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Ninety day adverse events following single level posterior lumbar interbody fusion in patients with sickle cell disease.
Dhodapkar, Meera M; Halperin, Scott J; Saifi, Comron; Whang, Peter; Grauer, Jonathan N; Varthi, Arya.
Afiliação
  • Dhodapkar MM; Department of Orthopaedics and Rehabilitation, Yale School of Medicine, 47 College St, New Haven, CT, USA.
  • Halperin SJ; Department of Orthopaedics and Rehabilitation, Yale School of Medicine, 47 College St, New Haven, CT, USA.
  • Saifi C; Department of Orthopaedic Surgery, Houston Methodist Hospital, Houston, TX, USA.
  • Whang P; Department of Orthopaedics and Rehabilitation, Yale School of Medicine, 47 College St, New Haven, CT, USA.
  • Grauer JN; Department of Orthopaedics and Rehabilitation, Yale School of Medicine, 47 College St, New Haven, CT, USA.
  • Varthi A; Department of Orthopaedics and Rehabilitation, Yale School of Medicine, 47 College St, New Haven, CT, USA. Electronic address: arya.varthi@yale.edu.
Spine J ; 2023 Dec 09.
Article em En | MEDLINE | ID: mdl-38081460
ABSTRACT
BACKGROUND CONTEXT Sickle cell disease (SCD) is an inherited disorder of red blood cells caused by mutation in the hemoglobin beta chain and is the most common inherited genetic disorder in the United States. Postoperative outcomes following single-level posterior lumbar interbody fusion (PLIF) in patients with SCD are not well characterized.

PURPOSE:

To examine 90-day postoperative outcomes among a matched cohort of patients with and without SCD who underwent single level PLIF utilizing a national administrative database. STUDY DESIGN/

SETTING:

Retrospective database study. PATIENT SAMPLE Adult patients without and with SCD who underwent single level PLIF from 2010 to 2021 Q1 were identified and matched 101 based on age, sex and ECI. Exclusion criteria included age <18 years old, recent history of infection, neoplasm, or trauma, as well as not being active in the database for 90 days following their procedure. OUTCOME

MEASURES:

Ninety-day postoperative adverse events and emergency department (ED) visits.

METHODS:

The matched cohorts were defined, and 90-day adverse event and ED visit rates were compared with univariable analyses and multivariable logistic regression, controlling for age, sex, and Elixhauser comorbidity index (ECI).

RESULTS:

Overall, 191,765 PLIF patients were identified, of which SCD was noted for 76 (0.04%). On multivariable analysis of the matched populations, patients with SCD were at increased odds ratio (OR) of the following (in decreasing OR order) transfusion (OR 17.69), pneumonia (OR 6.30), sepsis (OR 4.86), aggregated minor adverse events (OR 4.65), aggregated all adverse events (OR 3.87), ED visits (OR 3.53), and aggregated severe adverse events (OR 2.80) (p<.05 for all).

CONCLUSIONS:

The current study examined a relatively small, but largest to date, cohort of SCD patients undergoing PLIF. Patients with this condition were at greater odds of several perioperative adverse events, and these findings may be helpful for patient counselling and surgical planning.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Spine J Assunto da revista: ORTOPEDIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Spine J Assunto da revista: ORTOPEDIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos