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ASA class is associated with early revision and reoperation after total hip arthroplasty: an analysis of the Geneva and Swedish Hip Arthroplasty Registries

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ASA class is associated with early revision and reoperation after total hip arthroplasty: an analysis of the Geneva and Swedish Hip

Arthroplasty Registries

FERGUSON, Rory J, et al .

Abstract

Background and purpose - Data from several joint replacement registries suggest that the rate of early revision surgery after primary total hip arthroplasty (THA) is increasing. The ASA class, now widely recorded in arthroplasty registries, may predict early revision. We investigated the influence of ASA class on the risk of revision and other reoperation within 3 months and within 5 years of primary THA. Patients and methods - We used data from the Geneva and Swedish Hip Arthroplasty Registries, on primary elective THAs performed in 1996-2016 and 2008-2016, respectively. 5,319 and 122,241 THAs were included, respectively. Outcomes were all-cause revision and other reoperations evaluated using Kaplan-Meier survival and Cox regression analyses. Results - Within 3 months after surgery, higher ASA class was associated with greater risk of revision and other reoperation. 3-month cumulative incidences of revision by ASA class I, II, and III-IV respectively, were 0.6%, 0.7%, and 2.3% in Geneva and 0.5%, 0.8%, and 1.6% in Sweden. 3-month cumulative incidences of other reoperation were 0.4%, 0.7%, and 0.9% in Geneva and 0.2%, [...]

FERGUSON, Rory J, et al . ASA class is associated with early revision and reoperation after total hip arthroplasty: an analysis of the Geneva and Swedish Hip Arthroplasty Registries. Acta Orthopaedica , 2019, vol. 90

DOI : 10.1080/17453674.2019.1605785 PMID : 31035846

Available at:

http://archive-ouverte.unige.ch/unige:116919

Disclaimer: layout of this document may differ from the published version.

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Acta Orthopaedica 2019; 90 (DOI: 10.1080/17453674.2019.1605785) Supplementary data (1/2)

Supplementary data

Table 4. Associations with the risk of other reoperation (time-invari- ant HR unless specified)

GAR cohort SHAR cohort

Model HR (CI) HR (CI)

Univariable model

ASA I 1 (ref) 1 (ref)

ASA II 0.9 (0.5–1.8) 1.8 (1.3–2.4) a,f

1.2 (1.0–1.6) b,f

ASA III–IV 1.2 (0.6–2.5) 3.2 (2.3–4.3) a,f

1.6 (1.2–2.1) b,f

Multivariable model

ASA I 1 (ref) 1 (ref)

ASA II 0.9 (0.4–1.7) 1.7 (1.2–2.2) a,g

1.1 (0.9–1.5) b,g

ASA III–IV 1.1 (0.5–2.4) 2.7 (2.0–3.7) a,g

1.4 (1.0–1.8) b,g

Sex

Male 1 (ref) 1 (ref)

Female 0.8 (0.4–1.6) a,c 0.6 (0.5–0.8) a,h 1.8 (1.0–3.2) b,c 1.0 (0.8–1.2) b,h Diagnosis

Primary OA 1 (ref) 1 (ref) Secondary OA 3.1 (1.6–6.0) a,d 1.8 (1.5–2.2)

0.7 (0.4–1.5) b,d

BMI

< 35 1 (ref) 1 (ref)

≥ 35 4.5 (1.9–10.3) a,e 2.6 (1.9–3.4) a,i 1.1 (0.4–2.9) b,e 1.2 (0.8–1.7) b,i Age

< 85 y 1 (ref) 1 (ref) ≥ 85 y 0.9 (0.4–2.0) 1.9 (1.4–2.4)

a HR within the first 3 months.

b HR after 3 months and within 5 years.

c A change in HR within the first 3 months and after was suspected (p = 0.08).

d The change in HR within the first 3 months and after was statisti- cally significant (p = 0.003).

e A change in HR within the first 3 months and after was suspected (p = 0.05).

f The change in HR within the first 3 months and after was statisti- cally significant (ASA II: p = 0.05, ASA III–IV: p = 0.001).

g The change in HR within the first 3 months and after was statisti- cally significant for ASA II (p = 0.05) and close to statistical signifi- cance for ASA III–IV (p = 0.05).

h The change in HR within the first 3 months and after was statisti- cally significant (p < 0.001).

i The change in HR within the first 3 months and after was statisti- cally significant (p = 0.001).

Appendix

Checking of models

The proportionality of hazards was checked by plotting the complementary log-log of Kaplan-Meier’s survival (with cen- soring death) versus the log of the follow-up time. In addition, for each covariate (gender, age, BMI, diagnosis), univariate cause-specific Cox models were used to detect a variation of HRs within 3 months following primary THA and after 3 months. In cases where the proportional hazards assump- tion over follow-up time was violated, a time-varying HR was introduced in the model using a time-dependent variable and an interaction term.

Statistical method for the assessment of cause-spe- cific Cox models

For the analyses of the risk of revision, we ran a cause-specific Cox model with death as competing risk and with an interac- tion to allow a variation of the hazard ratio over follow-up time. For this purpose, we used the function coxph of R soft- ware (package Survival). Data were organized as follow:

TimeStart TimeStop Group

IdPatient (days) (days) Event ASA 2 ASA 3/4 Time

1 0 90 0 No Yes 0

1 90 540 1 No Yes 1

2 0 90 0 Yes No 0

2 90 120 2 Yes No 1

The coding of the variable “Event” was: 0=censor, 1=revi- sion, 2=death.

If a patient was censored or had a revision or died after 90 days, data were stored on two lines: one per period (first 3 months and after 3 months). The variable “GroupTime” indi- cated the period of time. The struture of database was consis- tent with the documentation of the R package Survival (see Therneau et al. https://cran.r-project.org/web/packages/sur- vival/vignettes/timedep.pdf ).

In Cox model, the hazard function for revision, hRevision (t), was modelled as follow:

hRevision(t) = hRevision,0(t) exp[ a I(ASA = 2) + b I(ASA = 2) Group- Time + g I(ASA = 3/4) + d I(ASA = 3/4) GroupTime]

were h0(t) is the baseline hazard of revision, a is the coef- ficient of ASA class = 2 (with ASA class = 1 as reference cate- gory), b is the coefficient of the interaction between ASA class

= 2 and the period of time, g is the coefficient of ASA class = 3 or 4 and d is the coefficient of the interaction between ASA class = 3/4 and the period of time. With this model, the cause

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Supplementary data (2/2) Acta Orthopaedica 2019; 90 (DOI: 10.1080/17453674.2019.1605785)

specific hazard ratio for the association between ASA class 2 and revision was exp(a) in the first 3 months and exp(a + b) after 3 months. The test of the null hypothesis b = 0 allowed testing that the hypothesis that the association between ASA class = 2 and revision was the same in the two periods of time.

Similarily, the cause specific hazard ratio for the association between ASA class 3 or 4 and revision was exp(g) in the first 3 months and exp(g + d) after 3 months.

The code written in software R to assess the regression coef- ficients was:

coxph(Surv(TimeStart,TimeStop, Event==1) ~ ASAClass2+

ASAClass2:GroupTime+ ASAClass3+ ASAClass3:GroupTime) For the additional models (with adjustment for sex, age and BMI and for the risk of other reoperation), a similar approach was followed.

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