Pub Date : 2026-03-01Epub Date: 2025-01-28DOI: 10.1177/17504589241305299
Francis X Cedeño-Rodriguez, Hans W Hess Arcelay, José I Acosta Julbe, Emil Varas-Rodríguez, Jerry Cruz, Francisco Otero, Kenneth Cintron, Julian Girod
Case: An active healthy 68-year-old male sustained a bilateral quadriceps tendon rupture while running. He underwent a simultaneous bilateral quadriceps tendon repair in a dual-surgeon approach. The right quadriceps tendon was repaired with a tourniquet, while the left quadriceps tendon tear was repaired without one. Postoperatively, the patient developed deep vein thrombosis in the right leg, which led to a bilateral pulmonary embolism. This case illustrates a potential complication of tourniquet use in patients undergoing quadriceps tendon repairs.
Conclusion: The use of tourniquets in orthopaedic surgeries may be associated with potential risks, such as development of venous thromboembolism including deep vein thrombosis and pulmonary embolism. This case highlights the importance of carefully considering tourniquet use for quadriceps tendon repairs and close postoperative monitoring, early mobility, and thromboprophylaxis to prevent severe complications.
{"title":"Pulmonary embolism following bilateral quadriceps tendon repair with unilateral tourniquet use: A case report.","authors":"Francis X Cedeño-Rodriguez, Hans W Hess Arcelay, José I Acosta Julbe, Emil Varas-Rodríguez, Jerry Cruz, Francisco Otero, Kenneth Cintron, Julian Girod","doi":"10.1177/17504589241305299","DOIUrl":"10.1177/17504589241305299","url":null,"abstract":"<p><strong>Case: </strong>An active healthy 68-year-old male sustained a bilateral quadriceps tendon rupture while running. He underwent a simultaneous bilateral quadriceps tendon repair in a dual-surgeon approach. The right quadriceps tendon was repaired with a tourniquet, while the left quadriceps tendon tear was repaired without one. Postoperatively, the patient developed deep vein thrombosis in the right leg, which led to a bilateral pulmonary embolism. This case illustrates a potential complication of tourniquet use in patients undergoing quadriceps tendon repairs.</p><p><strong>Conclusion: </strong>The use of tourniquets in orthopaedic surgeries may be associated with potential risks, such as development of venous thromboembolism including deep vein thrombosis and pulmonary embolism. This case highlights the importance of carefully considering tourniquet use for quadriceps tendon repairs and close postoperative monitoring, early mobility, and thromboprophylaxis to prevent severe complications.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"110-113"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143053706","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-02-18DOI: 10.1177/17504589251318229
Naqiya Noorain, Mohammed Ismail Nizami, Shibani Padhy, Kavitha Jayaram
Background: The incidence of perioperative cardiovascular morbidity and mortality in diabetic patients is due to impaired cardiovascular response to exercise caused by impairment in peripheral blood flow and oxygen diffusion to the exercising muscle. Preoperative bedside testing by 6-min walk for autonomic dysfunction in diabetic patients might reduce haemodynamic instability and cardiovascular complications.
Methods and materials: Sixty patients with American Society of Anaesthesiologists grade 1 classification and 60 diabetic patients (total of 120) of age 30-60 years, of either sex, undergoing elective surgery under general anaesthesia were recruited. A 6-min walk test, breath-holding time and five clinical bedside tests for autonomic dysfunction were performed. Based on that, patients were classified into non-diabetic patients (group C), diabetic patients without autonomic dysfunction (group D) and diabetic patients with autonomic dysfunction (group A).
Results: The incidence of autonomic dysfunction was 31.7%. Among all the parameters, breath-holding time, steps and distance covered by 6-min walk test was significantly less in group A. The incidence of intraoperative tachycardia and hypotension was significantly higher (78.9% and 57.9%, respectively) in group A.
Conclusion: The 6-min walk test can be used as one of the preliminary tests for detection of cardiac autonomic neuropathy in diabetes since it had association with distance covered and intraoperative haemodynamic disturbances.
{"title":"To assess the usefulness of 6-min walk test for determining autonomic dysfunction in diabetic patients compared with non-diabetic patients during preoperative evaluation: A prospective observational controlled study.","authors":"Naqiya Noorain, Mohammed Ismail Nizami, Shibani Padhy, Kavitha Jayaram","doi":"10.1177/17504589251318229","DOIUrl":"10.1177/17504589251318229","url":null,"abstract":"<p><strong>Background: </strong>The incidence of perioperative cardiovascular morbidity and mortality in diabetic patients is due to impaired cardiovascular response to exercise caused by impairment in peripheral blood flow and oxygen diffusion to the exercising muscle. Preoperative bedside testing by 6-min walk for autonomic dysfunction in diabetic patients might reduce haemodynamic instability and cardiovascular complications.</p><p><strong>Methods and materials: </strong>Sixty patients with American Society of Anaesthesiologists grade 1 classification and 60 diabetic patients (total of 120) of age 30-60 years, of either sex, undergoing elective surgery under general anaesthesia were recruited. A 6-min walk test, breath-holding time and five clinical bedside tests for autonomic dysfunction were performed. Based on that, patients were classified into non-diabetic patients (group C), diabetic patients without autonomic dysfunction (group D) and diabetic patients with autonomic dysfunction (group A).</p><p><strong>Results: </strong>The incidence of autonomic dysfunction was 31.7%. Among all the parameters, breath-holding time, steps and distance covered by 6-min walk test was significantly less in group A. The incidence of intraoperative tachycardia and hypotension was significantly higher (78.9% and 57.9%, respectively) in group A.</p><p><strong>Conclusion: </strong>The 6-min walk test can be used as one of the preliminary tests for detection of cardiac autonomic neuropathy in diabetes since it had association with distance covered and intraoperative haemodynamic disturbances.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"164-172"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143441929","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-07-22DOI: 10.1177/17504589251359164
José Miguel Seguro, Pedro Marques, Pedro Moura, Marisa Vicente, José Ferrão
Introduction: Prone positioning in surgery, commonly used in orthopaedics and neurosurgery, carries a high risk of positioning-related injuries. In patients with achondroplasia, anatomical differences present unique challenges for safe surgical positioning.
Case summary: This case report describes the perioperative management of a 48-year-old woman with achondroplasia undergoing spinal decompression and posterolateral arthrodesis. A detailed preoperative assessment was conducted, including patient participation in testing positions and equipment to ensure both safety and surgical accessibility. A balanced approach was achieved, and intraoperative positioning was continuously monitored. Postoperative evaluation revealed no positioning-related injuries.
Conclusions: This case highlights the critical role of preoperative planning and intraoperative vigilance in preventing complications. It also underscores the need for specific guidelines addressing the positioning of individuals with achondroplasia during surgery, particularly in the prone position, to be incorporated into international standards and best practice recommendations.
{"title":"Prone positioning for spinal surgery in achondroplasia: A case study report.","authors":"José Miguel Seguro, Pedro Marques, Pedro Moura, Marisa Vicente, José Ferrão","doi":"10.1177/17504589251359164","DOIUrl":"10.1177/17504589251359164","url":null,"abstract":"<p><strong>Introduction: </strong>Prone positioning in surgery, commonly used in orthopaedics and neurosurgery, carries a high risk of positioning-related injuries. In patients with achondroplasia, anatomical differences present unique challenges for safe surgical positioning.</p><p><strong>Case summary: </strong>This case report describes the perioperative management of a 48-year-old woman with achondroplasia undergoing spinal decompression and posterolateral arthrodesis. A detailed preoperative assessment was conducted, including patient participation in testing positions and equipment to ensure both safety and surgical accessibility. A balanced approach was achieved, and intraoperative positioning was continuously monitored. Postoperative evaluation revealed no positioning-related injuries.</p><p><strong>Conclusions: </strong>This case highlights the critical role of preoperative planning and intraoperative vigilance in preventing complications. It also underscores the need for specific guidelines addressing the positioning of individuals with achondroplasia during surgery, particularly in the prone position, to be incorporated into international standards and best practice recommendations.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"121-125"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12913700/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144691813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-07-29DOI: 10.1177/17504589251355395
Ghazanfar Khan, Aurangzeb Khan, Hamza Khan, Hajra Faheem, Mahnoor Shaukat
Uterine perforation is one of the serious complications associated with the use of an intrauterine contraceptive device, and its migration can lead to complications involving neighbouring organs, including the appendix. We report an unusual case of a 22-year-old Pakistani woman, who presented to the emergency department with pain in the right iliac fossa and was diagnosed as a case of foreign body appendicitis resulting from migration of an intrauterine contraceptive device and entering the lumen of the appendix. This case adds to the limited literature, with only 17 previously documented cases of intrauterine contraceptive device-related appendicitis. To our knowledge, it is the first reported instance of an intrauterine contraceptive device found inside the lumen of the appendix without causing its perforation, making it very rare. These occurrences highlight the need for vigilant monitoring of potential complications following intrauterine contraceptive device insertion.
{"title":"From contraception to complication: Copper-T intrauterine contraceptive device migration leading to foreign body appendicitis.","authors":"Ghazanfar Khan, Aurangzeb Khan, Hamza Khan, Hajra Faheem, Mahnoor Shaukat","doi":"10.1177/17504589251355395","DOIUrl":"10.1177/17504589251355395","url":null,"abstract":"<p><p>Uterine perforation is one of the serious complications associated with the use of an intrauterine contraceptive device, and its migration can lead to complications involving neighbouring organs, including the appendix. We report an unusual case of a 22-year-old Pakistani woman, who presented to the emergency department with pain in the right iliac fossa and was diagnosed as a case of foreign body appendicitis resulting from migration of an intrauterine contraceptive device and entering the lumen of the appendix. This case adds to the limited literature, with only 17 previously documented cases of intrauterine contraceptive device-related appendicitis. To our knowledge, it is the first reported instance of an intrauterine contraceptive device found inside the lumen of the appendix without causing its perforation, making it very rare. These occurrences highlight the need for vigilant monitoring of potential complications following intrauterine contraceptive device insertion.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"126-129"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144733585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: The choice of analgesic technique for total knee arthroplasty affects its rehabilitation and surgical outcomes. This study evaluates this choice on short-term postoperative quality of life.
Methods: In this prospective observational study, patients were categorised into two groups: epidural analgesia or peripheral nerve blocks. The medical and intraoperative data of 36 adult patients undergoing scheduled total knee arthroplasty was collected. The researchers applied the Knee Injury and Osteoarthritis Outcome Score (KOOS), EuroQoL 5 Dimension Score (EQ-5D) and Clinical Frailty Scale questionnaires, preoperatively and at 48 hours postoperatively.
Results: Both groups showed postoperative improvement in pain, mobility and perceived health status. However, no significant differences were observed between the groups across any of the outcome measures, suggesting comparable postoperative results.
Discussion: Although epidural analgesia has traditionally been favoured, no clear advantage was identified. These results support the consideration of both techniques in clinical practice and highlight the need for further research on long-term, patient-centred recovery indicators.
{"title":"Impact of analgesic technique on immediate patient-reported outcomes after total knee arthroplasty.","authors":"Luís Guilherme Casimiro, Beatriz Cunha, Catarina M Fernandes, Joselina Barbosa, Joana Mourão","doi":"10.1177/17504589251367127","DOIUrl":"10.1177/17504589251367127","url":null,"abstract":"<p><strong>Introduction: </strong>The choice of analgesic technique for total knee arthroplasty affects its rehabilitation and surgical outcomes. This study evaluates this choice on short-term postoperative quality of life.</p><p><strong>Methods: </strong>In this prospective observational study, patients were categorised into two groups: epidural analgesia or peripheral nerve blocks. The medical and intraoperative data of 36 adult patients undergoing scheduled total knee arthroplasty was collected. The researchers applied the Knee Injury and Osteoarthritis Outcome Score (KOOS), EuroQoL 5 Dimension Score (EQ-5D) and Clinical Frailty Scale questionnaires, preoperatively and at 48 hours postoperatively.</p><p><strong>Results: </strong>Both groups showed postoperative improvement in pain, mobility and perceived health status. However, no significant differences were observed between the groups across any of the outcome measures, suggesting comparable postoperative results.</p><p><strong>Discussion: </strong>Although epidural analgesia has traditionally been favoured, no clear advantage was identified. These results support the consideration of both techniques in clinical practice and highlight the need for further research on long-term, patient-centred recovery indicators.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"134-140"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145008470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Myocardial injury after non-cardiac surgery is due to ischaemia either during non-cardiac surgery or within 30 days after it. Our surveillance protocol includes hip fracture template and high-sensitivity troponin stratification, as recommended in European countries. Our retrospective study cohort included surgical patients for hip fracture at our hospital in Japan. The primary outcome was the rate of myocardial injury after non-cardiac surgery in comparison to patients managed with (213) and without (176) hip fracture template. The hip fracture template was used more in patients with myocardial injury after non-cardiac surgery than those without myocardial injury after non-cardiac surgery. When hip fracture template was used, patients had a higher likelihood of myocardial injury after non-cardiac surgery after adjusting for age, time to operation, diabetes mellitus, and chronic kidney disease (odds ratio 41.3; 95% confidence interval: 12.1, 259.6). Patients with myocardial injury after non-cardiac surgery had higher in-hospital mortality than those without myocardial injury after non-cardiac surgery, even in adjusted analysis. There was a high detection rate of myocardial injury after non-cardiac surgery when patients with hip fractures were managed with hip fracture template. Myocardial injury after non-cardiac surgery was associated with in-hospital mortality.
{"title":"Perioperative surveillance of myocardial injury after non-cardiac surgery in patients with hip fracture: A retrospective cohort study.","authors":"Naoto Ishimaru, Takahiro Waki, Toshio Shimokawa, Shimpei Mizuki, Jun Ohnishi, Yohei Kanzawa, Takahiro Nakajima, Tomonori Yano, Kenjiro Ito, Keisuke Oe, Saori Kinami","doi":"10.1177/17504589241268624","DOIUrl":"10.1177/17504589241268624","url":null,"abstract":"<p><p>Myocardial injury after non-cardiac surgery is due to ischaemia either during non-cardiac surgery or within 30 days after it. Our surveillance protocol includes hip fracture template and high-sensitivity troponin stratification, as recommended in European countries. Our retrospective study cohort included surgical patients for hip fracture at our hospital in Japan. The primary outcome was the rate of myocardial injury after non-cardiac surgery in comparison to patients managed with (213) and without (176) hip fracture template. The hip fracture template was used more in patients with myocardial injury after non-cardiac surgery than those without myocardial injury after non-cardiac surgery. When hip fracture template was used, patients had a higher likelihood of myocardial injury after non-cardiac surgery after adjusting for age, time to operation, diabetes mellitus, and chronic kidney disease (odds ratio 41.3; 95% confidence interval: 12.1, 259.6). Patients with myocardial injury after non-cardiac surgery had higher in-hospital mortality than those without myocardial injury after non-cardiac surgery, even in adjusted analysis. There was a high detection rate of myocardial injury after non-cardiac surgery when patients with hip fractures were managed with hip fracture template. Myocardial injury after non-cardiac surgery was associated with in-hospital mortality.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"141-147"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142005448","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-08-23DOI: 10.1177/17504589251366105
Bushu Harna, Shivali Arya, Tarkik Thami
Introduction: Effective postoperative wound care is essential in orthopaedic surgeries to minimise complications such as infection, swelling, and compartment syndrome. Postoperative oedema can delay healing and restrict mobility. SU-Mag ointment, known for its hygroscopic and anti-inflammatory properties, has been used in conditions like thrombophlebitis and intravenous infiltration, but its role in orthopaedic postoperative care is not well studied. This study evaluates the effectiveness of SU-Mag dressing in reducing postoperative oedema following limb fracture fixation surgeries.
Methodology: A 12-month prospective observational study was conducted at a tertiary care centre involving 233 patients undergoing upper or lower limb fracture fixation. Patients with open wounds, vascular disorders, immunosuppression, or hypersensitivity to SU-Mag components were excluded. Post-surgery, SU-Mag ointment was applied circumferentially around, but not on, the incision site, followed by sterile gauze, cotton padding, and a crepe bandage. The dressing was kept in place for 72 h unless an early change was needed.
Results: Among 233 patients (mean age 43.8 ± 13.2 years), 68.6% had no swelling and 31.7% had only mild oedema. Mean oedema score was 0.32 ± 0.12, with an average limb circumference difference of 0.42 ± 0.11 cm (p < 0.001). No major complications were noted.
Conclusion: SU-Mag dressing effectively reduced postoperative oedema and discomfort without adverse effects.
在骨科手术中,有效的术后伤口护理是必要的,以尽量减少并发症,如感染、肿胀和隔室综合征。术后水肿可延迟愈合并限制活动。SU-Mag软膏以其吸湿和抗炎特性而闻名,已用于血栓性静脉炎和静脉浸润等疾病,但其在骨科术后护理中的作用尚未得到很好的研究。本研究评估了SU-Mag敷料在肢体骨折固定手术后减少术后水肿的有效性。方法:在三级保健中心进行了一项为期12个月的前瞻性观察研究,涉及233例接受上肢或下肢骨折固定的患者。排除有开放性伤口、血管疾病、免疫抑制或对SU-Mag成分过敏的患者。术后,将SU-Mag软膏涂抹在切口周围,但不涂在切口上,然后用无菌纱布、棉絮和皱褶绷带包扎。敷料放置72小时,除非需要提前更换。结果:233例患者(平均年龄43.8±13.2岁)中,68.6%的患者无肿胀,31.7%的患者仅有轻度水肿。平均水肿评分为0.32±0.12,平均肢围差为0.42±0.11 cm (p)。结论:SU-Mag敷料可有效减轻术后水肿和不适,无不良反应。
{"title":"Role of SU-Mag dressing in postoperative orthopaedic surgeries: A prospective study.","authors":"Bushu Harna, Shivali Arya, Tarkik Thami","doi":"10.1177/17504589251366105","DOIUrl":"10.1177/17504589251366105","url":null,"abstract":"<p><strong>Introduction: </strong>Effective postoperative wound care is essential in orthopaedic surgeries to minimise complications such as infection, swelling, and compartment syndrome. Postoperative oedema can delay healing and restrict mobility. SU-Mag ointment, known for its hygroscopic and anti-inflammatory properties, has been used in conditions like thrombophlebitis and intravenous infiltration, but its role in orthopaedic postoperative care is not well studied. This study evaluates the effectiveness of SU-Mag dressing in reducing postoperative oedema following limb fracture fixation surgeries.</p><p><strong>Methodology: </strong>A 12-month prospective observational study was conducted at a tertiary care centre involving 233 patients undergoing upper or lower limb fracture fixation. Patients with open wounds, vascular disorders, immunosuppression, or hypersensitivity to SU-Mag components were excluded. Post-surgery, SU-Mag ointment was applied circumferentially around, but not on, the incision site, followed by sterile gauze, cotton padding, and a crepe bandage. The dressing was kept in place for 72 h unless an early change was needed.</p><p><strong>Results: </strong>Among 233 patients (mean age 43.8 ± 13.2 years), 68.6% had no swelling and 31.7% had only mild oedema. Mean oedema score was 0.32 ± 0.12, with an average limb circumference difference of 0.42 ± 0.11 cm (p < 0.001). No major complications were noted.</p><p><strong>Conclusion: </strong>SU-Mag dressing effectively reduced postoperative oedema and discomfort without adverse effects.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"130-133"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144972253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-01-19DOI: 10.1177/17504589241309534
Darcy Fay, Tayla Fay, Wayne Hoskins, Roger Bingham
Background: Tourniquet use is ubiquitous in the operating theatre. However, optimal tourniquet usage is unclear, including type, pressure, inflation time, or whether a tourniquet should be used at all. This study reports a literature review of tourniquet use, comparing type, pressure, duration, effectiveness, and the spectrum of complications in an adult surgical population.
Results: Data regarding population size, surgery performed, tourniquet type, tourniquet location, total tourniquet inflation time, timing of inflation and deflation, pressure, and complications were recorded. Postoperative tourniquet-related pain was the commonest adverse event. Other complications included venous thromboembolism, wound healing issues, neuropathy, and abrasions. Findings suggest that most surgeons use standardised pressures.
Conclusion: Tourniquets are associated with a spectrum of complications. It is unclear whether tourniquet use provides better surgical outcomes. If tourniquets are used, surgeons should minimise the application pressure and duration. This may be achieved through a patient-centred approach and careful use of padding.
{"title":"Appropriate tourniquet use in surgery: A literature review.","authors":"Darcy Fay, Tayla Fay, Wayne Hoskins, Roger Bingham","doi":"10.1177/17504589241309534","DOIUrl":"10.1177/17504589241309534","url":null,"abstract":"<p><strong>Background: </strong>Tourniquet use is ubiquitous in the operating theatre. However, optimal tourniquet usage is unclear, including type, pressure, inflation time, or whether a tourniquet should be used at all. This study reports a literature review of tourniquet use, comparing type, pressure, duration, effectiveness, and the spectrum of complications in an adult surgical population.</p><p><strong>Results: </strong>Data regarding population size, surgery performed, tourniquet type, tourniquet location, total tourniquet inflation time, timing of inflation and deflation, pressure, and complications were recorded. Postoperative tourniquet-related pain was the commonest adverse event. Other complications included venous thromboembolism, wound healing issues, neuropathy, and abrasions. Findings suggest that most surgeons use standardised pressures.</p><p><strong>Conclusion: </strong>Tourniquets are associated with a spectrum of complications. It is unclear whether tourniquet use provides better surgical outcomes. If tourniquets are used, surgeons should minimise the application pressure and duration. This may be achieved through a patient-centred approach and careful use of padding.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"96-105"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143013174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-02-13DOI: 10.1177/17504589251317325
Mohamed Askar, Yasmine Zedan, Owain Davies, Alun John
Background: Total hip replacement is a quality of life-enhancing procedure. Postoperative blood transfusion is a risk factor compromising the outcome of total hip replacement and increasing the risk of deep infection. The aim of this study is to determine the risk factors for postoperative blood transfusion after total hip replacement.
Methods: In this retrospective study, 3901 patients underwent primary total hip replacement, in the period between January 2015 and December 2023. The mean age of the participants was 67.3 (SD: 12.6) years, and 61% of them were females. Participants were divided into 'transfusion' and 'non-transfusion' groups.
Results: Forty-two patients (1.1%) received blood transfusion after total hip replacement. In a multivariable logistic regression analysis, preoperative haemoglobin was the only independent risk factor that reduced the odds of postoperative transfusion by 0.3 (95% confidence interval: 0.23-0.39) for every 1 g/dL increase.
Conclusion: Postoperative blood transfusion is a rare, yet potentially serious, occurrence after total hip replacement. In this study, preoperative haemoglobin level was the only independent risk factor associated with postoperative transfusion. We recommend aiming to achieve minimum preoperative haemoglobin level of 13 g/dL to minimise the risk of postoperative transfusion.
{"title":"Risk factors of blood transfusion following primary total hip replacement.","authors":"Mohamed Askar, Yasmine Zedan, Owain Davies, Alun John","doi":"10.1177/17504589251317325","DOIUrl":"10.1177/17504589251317325","url":null,"abstract":"<p><strong>Background: </strong>Total hip replacement is a quality of life-enhancing procedure. Postoperative blood transfusion is a risk factor compromising the outcome of total hip replacement and increasing the risk of deep infection. The aim of this study is to determine the risk factors for postoperative blood transfusion after total hip replacement.</p><p><strong>Methods: </strong>In this retrospective study, 3901 patients underwent primary total hip replacement, in the period between January 2015 and December 2023. The mean age of the participants was 67.3 (SD: 12.6) years, and 61% of them were females. Participants were divided into 'transfusion' and 'non-transfusion' groups.</p><p><strong>Results: </strong>Forty-two patients (1.1%) received blood transfusion after total hip replacement. In a multivariable logistic regression analysis, preoperative haemoglobin was the only independent risk factor that reduced the odds of postoperative transfusion by 0.3 (95% confidence interval: 0.23-0.39) for every 1 g/dL increase.</p><p><strong>Conclusion: </strong>Postoperative blood transfusion is a rare, yet potentially serious, occurrence after total hip replacement. In this study, preoperative haemoglobin level was the only independent risk factor associated with postoperative transfusion. We recommend aiming to achieve minimum preoperative haemoglobin level of 13 g/dL to minimise the risk of postoperative transfusion.</p>","PeriodicalId":35481,"journal":{"name":"Journal of perioperative practice","volume":" ","pages":"148-153"},"PeriodicalIF":1.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143415419","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}