for data extraction. If consensus was not reached, a third author was asked to complete the data extraction form.

Data Extraction and Data Items

The baseline characteristics obtained from each study were as follows: study, period, follow-up, region, type of study, location, number of patients, number of female patients, age, surgical technique, etiologies, and method of assessing pseudarthrosis. The main outcomes that could be compared were the incidence of non-union or pseudoarthrosis, as well as patient-reported outcome measures: Visual Analog Scale (VAS), Oswestry Disability Index (ODI), EQ-5D, SF-12/36 physical component (PCS), SF-12/36 mental component (MCS), return to work rates, satisfaction, and the minimally clinically important difference (MCID). The data extraction process was independently conducted by two reviewers. Any discrepancies between the extracted data were identified and resolved through discussions between the two reviewers. If consensus could not be reached, a third reviewer was consulted to assess the discrepant data items and make a final determination to arrive at an agreement.

Assessment of Risk of Bias in Included Studies

Two authors independently assessed the quality of the included studies using the Methodological Index for Non-Randomized Studies (MINORS) criteria, as shown in Table 1.⁴² The comparative studies had a maximum score of 24, whereas the non-comparative studies had a maximum score of 16. For non-comparative studies, scores ranging from 0 to 4 were categorized as very low quality, 5 to 7 as low quality, 8 to 12 as fair quality, and scores of 13 or higher as high quality. For comparative studies, scores ranging from 0 to 6 were considered very low quality, 7 to 10 as low quality, 11 to 15 as fair quality, and scores of 16 or higher as high quality.⁴²

Table 1.

Assessment of the Quality of Studies Through Methodological Index for Non-randomized Studies (MINORS)

Study	Clearly stated aim	Consecutive patients	Prospective collection data	Endpoints	Assessment endpoint	Follow-up period	Loss less than 5%	Study size	Adequate control group	Contemporary group	Baseline control	Statistical analyses	MINORS
Andersen et al 2001¹⁰	2	2	0	2	2	2	0	2	1	2	0	2	17
Behrend et al. 2012¹²	2	0	0	2	2	1	0	2	1	0	1	2	13
Boishardy et al 2022²⁰	2	2	0	2	2	2	0	2	2	2	2	2	20
Brown et al. 1985²¹	2	0	0	2	2	0	0	1	2	2	1	2	14
Bydon et al 2014²²	2	2	0	2	2	2	2	2	2	2	2	2	22
Cerier et al. 2019²³	2	2	0	2	2	1	2	1	2	2	2	2	20
Chapin et al 2015²⁴	2	2	2	2	1	2	2	1	1	2	0	2	18
Cho et al. 2021²⁵	2	2	0	2	2	2	2	1	2	2	2	2	21
Cole et al 2023²⁶	2	2	0	2	2	2	0	2	1	2	0	2	17
Gatot et al 2022²⁷	2	2	0	2	2	2	0	2	2	2	2	2	20
Glassman et al 2000¹¹	2	2	0	2	2	2	0	2	1	2	0	2	17
Hermann et al 2016²⁸	2	2	0	2	2	0	1	1	1	2	0	2	15
Hilibrand et al. 2001²⁹	2	2	0	2	2	2	0	1	0	2	0	2	15
Hofler et al. 2018¹⁶	2	2	1	2	2	0	0	2	1	2	0	2	16
Jazini et al 2017¹³	2	2	2	2	2	1	0	2	1	2	0	2	18
Kim et al 2006³⁰	2	2	0	2	2	2	0	1	0	2	0	2	15
Kuo et al. 2020³¹	2	2	0	2	2	2	0	1	1	2	1	2	17
Lau et al. 2014¹⁴	1	2	0	2	2	2	0	2	2	2	1	2	18
Lim et al 2023³²	2	2	2	2	2	2	0	2	0	2	0	2	18
Luszczyk et al. 2013³³	2	0	0	1	1	2	0	2	0	0	0	2	10
Macki et al 2016³⁴	2	0	0	2	2	2	0	1	1	0	2	2	14
Patel et al. 2019³⁵	2	2	0	2	2	1	2	1	2	2	2	2	20
Phan et al 2017¹⁵	2	1	2	2	2	2	0	1	2	1	2	2	19
Samartzis et al 2005³⁶	2	0	0	2	1	2	0	1	0	0	0	2	10
Sandén et al 2011³⁷	2	2	0	2	2	2	0	2	2	2	2	2	20
Toci et al 2022³⁸	2	2	0	2	2	0	0	2	1	2	0	2	15
Wang et al. 2021³⁹	2	2	0	2	2	2	0	2	2	2	2	2	20
Yoo et al 2014⁴⁰	2	2	0	2	2	1	0	1	2	2	2	2	18
Zhou et al. 2022⁴¹	2	2	0	2	2	1	0	2	1	2	1	2	17

Assessment of Results

The meta-analysis was conducted using the software Review Manager (RevMan, v5.4, Cochrane Collaboration). Odds ratios (OR) with 95% confidence intervals (CI) were calculated for dichotomous variables. Continuous variables were analyzed using mean differences (MD) with 95% confidence intervals (CI), except for variables that differed in scale or units, for which standard mean differences (SMD) with 95% CI were calculated. When individual studies presented risk factors as odds ratios, a generic inverse variance method was employed. To assess heterogeneity, both the chi-square test and I² statistic were used. I² values ranging from 0 to 100% were interpreted as indicative of low, moderate, and high heterogeneity at 25%, 50%, and 75% thresholds, respectively. In the absence of statistical evidence of heterogeneity, a fixed-effects model was used. A random-effects model was used when significant heterogeneity was detected. Whenever feasible, adjusted data derived from multivariate analyses were extracted to account for potential confounding variables. In cases where such information was not provided, unadjusted estimates from the univariate analyses were included in the meta-analysis. To extract precise information from figures within the articles, WebPlotDigitizer (version 4.5.0) was utilized. Missing data were managed according to the guidelines outlined in the Cochrane Handbook.⁴³

Risk of Bias Across the Studies

To evaluate the potential presence of publication bias, an assessment of small study effects was conducted through visual inspection of a funnel plot using RevMan, comparing each study’s effect size against its precision. A symmetrical distribution of points around the pooled estimate line would suggest a lack of bias, whereas asymmetry could indicate systematic non-publication of smaller trials with null or unfavorable results.

Additional Analyses

Subgroup analyses were conducted to explore sources of heterogeneity based on spinal region and smoking status classification. Information on smoking cessation, including its definition, timing relative to surgery, and potential impact on outcomes, was systematically collected from all included studies in which such data were available.

Sensitivity analyses, including a leave-one-out analysis using RevMan, were performed to assess the robustness of findings by iteratively removing the highest-weighted study from each meta-analysis.

In addition, Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) methodology was employed to systematically assess the certainty of evidence for key outcomes.⁴⁴ This system rates evidence quality, with randomized trials considered high-quality but subject to downgrading for bias, inconsistency, or imprecision. Observational studies begin as low quality but may be upgraded based on large effects or minimal validity threats.

Results

Study Selection

A systematic search of PubMed, EMBASE, Scopus, and Cochrane Collaboration Library yielded 558 citations. After reviewing the titles and abstracts, 500 studies were excluded because they did not focus on smoking or were not comparative. The full texts of the remaining 58 citations were examined in detail; 35 studies did not meet the inclusion criteria, resulting in 23 studies. Six additional studies were identified by reviewing the references in the included articles. Ultimately, 29 studies were included in this meta-analysis (Figure 1).^{10–16,20–41}

Study Characteristics

The main characteristics of the included studies are shown in Table 2. A total of 29 studies with 305 694 patients were included. The majority (62.1%) of the studies were conducted in the United States. The publication dates ranged from 1985 to 2023. The study designs included 28 retrospective and prospective cohort studies, as well as 1 case-control investigation. The follow-up duration, sex distribution, mean age, surgical techniques, and underlying diagnoses of patients in each study are detailed in Table 2. The assessment of pseudarthrosis in individual studies is shown in Supplemental Table 1. Definitions of smoking used in the included studies are presented in Supplemental Table 2.

Table 2.

Baseline Characteristic of the 29 Included Studies

Study	Period	Follow-up (years)	Region	Type of study	Location	n patients (Smoke/Control)	n Female (Smoke/Control)	Age (Smoke/Control)	Surgical technique	Etiologies
Andersen et al 2001¹⁰	1993 to 1997	2.0	Denmark	Retrospective cohort	Lumbar	396 (216/180)	237 (119/118)	NS	LF	NS
Behrend et al. 2012¹²	NS	0.7	USA	Retrospective cohort	Spine	5333 (2699/2634)	2925 (1608/1317)	(51/52)	Spine surgery	NS
Boishardy et al 2022²⁰	2010 to 2020	2.1	France	Retrospective cohort	ASD	1094 (209/885)	NS	NS	NS	ASD
Brown et al. 1985²¹	1977 to 1078	NS	UK	Case-control study	Lumbar	100 (50/50)	50 (24/26)	(42/43)	Laminectomy and fusion	NS
Bydon et al 2014²²	1990 to 2011	3.0	USA	Retrospective cohort	Lumbar	281 (50/231)	156 (29/127)	(59/59)	PLF	Spinal stenosis, spondylolisthesis, degenerative disc disease
Cerier et al. 2019²³	2013 to 2015	1.0	USA	Retrospective cohort	Cervical	51 (23/28)	29 (12/17)	(48/52)	ACDF	Radiculopathy and/or myelopathy
Chapin et al 2015²⁴	NS	1.0	USA	Prospective cohort	Lumbar	165 (43/122)	NS	NS	Lumbar spine surgeries	NS
Cho et al. 2021²⁵	2014 to 2018	2.0	South Korea	Retrospective cohort	Lumbar	76 (11/65)	NS	NS	PLIF	Spinal stenosis or spondylolisthesis
Cole et al 2023²⁶	2010 to 2021	2.0	USA	Retrospective cohort	Lumbar	154869 (44894/109975)	NS	NS	Anterior and posterior primary fusion and included patients undergoing both single-level fusions and those undergoing multilevel fusions	NS
Gatot et al 2022²⁷	2012 to 2014	2.0	Singapore	Retrospective cohort	Lumbar	188 (26/162)	62 (41/21)	(54/62)	MIS-TLIF	Degenerative spondylolisthesis, degenerative disk disease causing central herniation or foraminal-lateral herniation, and central stenosis or foraminal/lateral stenosis
Glassman et al 2000¹¹	1992 to 1996	4.1	USA	Retrospective cohort	Lumbar	357 (188/169)	155 (76/79)	41/47	LF	Spinal stenosis, pseudarthrosis, mechanical low back pain, discogenic low back pain, or spinal instability
Hermann et al 2016²⁸	2010 to 2012	NS	Germany	Retrospective cohort	Lumbar	50 (16/34)	27 (9/18)	(42/58)	NS	Spondylodesis
Hilibrand et al. 2001²⁹	1973 to 1992	5.7	USA	Retrospective study	Cervical	190 (135/55)	NS	NS	ACDF	Spondylosis with compression of nerve roots or the spinal cord, or both
Hofler et al. 2018¹⁶	2009 to 2011	NS	USA	Retrospective cohort	Spine	107650 (29521/78129)	NS	NS	Spinal fusions	NS
Jazini et al 2017¹³	NS	1.0	USA	Prospective cohort	Lumbar	272 (102/170)	85 (29/56)	(57/57)	Decompression with fusion	Adjacent segment disease, spondylolisthesis, spinal stenosis, mechanical disc collapse or disc herniation
Kim et al 2006³⁰	1985 to 2022	3.9	USA	Retrospective cohort	Lumbar	178 (17/161)	NS	NS	PSF	ASD
Kuo et al. 2020³¹	2006 to 2015	3.7	Taiwan	Retrospective cohort	Lumbar	306 (34/272)	140 (9/131)	(57/61)	Posterior laminectomy decompression and placement of a 1- or 2-level	Spinal stenosis with hypertrophy of the ligamentum flavum, facet degeneration, minimal Or mild spondylolisthesis, degenerative disc disease And recurrent disc herniation
Lau et al. 2014¹⁴	2006 to 2011	1.0	USA	Retrospective cohort	Cervical	160 (40/120)	67 (11/56)	(52/54)	Anterior cervical corpectomy with cage or structural allograft	Degenerative, trauma, tumor, infection
Lim et al 2023³²	2017 to 2020	2.0	USA	Retrospective cohort	Cervical and lumbar	27187 (4947/22240)	13333 (2380/10953)	(53/60)	Spine surgery	Degenerative disease
Luszczyk et al. 2013³³	NS	2.0	USA	Retrospective cohort	Cervical	573 (156/417)	NS	NS	Single-level ACDF with allograft and locked plate fixation	NS
Macki et al 2016³⁴	NS	4.9	USA	Retrospective cohort	Lumbar	110 (28/82)	63 (11/52)	(54/61)	First-time posterolateral, instrumented fusion of the lumbar spine	Degenerative spinal disease
Patel et al. 2019³⁵	2013 to 2018	0.5	USA	Retrospective cohort	Cervical	192 (25/167)	77 (13/64)	(47/50)	Primary 1-Level, or 2-level ACDF	Degenerative pathology
Phan et al 2017¹⁵	NS	1.0	Australia	Retrospective cohort	Lumbar	137 (23/114)	NS	(53/57)	ALIF	Degenerative disk disease without radiculopathy, degenerative disk disease with radiculopathy, spondylolisthesis, failed posterior Fusion, adjacent-segment disease, and scoliosis requiring correction
Samartzis et al 2005³⁶	NS	1.0	USA	Retrospective cohort	Cervical	66 (NS/NS)	24 (NS/NS)	NS	One-level ACDF with rigid anterior plate fixation who had either allograft or autograft	Radiculopathy, myelopathy, or myeloradiculopathy stemming from a herniated nucleus pulposus Or spondylosis
Sandén et al 2011³⁷	NS	2.0	Sweeden	Retrospective cohort	Lumbar	4555 (758/3797)	2535 (444/2091)	(65/70)	Surgical procedures for degenerative lumbar spine disorders	Degenerative lumbar spine disorders
Toci et al 2022³⁸	2013 to 2020	1.0	USA	Retrospective cohort	Cervical	195 (94/101)	75 (38/37)	(61/62)	PCF	NS
Wang et al. 2021³⁹	NS	3.4	China	Retrospective cohort	Cervical	153 (74/79)	102 (34/68)	(51/50)	Two- and three-level hybrid surgery using the Prestige-LP artificial cervical disc	Cervical myelopathy or radiculopathy or both
Yoo et al 2014⁴⁰	2004 to 2009	0.5	Korea	Retrospective cohort	Cervical	58 (22/36)	26 (NS/NS)	NS	Stand-alone cages	Radiculopathy and/or myelopathy
Zhou et al. 2022⁴¹	2016 to 2020	0.5	China	Retrospective cohort	Cervical	750 (284/466)	392 (NS/NS)	NS	ACDF	Cervical spondylotic disease

ACDF: Anterior cervical discectomy and fusion; AIS: Adult idiopathic scoliosis; ALIF: Anterior lumbar interbody fusion; ASD: Adult spinal deformity; LF: Lumbar fusion; MD: Microdiscectomy; MIS: Minimally invasive surgery; NA: Not applicable; NS: Not specified; PCF: Posterior cervical fusion; PLIF: Posterior lumbar interbody fusion; PSF: Posterior spine fusion; TLIF: Transforaminal lumbar interbody fusion.

Pseudoarthrosis

The unadjusted incidence of pseudarthrosis was significantly higher in the smoking group (OR1.97, 95%CI 1.55 to 2.52; studies = 22) (Figure 2). Significant differences were observed at the cervical (OR2.09, 95%CI 1.27 to 3.44; studies = 9) and lumbar (OR1.97, 95%CI 1.45 to 2.68; studies = 13) levels. When the adjusted incidence of pseudarthrosis was analyzed (considering comorbidities, demographics and type of surgery), smokers continued to show a significantly higher incidence (OR1.38, 95%CI 1.12 to 1.72; studies = 7) (Figure 3). When subgroup analyses were performed using the adjusted incidence at the cervical level, no significant differences were observed (OR1.28, 95%CI 0.46 to 3.58; studies = 3). In contrast, at the lumbar level, smokers had a higher frequency of adjusted incidence of pseudarthrosis (OR1.48, 95%CI 1.02 to 2.16; studies = 4).

Figure 2.

Forest Plot Showing Smoking Patients (Smoke) had Twice the Risk of Cervical and Lumbar Pseudarthrosis than Non-smoking Patients (Control)

Figure 3.

Forest Plot Showing Adjusted Risk of Pseudarthrosis. In Total, Smoking Patients (Smoke) Were Found to Have a Significantly Higher Risk than Non-smokers (Control) (OR 1.38, 95% CI 1.12 to 1.72, P < 0.01)

Patient Reported Outcome Measures

Table 3 shows a summary of PROMs according to the follow-up time and spine location. Postoperatively, there were no significant differences in the ODI scores between smokers and non-smokers (MD1.43, 95%CI -1.48 to 4.35; participants = 653; studies = 5; I² = 56%). However, sensitivity analysis showed differences when removing the highest-weighted study (MD5.60, 95%CI 1.58 to 9.61; participants = 603; studies = 5; I² = 0%). ODI scores at 3-6 months showed worse results in the smoking group (MD6.34, 95%CI 3.34 to 9.34; participants = 735; studies = 3; I² = 0%), and at the final follow-up, the smoking group showed worse results for the lumbar spine (MD5.39, 95%CI 2.87 to 7.91; participants = 5081; studies = 4; I² = 4%) (Figure 4A). Sensitivity analysis showed consistency for the ODI scores at 3-6 months and at the final follow-up.

Table 3.

Patient-Reported Outcome Measures

Effect size	n studies	n participants	Fixed effect model (MD/SMD 95% CI)	I² (%)	P-value
ODI postoperative	5	653	MD 1.43, 95% CI -1.48 to 4.35	56%	0.34
Cervical	1	144	MD 6.20, 95% CI -2.01 to 14.41	N/E	0.14
Lumbar	4	509	MD 0.74, 95% CI -2.38 to 3.86	60%	0.64
ODI 3-6 months	3	735	MD 6.34, 95% CI 3.34 to 9.34	0%	<0.0001
ODI final follow-up	5	5200	^aMD 4.11, 95% CI -0.14 to 8.35	82%	0.06
Cervical	1	119	MD -0.87, 95% CI -2.28 to 0.54	N/E	0.23
Lumbar	4	5081	MD 5.39, 95% CI 2.87 to 7.91	4%	<0.0001
VAS arm/leg postoperative	3	722	^aMD 0.17, 95% CI -1.85 to 2.19	95%	0.87
VAS arm/leg 3-6 months	2	570	^aMD 1.36, 95% CI 0.05 to 2.68	83%	0.04
VAS arm/leg final follow-up	4	5244	^aSMD 0.29, 95% CI 0.01 to 0.57	79%	0.04
Cervical	1	119	SMD 0.00, 95% CI -0.38 to 0.38	N/E	1.00
Lumbar	3	5125	^aSMD 0.37, 95% CI 0.03 to 0.72	85%	0.04
VAS back/neck postoperative	2	N/A	OR 1.99, 95% CI 1.23 to 3.21	62%	0.93
Cervical	4	N/A	^aOR 1.46, 95% CI 1.10 to 1.95	88%	0.85
Lumbar	6	298298	^aOR 1.89, 95% CI 1.67 to 2.13	90%	0.98
VAS back/neck 3-6 months	2	570	MD 1.54, 95% CI 0.97 to 2.12	0%	<0.00001
VAS back/neck final follow-up	4	5244	SMD 0.31, 95% CI 0.11 to 0.50	58%	0.002
Cervical	1	119	SMD 0.08, 95% CI -0.30 to 0.46	N/E	0.68
Lumbar	3	5125	SMD 0.36, 95% CI 0.12 to 0.60	68%	0.003
EQ-5D final follow-up	2	4684	^aMD -0.10, 95% CI -0.17 to −0.03	94%	0.006
SF-12/36 PCS postoperative	3	553	SMD -0.18, 95% CI -0.38 to 0.03	0%	0.09
SF-12/36 PCS final follow-up	2	4742	SMD -0.12, 95% CI -0.20 to −0.04	0%	0.002
SF-12/36 MCS postoperative	3	553	SMD -0.34, 95% CI -0.55 to −0.14	53%	0.001

^aRandom effect model; N/E: Not estimable.

Figure 4.

Forest Plots Comparing Smokers (Smoke) With Non-smokers (Control) for Each of the PROMs Studied at the Final Follow-up

The postoperative VAS arm/leg did not show significant differences between smokers and non-smokers (MD0.17, 95% CI -1.85 to 2.19; participants = 722; studies = 3; I² = 95%). However, at 3-6 months (MD1.36, 95% CI 0.05 to 2.68; participants = 570; studies = 2; I² = 83%) and at the final follow-up (SMD0.29, 95% CI 0.01 to 0.57; participants = 5244; studies = 4; I² = 79%), smokers experienced significantly more pain (Figure 4B). Sensitivity analysis did not show any differences at the final follow-up (MD1.73, 95%CI -0.33 to 3.79; participants = 4861; studies = 4; I² = 93%).

The postoperative VAS back/neck scores did not show significant differences between smokers and non-smokers (SMD-0.02, 95%CI -0.38 to 0.35; participants = 772; studies = 4; I² = 72%). However, at 3-6 months (MD1.54, 95% CI 0.97 to 2.12; participants = 570; studies = 2; I² = 0%) and at the final follow-up (SMD0.31, 95% CI 0.11 to 0.50; participants = 5244; studies = 4; I² = 58%), the smoking group experienced significantly more pain (Figure 4C). Sensitivity analysis did not show any differences at the final follow-up (MD0.35, 95% CI -0.03 to 0.66; participants = 689; studies = 3; I² = 59%).

The EQ-5D showed worse results in the smoking group (MD-0.12, 95% CI -0.13 to −0.11; participants = 4684; studies = 2; I² = 94%) (Figure 4D).

Postoperative SF-12/36 PCS did not show significant differences (SMD-0.18, 95% CI -0.38 to 0.03; participants = 553; studies =; I² = 0%), but the smoking group showed worse results at the final follow-up (SMD-0.12, 95% CI -0.20, −0.04; participants = 4742; studies = 2; I² = 0%) (Figure 4E). SF-12/36 MCS could only be analyzed postoperatively and did not show significant differences (SMD-0.34, 95% CI -0.55 to −0.14; participants = 553; studies = 3; I² = 53%). Sensitivity analyses of these variables showed consistency and did not change the direction of the results.

Table 4 shows the MCIDs that can be compared for the PROMs. Non-smokers achieved the MCID significantly more frequently than smokers with respect to the PROMs: VAS back/neck postoperative (OR0.65, 95% CI 0.40 to 1.04; participants = 416; studies = 2; I² = 0%), VAS back/neck final follow-up (OR0.79, 95% CI 0.40 1. 04; participants = 416; studies = 2; I² = 0%), VAS back/neck final follow-up (OR0.79, 95% CI 0.66 to 0.95; participants = 4560; studies = 2; I² = 0%), and ODI postoperatively (OR0.53, 95% CI 0.31 to 0.89; participants = 416; studies = 2; I² = 0%).

Table 4.

Assessment of the Minimally Clinical Important Difference (MCID)

Effect size	n studies	n participants	Fixed effect model (MD 95% CI)	I² (%)	P-value
SF-12/36 - PCS	2	416	OR 0.75, 95% CI 0.46 to 1.19	0%	0.22
SF-12/36 - MCS	2	416	OR 0.82, 95% CI 0.50 to 1.33	54%	0.41
VAS a/l postoperative	2	416	OR 0.80, 95% CI 0.50 to 1.28	0%	0.35
VAS a/l FFU	2	4560	OR 0.89, 95% CI 0.74 to 1.08	0%	0.24
VAS b/n/global postoperative	2	416	OR 0.65, 95% CI 0.40 to 1.04	0%	0.07
VAS b/n/global FFU	2	4560	OR 0.79, 95% CI 0.66 to 0.95	0%	0.01
ODI postoperative	2	416	OR 0.53, 95% CI 0.31 to 0.89	0%	0.02

Smokers had a lower return to work frequency (OR0.70, 95% CI 0.54 to 0.90; participants = 2065; studies = 2; I² = 0%) (Figure 5A). Satisfaction at the final follow-up was also lower in the smoking group (OR0.40, 95% CI 0.15 to 1.08; participants = 4997; studies = 3; I² = 82%) (Figure 5B).

Figure 5.

Forest Plot Comparing Return to Work (5a) and Satisfaction (5b) Between Smoking (Smoke) and Non-smoking (Control) Patients. In Total, a Significant Difference was Observed With 66.3% of Smokers, as Compared to 75.4% of Non-smokers, Returning to work. In Addition, a Significant Difference was Found With 66.1% of Smokers and 78.7% of Non-smokers Reporting Being Satisfied

Effect of Smoking Cessation

Data on the effect of smoking cessation were extracted from eight studies (Supplemental Table 3). In lumbar surgery, quitting smoking was associated with higher fusion rates (e.g., Andersen et al, 86.6% vs 77.4%) and a trend toward reduced nonunion even when cessation occurred just 1 month before surgery (Glassman et al). In cervical fusion, lower pseudarthrosis rates were observed in quitters (8.1% vs 16.0%; Lau et al). Improvements in pain scores were inconsistently reported, although some studies noted greater pain reduction or correlation between longer cessation and lower pain (Behrend et al, Jazini et al). The definition of cessation timing varied substantially across studies, ranging from ≥2 weeks to ≥1 year before surgery.

Publication Bias

Publication bias was assessed using funnel plot analysis of the primary outcomes (Figure 6). Upon visual inspection of funnel plots, with effect estimates plotted on the x-axis against their standard errors on the y-axis, asymmetry was observed. This suggests the potential for publication bias, such that smaller or non-significant studies may not have been published. However, funnel plot analysis alone cannot provide conclusive evidence of bias, as asymmetry could arise due to heterogeneity across the included studies. Nonetheless, the possibility of publication bias should be considered when interpreting the findings, as biased literature can overestimate true effects.

Figure 6.

Funnel Plots Examining Publication Bias for the Main Outcomes

GRADE

The GRADE summary of the results of these three comparisons is shown in Table 5. There was high certainty for the return to work variable, moderate certainty for the pseudoarthrosis-unadjusted variable and satisfaction at the final follow-up, and low certainty for pseudoarthrosis-adjusted, ODI, and VAS outcomes.

Table 5.

GRADE Assessment of the Quality of the Evidence and the Strength of the Recommendations

Certainty assessment							№ of patients		Effect		Certainty	Importance
№ of studies	Study design	Risk of bias	Inconsistency	Indirectness	Imprecision	Other considerations	Fusion/PROMs	Never	Relative (95% CI)	Absolute (95% CI)	Certainty	Importance
Pseudoarthrosis unadjusted
21	Observational studies	not serious	not serious	serious^a	not serious	Publication bias strongly suspected Very strong association Dose response gradient^b	-/0	-/0	OR 1.97 (1.55 to 2.52)	2 fewer per 1000 (from 3 fewer to 2 fewer)	⨁⨁⨁◯ Moderate	CRITICAL
Pseudoarthrosis adjusted
6	Observational studies	not serious	not serious	serious^a	not serious	Publication bias strongly suspected Strong association Dose response gradient^b	-/0	-/0	OR 1.38 (1.12 to 1.72)	1 fewer per 1000 (from 2 fewer to 1 fewer)	⨁⨁◯◯ Low	CRITICAL
ODI/NDI FFU
5	Observational studies	not serious	not serious	serious^a	not serious	Publication bias strongly suspected Strong association Dose response gradient^b	897	4303	-	MD 4.11 higher (0.14 lower to 8.35 higher)	⨁⨁◯◯ Low	CRITICAL
VAS a/l FFU
4	Observational studies	not serious	not serious	serious^a	not serious	Publication bias strongly suspected Strong association Dose response gradient^b	899	4345	-	MD 1.79 higher (0.15 higher to 3.42 higher)	⨁⨁◯◯ Low	CRITICAL
VAS b/n/global FFU
4	Observational studies	not serious	not serious	serious^a	not serious	Publication bias strongly suspected Strong association Dose response gradient^b	899	4345	-	MD 1.71 higher (0.21 higher to 3.22 higher)	⨁⨁◯◯ Low	CRITICAL
Return to work
2	Observational studies	not serious	not serious	not serious	not serious	Strong association Dose response gradient	273/412 (66.3%)	1247/1653 (75.4%)	OR 0.70 (0.54 to 0.90)	72 fewer per 1000 (from 131 fewer to 20 fewer)	⨁⨁⨁⨁ High	IMPORTANT
Satisfaction FFU
3	Observational studies	not serious	not serious	serious^a	not serious	Publication bias strongly suspected Very strong association Dose response gradient^b	467/632 (73.9%)	3436/4365 (78.7%)	OR 0.40 (0.15 to 1.08)	190 fewer per 1000 (from 430 fewer to 13 more)	⨁⨁⨁◯ Moderate	IMPORTANT

CI: confidence interval; MD: mean difference; OR: odds ratio; a. Differences in surgical procedure, location, etiology.; b. Publication bias assessed by funnel plot.

Discussion

This meta-analysis found that smokers have a higher incidence of pseudarthrosis after spinal surgery compared to non-smokers. Smoking is also linked to greater pain, worse functionality, delayed return to work, and lower satisfaction post-spinal fusion. The quality of the included studies was generally high, but the evidence certainty was moderate to low for most outcomes. Variability in the definition and diagnosis of pseudarthrosis across studies must be considered, as some used clinical symptoms while others relied on imaging modalities like CT or X-rays. Standardizing diagnostic criteria would improve future analyses. The definition of smoking was not standardized or was unspecified in several of the included studies. Of the studies included, 13 did not provide a formal definition of smoking status. Among those that did, definitions varied considerably: some classified smokers based on the number of cigarettes consumed, while others used temporal criteria such as smoking within 2 weeks, 6 weeks, 6 months, or 1 year before surgery. A few distinguished between current, former, and never smokers using predefined cessation cut-offs. One study identified tobacco use exclusively through diagnostic codes, and another focused on chewing tobacco rather than smoking. This variability underscores the lack of standardization in assessing smoking status across the included literature.

Smoking’s negative impact on fusion outcomes may also depend on the type of implant material used; for instance, smokers had worse results with PEEK interbody cages.⁴⁵ Microvascular impairment, caused by nicotine-induced vasoconstriction, reduces blood flow and nutrient availability, leading to pseudarthrosis.⁴ Smoking is also associated with lower vitamin D levels⁴⁶ and comorbidities like diabetes and hypertension, further increasing pseudarthrosis risk.⁴⁷

Smokers undergoing spinal fusion were, on average, younger than non-smokers in the studies, suggesting that smoking accelerates spinal degeneration. This aligns with the concept of “accelerated aging”, which is observed in cardiovascular, lung, and other organ systems. Consistent with prior studies, multilevel fusion procedures were linked to higher pseudarthrosis rates compared to single-level surgeries.⁴⁸ Increased instability over a larger bony surface area may make fusion more vulnerable to smoking-induced microvascular changes, possibly indicating a dose-response relationship. Regarding minimally invasive techniques (MIS), Emami et al. found that pseudarthrosis could also occur after MIS transforaminal lumbar interbody fusion (MIS TLIF). This suggests that pseudarthrosis is more influenced by physiological factors such as smoking, obesity, diabetes, and age, rather than the type of surgical procedure.⁴⁹

Kim et al suggested that the thoracolumbar area is at higher risk of pseudarthrosis, recommending additional grafts in this region.³⁰ However, this meta-analysis found no significant differences in pseudarthrosis rates between the thoracolumbar and cervical spine, despite the cervical spine being more vascularized.⁵⁰ For grafts to function properly, adequate vascularization is necessary, but smoking-induced vascular impairment can hinder this.³⁴ Regarding modern graft options, Advanced graft technologies may deliver options for improving fusion success, mitigating some of the negative effects reported with smoking.⁴⁶ Additionally, no differences were found in pseudarthrosis incidence based on study definitions or imaging tests (CT or X-ray).

Smokers undergoing spinal surgery reported worse pain and functional outcomes. This could be due to nicotine’s neurophysiological effects, mental health issues,⁵¹ and reduced regenerative capacity.⁵² Smoking may impede nerve recovery, increase psychological distress, and delay tissue healing, worsening clinical outcomes. Unresolved pseudarthrosis can also cause persistent pain.⁵³

Regarding return to work, the studies included in this meta-analysis only reported the incidence of patients resuming work and did not provide information on how other factors might influence this outcome. In spinal surgery, factors such as older age, higher body mass index (BMI), physically demanding jobs, pain, and worker’s compensation status have been shown to affect return to work. Additionally, none of the studies in this meta-analysis reported the average time to return to work, though some mentioned a timeframe around 9 months.^54–56

Regarding smoking cessation, there is limited and heterogeneous evidence across the included studies, but the available data consistently point toward clinical benefits that warrant strong surgical recommendations (Supplemental Table 3). Smoking cessation was generally associated with higher fusion rates, with several studies reporting absolute improvements of 8-9% compared to continued smokers (e.g., Andersen et al, 86.6% vs 77.4% in lumbar cases; Lau et al, pseudarthrosis 8.1% vs 16.0% in cervical procedures). Glassman et al demonstrated a dose–response relationship particularly in lumbar fusion, where patients who quit even 1 month before surgery had lower nonunion rates than those who continued smoking, and quitting 6 months prior yielded the best return-to-work outcomes. Overall, the data on lumbar surgery are more extensive and consistent, while evidence for cervical fusion is less abundant but suggests a similar positive trend with smoking cessation. Effects on patient-reported measures (PROMs) were more variable: Andersen et al found no significant change in satisfaction primarily in lumbar cases, whereas Behrend et al (spine overall) observed greater reductions in worst pain among quitters, and Jazini et al reported that longer postoperative cessation correlated with lower pain scores at 12 months in lumbar patients. Definitions of cessation timing varied widely across locations (≥2 weeks, ≥6 weeks, ≥6 months, ≥1 year), yet the overall trend suggests that earlier and sustained quitting—ideally several weeks to months before surgery—maximizes the likelihood of solid fusion and may enhance pain outcomes regardless of spinal region. Based on this evidence, spine surgeons should actively integrate structured, early smoking cessation programs into preoperative management, clearly communicating that continued smoking increases the risk of pseudarthrosis, persistent pain, delayed functional recovery, and higher postoperative analgesic needs.^52,53,57,58 Combining cessation counseling with optimized perioperative pain control may improve both structural and patient-reported outcomes across lumbar and cervical spine surgeries.

Can be high, but Andersen et al found that only 13% quit despite being warned of the risks.^10,11 The studies included in our meta-analysis did not distinguish between the effects of cigarette smoking and smokeless tobacco use on spinal fusion rates; typically, “smoking” herein refers to combusted tobacco products. Only 1 study specifically assessed chewing tobacco, finding that its use was associated with a risk of pseudoarthrosis similar to that observed for cigarette smokers (OR 2.15, 95% CI 2.09-2.21), aligning closely with the global risk reported in our meta-analysis (Cole et al).²⁶

Emerging evidence suggests that other non-combustible nicotine products such as vapes and e-cigarettes may confer similar surgical risks to smoking, including impaired wound healing and bone health. For example, nicotine exposure from vaping in adolescents has been shown to be comparable to that of traditional smoking, particularly when nicotine salt products are used (Hammond et al).⁵⁹

Vaping is linked to postoperative complications such as delayed wound healing and increased infection risk, as highlighted in systematic reviews and clinical observations (Ashour et al).⁶⁰ E-liquids contain toxins such as cadmium and aromatic flavorings, which can impair osteoblast function, reduce bone mineral density, and increase susceptibility to osteoporosis and delayed fracture healing, all of which could theoretically contribute to spinal fusion failure (Fiani et al; Nicholson et al).^61,62

Although the literature in spine and orthopedic surgery is still limited, recent data consistently show that use of non-tobacco nicotine products—including vaping and chewing tobacco—can substantially increase perioperative risks. A pioneering study demonstrated that vaping was associated with longer surgical times and increased readmissions in joint arthroplasty patients (Bieganowski et al).⁶³

On the other hand, substances such as cannabis have been shown to negatively impact spine surgery outcomes, both in lumbar and cervical fusions, by significantly increasing the rate of pseudarthrosis. Cannabis use is also associated with a three to fourfold increase in the risk of revision surgeries, along with higher opioid consumption and longer hospital stays.⁶⁴

Moreover, both nicotine and cannabis use have been shown to further complicate recovery following orthopedic and spinal surgery. Preoperative identification and management of these risk factors are essential for optimizing wound healing and improving functional outcomes (Shore et al 2021).⁶⁵

Limitations

This study has several limitations that should be considered when interpreting the results. Most included studies were retrospective, which can introduce bias and limit the validity of findings. Additionally, variations in the definition of pseudarthrosis hinder comparisons across studies. The lack of a standardized definition of smoking status across the included studies, with many not reporting it and others using highly variable criteria, prevented its inclusion in subgroup analyses. Another limitation of this meta-analysis was the inability to differentiate between the effects of cigarette smoking and other forms of nicotine use, such as smokeless tobacco or vaping, on fusion outcomes, as none of the included studies provided separate or specific data on these alternative nicotine products. Few studies focused on cervical-level assessments, limiting comparisons in this area, and most did not use Patient-Reported Outcome Measures (PROMs). Future studies should include additional PROMs, such as PROMIS, and provide more detailed information on return-to-work outcomes, emphasizing the type of occupation as well as the influence of factors such as spinal level. There was also variability in follow-up periods, with some studies having 1-year follow-ups while others had longer periods, affecting result comparability. Different functional scales using various instruments were combined, introducing potential bias. Some variables were based on only two studies, highlighting the need for larger sample sizes in future research. Furthermore, many studies compared smokers and non-smokers without distinguishing between current and former smokers, limiting the understanding of smoking’s impact. Few studies clearly defined smoking categories, complicating interpretation. Additionally, the heterogeneity of etiologies and procedures used in the studies limits the generalizability of results. Most studies lacked adjusted effect estimates or did not specify covariates, and the majority were conducted in the United States, limiting extrapolation to other countries and healthcare systems.

Conclusions

This study found that smokers had a significantly higher incidence of pseudarthrosis and worse patient-reported outcomes at both cervical and lumbar levels compared to non-smokers. These differences were more pronounced at 3-6 months and at final follow-up, with smokers also experiencing lower return-to-work rates and satisfaction. Prospective studies are needed to reduce bias, and a consensus on pseudarthrosis definitions should be established. Smoking cessation should be encouraged to improve clinical outcomes and health.

Supplemental Material

Supplemental Material - Adverse Impact of Smoking on Spine Fusion and Patient-Reported Outcomes: A Systematic Review and Meta-Analysis

Supplemental Material for Adverse Impact of Smoking on Spine Fusion and Patient-Reported Outcomes: A Systematic Review and Meta-Analysis by P.M. Arnold, J.S. Harrop, G. Mariscal, R.C. Sasso, M.P. Steinmetz, C.D. Chaput, W.B. Jacobs, C.D. Witiw, J.E. O'Toole in Global Spine Journal.

Footnotes

ORCID iDs

P.M. Arnold

G. Mariscal

Ethical Considerations

As this research is a meta-analysis, it does not involve any direct human or animal subjects and therefore does not require ethical approval from an Institutional Review Board (IRB).

Author Contributions

Conceptualization; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Data curation; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Formal analysis; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Funding acquisition; C.D.C.; C.D.W.; Investigation; P.M.A.; J.S.H.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Methodology; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Project administration; P.M.A.; C.D.C.; C.D.W.; Resources; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Software; Supervision; P.M.A.; G.M.; Validation; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Visualization; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; Roles/Writing - original draft; P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.; and Writing - review & editing: P.M.A.; J.S.H.; G.M.; R.C.S.; M.P.S.; C.D.C.; W.B.J.; C.D.W.; J.E.O.

Funding

The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was funded by Cerapedics Inc.

Declaration of conflicting interests

The authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article:

Dr M.P. Steinmetz received royalties from Elsevier and Globus Medical, Inc an honorarium from Globus Medical, Inc and consulting fees from Cerapedics Inc.

Dr J.S. Harrop is a scientific advisor to Johnson & Johnson, Spiderwort Inc, and Kringle Pharma, Inc.

Dr C.D. Witiw received institutional research funding from the Canadian Institutes of Health Research and Cerapedics Inc, as well as speaking and consulting fees from Stryker Corp.

Dr J.E. O’Toole received consulting fees and royalties from Globus Medical, Inc, consulting fees from Cerapedics Inc, royalties from Medtronic plc and NuVasive, Inc and owns stock in Viseon Inc.

Dr C.D. Chaput received institutional research funding from Cerapedics Inc, Kuros Biosciences A.G., and Nuvasive, Inc and received royalties from Globus Medical, Inc.

Dr W.B. Jacobs received consulting and speaking fees from DePuy-Synthes, Inc, Stryker Corp, and Cerapedics Inc.

Dr R.C. Sasso received royalties from Medtronic plc and NuVasive, Inc.

Dr G. Mariscal received consulting fees from Cerapedics Inc.

Dr P.M. Arnold has no relevant financial or non-financial interests to disclose.

Data Availability Statement

All data relevant to the study are included in the article or uploaded as online supplemental information. Data may be available upon reasonable request.*

Supplemental Material

Supplemental material for this article is available online.

References

Martin

Mirza

Comstock

Gray

Kreuter

Deyo

. Reoperation rates following lumbar spine surgery and the influence of spinal fusion procedures. Spine. 2007;32(3):382-387.

Adogwa

Parker

Shau

, et al. Cost per qualityadjusted life year gained of revision lumbar pseudoarthrosis: defining the value of surgery. J Spinal Disord Tech. 2015;28:101-105.

Shriver

Lewis

Kshettry

Rosenbaum

Benzel

Mroz

. Pseudoarthrosis rates in anterior cervical discectomy and fusion: a metaanalysis. Spine J. 2015;15(9):2016-2027.

Theiss

Boden

Hair

Titus

Morone

Ugbo

. The effect of nicotine on gene expression during spine fusion. Spine. 2000;25:2588-2594.

Wing

Fisher

O’Connell

Wing

. Stopping nicotine exposure before surgery: the effect on spinal fusion in a rabbit model. Spine. 2000;25:30-34.

Sørensen

. Wound healing and infection in surgery. The clinical impact of smoking and smoking cessation: a systematic review and meta-analysis. Arch Surg. 2012;147(4):373-383.

Ditre

Brandon

Zale

Meagher

. Pain, nicotine, and smoking: research findings and mechanistic considerations. Psychol Bull. 2011;137(6):1065-1693.

Ditre

Brandon

Zale

Meagher

. Pain, nicotine, and smoking: research findings and mechanistic considerations. Psychol Bull. 2011;137(6):1065-1093.

Creamer

Wang

Babb

, et al. Tobacco product use and cessation indicators among adults - united States, 2018. MMWR Morb Mortal Wkly Rep. 2019;68(45):1013-1019.

10.

Andersen

Christensen

Laursen

Høy

Hansen

Bünger

. Smoking as a predictor of negative outcome in lumbar spinal fusion. Spine. 2001;26(23):2623-2628.

11.

Glassman

Anagnost

Parker

Burke

Johnson

Dimar

. The effect of cigarette smoking and smoking cessation on spinal fusion. Spine. 2000;25(20):2608-2615.

12.

Behrend

Prasarn

Coyne

Horodyski

Wright

Rechtine

. Smoking cessation related to improved patient-reported pain scores following spinal care. J Bone Joint Surg Am. 2012;94(23):2161-2166.

13.

Jazini

Glassman

Bisson

Potts

Carreon

. Do former smokers exhibit a distinct profile before and after lumbar spine surgery? Spine. 2018;43(3):201-206.

14.

Lau

Chou

Ziewacz

Mummaneni

. The effects of smoking on perioperative outcomes and pseudarthrosis following anterior cervical corpectomy: clinical article. J Neurosurg Spine. 2014;21(4):547-558.

15.

Phan

Fadhil

Chang

Giang

Gragnaniello

Mobbs

. Effect of smoking status on successful arthrodesis, clinical outcome, and complications after anterior lumbar interbody fusion (ALIF). World Neurosurg. 2018;110:e998-e1003.

16.

Hofler

Swong

Martin

Wemhoff

Jones

. Risk of pseudoarthrosis after spinal fusion: analysis from the healthcare cost and utilization project. World Neurosurg. 2018;120:e194-e202.

17.

Grabowski

Robertson

. Bone allograft with mesenchymal stem cells: a critical review of the literature. Hard Tissue. 2013;2(2):20.

18.

Jackson

Devine

. The effects of smoking and smoking cessation on spine surgery: a systematic review of the literature. Glob Spine J. 2016;6(7):695-701.

19.

Page

McKenzie

Bossuyt

, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71.

20.

Boishardy

Bouyer

Boissière

, et al. Surgical site infection is a major risk factor of pseudarthrosis in adult spinal deformity surgery. Spine J. 2022;22(12):2059-2065.

21.

Brown

Orme

Richardson

. The rate of pseudarthrosis (surgical nonunion) in patients who are smokers and patients who are nonsmokers: a comparison study. Spine. 1986;11(9):942-943.

22.

Bydon

De la Garza-Ramos

Abt

, et al. Impact of smoking on complication and pseudarthrosis rates after single- and 2-level posterolateral fusion of the lumbar spine. Spine. 2014;39(21):1765-1770.

23.

Cerier

Jain

Lenobel

Niedermeier

Stammen

. Smoking is associated with 1-year suboptimal patient-reported outcomes after 2-level anterior cervical fusion. Clin Spine Surg. 2019;32(4):175-178.

24.

Chapin

Ward

Ryken

. Preoperative depression, smoking, and employment status are significant factors in patient satisfaction after lumbar spine surgery. Clin Spine Surg. 2017;30(6):E725-E732.

25.

Cho

Hwang

Lee

. Clinical and radiological outcomes in patients who underwent posterior lumbar interbody fusion: comparisons between unilateral and bilateral cage insertion. BMC Muscoskelet Disord. 2021;22(1):963.

26.

Cole

Collins

Waters

Salas

Sherman

Cyriac

. Put Down the tin: chewing tobacco use is associated with worse outcomes after primary lumbar fusion. Clin Spine Surg. 2023;36(7):E332-E338.

27.

Gatot

Liow

MHL

Goh

, et al. Smoking is associated with lower satisfaction in nondiabetic patients undergoing minimally invasive single-level transforaminal lumbar interbody fusion. Clin Spine Surg. 2022;35(1):E19-E25.

28.

Hermann

Webler

Bornemann

, et al. Influence of smoking on spinal fusion after spondylodesis surgery: a comparative clinical study. Technol Health Care. 2016;24(5):737-744.

29.

Hilibrand

Fye

Emery

Palumbo

Bohlman

. Impact of smoking on the outcome of anterior cervical arthrodesis with interbody or strut-grafting. J Bone Joint Surg Am. 2001;83(5):668-673.

30.

Kim

Bridwell

Lenke

Rhim

Cheh

. Pseudarthrosis in long adult spinal deformity instrumentation and fusion to the sacrum: prevalence and risk factor analysis of 144 cases. Spine. 2006;31(20):2329-2336.

31.

Kuo

Chang

, et al. Effects of smoking on pedicle screw-based dynamic stabilization: radiological and clinical evaluations of screw loosening in 306 patients. J Neurosurg Spine. 2020;33:1-8.

32.

Lim

Schultz

Zakko

, et al. The potential negative effects of smoking on cervical and lumbar surgery beyond pseudarthrosis: a Michigan spine surgery improvement collaborative study. World Neurosurg. 2023;173:e241-e249.

33.

Luszczyk

Smith

Fischgrund

, et al. Does smoking have an impact on fusion rate in single-level anterior cervical discectomy and fusion with allograft and rigid plate fixation? Clinical article. J Neurosurg Spine. 2013;19(5):527-531.

34.

Macki

Syeda

Rajjoub

, et al. The effect of smoking status on successful arthrodesis after lumbar instrumentation supplemented with rhBMP-2. World Neurosurg. 2017;97:459-464.

35.

Patel

Yoo

Lamoutte

Karmarkar

Singh

. The effect of tobacco use on postoperative pain following anterior cervical discectomy and fusion. Clin Spine Surg. 2019;32(10):E440-E443.

36.

Samartzis

Shen

Goldberg

. Is autograft The Gold standard in achieving radiographic fusion in one-level anterior cervical discectomy and fusion with rigid anterior plate fixation? Spine. 2005;30(15):1756-1761.

37.

Sandén

Försth

Michaëlsson

. Smokers show less improvement than nonsmokers two years after surgery for lumbar spinal stenosis: a study of 4555 patients from the Swedish spine register. Spine. 2011;36(13):1059-1064.

38.

Toci

Karamian

Lambrechts

, et al.

What is the impact of smoking on patient-reported outcomes following posterior cervical decompression and fusion?

World Neurosurg. 2022;162:e319-e327.

39.

Wang

Meng

Liu

Wang

Hong

. The impact of smoking on outcomes following anterior cervical fusion-nonfusion hybrid surgery: a retrospective single-center cohort study. BMC Muscoskelet Disord. 2021;22(1):612.

40.

Yoo

Kim

Hyun

Kim

Jahng

Kim

. Comparison between two different cervical interbody fusion cages in one level stand-alone ACDF: carbon fiber composite frame cage versus polyetheretherketone cage. Korean J Spine. 2014;11(3):127-1235.

41.

Zhou

Pang

Tang

Liu

. Predictive nomogram of cage nonunion after anterior cervical discectomy and fusion: a retrospective study in a spine surgery center. Medicine (Baltim). 2022;101(39):e30763.

42.

Slim

Nini

Forestier

Kwiatkowski

Panis

Chipponi

. Methodological index for non-randomized studies (minors): development and validation of a new instrument. ANZ J Surg. 2003;73(9):712-716.

43.

Higgins

Thomas

Chandler

, et al. Cochrane Handbook for Systematic Reviews of Interventions. John Wiley & Sons; 2019.

44.

Guyatt

Thorlund

Oxman

, et al. GRADE guidelines: 13. Preparing summary of findings tables and evidence profiles-continuous outcomes. J Clin Epidemiol. 2013;66(2):173-183.

45.

Bergin

Wang

Park

, et al. Pseudarthrosis rate following anterior cervical discectomy with fusion using an allograft cellular bone matrix: a multi-institutional analysis. Neurosurg Focus. 2021;50(6):E6.

46.

Russo

Park

Lansford

, et al. Impact of surgical risk factors for non-union on lumbar spinal fusion outcomes using cellular bone allograft at 24-months follow-up. BMC Muscoskelet Disord. 2024;25(1):351.

47.

Rao

, et al. Associations among vitamin D, tobacco smoke, and hypertension: a cross-sectional study of the NHANES 2001-2016. Hypertens Res. 2022;45(12):1986-1996.

48.

Emery

Fisher

Bohlman

. Three-level anterior cervical discectomy and fusion: radiographic and clinical results. Spine. 1997;22:2622-2624.

49.

Emami

Faloon

Sahai

, et al. Risk factors for pseudarthrosis in minimally-invasive transforaminal lumbar interbody fusion. Asian Spine J. 2018;12(5):830-838.

50.

Moazzeni

Kazemi

Khanmohammad

Eslamian

Rostami

Faghih-Jouibari

. Comparison of surgical outcome between diabetic versus nondiabetic patients after lumbar fusion. Int J Spine Surg. 2018;12(4):528-532.

51.

Taylor

McNeill

Girling

Farley

Lindson-Hawley

Aveyard

. Change in mental health after smoking cessation: systematic review and meta-analysis. BMJ. 2014;348:g1151.

52.

Ueha

Sakamoto

, et al. Cigarette smoke delays regeneration of the olfactory epithelium in mice. Neurotox Res. 2016;30(2):213-224.

53.

Raizman

O'Brien

Poehling-Monaghan

. Pseudarthrosis of the spine. J Am Acad Orthop Surg. 2009;17(8):494-503.

54.

Mirzamohammadi

Qasemian

Kassiri

Mohammadi

Hatam

Ghandhari

. Return-to-Work status following One- and two-level anterior cervical discectomy and fusions: a prospective cohort study. Cureus. 2022;14(8):e27546.

55.

Mullerpatan

Jadhav

. Trends in work-absenteeism and return-to-work among people with spine pain in middle income countries: a need for evidence. Work. 2025;80(4):1983-1989.

56.

Hani

Monk

Pfortmiller

, et al. Effect of workers' compensation status on pain, disability, quality of life, and return to work after lumbar spine surgery: a 1-year propensity-matched analysis. J Neurosurg Spine. 2023;39(1):47-57.

57.

Steinmiller

Diederichs

Roehrs

Hyde-Nolan

Roth

Greenwald

. Postsurgical patient controlled opioid self-administration is greater in hospitalized abstinent smokers than nonsmokers. J Opioid Manag. 2012;8:227-235.

58.

Lindström

Sadr Azodi

Wladis

, et al. Effects of a perioperative smoking cessation intervention on postoperative complications: a randomized trial. Ann Surg. 2008;248(5):739-745.

59.

Hammond

Reid

Goniewicz

, et al. Nicotine exposure from smoking tobacco and vaping among adolescents. JAMA Netw Open. 2025;8(3):e2462544.

60.

Ashour

Al-Huneidy

Noordeen

. The implications of vaping on surgical wound healing: a systematic review. Surgery. 2023;173(6):1452-1462.

61.

Fiani

Noblett

Nanney

, et al. The impact of “vaping” electronic cigarettes on spine health. Cureus. 2020;12(6):e8907.

62.

Nicholson

Scott

Newton Ede

Jones

. Do E-cigarettes and vaping have a lower risk of osteoporosis, nonunion, and infection than tobacco smoking? Bone Joint Res. 2021;10(3):188-191.

63.

Bieganowski

Singh

Kugelman

Rozell

Schwarzkopf

Lajam

. Vaping trends and outcomes in primary total joint arthroplasty patients: an analysis of 21,341 patients. J Am Acad Orthop Surg Glob Res Rev. 2023;7(1):e22.

64.

Chaliparambil

Mittal

Gibson

Ahuja

Dahdaleh

El Tecle

. Association between preoperative cannabis use and increased rate of revision surgery following spinal fusion: a systematic review and meta-analysis. Cureus. 2024;16(6):e61828.

65.

Shore

Flaugh

Shannon

Curran

Hogue

. Preoperative considerations for teenagers undergoing orthopaedic surgery: VTE prevention, mental health assessment, vaping, and drug addiction. J Pediatr Orthop. 2021;41(Suppl 1):S64-S69.

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.15 MB