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1.
Arthroplast Today ; 6(2): 278-282, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32577478

ABSTRACT

Crystalline arthropathies are well-known pathologies in a native knee; however, the literature is scarce with regards to crystalline arthropathies in a total knee arthroplasty (TKA). The presentation of crystalline arthropathy in a TKA can be similar to a periprosthetic joint infection (PJI), making it difficult to distinguish between the 2 diagnoses. We present 1 case highlighting the similarity between crystalline arthropathy and PJI. A 71-year-old man with a history of bilateral TKAs presented with bilateral painful knee effusions and was initially presumed to have PJIs; however, he was later diagnosed with gout and successfully treated medically. A complete review of the literature demonstrates that crystalline arthropathies after TKA are infrequently reported and can be difficult to decipher from PJIs, and there is a lack of standardized treatment.

2.
Clin Orthop Relat Res ; 473(8): 2639-43, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25991434

ABSTRACT

BACKGROUND: Tranexamic acid (TXA) has shown safety and efficacy in reducing blood loss associated with various surgical procedures. However, to our knowledge there are no studies evaluating the effect of TXA on blood loss and transfusion requirements associated with periacetabular osteotomy (PAO). QUESTIONS/PURPOSES: The main purpose of this study is to determine whether TXA reduces blood loss and transfusion use in patients undergoing PAO for symptomatic acetabular dysplasia. Our secondary purpose was to compare the frequency of symptomatic thromboembolic events between patients undergoing surgery with and without TXA. METHODS: A consecutive series of 100 periacetabular osteotomies performed by one surgeon was reviewed to compare the groups immediately before and after implementation of routine use of tranexamic acid (two retrospective cohorts). TXA dosing followed an established protocol with a standard dose of 1 g infused intravenously during 10 minutes before skin incision and an additional 1 g intravenously at wound closure. Outcome measures include total estimated blood loss perioperatively and transfusion requirements. Total estimated blood loss was calculated using a formula built from the National Surgical Quality Improvement Program data regarding surgical blood loss. RESULTS: The mean perioperative total estimated blood loss was less in the patients receiving TXA compared with blood loss in patients who did not receive TXA (706 mL versus 1021 mL; p<0.001; 95% CI, -495 to -134). Twenty-six (52%) of the 50 patients who did not receive TXA had postoperative blood transfusions compared with 15 (30%) of 50 who received TXA (odds ratio, 0.395; 95% CI, 0.174-0.899; p=0.0414). No symptomatic deep vein thromboses or symptomatic pulmonary emboli were identified in either group. CONCLUSIONS: TXA reduces estimated blood loss and the frequency of transfusions in patients undergoing PAO for treatment of symptomatic acetabular dysplasia. Future prospective studies should confirm our findings to determine whether patients undergoing PAO should receive routine perioperative TXA. LEVEL OF EVIDENCE: Level III, therapeutic study.


Subject(s)
Acetabulum/surgery , Antifibrinolytic Agents/administration & dosage , Blood Loss, Surgical/prevention & control , Blood Transfusion , Hip Dislocation/surgery , Osteotomy/adverse effects , Postoperative Hemorrhage/prevention & control , Tranexamic Acid/administration & dosage , Adolescent , Adult , Antifibrinolytic Agents/adverse effects , Drug Administration Schedule , Female , Hip Dislocation/diagnosis , Humans , Infusions, Intravenous , Male , Middle Aged , Odds Ratio , Postoperative Hemorrhage/etiology , Pulmonary Embolism/etiology , Pulmonary Embolism/prevention & control , Retrospective Studies , Risk Factors , Time Factors , Tranexamic Acid/adverse effects , Treatment Outcome , Venous Thrombosis/etiology , Venous Thrombosis/prevention & control , Young Adult
3.
Foot Ankle Int ; 34(10): 1355-63, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23832712

ABSTRACT

BACKGROUND: The literature supports fusion as the surgical treatment of choice for stage III posterior tibial tendon dysfunction (PTTD). The present study reports the radiographic correction following a modified triple arthrodesis (fusions of the subtalar, talonavicular, and first tarsometatarsal joints) in patients with stage III PTTD. METHODS: An institutional review board-approved retrospective study was performed to assess the radiographic outcome of a modified triple arthrodesis in 21 patients (22 feet). Pre- and postoperative weight-bearing radiographs were reviewed in a blinded fashion by clinicians of varying levels of training. The talo-first metatarsal, talocalcaneal, and talonavicular coverage angles were measured on anteroposterior views. On lateral views, the talo-first metatarsal (Meary's), talocalcaneal, calcaneal pitch, and talar declination angles and the medial cuneiform to floor distance were measured. Statistical analysis was performed to compare pre- and postoperative measurements, assess the degree of correction, and determine interobserver reliability of the radiographic measurements. RESULTS: All measurements improved significantly after treatment with a modified triple arthrodesis (P ≤ .001). The medial cuneiform to floor distance (0.910), talonavicular coverage angle (0.896), and lateral talo-first metatarsal angle (0.873) were the most reproducible between observers. Postoperatively, 100% of feet were corrected to normal medial cuneiform to floor distance and talonavicular coverage angle, and 90.9% were corrected to a normal lateral talo-first metatarsal angle. CONCLUSION: The modified triple arthrodesis resulted in a reliable and reproducible correction of the deformity seen in rigid stage III PTTD. LEVEL OF EVIDENCE: Level IV, case series.


Subject(s)
Arthrodesis/methods , Foot Bones/diagnostic imaging , Posterior Tibial Tendon Dysfunction/diagnostic imaging , Posterior Tibial Tendon Dysfunction/surgery , Aged , Aged, 80 and over , Female , Humans , Male , Metatarsal Bones/diagnostic imaging , Middle Aged , Radiography , Tarsal Bones/diagnostic imaging , Treatment Outcome
4.
Orthop Clin North Am ; 42(1): 115-21, vii, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21095440

ABSTRACT

There has been a significant increase in the prevalence of obesity in the United States over the last 20 years, with the highest percentage in Mississippi. The percentage of obese patients undergoing total hip arthroplasty (THA) appears to be increasing at an even faster rate. Orthopedic surgeons performing hip arthroplasty need to be aware of potential issues to minimize complications associated with this population. This article outlines preoperative and postoperative care and describes current techniques and tools used by surgeons in obese patients to facilitate soft tissue dissection, exposure, implant placement, and closure.


Subject(s)
Arthroplasty, Replacement, Hip/methods , Osteoarthritis, Hip/surgery , Humans , Morbidity , Obesity/complications , Obesity/epidemiology , Osteoarthritis, Hip/complications , Osteoarthritis, Hip/epidemiology , United States/epidemiology
5.
J Spinal Disord Tech ; 22(7): 473-8, 2009 Oct.
Article in English | MEDLINE | ID: mdl-20075809

ABSTRACT

STUDY DESIGN: A novel degenerative disc disease model and sustained delivery method for corticosteroid in male Sprague-Dawley albino rats. OBJECTIVES: To develop a model of degenerative disc disease and to determine the effect of continuous sustained release of corticosteroid on the process of degeneration within the traumatized disc. SUMMARY OF BACKGROUND DATA: The current modalities of treating symptomatic degenerative disc disease are either conservative or surgical. However, there is no cure for the degenerative process and prevention, therefore, is the ideal treatment. An understanding of the mechanisms involved in disc degeneration is crucial to develop new methods for prevention and treatment, including appropriate delivery systems and dosages of repair factors. METHODS: The L5-L6 intervertebral disc was pierced with a 23-gauge needle in 18 rats. The animals received either sham or corticosterone-charged tricalcium phosphate ceramic capsules. The rats were euthanized at 4 weeks. Chondrocytes in the transition zone areas were counted and compared statistically. RESULTS: The surgical technique induced degeneration of the nucleus without evidence of inflammation at adjacent levels when compared with nontraumatized controls. The number of chondrocytes per area was significantly less in the sham group than in the control group. Corticosteroid treatment showed chondrocyte numbers similar to control in 4 of 5 different views of the disc. The anterior region of the disc had 50% less chondrocytes per area than the control; however, the chondrocyte numbers were 50% greater than in the same site from discs of sham animals. CONCLUSIONS: The results show the development of a degenerative disc animal model that can be used to test the effects of growth enhancing factors in disc repair. Administration of continuous sustained release of corticosterone can slow the process of degeneration within the traumatized disc in the rat model.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Corticosterone/pharmacology , Intervertebral Disc Degeneration/drug therapy , Intervertebral Disc/drug effects , Animals , Anti-Inflammatory Agents/therapeutic use , Biocompatible Materials/pharmacology , Biocompatible Materials/therapeutic use , Calcium Phosphates/pharmacology , Calcium Phosphates/therapeutic use , Cell Count , Chondrocytes/cytology , Chondrocytes/drug effects , Chondrocytes/physiology , Corticosterone/therapeutic use , Disease Models, Animal , Drug Administration Schedule , Fibrocartilage/cytology , Fibrocartilage/drug effects , Fibrocartilage/physiology , Inflammation/drug therapy , Inflammation/pathology , Inflammation/physiopathology , Intervertebral Disc/cytology , Intervertebral Disc/physiology , Intervertebral Disc Degeneration/pathology , Intervertebral Disc Degeneration/physiopathology , Male , Rats , Rats, Sprague-Dawley , Regeneration/drug effects , Regeneration/physiology , Treatment Outcome
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