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  1. AU="Moushmoush, Obadah"
  2. AU="Fernández-Bello, Ihosvany"
  3. AU="Tschumi, Fabian"
  4. AU="Cirillo, Valerio"
  5. AU="Yao, Yaling"
  6. AU=Saburi Amin
  7. AU="Wang, Jinwang" AU="Wang, Jinwang"
  8. AU="Jeffrey Rea"
  9. AU="Miskulin, Dana C"
  10. AU="Srikantha, Thyagarajan"
  11. AU="Sang-Yun Lee"
  12. AU="Gardiner, Karen"
  13. AU="Turias, Ignacio"
  14. AU="Xueming Li"
  15. AU="Felsch, Torsten"
  16. AU="Ferreira Camargo, Carlos Henrique"
  17. AU="Kory Johnson"
  18. AU="Espinoza, Gonzalo"
  19. AU=Batterham Rachel L.
  20. AU="Kojima, Fumiaki"
  21. AU="Saintigny, Pierre"
  22. AU="Winslow, Christopher J"

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  1. Artikel ; Online: Randomized Trial of Postoperative Venous Thromboembolism Prophylactic Compliance: Aspirin and Mobile Compression Pumps.

    Dietz, Matthew J / Moushmoush, Obadah / Frye, Benjamin M / Lindsey, Brock A / Murphy, T Ryan / Klein, Adam E

    The Journal of the American Academy of Orthopaedic Surgeons

    2022  Band 30, Heft 20, Seite(n) e1319–e1326

    Abstract: Background: Aspirin, as a routine venous thromboembolism (VTE) prophylaxis, is approved along with pneumatic compression pumps by the American College of Chest Physicians. We assessed compliance of aspirin and pump use after total joint arthroplasty.: ...

    Abstract Background: Aspirin, as a routine venous thromboembolism (VTE) prophylaxis, is approved along with pneumatic compression pumps by the American College of Chest Physicians. We assessed compliance of aspirin and pump use after total joint arthroplasty.
    Methods: A randomized trial of aspirin alone or aspirin/mobile compression pumps after total joint arthroplasty was performed. Aspirin and pump compliance, VTE events, and satisfaction with pump use were collected. Compliance was assessed through an internal device monitor and drug log book. Patients were also contacted 90 days postoperatively for reported symptomatic VTEs.
    Results: Each group had 40 patients and greater than 94% compliance with aspirin use, with no difference between groups (P = 0.55). Overall pump compliance during the first 14 days after hospital discharge was 51% (SD ± 33), which was significantly worse than aspirin compliance at 99% (SD ± 4.1) (P < 0.0001). Only 10 patients were compliant (>20 hr/d) with recommended pump use throughout the entire recommended period. There was no notable association between aspirin compliance and VTE within 90 days. There was no notable association between pump compliance and VTE at 90 days. However, average pump use compliance was 20% in patients with VTE and 54% in patients without VTE within 90 days. With the numbers available in this compliance study, there was no significant difference (P = 0.11).
    Discussion: Aspirin compliance was notably greater than pump compliance. In this study, we found that pump compliance was not associated with lower VTE risk. In fact, no increased risk was recognized in patients with an average pump usage of >50%. Further study is warranted to define the duration of pump use required for clinical significance. The recommended use of compression pumps should continue to be examined.
    Mesh-Begriff(e) Anticoagulants/therapeutic use ; Arthroplasty, Replacement, Hip/adverse effects ; Aspirin/therapeutic use ; Humans ; Postoperative Period ; Venous Thromboembolism/etiology ; Venous Thromboembolism/prevention & control
    Chemische Substanzen Anticoagulants ; Aspirin (R16CO5Y76E)
    Sprache Englisch
    Erscheinungsdatum 2022-06-29
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Randomized Controlled Trial
    ZDB-ID 1200524-1
    ISSN 1940-5480 ; 1067-151X
    ISSN (online) 1940-5480
    ISSN 1067-151X
    DOI 10.5435/JAAOS-D-21-01063
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Describing Adverse Events Associated with Bilateral Same-Day Intravitreal Dexamethasone Implants.

    Dinh, Russel H / Moushmoush, Obadah / Kolyvas, Peter / Jacobsen, Brad A / Mathai, Mariam / Sanghavi, Kavya / Levinson, Joshua D / Do, Brian K

    Ophthalmic surgery, lasers & imaging retina

    2022  Band 53, Heft 11, Seite(n) 612–618

    Abstract: Background and objectives: To explore the incidence of adverse events after bilateral same-day intravitreal 0.7-mg dexamethasone implant (SDIDI) injections.: Materials and methods: We performed an IRB approved, single-center, retrospective review of ... ...

    Abstract Background and objectives: To explore the incidence of adverse events after bilateral same-day intravitreal 0.7-mg dexamethasone implant (SDIDI) injections.
    Materials and methods: We performed an IRB approved, single-center, retrospective review of patients receiving bilateral SDIDI injections from January 1, 2016 to October 31, 2021 and reviewed adverse events that occurred within 3 months of injection.
    Results: A total of 206 bilateral (412 eyes) SDIDI injections were performed in 59 patients. Ocular hypertension or the addition of intraocular pressure (IOP) lowering drops occurred in 121 (29.4%) eyes after IDI. Two (0.5%) eyes required glaucoma drainage surgeries. Of the 117 phakic eyes, 32 (27.4%) had progression of cataract or cataract extraction. There were two (0.5%) episodes of vitreous hemorrhage and one (0.2%) retinal tear with retinal detachment. There were no cases of endophthalmitis.
    Conclusion: Serious complication rates after bilateral same-day IDI injections appears low. Increased IOP that requires intervention can occur.
    Mesh-Begriff(e) Humans ; Macular Edema/diagnosis ; Macular Edema/drug therapy ; Macular Edema/etiology ; Dexamethasone/adverse effects ; Intravitreal Injections ; Glucocorticoids/adverse effects ; Drug Implants/adverse effects ; Visual Acuity ; Intraocular Pressure ; Glaucoma/etiology ; Retrospective Studies
    Chemische Substanzen Dexamethasone (7S5I7G3JQL) ; Glucocorticoids ; Drug Implants
    Sprache Englisch
    Erscheinungsdatum 2022-11-01
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2701167-7
    ISSN 2325-8179 ; 2325-8160
    ISSN (online) 2325-8179
    ISSN 2325-8160
    DOI 10.3928/23258160-20221018-04
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Distal Radius Fractures: Does Obesity Affect Fracture Pattern, Treatment, and Functional Outcomes?

    Montague, Michael D / Lewis, Jesse T / Moushmoush, Obadah / Ryu, Jaiyoung

    Hand (New York, N.Y.)

    2018  Band 14, Heft 3, Seite(n) 398–401

    Abstract: Background: Distal radius fractures (DRFs) are 16% of fractures treated by orthopedic surgeons. Obesity's influence on DRF complexity has not been studied. This study was undertaken to determine if body mass index (BMI) affects DRF pattern, treatment, ... ...

    Abstract Background: Distal radius fractures (DRFs) are 16% of fractures treated by orthopedic surgeons. Obesity's influence on DRF complexity has not been studied. This study was undertaken to determine if body mass index (BMI) affects DRF pattern, treatment, and functional outcomes.
    Methods: Part 1 was a retrospective review of patients who sustained a DRF after a fall from standing height with no prior reduction or treatment. Radiographs were classified as "simple" or "complex." Part 2 consisted of contacting patients from Part 1 and obtaining a Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) score. Retrospective review also identified patients who failed initial nonoperative treatment. Fracture pattern, failure of nonoperative treatment, and QuickDASH scores were compared with BMI at the time of injury.
    Results: For Part 1, 130 patients (132 wrists) were identified. Average age was 57 years, 77% were female, and average BMI was 28.2 kg/m
    Conclusions: A higher BMI increases the odds of a complex DRF. Despite more complex fractures, overweight patients may experience less disability after sustaining a DRF.
    Mesh-Begriff(e) Accidental Falls/statistics & numerical data ; Adult ; Aged ; Aged, 80 and over ; Body Mass Index ; Case-Control Studies ; Female ; Humans ; Incidence ; Male ; Middle Aged ; Obesity/complications ; Obesity/epidemiology ; Radiography/methods ; Radius Fractures/classification ; Radius Fractures/diagnostic imaging ; Radius Fractures/epidemiology ; Radius Fractures/therapy ; Range of Motion, Articular/physiology ; Retrospective Studies ; Treatment Outcome
    Sprache Englisch
    Erscheinungsdatum 2018-01-07
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2277325-3
    ISSN 1558-9455 ; 1558-9447
    ISSN (online) 1558-9455
    ISSN 1558-9447
    DOI 10.1177/1558944717750915
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: The Effect Of Increasing Femoral Head Size On The Force Required For Dislocation.

    Dietz, Matthew J / Moushmoush, Obadah / Samora, Walter P / Kish, Vincent L / Hamlin, Brian R

    Surgical technology international

    2019  Band 35, Seite(n) 426–429

    Abstract: Alternative bearings allow for the increased utilization of large femoral heads in total hip arthroplasty. This study demonstrated the effect of increasing femoral head size on the force required for dislocation during intraoperative assessment. Using a ... ...

    Abstract Alternative bearings allow for the increased utilization of large femoral heads in total hip arthroplasty. This study demonstrated the effect of increasing femoral head size on the force required for dislocation during intraoperative assessment. Using a standard posterior approach, 10 cadaver hips underwent total hip arthroplasty; components were implanted in a standard fashion. The extremity was attached to a custom jig to replicate intraoperative assessment (internal rotation with 90° of hip flexion/neutral adduction). This range of motion (ROM) was repeated in triplicate using femoral head sizes of 28mm, 32mm, 36mm, 40mm, and 44mm. The ROM to dislocation (degrees) and torque (N*m) required were recorded. With increasing head sizes, there was a significant increase in torque required for dislocation (p<0.0001). The least square means torques (N*m) for each femoral head size (28-44mm) were 2.07, 2.15, 2.42, 2.74, and 3.65N*m. The corresponding least square means ROMs prior to dislocation were 43.5°, 46.2°, 50.8°, 54.3°, and 59.5°. There was a significant difference in ROM between nonadjacent head sizes (i.e., 28mm and 44mm) (p<0.0001). Total hip implant stability is multifactorial. Increasing femoral head size may confer stability during intraoperative assessment by increasing both the ROM prior to dislocation and the force required for dislocation.
    Mesh-Begriff(e) Arthroplasty, Replacement, Hip/adverse effects ; Cadaver ; Femur Head/physiopathology ; Femur Head/surgery ; Hip Dislocation/etiology ; Hip Dislocation/physiopathology ; Hip Joint/physiopathology ; Hip Joint/surgery ; Hip Prosthesis/adverse effects ; Humans ; Prosthesis Design ; Range of Motion, Articular ; Torque
    Sprache Englisch
    Erscheinungsdatum 2019-06-17
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 1225512-9
    ISSN 1090-3941
    ISSN 1090-3941
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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