Literature DB >> 19787790

Outcomes of inpatients with and without sickle cell disease after high-volume surgical procedures.

Michaela A Dinan1, Chia-Hung Chou, Bradley G Hammill, Felicia L Graham, Kevin A Schulman, Marilyn J Telen, Shelby D Reed.   

Abstract

In this study, we examined differences in inpatient costs, length of stay, and in-hospital mortality between hospitalizations for patients with and without sickle cell disease (SCD) undergoing high-volume surgical procedures. We used Clinical Classification Software (CCS) codes to identify discharges in the 2002-2005 Nationwide Inpatient Sample of the Healthcare Cost and Utilization Project for patients who had undergone either cholecystectomy or hip replacement. We limited the non-SCD cohort to hospitals where patients with SCD had undergone the same procedure. We compared inpatient outcomes using summary statistics and generalized linear regression analysis to adjust for patient, hospital, and procedural characteristics. Overall, the median age of surgical patients with SCD was more than three decades less than the median age of patients without SCD undergoing the same procedure. In recognition of the age disparity, we limited the analyses to patients aged 18 to 64 years. Nonetheless, patients with SCD undergoing cholecystectomy or hip replacement were 12.1 and 14.4 years younger, had inpatient stays that were 73% and 82% longer, and incurred costs that were 46% and 40% higher per discharge than patients without SCD, respectively. Inpatient mortality for these procedures was low, approximately 0.6% for cholecystectomy and 0.2% for hip replacement and did not differ significantly between patients with and without SCD. Multivariable regression analyses revealed that higher inpatient costs among patients with SCD were primarily attributable to longer hospital stays. Patients with SCD who underwent cholecystectomy or hip replacement required more health care resources than patients without SCD. Am. J. Hematol. 2009. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19787790      PMCID: PMC2783350          DOI: 10.1002/ajh.21520

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  17 in total

Review 1.  Preoperative blood transfusions for sickle cell disease.

Authors:  C Riddington; L Williamson
Journal:  Cochrane Database Syst Rev       Date:  2001

2.  Surgery in patients with sickle cell disease.

Authors:  A Spigelman; M J Warden
Journal:  Arch Surg       Date:  1972-06

3.  The perioperative complication rate of orthopedic surgery in sickle cell disease: report of the National Sickle Cell Surgery Study Group.

Authors:  E P Vichinsky; L D Neumayr; C Haberkern; A N Earles; J Eckman; M Koshy; D M Black
Journal:  Am J Hematol       Date:  1999-11       Impact factor: 10.047

4.  Cholecystectomy in sickle cell anemia patients: perioperative outcome of 364 cases from the National Preoperative Transfusion Study. Preoperative Transfusion in Sickle Cell Disease Study Group.

Authors:  C M Haberkern; L D Neumayr; E P Orringer; A N Earles; S M Robertson; D Black; M R Abboud; M Koshy; O Idowu; E P Vichinsky
Journal:  Blood       Date:  1997-03-01       Impact factor: 22.113

5.  Surgical and obstetric outcomes in adults with sickle cell disease.

Authors:  Soheir Adam; Jude Jonassaint; Hillary Kruger; Melanie Kail; Eugene P Orringer; James R Eckman; Allison Ashley-Koch; Marilyn J Telen; Laura M De Castro
Journal:  Am J Med       Date:  2008-10       Impact factor: 4.965

6.  Surgery and anesthesia in sickle cell disease. Cooperative Study of Sickle Cell Diseases.

Authors:  M Koshy; S J Weiner; S T Miller; L A Sleeper; E Vichinsky; A K Brown; Y Khakoo; T R Kinney
Journal:  Blood       Date:  1995-11-15       Impact factor: 22.113

7.  Sickle cell disease as a cause of osteonecrosis of the femoral head.

Authors:  P F Milner; A P Kraus; J I Sebes; L A Sleeper; K A Dukes; S H Embury; R Bellevue; M Koshy; J W Moohr; J Smith
Journal:  N Engl J Med       Date:  1991-11-21       Impact factor: 91.245

8.  A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. The Preoperative Transfusion in Sickle Cell Disease Study Group.

Authors:  E P Vichinsky; C M Haberkern; L Neumayr; A N Earles; D Black; M Koshy; C Pegelow; M Abboud; K Ohene-Frempong; R V Iyer
Journal:  N Engl J Med       Date:  1995-07-27       Impact factor: 91.245

Review 9.  Osteonecrosis of the hip in sickle cell hemoglobinopathy.

Authors:  M C Moran
Journal:  Am J Orthop (Belle Mead NJ)       Date:  1995-01

10.  Prevalence, clinical features, and risk factors of osteonecrosis of the femoral head among adults with sickle cell disease.

Authors:  M Mukisi-Mukaza; A Elbaz; Y Samuel-Leborgne; L Kéclard; C Le Turdu-Chicot; E Christophe-Duchange; G Mérault
Journal:  Orthopedics       Date:  2000-04       Impact factor: 1.390

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  3 in total

1.  Costs and length of stay for patients with and without sickle cell disease after hysterectomy, appendectomy, or knee replacement.

Authors:  Shital Kamble; Marilyn J Telen; Michaela A Dinan; Chelsea A Grussemeyer; Shelby D Reed
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

2.  The accuracy of hospital ICD-9-CM codes for determining Sickle Cell Disease genotype.

Authors:  Angela B Snyder; Peter A Lane; Mei Zhou; Susan T Paulukonis; Mary M Hulihan
Journal:  J Rare Dis Res Treat       Date:  2017-07-28

3.  A case series of cholecystectomy in Jamaican sickle cell disease patients - The need for a new strategy.

Authors:  Pierre-Anthony Leake; Marvin Reid; Joseph Plummer
Journal:  Ann Med Surg (Lond)       Date:  2017-02-04
  3 in total

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