Total hip replacement in patients with sickle-cell disease

1977 ◽  
Vol 59 (6) ◽  
pp. 760-762 ◽  
Author(s):  
C Gunderson ◽  
RD DʼAmbrosia ◽  
H Shoji
2002 ◽  
Vol 26 (3) ◽  
pp. 157-161 ◽  
Author(s):  
Al-Mousawi F. ◽  
Malki A. ◽  
Al-Aradi A. ◽  
Al-Bagali M. ◽  
Al-Sadadi A. ◽  
...  

SICOT-J ◽  
2018 ◽  
Vol 4 ◽  
pp. 22 ◽  
Author(s):  
Udo Ego Anyaehie ◽  
Gabriel Okey Eyichukwu ◽  
Cajetan Uwatoronye Nwadinigwe ◽  
Amechi Uchenna Katchy

Introduction: Total hip replacement (THR) surgery is still evolving in Nigeria with increasing awareness as more cases are being done. This has attraction for individuals who hitherto had no solutions for their hip pathologies. These are mostly complex primary hips which present challenging technical difficulties with increased risk of complications, thus requiring detailed planning to ensure successful operation. This work aims to present the pattern of complex primary hips presenting for THR, the challenges and complications. Methodology: Data collected over a seven year period, of patients who presented for THR, were analyzed for age, sex, diagnosis, type of hip, complications, duration of surgery, blood loss and transfusions, challenges and outcome. Results: Fifty-nine (43.4%) of the 136 cases of THR done were complex primary hip replacement surgeries. Avascular necrosis of femoral head amongst sickle cell disease patients (23.7%) was the commonest cause of complex primary hips in our series. Most of them had absent/tight medullary canals. This is followed by old unreduced hip dislocation and non-united hip fractures with an incidence of 10.1% each. The major peri operative complication noted was calcar split in 10 patients (16.9%) Discussion: Sickle cell disease patients presented more with complex primary hips and the commonest difficulty was recreating medullary canals. Increased operation time and blood loss alongside technical difficulties should be anticipated and measures put in place to avert complications.


2015 ◽  
Vol 26 (2) ◽  
pp. 186-192 ◽  
Author(s):  
Christopher M. Jack ◽  
Jo Howard ◽  
Emad S. Aziz ◽  
Rachel Kesse-Adu ◽  
Marcus J. Bankes

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 2904-2904
Author(s):  
France Noizat-Pirenne ◽  
Philippe Chadebech ◽  
Marc Michel ◽  
Dora Bachir ◽  
Frederic Galacteros ◽  
...  

Abstract Background: Delayed hemolytic transfusion reaction (DHTR) is a life-threatening complication frequently reported in sickle cell disease patients (SCD) patients. The hallmarks of DHTR in SCD are a dramatic drop in post-transfusion hemoglobin (Hb) caused by destruction of both donor and recipient red blood cells (RBCs) and hemolysis exacerbation by further transfusion. Destruction of autologous and transfused RBCs can be triggered by auto-antibodies produced as a result of transfusion. As rituximab specifically targets circulating B cells and is successfully used to treat several auto-immune diseases, we thought that it could be beneficial in preventing this immune-mediated transfusion complication. We report the case of a SCD patient who already experienced many DHTR due to auto-antibodies and who needed again transfusion for surgery. Rituximab was administered prior transfusion. Patient and method: The SCD patient was a poly-immunized 33-year-old man who had experienced 2 life-threatening DHTR with auto and allo-antibodies following transfusion for orthopedic surgery. He was scheduled again in 2005 and 2007 for hip replacement. In 2007, he received 1000 mg of rituximab 3 days before surgery and transfusion and 7 days after the procedure. For both episodes, routine serological evaluation, hematologic parameters and lymphocyte subsets were determined. IL-10 transcripts were quantified. IL6 and TNFα were evaluated in sera after rituximab infusion. Results: In 2005, the patient received 7 crossmatched-compatible units at day 0 of surgery and developed a severe auto-immune haemolytic anemia at day 13 as demonstrated by serological evaluation revealing RBC auto-antibodies without new allo-antibodies, a positive direct antiglobulin test (DAT) with anti-C3d/anti-IgG. Hb dropped to 2 g/dL and patient consciousness was impaired. Renal failure ensued. Then, he received 6 more units compatible with the known allo-antibodies, and was given steroids, cyclophosphamide and erythropoietin. The patient clinical status gradually improved. Lymphocyte subsets increased on day 14. Natural killer cells increased ten times. IL10 transcripts were over 900 copies at day 15 and around 50 copies at day 32. In 2007, as transfusion was absolutely necessary for hip replacement, we thought that rituximab could prevent recurrence of DHTR for this patient by inhibiting development of auto-antibodies. Seven crossmatched-compatible units were transfused. Sera remained compatible with transfused RBCs, DAT and eluate remained negative. Hb A rose up to 40% after transfusion and decreased slowly to reach 17% on day 21. Rituximab treatment resulted in marked depletion of B cells. Existing allo-antibodies (anti-C, anti-Fya, anti-S) and levels of total IgG, IgM and IgA remained stable. Dosage of IL6 and TNFα after rituximab infusions did not reveal any cytokine-release syndrome attesting the immediate safety of the procedure. Three months after treatment, the patient was in good condition. Conclusion: This observation shows for the first time that DHTR can be prevented. We believe that the use of rituximab should be considered when a new transfusion seems inevitable in patients with SCD and a prior history of life-threatening DHTR with production of auto-antibodies. In this setting, rituximab prevented DHTR without causing significant side-effects.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 2489-2489 ◽  
Author(s):  
Oyebimpe O Adesina ◽  
Ann M Brunson ◽  
Jason R. Gotlib ◽  
Theresa Keegan ◽  
Ted Wun

Abstract Introduction Osteonecrosis of the femoral head (ONFH) is characterized by insidious onset of hip joint pain, limited range of motion and disability in sickle cell disease (SCD) patients. Prevalence of ONFH, rates of hip replacement surgery and post-operative course have not been previously described in population-based cohort studies. We retrospectively reviewed a large SCD patient cohort from California's Office of Statewide Planning and Development (OSHPD) Patient Discharge Database (PDD), and report the risk factors and clinical outcomes for SCD patients with ONFH. Methods Patients were ascertained from the PDD from 1991 to 2013, through an iterative search algorithm using ICD-9 codes. In addition to descriptive statistics and univariate comparisons with the chi-square test, we used multivariable Cox proportional hazards models (with age as the time scale), to analyze factors associated with ONFH diagnosis, including sex, SCD severity and antecedent acute chest syndrome (ACS; data available from 2003-2013). Patients with more severe SCD were defined as those who averaged 3 of more hospitalizations per year. Antecedent ACS was considered as a time-dependent covariate to first ONFH diagnosis after 2003. We estimated the cumulative incidence of ONFH, accounting for the competing risk of death, by SCD severity and antecedent ACS diagnoses, with differences assessed by the Gray's test for equality. We also determined rates of all re-admissions to the PDD and emergency department within 30-90 days after hip replacement surgery, including re-admissions for venous thromboembolism (VTE) and painful vasoocclusive crises (VOC). All data were analyzed using SAS 9.4 software, and results presented as hazard ratios (HR) and 95% confidence intervals (CI). Results Of the 6,237 SCD patients identified, 1,356 (22%) were diagnosed with ONFH (Table 1). Three hundred and eight of the SCD patients with ONFH underwent hip arthroplasty. The median ages of ONFH diagnosis and hip replacement surgery were 27 and 36 years, respectively. In Cox regression analyses over the entire study period, both males (HR 1.13, CI 1.01 - 1.27) and SCD severity (HR 2.75, CI 2.44 - 3.11) were associated with ONFH. In Cox regression analyses from 2003-2013, SCD severity (HR 2.89, CI 2.48 - 3.36) and antecedent ACS (HR 1.56, CI 1.31 - 1.84) were independently associated with ONFH diagnosis. The cumulative incidence curves corroborate the association between SCD severity, antecedent ACS, and ONFH (Figures 1 and 2; p<0.0001)). By 40 years of age, 36% of patients with severe SCD (vs. 14% without severe disease) and 36% with antecedent ACS (vs. 12% without ACS) had developed ONFH. Among SCD patients with ONFH, 43%, 51% and 58% were re-admitted postoperatively within 30, 60 and 90 days, respectively. At 60 and 90 days after discharge for hip arthroplasty, 22% and 28% were readmitted for VOC, respectively. Conclusions The overall prevalence of ONFH in this SCD cohort was 22%, and approximately 23% of the ONFH patients underwent hip arthroplasty (5% of the entire SCD cohort). Thus, ONFH is a common complication of SCD, which often requires surgical intervention. ONFH was independently associated with SCD severity and ACS, as has been previously suggested (Kato, Gladwin et al. 2007). Readmission within 30-60 days after hip surgery was common in this SCD cohort, and often due to painful VOC. Of the 144 readmissions within 90 days of discharge from hip replacement surgery, only 2 (~1%) were due to VTE, which is lower than reported in non-sickle cell patients undergoing hip replacement surgery. Our large, populations-based cohort study provides insight into the frequency and risk factors of ONFH in SCD patients, and also reveals that post-operative readmissions are common. References Kato, G. J., M. T. Gladwin and M. H. Steinberg (2007). "Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes." Blood Rev 21(1): 37-47. Cumulative incidence of ONFH among SCD patients in the Patient Discharge Database, 1991-2013 (n=6,237) Cumulative incidence of ONFH among SCD patients in the Patient Discharge Database, 1991-2013 (n=6,237) Figure 1 Cumulative incidence of ONFH among SCD patients entering the Patient Discharge Database after 10/1/2003 (n=1,538) Figure 1. Cumulative incidence of ONFH among SCD patients entering the Patient Discharge Database after 10/1/2003 (n=1,538) Figure 2 Figure 2. Disclosures Adesina: bluebird bio: Honoraria.


Sign in / Sign up

Export Citation Format

Share Document