Pub Date : 2025-03-01Epub Date: 2024-09-20DOI: 10.1016/j.surg.2024.06.055
William R Lorenz, Alexis M Holland, Samantha W Kerr, Sully A Ayuso, Monica E Polcz, Gregory T Scarola, Kent W Kercher, B Todd Heniford, Vedra A Augenstein
Introduction: The choice of biologic compared with synthetic mesh in abdominal wall reconstruction remains controversial, especially in Centers for Disease Control and Prevention class 1 and 2 wounds. This study evaluated wound complications and hernia recurrence with a 2:1 propensity-matched sample and extended follow-up.
Methods and procedures: A prospectively maintained abdominal wall reconstruction database was queried for patients undergoing open abdominal wall reconstruction using biologic or synthetic mesh in Centers for Disease Control and Prevention class 1 and 2 wounds. Patients receiving synthetic or biologic mesh were propensity score matched in a 2:1 fashion. Univariate, bivariate, and inferential analyses were conducted. Unless stated, data are reported as biologic compared with synthetic.
Results: In total, 519 patients were compared, 173 with biologic and 346 with synthetic mesh. Defect size (215.2 ± 153.6 cm2 vs 251.5 ± 284.3 cm2), body mass index (33.6 ± 9 kg/m2 vs 34 ±17.7 kg/m2), and comorbidities were well matched (all P > .05). Although Centers for Disease Control and Prevention wound class was used in the match, it was significantly different between groups (Centers for Disease Control and Prevention 1:43.4% vs 81.2%, Centers for Disease Control and Prevention 2:56.6% vs 18.8%; P < .001). The rate of component separation (40.1% vs 44.2%; P = .397), fascial closure (97.7% vs 98.3%; P = .738), and panniculectomy (33.5% vs 29.2%; P = .315) were similar. Mesh size was also similar (816.4 ± 555.5 vs 892.2 ± 487.8 cm2; P = .112). Wound complications were equal, including wound breakdown (10.5% vs 7.5%; P = .315), wound cellulitis (5.2% vs 5.8%; P = .843), wound infection (7.5% vs 4.6%; P = .223), seroma requiring intervention (6.4% vs 7.8%; P = .597), and mesh infection (1.2% vs 0.9%; P > .999). The biologic group had an increased length of stay (6.8 ± 5.5 days vs 5.4 ± 2.3 days; P < .001) and greater hospital charges ($82,181 ± 50,356 vs $62,221 ± 26,817 USD; P < .001). Mean follow-up after biologic repair was longer (33.9 ± 36.6 months vs 23.3 ± 32.3 months; P < .001). Hernia recurrence between the biologic and synthetic groups was not significantly different (2.9% vs 1.4%; P = .313). On multivariable regression, wound complications were predictive of recurrence, and panniculectomy was predictive of wound complications.
Conclusion: In a 2:1 matched analysis of Centers for Disease Control and Prevention 1 and 2 wounds with nearly 3-years of follow-up, biologic and synthetic mesh had similar rates of wound complications and recurrence in abdominal wall reconstruction.
导言:在腹壁重建中,选择生物网片还是合成网片仍存在争议,尤其是在美国疾病控制和预防中心评定的 1 级和 2 级伤口中。本研究通过2:1倾向匹配样本和长期随访评估了伤口并发症和疝气复发情况:我们在前瞻性维护的腹壁重建数据库中查询了在疾病控制和预防中心1级和2级伤口中使用生物或合成网片进行开放式腹壁重建的患者。接受合成网片或生物网片的患者按 2:1 的比例进行倾向评分匹配。进行了单变量、双变量和推理分析。除非另有说明,否则数据均以生物网片与合成网片的比较进行报告:共有 519 例患者进行了比较,其中 173 例使用生物网片,346 例使用合成网片。缺陷大小(215.2 ± 153.6 cm2 vs 251.5 ± 284.3 cm2)、体重指数(33.6 ± 9 kg/m2 vs 34 ± 17.7 kg/m2)和合并症的匹配度很高(P 均大于 0.05)。虽然匹配中使用了美国疾病控制和预防中心的伤口等级,但组间差异显著(美国疾病控制和预防中心 1:43.4% vs 81.2%,美国疾病控制和预防中心 2:56.6% vs 18.8%;P < .001)。组件分离率(40.1% vs 44.2%;P = .397)、筋膜闭合率(97.7% vs 98.3%;P = .738)和脓肿切除率(33.5% vs 29.2%;P = .315)相似。网片大小也相似(816.4 ± 555.5 vs 892.2 ± 487.8 cm2;P = .112)。伤口并发症相同,包括伤口破裂(10.5% vs 7.5%;P = .315)、伤口蜂窝组织炎(5.2% vs 5.8%;P = .843)、伤口感染(7.5% vs 4.6%;P = .223)、需要干预的血清肿(6.4% vs 7.8%;P = .597)和网片感染(1.2% vs 0.9%;P > .999)。生物组的住院时间延长(6.8 ± 5.5 天 vs 5.4 ± 2.3 天;P < .001),住院费用增加(82,181 ± 50,356 美元 vs 62,221 ± 26,817 美元;P < .001)。生物修复术后的平均随访时间更长(33.9 ± 36.6 个月 vs 23.3 ± 32.3 个月;P < .001)。生物组和合成组的疝气复发率差异不大(2.9% vs 1.4%; P = .313)。在多变量回归中,伤口并发症是复发的预测因素,而泛影葡胺切除术是伤口并发症的预测因素:结论:在对美国疾病控制和预防中心 1 级和 2 级伤口进行的 2:1 匹配分析中,在近 3 年的随访中,生物网片和合成网片在腹壁重建中的伤口并发症和复发率相似。
{"title":"Outcomes of synthetic and biologic mesh in abdominal wall reconstruction: A propensity-matched analysis in Centers for Disease Control and Prevention class 1 and 2 wounds.","authors":"William R Lorenz, Alexis M Holland, Samantha W Kerr, Sully A Ayuso, Monica E Polcz, Gregory T Scarola, Kent W Kercher, B Todd Heniford, Vedra A Augenstein","doi":"10.1016/j.surg.2024.06.055","DOIUrl":"10.1016/j.surg.2024.06.055","url":null,"abstract":"<p><strong>Introduction: </strong>The choice of biologic compared with synthetic mesh in abdominal wall reconstruction remains controversial, especially in Centers for Disease Control and Prevention class 1 and 2 wounds. This study evaluated wound complications and hernia recurrence with a 2:1 propensity-matched sample and extended follow-up.</p><p><strong>Methods and procedures: </strong>A prospectively maintained abdominal wall reconstruction database was queried for patients undergoing open abdominal wall reconstruction using biologic or synthetic mesh in Centers for Disease Control and Prevention class 1 and 2 wounds. Patients receiving synthetic or biologic mesh were propensity score matched in a 2:1 fashion. Univariate, bivariate, and inferential analyses were conducted. Unless stated, data are reported as biologic compared with synthetic.</p><p><strong>Results: </strong>In total, 519 patients were compared, 173 with biologic and 346 with synthetic mesh. Defect size (215.2 ± 153.6 cm<sup>2</sup> vs 251.5 ± 284.3 cm<sup>2</sup>), body mass index (33.6 ± 9 kg/m<sup>2</sup> vs 34 ±17.7 kg/m<sup>2</sup>), and comorbidities were well matched (all P > .05). Although Centers for Disease Control and Prevention wound class was used in the match, it was significantly different between groups (Centers for Disease Control and Prevention 1:43.4% vs 81.2%, Centers for Disease Control and Prevention 2:56.6% vs 18.8%; P < .001). The rate of component separation (40.1% vs 44.2%; P = .397), fascial closure (97.7% vs 98.3%; P = .738), and panniculectomy (33.5% vs 29.2%; P = .315) were similar. Mesh size was also similar (816.4 ± 555.5 vs 892.2 ± 487.8 cm<sup>2</sup>; P = .112). Wound complications were equal, including wound breakdown (10.5% vs 7.5%; P = .315), wound cellulitis (5.2% vs 5.8%; P = .843), wound infection (7.5% vs 4.6%; P = .223), seroma requiring intervention (6.4% vs 7.8%; P = .597), and mesh infection (1.2% vs 0.9%; P > .999). The biologic group had an increased length of stay (6.8 ± 5.5 days vs 5.4 ± 2.3 days; P < .001) and greater hospital charges ($82,181 ± 50,356 vs $62,221 ± 26,817 USD; P < .001). Mean follow-up after biologic repair was longer (33.9 ± 36.6 months vs 23.3 ± 32.3 months; P < .001). Hernia recurrence between the biologic and synthetic groups was not significantly different (2.9% vs 1.4%; P = .313). On multivariable regression, wound complications were predictive of recurrence, and panniculectomy was predictive of wound complications.</p><p><strong>Conclusion: </strong>In a 2:1 matched analysis of Centers for Disease Control and Prevention 1 and 2 wounds with nearly 3-years of follow-up, biologic and synthetic mesh had similar rates of wound complications and recurrence in abdominal wall reconstruction.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108795"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142296013","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-09-20DOI: 10.1016/j.surg.2024.07.058
Alexandra Jones, Matthew Benns, Russell Farmer
Objective: To determine whether performance on Step 2 CK can be used to predict adverse academic outcomes in surgical residency.
Methods: Surgical resident data from a single institution was used. Step 2 scores of each resident were normalized against the average Step 2 CK score for each cohort's application cycle (ie, resident who scored 246 on a year with a national average of 246 would have a normed score of 1; resident with a score >246 would have a normed score >1 etc). All adverse events were classified, and logistic regression analysis was used to determine the effects of the Step 2 scores. Adverse academic outcomes were defined.
Results: Ninety-two surgical residents were evaluated with 7,182 faculty evaluations reviewed. Lower Step 2 CK scores demonstrated an increased likelihood of lower American Board of Surgery In-Training Examination performance <25% (P = .011). The remaining adverse events, including passing the Qualifying Examination (P = .998), passing the Certifying Examination (P = .778), early withdrawal from the surgical residency program (P = .565), failure on mock orals during postgraduate years 4 and 5 (P = .731; P = .600), as well as selection of administrative chiefs (P = .565), all demonstrated no correlation.
Conclusion: Emphasis has historically been placed on board examinations like Step 2 CK to predict overall success in residency and is used as an important metric during the interview process. However, these findings demonstrate that although lower scores on Step 2 CK correlate with a lower quartile on the American Board of Surgery In-Training Examination during general surgery residency, the examination cannot predict success in all areas of surgical residency.
目的确定第 2 步 CK 考试成绩是否可用于预测外科住院医师的不良学习结果:方法: 使用来自单一机构的外科住院医师数据。每位住院医师的第 2 步得分均与每个组群申请周期的第 2 步 CK 平均得分进行了标准化处理(即,在全国平均分为 246 分的年份获得 246 分的住院医师的标准化得分为 1 分;得分大于 246 分的住院医师的标准化得分大于 1 分等)。对所有不良事件进行分类,并使用逻辑回归分析确定第 2 步评分的影响。结果:对 92 名外科住院医师进行了评估,审查了 7,182 份教师评估报告。第 2 步 CK 分数越低,美国外科学委员会住院医师培训考试成绩越低:第 2 步 CK 等委员会考试历来是预测住院医师培训总体成功与否的重点,也是面试过程中的重要指标。然而,这些研究结果表明,虽然第 2 步 CK 考试的较低分数与普外科住院医师培训期间美国外科学委员会培训考试的较低四分位数相关,但该考试并不能预测外科住院医师培训所有领域的成功。
{"title":"Using resident performance on Step 2 to predict surgical residency success.","authors":"Alexandra Jones, Matthew Benns, Russell Farmer","doi":"10.1016/j.surg.2024.07.058","DOIUrl":"10.1016/j.surg.2024.07.058","url":null,"abstract":"<p><strong>Objective: </strong>To determine whether performance on Step 2 CK can be used to predict adverse academic outcomes in surgical residency.</p><p><strong>Methods: </strong>Surgical resident data from a single institution was used. Step 2 scores of each resident were normalized against the average Step 2 CK score for each cohort's application cycle (ie, resident who scored 246 on a year with a national average of 246 would have a normed score of 1; resident with a score >246 would have a normed score >1 etc). All adverse events were classified, and logistic regression analysis was used to determine the effects of the Step 2 scores. Adverse academic outcomes were defined.</p><p><strong>Results: </strong>Ninety-two surgical residents were evaluated with 7,182 faculty evaluations reviewed. Lower Step 2 CK scores demonstrated an increased likelihood of lower American Board of Surgery In-Training Examination performance <25% (P = .011). The remaining adverse events, including passing the Qualifying Examination (P = .998), passing the Certifying Examination (P = .778), early withdrawal from the surgical residency program (P = .565), failure on mock orals during postgraduate years 4 and 5 (P = .731; P = .600), as well as selection of administrative chiefs (P = .565), all demonstrated no correlation.</p><p><strong>Conclusion: </strong>Emphasis has historically been placed on board examinations like Step 2 CK to predict overall success in residency and is used as an important metric during the interview process. However, these findings demonstrate that although lower scores on Step 2 CK correlate with a lower quartile on the American Board of Surgery In-Training Examination during general surgery residency, the examination cannot predict success in all areas of surgical residency.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108801"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142296028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-09-27DOI: 10.1016/j.surg.2024.07.057
Signe Braafladt, Hannah Allison, Jeanette Chung, Cary N Mariash, Oindrila Bhattacharyya, Alexandria D McDow, David A Haggstrom
Background: Long-term survival for patients with differentiated (papillary, follicular, and Hürthle cell) thyroid cancer exceeds 95% but self-reported health-related quality of life scores remain low compared with survivors of cancers with worse prognoses. There are reports that thyroid hormone replacement therapy is associated with lower health-related quality of life. This hypothesis was tested in a sample of Medicare Advantage survivors of differentiated thyroid cancer.
Methods: Data were obtained from the linked 2007-2017 Surveillance, Epidemiology and End Results-Medicare Health Outcomes Survey for patients with differentiated thyroid cancer to conduct a cross-sectional study. Levothyroxine 6-month defined daily dose was calculated from claims data. Defined daily dose was classified as low, average, or high on the basis of standard deviations around body mass index-specific means. Veterans RAND 12-item Quality of Life Survey measures were categorized by T score as low health-related quality of life (T scores ≤25), moderately low (25< T scores ≤50), and high (T scores >50). The association of defined daily dose and health-related quality of life was tested using multinomial logistic regression.
Results: Among patients with differentiated thyroid cancer (n = 782), 67.5% were prescribed levothyroxine for thyroid hormone replacement therapy (mean defined daily dose 123 μg; standard deviation 44.1 μg). Greater defined daily dose was associated with greater relative risk of low (compared with moderately low) health-related quality of life on several measures including Role Limitation (relative risk, 4.9, 95% confidence interval, 2.1-11.6) and Social Functioning (relative risk, 5.6, 95% confidence interval, 2.5-12.5), as well as greater relative risk of multiple low-scoring health-related quality of life measures.
Conclusion: Results suggest greater-than-average thyroid hormone replacement therapy dosages may be associated with lower health-related quality of life among survivors of differentiated thyroid cancer. Given the prevalence of thyroid hormone replacement therapy among survivors of differentiated thyroid cancer, thyroid hormone replacement therapy dose adjustment warrants close attention to address the functional and psychosocial well-being of patients.
背景:分化型(乳头状细胞、滤泡细胞和Hürthle细胞)甲状腺癌患者的长期生存率超过95%,但与预后较差的癌症幸存者相比,自我报告的健康相关生活质量得分仍然较低。有报道称,甲状腺激素替代治疗与较低的健康相关生活质量有关。我们在医疗保险优势计划(Medicare Advantage)的分化型甲状腺癌幸存者样本中检验了这一假设:我们从 2007-2017 年监测、流行病学和最终结果-医疗保险健康结果调查中获取了分化型甲状腺癌患者的相关数据,从而开展了一项横断面研究。根据理赔数据计算左甲状腺素 6 个月的定义日剂量。根据身体质量指数特定平均值的标准偏差,将限定日剂量分为低、平均和高三个等级。退伍军人兰德 12 项生活质量调查指标按 T 值分为健康相关生活质量低(T 值≤25)、中低(25< T 值≤50)和高(T 值>50)。采用多项式逻辑回归法检验了规定日剂量与健康相关生活质量的关系:在分化型甲状腺癌患者(n = 782)中,67.5%的患者服用左甲状腺素进行甲状腺激素替代治疗(平均规定日剂量为123微克;标准差为44.1微克)。在包括角色限制(相对风险为4.9,95%置信区间为2.1-11.6)和社会功能(相对风险为5.6,95%置信区间为2.5-12.5)在内的几项健康相关生活质量测量中,明确规定的日剂量越大,健康相关生活质量越低(与中低相比)的相对风险也越大:结果表明,甲状腺激素替代治疗剂量高于平均水平可能与分化型甲状腺癌幸存者较低的健康相关生活质量有关。鉴于甲状腺激素替代疗法在分化型甲状腺癌幸存者中的普遍性,甲状腺激素替代疗法的剂量调整值得密切关注,以解决患者的功能和社会心理健康问题。
{"title":"Dose-dependent relationship between levothyroxine and health-related quality of life in survivors of differentiated thyroid cancer.","authors":"Signe Braafladt, Hannah Allison, Jeanette Chung, Cary N Mariash, Oindrila Bhattacharyya, Alexandria D McDow, David A Haggstrom","doi":"10.1016/j.surg.2024.07.057","DOIUrl":"10.1016/j.surg.2024.07.057","url":null,"abstract":"<p><strong>Background: </strong>Long-term survival for patients with differentiated (papillary, follicular, and Hürthle cell) thyroid cancer exceeds 95% but self-reported health-related quality of life scores remain low compared with survivors of cancers with worse prognoses. There are reports that thyroid hormone replacement therapy is associated with lower health-related quality of life. This hypothesis was tested in a sample of Medicare Advantage survivors of differentiated thyroid cancer.</p><p><strong>Methods: </strong>Data were obtained from the linked 2007-2017 Surveillance, Epidemiology and End Results-Medicare Health Outcomes Survey for patients with differentiated thyroid cancer to conduct a cross-sectional study. Levothyroxine 6-month defined daily dose was calculated from claims data. Defined daily dose was classified as low, average, or high on the basis of standard deviations around body mass index-specific means. Veterans RAND 12-item Quality of Life Survey measures were categorized by T score as low health-related quality of life (T scores ≤25), moderately low (25< T scores ≤50), and high (T scores >50). The association of defined daily dose and health-related quality of life was tested using multinomial logistic regression.</p><p><strong>Results: </strong>Among patients with differentiated thyroid cancer (n = 782), 67.5% were prescribed levothyroxine for thyroid hormone replacement therapy (mean defined daily dose 123 μg; standard deviation 44.1 μg). Greater defined daily dose was associated with greater relative risk of low (compared with moderately low) health-related quality of life on several measures including Role Limitation (relative risk, 4.9, 95% confidence interval, 2.1-11.6) and Social Functioning (relative risk, 5.6, 95% confidence interval, 2.5-12.5), as well as greater relative risk of multiple low-scoring health-related quality of life measures.</p><p><strong>Conclusion: </strong>Results suggest greater-than-average thyroid hormone replacement therapy dosages may be associated with lower health-related quality of life among survivors of differentiated thyroid cancer. Given the prevalence of thyroid hormone replacement therapy among survivors of differentiated thyroid cancer, thyroid hormone replacement therapy dose adjustment warrants close attention to address the functional and psychosocial well-being of patients.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108799"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142354258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-10-29DOI: 10.1016/j.surg.2024.06.084
Alexis M Holland, William R Lorenz, Namratha Mylarapu, Samantha W Kerr, Brittany S Mead, Sullivan A Ayuso, Gregory T Scarola, Vedra A Augenstein, Kent W Kercher, B Todd Heniford
Background: Conflicting literature suggests that larger defects in abdominal wall reconstruction both increase the risk of recurrence and have no impact on recurrence. In our prior work, hernias with defect areas ≥100 cm2 were associated with increased discomfort, operative time, and length of stay but not recurrence or reoperation. Our goal was to determine if defect size, even in giant hernias, would impact recurrence after mesh repair with complete fascial closure.
Methods: A prospectively maintained hernia database was reviewed for clean, abdominal wall reconstruction with fascial closure and synthetic mesh. Patients were grouped and compared by defect area: moderate hernias <200 cm2 (LT200) and giant hernias ≥200 cm2 (GT200).
Results: Of 984 patients, 607 LT200 (average area: 92.8 ± 60.8 cm2) were compared with 377 GT200 (average area: 363.2 ± 196.7 cm2). LT200 and GT200 had similar mean age, body mass index, and smoking rate, but GT200 had higher rates of diabetes (22.1% vs 27.9%; P = .040), recurrent hernias (52.7% vs 63.4%; P = .001), preoperative Botox (0.7% vs 8.8%; P < .001), component separation (23.4% vs 59.9%; P < .001), panniculectomy (8.7% vs 15.4%; P = .001), and negative-pressure incisional vacuum placement (5.9% vs 13.5%; P < .001). GT200 had increased mesh size (753.5 ± 367.1 vs 1168.2 ± 412.0 cm2; P < .001), operative time (147.8 ± 55.7 vs 205.3 ± 59.9 minutes; P < .001), and length of stay (5.1 ± 3.2 vs 6.9 ± 4.4 days; P < .001). GT200 had more wound complications (24.7% vs 36.1%; P < .001) and readmissions (9.1% vs 15.1%; P = .004) but similar recurrence rates (3.0% vs 3.7%; P = .520) over the mean follow-up of 30.1 ± 38.9 and 23.0 ± 33.6 months for LT200 and GT200, respectively. On multivariable regression, previous abdominal wall reconstruction, lightweight mesh, and wound complications independently predicted recurrence; component separation was protective, but defect size was not predictive of recurrence.
Conclusion: GT200 required more complex measures to achieve fascial closure and resulted in increased length of stay, wound complications, and readmissions; however, GT200 had the same recurrence rate as smaller defects when fascial closure was achieved.
背景:相互矛盾的文献表明,腹壁重建中较大的缺损既会增加复发风险,也不会影响复发。在我们之前的研究中,缺损面积≥100 平方厘米的疝与不适感、手术时间和住院时间增加有关,但与复发或再次手术无关。我们的目标是确定即使是巨大的疝气,其缺损面积是否会影响完全筋膜闭合的网片修复术后的复发:方法:我们对一个前瞻性维护的疝气数据库进行了审查,该数据库中的患者都是采用筋膜闭合和合成网片进行腹壁重建的清洁患者。按缺损面积对患者进行分组和比较:中度疝气 2(LT200)和巨大疝气≥200 平方厘米(GT200):在 984 例患者中,607 例 LT200(平均面积:92.8 ± 60.8 cm2)与 377 例 GT200(平均面积:363.2 ± 196.7 cm2)进行了比较。LT200 和 GT200 的平均年龄、体重指数和吸烟率相似,但 GT200 的糖尿病(22.1% vs 27.9%;P = .040)、复发性疝(52.7% vs 63.4%;P = .001)、术前肉毒杆菌(0.7% vs 8.8%;P < .001)、组件分离(23.4% vs 59.9%;P < .001)、脓肿切除术(8.7% vs 15.4%;P = .001)和负压切口真空放置(5.9% vs 13.5%;P < .001)。GT200 增加了网片尺寸(753.5 ± 367.1 vs 1168.2 ± 412.0 平方厘米;P < .001)、手术时间(147.8 ± 55.7 vs 205.3 ± 59.9 分钟;P < .001)和住院时间(5.1 ± 3.2 vs 6.9 ± 4.4 天;P < .001)。GT200的伤口并发症(24.7% vs 36.1%;P < .001)和再住院率(9.1% vs 15.1%;P = .004)更高,但在LT200和GT200分别为30.1 ± 38.9个月和23.0 ± 33.6个月的平均随访期间,复发率(3.0% vs 3.7%;P = .520)相似。在多变量回归中,既往腹壁重建、轻质网片和伤口并发症可独立预测复发;组件分离具有保护作用,但缺损大小不能预测复发:结论:GT200需要更复杂的措施来实现筋膜闭合,并导致住院时间、伤口并发症和再入院率的增加;然而,当实现筋膜闭合时,GT200的复发率与较小的缺损相同。
{"title":"Does defect size matter in abdominal wall reconstruction with successful fascial closure?","authors":"Alexis M Holland, William R Lorenz, Namratha Mylarapu, Samantha W Kerr, Brittany S Mead, Sullivan A Ayuso, Gregory T Scarola, Vedra A Augenstein, Kent W Kercher, B Todd Heniford","doi":"10.1016/j.surg.2024.06.084","DOIUrl":"10.1016/j.surg.2024.06.084","url":null,"abstract":"<p><strong>Background: </strong>Conflicting literature suggests that larger defects in abdominal wall reconstruction both increase the risk of recurrence and have no impact on recurrence. In our prior work, hernias with defect areas ≥100 cm<sup>2</sup> were associated with increased discomfort, operative time, and length of stay but not recurrence or reoperation. Our goal was to determine if defect size, even in giant hernias, would impact recurrence after mesh repair with complete fascial closure.</p><p><strong>Methods: </strong>A prospectively maintained hernia database was reviewed for clean, abdominal wall reconstruction with fascial closure and synthetic mesh. Patients were grouped and compared by defect area: moderate hernias <200 cm<sup>2</sup> (LT200) and giant hernias ≥200 cm<sup>2</sup> (GT200).</p><p><strong>Results: </strong>Of 984 patients, 607 LT200 (average area: 92.8 ± 60.8 cm<sup>2</sup>) were compared with 377 GT200 (average area: 363.2 ± 196.7 cm<sup>2</sup>). LT200 and GT200 had similar mean age, body mass index, and smoking rate, but GT200 had higher rates of diabetes (22.1% vs 27.9%; P = .040), recurrent hernias (52.7% vs 63.4%; P = .001), preoperative Botox (0.7% vs 8.8%; P < .001), component separation (23.4% vs 59.9%; P < .001), panniculectomy (8.7% vs 15.4%; P = .001), and negative-pressure incisional vacuum placement (5.9% vs 13.5%; P < .001). GT200 had increased mesh size (753.5 ± 367.1 vs 1168.2 ± 412.0 cm<sup>2</sup>; P < .001), operative time (147.8 ± 55.7 vs 205.3 ± 59.9 minutes; P < .001), and length of stay (5.1 ± 3.2 vs 6.9 ± 4.4 days; P < .001). GT200 had more wound complications (24.7% vs 36.1%; P < .001) and readmissions (9.1% vs 15.1%; P = .004) but similar recurrence rates (3.0% vs 3.7%; P = .520) over the mean follow-up of 30.1 ± 38.9 and 23.0 ± 33.6 months for LT200 and GT200, respectively. On multivariable regression, previous abdominal wall reconstruction, lightweight mesh, and wound complications independently predicted recurrence; component separation was protective, but defect size was not predictive of recurrence.</p><p><strong>Conclusion: </strong>GT200 required more complex measures to achieve fascial closure and resulted in increased length of stay, wound complications, and readmissions; however, GT200 had the same recurrence rate as smaller defects when fascial closure was achieved.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108894"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142547586","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-11-29DOI: 10.1016/j.surg.2024.06.087
Sergio Mazzola Poli de Figueiredo, Sara M Maskal, Ryan C Ellis, Zubin Mishra, Aldo Fafaj, Nir Messer, David M Krpata, Benjamin T Miller, Lucas R A Beffa, Clayton C Petro, Ajita S Prabhu, Michael J Rosen
Background: Traumatic abdominal wall hernias are rare and commonly involve the lateral abdominal wall due to shearing off the oblique and transversus abdominis muscles from the iliac crest. The vast majority of the current literature focuses on the index trauma admission, includes few patients, and provides little to no detail about the hernia repair itself. We aim to report our center's high-volume experience with a definitive repair of chronic traumatic lateral abdominal wall hernias.
Methods: All patients who underwent lateral abdominal wall hernia repair performed at our institution from January 2015 through August 2023 were identified in the Abdominal Core Health Quality Collaborative. Only patients with blunt trauma etiology were included. Hernia characteristics, operative techniques, postoperative outcomes, and long-term patient-reported outcomes were extracted from the Abdominal Core Health Quality Collaborative database and supplemented with a manual chart review.
Results: Forty-three patients with traumatic lateral abdominal wall hernias underwent repair within the study period. Elective repair occurred at a median of 3 years after a traumatic event. Nearly half of the patients had a recurrent hernia (41.9%) and most had a lumbar (L4) component (79.1%). The mean hernia width was 16.2 cm, and 30.2% had concomitant midline defects. Transversus abdominis release was performed in 88.4% of patients; 74.5% had heavy-weight polypropylene mesh placed and 76.7% had mesh fixation. Superficial surgical site infection occurred in 11.6% of patients, and 7% had a surgical site occurrence. At a mean follow-up of 1.9 years, 3 patients (7%) developed a hernia recurrence, which was noted on physical examination or imaging. One patient was reoperated on for recurrence, and 1 patient underwent partial mesh removal because of a chronic mesh infection.
Conclusion: In the largest series of definitive repairs of complex lateral abdominal wall post-traumatic hernias to date, elective open complex abdominal wall reconstruction is safe and associated with low morbidity and hernia recurrence rates.
{"title":"Complex blunt traumatic abdominal wall hernias: Experience from a high-volume abdominal core health center.","authors":"Sergio Mazzola Poli de Figueiredo, Sara M Maskal, Ryan C Ellis, Zubin Mishra, Aldo Fafaj, Nir Messer, David M Krpata, Benjamin T Miller, Lucas R A Beffa, Clayton C Petro, Ajita S Prabhu, Michael J Rosen","doi":"10.1016/j.surg.2024.06.087","DOIUrl":"10.1016/j.surg.2024.06.087","url":null,"abstract":"<p><strong>Background: </strong>Traumatic abdominal wall hernias are rare and commonly involve the lateral abdominal wall due to shearing off the oblique and transversus abdominis muscles from the iliac crest. The vast majority of the current literature focuses on the index trauma admission, includes few patients, and provides little to no detail about the hernia repair itself. We aim to report our center's high-volume experience with a definitive repair of chronic traumatic lateral abdominal wall hernias.</p><p><strong>Methods: </strong>All patients who underwent lateral abdominal wall hernia repair performed at our institution from January 2015 through August 2023 were identified in the Abdominal Core Health Quality Collaborative. Only patients with blunt trauma etiology were included. Hernia characteristics, operative techniques, postoperative outcomes, and long-term patient-reported outcomes were extracted from the Abdominal Core Health Quality Collaborative database and supplemented with a manual chart review.</p><p><strong>Results: </strong>Forty-three patients with traumatic lateral abdominal wall hernias underwent repair within the study period. Elective repair occurred at a median of 3 years after a traumatic event. Nearly half of the patients had a recurrent hernia (41.9%) and most had a lumbar (L4) component (79.1%). The mean hernia width was 16.2 cm, and 30.2% had concomitant midline defects. Transversus abdominis release was performed in 88.4% of patients; 74.5% had heavy-weight polypropylene mesh placed and 76.7% had mesh fixation. Superficial surgical site infection occurred in 11.6% of patients, and 7% had a surgical site occurrence. At a mean follow-up of 1.9 years, 3 patients (7%) developed a hernia recurrence, which was noted on physical examination or imaging. One patient was reoperated on for recurrence, and 1 patient underwent partial mesh removal because of a chronic mesh infection.</p><p><strong>Conclusion: </strong>In the largest series of definitive repairs of complex lateral abdominal wall post-traumatic hernias to date, elective open complex abdominal wall reconstruction is safe and associated with low morbidity and hernia recurrence rates.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108941"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142755680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-10-30DOI: 10.1016/j.surg.2024.09.042
Catherine G Pratt, Szu-Aun Long, Jenna N Whitrock, Tammy M Holm
Background: Surgery is the mainstay of therapy for thyroid cancer. A rising number of patients decline recommended surgical intervention. This study aimed to identify factors associated with the decision to decline surgery for well-differentiated thyroid cancer.
Methods: Patients with papillary or follicular thyroid cancer diagnosed between 2004 and 2017 were identified from the National Cancer Database. Patients were grouped based on patient-documented refusal of recommended surgery and patients who successfully completed surgery. Baseline characteristic comparison, univariable and multivariable logistic regression, and survival analyses were performed.
Results: A total of 221,664 patients met inclusion criteria: 565 (0.3%) patients declined and 221,099 (99.7%) underwent recommended surgery. Patients who declined surgery were older, male, Black or Asian, and not privately insured. They more frequently had Charlson-Deyo scores ≥3, were diagnosed at academic centers, and presented with larger tumors and advanced clinical stage. Multivariable modeling demonstrated that older age, Black or Asian race, diagnosis at an academic center, no insurance or lack of private insurance, clinical N stage ≥1a, and clinical M stage >0 were associated with higher odds of declining surgery (P < .001). A mean survival of 10 years was found among patients who declined surgery versus 16 years among patients who underwent surgery (P < .0001).
Conclusion: Most patients diagnosed with well-differentiated thyroid cancer undergo physician-recommended surgical intervention. Declining surgery is associated with worse overall survival and is more likely in older, male, Black, or Asian patients with socioeconomic disadvantage. This study underscores the importance of understanding barriers to thyroid cancer surgery and opportunities to optimize outcomes and reduce disparities for these populations.
{"title":"\"Thanks, but no thanks\": Factors associated with patients who decline surgical intervention for thyroid cancer.","authors":"Catherine G Pratt, Szu-Aun Long, Jenna N Whitrock, Tammy M Holm","doi":"10.1016/j.surg.2024.09.042","DOIUrl":"10.1016/j.surg.2024.09.042","url":null,"abstract":"<p><strong>Background: </strong>Surgery is the mainstay of therapy for thyroid cancer. A rising number of patients decline recommended surgical intervention. This study aimed to identify factors associated with the decision to decline surgery for well-differentiated thyroid cancer.</p><p><strong>Methods: </strong>Patients with papillary or follicular thyroid cancer diagnosed between 2004 and 2017 were identified from the National Cancer Database. Patients were grouped based on patient-documented refusal of recommended surgery and patients who successfully completed surgery. Baseline characteristic comparison, univariable and multivariable logistic regression, and survival analyses were performed.</p><p><strong>Results: </strong>A total of 221,664 patients met inclusion criteria: 565 (0.3%) patients declined and 221,099 (99.7%) underwent recommended surgery. Patients who declined surgery were older, male, Black or Asian, and not privately insured. They more frequently had Charlson-Deyo scores ≥3, were diagnosed at academic centers, and presented with larger tumors and advanced clinical stage. Multivariable modeling demonstrated that older age, Black or Asian race, diagnosis at an academic center, no insurance or lack of private insurance, clinical N stage ≥1a, and clinical M stage >0 were associated with higher odds of declining surgery (P < .001). A mean survival of 10 years was found among patients who declined surgery versus 16 years among patients who underwent surgery (P < .0001).</p><p><strong>Conclusion: </strong>Most patients diagnosed with well-differentiated thyroid cancer undergo physician-recommended surgical intervention. Declining surgery is associated with worse overall survival and is more likely in older, male, Black, or Asian patients with socioeconomic disadvantage. This study underscores the importance of understanding barriers to thyroid cancer surgery and opportunities to optimize outcomes and reduce disparities for these populations.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108900"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142558838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-09-20DOI: 10.1016/j.surg.2024.07.054
Ryan C Chae, Stephanie Sisak, Christopher Q Nguyen, Lindsey J Wattley, Bernadin Joseph, Lisa England, Rebecca Schuster, Alex B Lentsch, Charles C Caldwell, Michael D Goodman, Timothy A Pritts
Background: The use of whole blood compared with a balanced ratio of components in trauma resuscitation remains an area of ongoing investigation. One factor that may affect outcomes is the age of the blood product transfused. We used a murine model of blood banking and hemorrhagic shock resuscitation to compare the effect of storage duration in whole blood and packed red blood cells on the recipient inflammatory response.
Methods: Murine whole blood or packed red blood cells were evaluated for the red blood cells storage lesion up to 14 days. Mice underwent hemorrhagic shock followed by resuscitation with whole blood or packed red blood cells combined with equal volume of thawed plasma (1:1) stored for 1, 7, or 14 days. Serum and lung cytokine/chemokine levels were measured and leukocyte infiltration determined via immunohistochemistry.
Results: Both whole blood and packed red blood cells develop a blood storage lesion. Four hours after resuscitation, mice resuscitated with either day 14 whole blood or 1:1 demonstrated increased inflammatory cytokines and chemokines with similar findings within lung tissue compared with mice resuscitated with whole blood and 1:1 products stored for 1 or 7 days.
Conclusions: Resuscitation with murine packed red blood cells or whole blood stored for 14 days produces a pronounced recipient inflammatory response compared with those units stored for lesser durations. Given the shorter storage duration of human whole blood to packed RBCs, resuscitation with whole blood within current storage limits may represent an advantageous resuscitation strategy compared with older packed red blood cells.
{"title":"Age above all: The impact of storage duration in mice resuscitated with whole blood or packed red blood cells and plasma in a hemorrhagic shock model.","authors":"Ryan C Chae, Stephanie Sisak, Christopher Q Nguyen, Lindsey J Wattley, Bernadin Joseph, Lisa England, Rebecca Schuster, Alex B Lentsch, Charles C Caldwell, Michael D Goodman, Timothy A Pritts","doi":"10.1016/j.surg.2024.07.054","DOIUrl":"10.1016/j.surg.2024.07.054","url":null,"abstract":"<p><strong>Background: </strong>The use of whole blood compared with a balanced ratio of components in trauma resuscitation remains an area of ongoing investigation. One factor that may affect outcomes is the age of the blood product transfused. We used a murine model of blood banking and hemorrhagic shock resuscitation to compare the effect of storage duration in whole blood and packed red blood cells on the recipient inflammatory response.</p><p><strong>Methods: </strong>Murine whole blood or packed red blood cells were evaluated for the red blood cells storage lesion up to 14 days. Mice underwent hemorrhagic shock followed by resuscitation with whole blood or packed red blood cells combined with equal volume of thawed plasma (1:1) stored for 1, 7, or 14 days. Serum and lung cytokine/chemokine levels were measured and leukocyte infiltration determined via immunohistochemistry.</p><p><strong>Results: </strong>Both whole blood and packed red blood cells develop a blood storage lesion. Four hours after resuscitation, mice resuscitated with either day 14 whole blood or 1:1 demonstrated increased inflammatory cytokines and chemokines with similar findings within lung tissue compared with mice resuscitated with whole blood and 1:1 products stored for 1 or 7 days.</p><p><strong>Conclusions: </strong>Resuscitation with murine packed red blood cells or whole blood stored for 14 days produces a pronounced recipient inflammatory response compared with those units stored for lesser durations. Given the shorter storage duration of human whole blood to packed RBCs, resuscitation with whole blood within current storage limits may represent an advantageous resuscitation strategy compared with older packed red blood cells.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108792"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142295904","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-10-28DOI: 10.1016/j.surg.2024.06.077
R Matthew Walsh
{"title":"Othered.","authors":"R Matthew Walsh","doi":"10.1016/j.surg.2024.06.077","DOIUrl":"10.1016/j.surg.2024.06.077","url":null,"abstract":"","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108877"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142508442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-10-09DOI: 10.1016/j.surg.2024.08.047
Jenna N Whitrock, Catherine G Pratt, Szu-Aun Long, Michela M Carter, Jaime D Lewis, Alicia A Heelan
Objectives: In 2016, the Choosing Wisely campaign published guidelines recommending omission of sentinel lymph node biopsy in clinically node-negative women ≥70 years with early-stage (cT1-2), hormone receptor-positive, and human epidermal growth factor receptor 2-negative breast cancers. This study aimed to evaluate the implementation of this guideline.
Methods: The National Cancer Database was queried from 2017 to 2020. All patients who met criteria for lymph node surgery omission were included and compared with those who underwent lymph node surgery.
Results: Of 138,648 patients who met criteria for lymph node surgery omission, 26,070 (21.0%) had lymph node surgery omission and 109,482 (79.0%) underwent lymph node surgery. Those who had lymph node surgery omission were older (median 79 [75-84] vs 75 [72-79] years, P < .01) and had increased comorbidities (28.3% with Charlson/Deyo score ≥3 had lymph node surgery omission vs 20.2% with score 0, P < .01). Academic/research institutions most frequently practiced lymph node surgery omission (25.8% vs 16.5% community cancer programs, 19.3% comprehensive community cancer programs, and 20.6% integrated network cancer programs, P < .01). A greater percentage of lymph node surgery omission was noted with ductal carcinoma (21.4% vs 17.6% lobular and 19.4% mixed, P < .01) and lower-grade tumors (21.7% of grade 1 vs 19.4% of grade 2 and 17.8% of grade 3, P < .01). Throughout the period studied, the overall rate of lymph node surgery omission increased from 17.7% in 2017 to 23.1% in 2020 (P < .01).
Conclusion: Despite the evidence-based Choosing Wisely guideline recommending lymph node surgery omission in selected patients with breast cancer, more than 75% of patients meeting criteria were still being subjected to lymph node surgery as of 2020. Future work is warranted to determine factors affecting implementation of the Choosing Wisely guideline.
{"title":"Implementation of Choosing Wisely guidelines: Omission of lymph node surgery.","authors":"Jenna N Whitrock, Catherine G Pratt, Szu-Aun Long, Michela M Carter, Jaime D Lewis, Alicia A Heelan","doi":"10.1016/j.surg.2024.08.047","DOIUrl":"10.1016/j.surg.2024.08.047","url":null,"abstract":"<p><strong>Objectives: </strong>In 2016, the Choosing Wisely campaign published guidelines recommending omission of sentinel lymph node biopsy in clinically node-negative women ≥70 years with early-stage (cT1-2), hormone receptor-positive, and human epidermal growth factor receptor 2-negative breast cancers. This study aimed to evaluate the implementation of this guideline.</p><p><strong>Methods: </strong>The National Cancer Database was queried from 2017 to 2020. All patients who met criteria for lymph node surgery omission were included and compared with those who underwent lymph node surgery.</p><p><strong>Results: </strong>Of 138,648 patients who met criteria for lymph node surgery omission, 26,070 (21.0%) had lymph node surgery omission and 109,482 (79.0%) underwent lymph node surgery. Those who had lymph node surgery omission were older (median 79 [75-84] vs 75 [72-79] years, P < .01) and had increased comorbidities (28.3% with Charlson/Deyo score ≥3 had lymph node surgery omission vs 20.2% with score 0, P < .01). Academic/research institutions most frequently practiced lymph node surgery omission (25.8% vs 16.5% community cancer programs, 19.3% comprehensive community cancer programs, and 20.6% integrated network cancer programs, P < .01). A greater percentage of lymph node surgery omission was noted with ductal carcinoma (21.4% vs 17.6% lobular and 19.4% mixed, P < .01) and lower-grade tumors (21.7% of grade 1 vs 19.4% of grade 2 and 17.8% of grade 3, P < .01). Throughout the period studied, the overall rate of lymph node surgery omission increased from 17.7% in 2017 to 23.1% in 2020 (P < .01).</p><p><strong>Conclusion: </strong>Despite the evidence-based Choosing Wisely guideline recommending lymph node surgery omission in selected patients with breast cancer, more than 75% of patients meeting criteria were still being subjected to lymph node surgery as of 2020. Future work is warranted to determine factors affecting implementation of the Choosing Wisely guideline.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108843"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142393507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-01Epub Date: 2024-11-05DOI: 10.1016/j.surg.2024.07.090
Jessica E Schucht, Shayan Rakhit, Michael C Smith, Jin H Han, Joshua B Brown, Areg Grigorian, Stephen P Gondek, Jason W Smith, Mayur B Patel, Amelia W Maiga
Introduction: Early identification of traumatic brain injury followed by timely, targeted treatment is essential. We aimed to establish the ability of prehospital Glasgow Coma Scale score alone and combined with vital signs to predict hospital-diagnosed traumatic brain injury.
Methods: This study included adults from the 2017-2020 Trauma Quality Improvement Program data set with blunt mechanism. We calculated test characteristics of prehospital Glasgow Coma Scale score ≤12 alone and Glasgow Coma Scale score combined with heart rate and systolic blood pressure for predicting (1) any traumatic brain injury and (2) moderate to severe traumatic brain injury. Diagnostic performances were calculated in all patients and older adults (≥55 years). We used decision curve analysis to determine the net diagnostic benefit of prehospital Glasgow Coma Scale score combined with heart rate + systolic blood pressure over Glasgow Coma Scale score alone.
Results: Of 1,687,336 patients, 39.1% had any traumatic brain injury, 3.7% had moderate to severe traumatic brain injury, and 9.1% had a prehospital Glasgow Coma Scale score ≤12. Prehospital Glasgow Coma Scale score ≤12 alone had a sensitivity 83.1%, specificity 93.7%, negative predictive value 99.3%, and positive predictive value 33.7% for predicting moderate to severe traumatic brain injury. Adding prehospital heart rate <65/min and systolic blood pressure >150 mm Hg to Glasgow Coma Scale score ≤12 improved the positive predictive value for moderate to severe traumatic brain injury (55.3%), with a preserved negative predictive value of 96.4%. Decision curve analysis showed the traumatic brain injury prediction model including prehospital heart rate and systolic blood pressure had the greatest net benefit across most threshold probabilities.
Conclusion: Less than a third of adult blunt trauma patients with a prehospital Glasgow Coma Scale score ≤12 have moderate to severe traumatic brain injury. Supplementing Glasgow Coma Scale score with prehospital vital signs improves diagnostic accuracy, potentially by filtering out patients with altered consciousness due to shock. Future work should better identify patients for traumatic brain injury-specific treatments in prehospital settings, including triage destination.
{"title":"Beyond Glasgow Coma Scale: Prehospital prediction of traumatic brain injury.","authors":"Jessica E Schucht, Shayan Rakhit, Michael C Smith, Jin H Han, Joshua B Brown, Areg Grigorian, Stephen P Gondek, Jason W Smith, Mayur B Patel, Amelia W Maiga","doi":"10.1016/j.surg.2024.07.090","DOIUrl":"10.1016/j.surg.2024.07.090","url":null,"abstract":"<p><strong>Introduction: </strong>Early identification of traumatic brain injury followed by timely, targeted treatment is essential. We aimed to establish the ability of prehospital Glasgow Coma Scale score alone and combined with vital signs to predict hospital-diagnosed traumatic brain injury.</p><p><strong>Methods: </strong>This study included adults from the 2017-2020 Trauma Quality Improvement Program data set with blunt mechanism. We calculated test characteristics of prehospital Glasgow Coma Scale score ≤12 alone and Glasgow Coma Scale score combined with heart rate and systolic blood pressure for predicting (1) any traumatic brain injury and (2) moderate to severe traumatic brain injury. Diagnostic performances were calculated in all patients and older adults (≥55 years). We used decision curve analysis to determine the net diagnostic benefit of prehospital Glasgow Coma Scale score combined with heart rate + systolic blood pressure over Glasgow Coma Scale score alone.</p><p><strong>Results: </strong>Of 1,687,336 patients, 39.1% had any traumatic brain injury, 3.7% had moderate to severe traumatic brain injury, and 9.1% had a prehospital Glasgow Coma Scale score ≤12. Prehospital Glasgow Coma Scale score ≤12 alone had a sensitivity 83.1%, specificity 93.7%, negative predictive value 99.3%, and positive predictive value 33.7% for predicting moderate to severe traumatic brain injury. Adding prehospital heart rate <65/min and systolic blood pressure >150 mm Hg to Glasgow Coma Scale score ≤12 improved the positive predictive value for moderate to severe traumatic brain injury (55.3%), with a preserved negative predictive value of 96.4%. Decision curve analysis showed the traumatic brain injury prediction model including prehospital heart rate and systolic blood pressure had the greatest net benefit across most threshold probabilities.</p><p><strong>Conclusion: </strong>Less than a third of adult blunt trauma patients with a prehospital Glasgow Coma Scale score ≤12 have moderate to severe traumatic brain injury. Supplementing Glasgow Coma Scale score with prehospital vital signs improves diagnostic accuracy, potentially by filtering out patients with altered consciousness due to shock. Future work should better identify patients for traumatic brain injury-specific treatments in prehospital settings, including triage destination.</p>","PeriodicalId":22152,"journal":{"name":"Surgery","volume":" ","pages":"108893"},"PeriodicalIF":3.2,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142590729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}