Skip to main content
Journal of Applied Statistics logoLink to Journal of Applied Statistics
. 2020 Dec 14;49(5):1252–1276. doi: 10.1080/02664763.2020.1859466

Bivariate Birnbaum-Saunders accelerated lifetime model: estimation and diagnostic analysis

Maria Ioneris Oliveira a, Michelli Barros b,CONTACT, Joelson Campos b, Francisco José A Cysneiros a
PMCID: PMC9042005  PMID: 35707503

Abstract

In this paper, we discuss the bivariate Birnbaum-Saunders accelerated lifetime model, in which we have modeled the dependence structure of bivariate survival data through the use of frailty models. Specifically, we propose the bivariate model Birnbaum-Saunders with the following frailty distributions: gamma, positive stable and logarithmic series. We present a study of inference and diagnostic analysis for the proposed model, more concisely, are proposed a diagnostic analysis based in local influence and residual analysis to assess the fit model, as well as, to detect influential observations. In this regard, we derived the normal curvatures of local influence under different perturbation schemes and we performed some simulation studies for assessing the potential of residuals to detect misspecification in the systematic component, the presence in the stochastic component of the model and to detect outliers. Finally, we apply the methodology studied to real data set from recurrence in times of infections of 38 kidney patients using a portable dialysis machine, we analyzed these data considering independence within the pairs and using the bivariate Birnbaum-Saunders accelerated lifetime model, so that we could make a comparison and verify the importance of modeling dependence within the times of infection associated with the same patient.

Keywords: Dependence, frailty, local influence, residual analysis, survival data

2010 Mathematics Subject Classifications: 62N01, 62N02, 62J20

1. Introduction

The Birnbaum-Saunders (BS) distribution is a lifetime distribution developed by Birnbaum and Saunders [2] to analyze material fatigue data. From its origin to the present day, this distribution has been studied under different aspects, besides gaining prominence through applications in other areas of knowledge (see, for example, [18]). According to [30], most of the works related to the BS models were developed assuming that the experimental units are independent. However, some works on correlated BS data has been developed in recent years, for example, Marchant et al. [20] developed multivariate logarithmic generalized BS distributions and multivariate generalized BS regression models for describing fatigue data. Multivariate generalized BS regression models and diagnostic measures were developed by Marchant et al. [21]. An alternative approach for analyzing multivariate (correlated) BS data based on estimating equations was developed by Tsuyuguchi et al. [30]. Specifically, for the bivariate case, the bivariate BS distribution and some inferential aspects were introduced by Kundu et al. [14], and Vilca et al. [31] derived a robust extension of the bivariate BS distribution. Also, Saulo et al. [29] introduced a bivariate BS distribution based on the reparameterized BS distribution proposed by Santos-Neto et al. [28]. Kundu [15] developed the bivariate log BS distribution and different properties were obtained using copula structure. Vilca et al. [33] proposed a bivariate BS regression model through the use of bivariate sinh-normal (SN) distribution, and [32] defined the bivariate Sinh-Elliptical distribution and discussed some of its properties.

Frailty models have been receiving special attention in recent decades to model dependence. For instance, Hougaard [12] presented a general approach to frailty models for survival data, Giussani and Bonetti [8] investigated a new family of parametric bivariate frailty models, Oakes [24] discussed bivariate survival models induced by frailties, Liu et al. [19] proposed frailty proportional hazards models for the recurrent event processes where the dependence is modeled by conditioning on shared frailty included in both hazard functions, Sankaran and Anisha [27] presented a shared frailty model for gap time distributions of recurrent events with multiple causes, Sahu et al. [26] considered a Weibull regression model with gamma frailties for multivariate survival data, Leão et al. [16] proposed a methodology based on a BS frailty regression model that can be applied to censored or uncensored data and [17] proposed a survival model with frailty based on the BS distribution. Furthermore, Choi and Matthews [4] proposed a bivariate accelerated lifetime model, where the gamma, positive stable, power series, logarithmic series, and lognormal frailty distributions are considered. However, for the bivariate BS regression model, there is no study using the frailty approach given in [4].

This paper aims to propose a bivariate BS accelerated lifetime model (bivariate BSAL model) with a dependence structure modeled via the frailty approach and present diagnostic methods based on local influence and residual analysis for the proposed model.

This paper is organized as follows. In Section 2, we present the BS distribution and its relationship with the SN distribution. We also propose the bivariate BSAL model and discuss inferential procedures based on the maximum likelihood method for such a model. In Section 3, we derive some diagnostic procedures based on residuals and local influence. In Section 4, we perform some Monte Carlo simulation studies for assessing the potential of the residuals to detect misspecification. In Section 5, we present and explore an empirical application to show the applicability of the proposed model. Some concluding remarks are given in Section 6. Finally, some derivations are presented in the Appendix.

2. Modeling

In this section, we present a brief review about the BS distribution. We introduce the bivariate BSAL model as well as we also present estimation method and we discuss asymptotic inference aspects.

2.1. The BS distribution

Let T be a continuous nonnegative random variable, we say that T has BS distribution with parameters α and β, which we will denote by TBS(α,β), if its probability density function (pdf) is given by:

f(t)=12πexp12α2tβ+βt2t32(t+β)2αβ, t>0.

In this case, α>0 is the shape parameter and β>0 is the scale parameter. It can be shown that the survival function of the BS distribution is given by

S(t)=1Φ1αtββt,

where Φ() denotes the cumulative distribution function (cdf) of the standard normal distribution.

Hence, an important property establishes a relationship between the BS distribution and the SN distribution. Such property says that if TBS(α,β) then Y=log(T)SN(α,μ,2), whose pdf and cdf are given, respectively, by

f(y)=1αcoshyμ2ϕ2αsinhyμ2

and

F(y)=Φ2αsinhyμ2,

where ϕ() pdf of the standard normal distribution and μ=log(β), with α,σ>0 and yR.

Due to the relationship established between the above distributions, the distribution of Y=log(T) is also called the log-Birnbaum-Saunders distribution (log-BS). For more details see [25].

2.2. Accelerated lifetime model

Assuming that the survival time of the ith subject ( i=1,,n) in the jth group (j = 1, 2) is denoted by Tij, with TijBS(α,exp(xijβ)), where xij denotes the observations on k explanatory variables and β=(β0,β1,,βk) denotes the vector of regression coefficients, we consider log-linear regression model

Yij=log(Tij)=xijβ+Wij, (1)

where Wij=log(ϵij)logBS(α,0,2). So, we will assume independence among the subjects and dependence within groups. To model this dependence, we will consider the frailty model, defined in [24], for (Wi1,Wi2) and thus, the bivariate survival function of the log-BS model stochastic components is given by

S(wi1,wi2)=Llog1Φξ21log1Φξ22, (2)

where ξ2j=(2/α)sinh(wij/2) and L is the Laplace transform of the distribution of the pair-specific frailties, which depends on a frailty parameter, κ. In this paper, we will use the following frailty distributions: gamma, positive stable and logarithmic series. Moreover, to measure dependence within groups we used the Kendall's tau, given by τ=140vL(g)2dgdv, where g=log[1Φ(ξ21)]log[1Φ(ξ22)] (see, [3]). The expressions for Kendall's tau and Laplace tranforms of the frailty variable may be found in [3,11].

Let (y1j,δ1j),,(ynj,δnj) be an observed sample of n independent observations, where yij is the logarithm of response measurement j in pair i and δij is the failure indicator variable, with i=1,,n and j = 1, 2. Then, the log-likelihood function is given by

l(θ)=i=1nδi1δi2log(f(wi1,wi2))+δi1(1δi2)logS(wi1,wi2)wi1+(1δi1)δi2logS(wi1,wi2)wi2+(1δi1)(1δi2)logS(wi1,wi2),

where wij=yij(xijβ), θ=(β,κ,α), f(wi1,wi2)=ξ11ξ12K(ξ21)K(ξ22)L{log(1Φ(ξ21))log[1Φ(ξ22)]} and /wij(S(wi1,wi2))=ξ1jK(ξ2j)L{log(1Φ(ξ21))log[1Φ(ξ22)]}, with ξ1j=(2/α)cosh(wij/2) and K(ξ2j)=ϕ(ξ2j)/{2[1Φ(ξ2j)]}.

The score functions for β, κ and α are, respectively, given by

Uβ(θ)=X1D(a1)+X2D(a2)Z,Uκ(θ)=tr(D(b))

and

Uα(θ)=tr(D(c)),

where Xj is a matrix of dimension n×(k+1), with the ith line given by xij=(xij0,,xijk), Z=[1,,1] and D() represents a diagonal matrix. The quantities a1(), a2(), b() and c() may be found in the Appendix.

The maximum likelihood estimates are solutions of the equation system Uβ(θ)=0, Uκ(θ)=0 and Uα(θ)=0. On the other hand, such equations do not present closed solutions and the use of iterative methods is necessary to find the roots. In this study, we used the BFGS method from the maxLik package of the software R. As initial values we have considered the least squares estimates for β, for κ we obtained as a function of the initial value for the Kendall's tau and, finally, for α we used the expression

α~=4ni=1nsinh2yi1xi1β2+sinh2yi2xi2β212. (3)

So, the inference for the parameter vector θ can be based on the asymptotic distribution of the maximum likelihood estimator, θˆ, that under suitable regularity conditions (see [6]), is given by

θˆaNk+30,Σθ, (4)

where Σθ denotes the asymptotic variance-covariance matrix for θˆ, which may be approximated by the observed information matrix evaluated at θˆ, given in the Appendix.

3. Diagnostic analysis

Indeed, an important step in the validation of a regression model is the verification of possible departures from the model assumptions, more specifically from the stochastic and systematic components of the model, as well as, to detect discrepant observations (outliers) that present some influence on the parameter estimates that may cause inferential changes. In this regard, Cook [5] presents the local influence method as a general way for assessing the joint influence of observations, under small perturbations in the model or data. Then, we will define some residuals for assessing the fit of the model proposed and we will make a study of local influence, for some perturbation schemes.

3.1. Residual analysis

In order to verify the quality of the fit of the bivariate BSAL model, we will consider the V-residuals and K-residuals proposed by Choi and Matthews [4]. The V-residuals are defined by

Vˆi=LlogS1Wˆi1logS2Wˆi2=LL1(Uˆi1)+L1(Uˆi2), (5)

where Uˆij=L{log[Sj(Wˆij)]}, with Sj(Wˆij)=1(2/α)sinh(Wˆij/2) and Wˆij=yijxijβˆ, for i=1,,n and j = 1, 2. Furthermore, L1 denotes the inverse of the Laplace transform of the considered frailty distribution.

Note that C(uˆi1,uˆi2) have the form of an Archimedean copula with generator φ=L1. Hence, choosing a frailty distribution that satisfies the conditions required for C(uˆi1,uˆi2) to be an Archimedean copula, it follows from a result presented in [7] that the V-residuals have a distribution given by

G(vi)=P(Vi<vi)=viφ(vi)φ(vi),

which depends on a frailty parameter κ.

Since the distribution of the V-residuals is not fully specified, as it depends on the frailty parameter κ, the authors suggest a new residual defined by an integral probability transformation of the V-residuals, i.e. Kˆi=G(Viˆ). Thus, it follows from the Total Probability Theorem that K-residuals have uniform distribution in the interval [0,1].

In the presence of right censoring, we consider V-residuals and adapted K-residuals, as in [4], given by

Vˆiadap=L{L1(Uˆi1adap)+(Uˆi2adap)}

and

Kˆiadap=G(Vˆiadap), (6)

with

Uˆijadap=Uˆij+12(δij1)Uˆij, (7)

where δij is the failure indicator variable. More details may be found in [4].

3.2. Local influence

The local influence, proposed by Cook [5], corresponds to one of the most modern diagnostic methods. The main idea of this method is to perform small perturbations on data or model and analyze the behavior of a specific measure associated with those perturbations. For this, we consider the log-likelihood function of a given model, l(θ), where θ is a vector of dimension p. Moreover, we consider λ a n×1 perturbation vector restricted to some open subset ΩRn. Thereby, the log-likelihood function of the perturbed model is denoted by l(θ|λ). Let λ0 be a non-perturbation vector, we have l(θ|λ0)=l(θ). Hence, the likelihood displacement LD(λ)=2[l(θˆ)l(θˆ|λ)] is used as a measure of influence, where θˆ|λ denotes the maximum likelihood estimate under the perturbed model. Further, using the concepts of Differential Geometry, Cook [5] shows that the normal curvature in the unit direction d is given by Cd(θ)=2|dΔL¨θθ1Δd|, where L¨θθ1 is the observed information matrix associated with the considered model and Δ is a p×n matrix that depends on the perturbation scheme with elements Δrs=2l(θ|λ)/θrλs, with r=1,,p and s=1,,n, evaluated at θˆ and λ0. So, Cook [5] suggests using the dmax direction, which corresponds to the largest curvature, Cdmax(θ).

Some diagnostic plots are suggested, for example, the plot of Cdr(θ) against the order of observations, where dr is a vector n×1 composed of one in the rth row and zero in the others. Such curvature is denoted by Cr(θ) and is given by Cr(θ)=2|ΔrL¨θθ1Δr|, where Δr is the rth row of Δ. Besides, a careful note observation in the observations is suggested such that Cr(θ)>2C¯, where C¯=(1/n)r=1nCr(θ).

As follows, we will calculate for the perturbation schemes considered, the expressions for the matrix components

Δ=2l(θ|λ)θλ,

considering the model defined in (1) and (2) and its log-likelihood function given by (3).

Case-weights perturbation: Let λ=(λ1,,λn) be the vector of perturbation. In this context, perturbed log-likelihood function is given by

l(θ|λ)=i=1nλili(wi;θ),

with 0λi1, λ0=(1,,1) and

liwi;θ=δi1δi2log(f(wi1,wi2))+δi1(1δi2)logS(wi1,wi2)wi1+δi2×(1δi1)logS(wi1,wi2)wi2+(1δi1)(1δi2)logS(wi1,wi2),

where wi=(wi1,wi2). In this case Δ=(Δβ,Δκ,Δα), with Δβ=[X1D(a1)+X2D(a2)], Δκ=(b1(w1,θ), ,bn(wn,θ)) and Δα =(c1(w1,θ),,cn(wn,θ)), where Xj, D(), aij(), bi() and ci() are given in the Appendix, for i=1,,n and j = 1, 2, with aij(), bi() and ci() evaluated at θˆ and λ0.

Perturbation of the response variable: Consider that each wi1 and wi2 is perturbed as wi1(λ)=wi1+λi and wi2(λ)=wi2+λi, respectively, where wij=yij(xijβ), with i=1,,n and j = 1, 2. Thus, perturbed log-likelihood function is given by

l(θ|λ)=i=1nli(wi(λ);θ),

with wi(λ)=(wi1(λ),wi2(λ)) and λ0=(0,,0) is the non-perturbation vector. Hence, the components of matrix Δ are Δβ=[X1D(k1)+X2D(k2)], Δκ=(l1,,ln) and Δα=(m1,,mn), with D(kj)=diag{k1j,,knj}, for kij=/λi[aij(wi(λ);θ)], li=/λi[bi(wi(λ);θ)] and mi=/λi[ci(wi(λ);θ)], where aij(), bi() and ci() are given in the Appendix and evaluated at θˆ and λ0.

We can perturb the response variable only in one coordinate. To do so, we must consider wi(λ)=(wi1+λi;wi2) or wi(λ)=(wi1;wi2+λi).

Explanatory variable perturbation: Consider now an additive perturbation on a particular continuous explanatory variable, namely xijs, by making xi1s(λ)=xi1s+λi and xi2s(λ)=xi2s+λi, where λ=(λ1,,λn). In this regard, λ0=(0,,0) and wij(λ)=yij(xij(λ)β), with xij(λ)=(xij0,,(xijs+λi),,xijk). Then, the perturbed log-likelihood function takes here the form

l(θ|λ)=i=1nli(wi(λ);θ),

where wi(λ)=(wi1(λ),wi2(λ)), with i=1,,n and j = 1, 2. Thereby, the components of matrix Δ are Δβ=[X1D(k1)+X2D(k2)], Δκ=(l1,,ln) and Δα=(m1,,mn), with D(kj)=diag{k1j,,knj}, for kij=/λi[aij(wi(λ);θ)], li=/λi[bi(wi(λ);θ)] and mi=/λi[ci(wi(λ);θ)], where aij(), bi() and ci() are given in the Appendix and evaluated at θˆ and λ0.

4. Numerical study

In this section, we performed some simulation studies for assessing the potential of K-residuals to detect misspecification in the systematic component, the presence in the stochastic component of the model, as well as, to detect outliers. The results were obtained through a computational routine implemented in R statistical software. Codes can be obtained from the authors upon request.

4.1. The algorithm

Firstly, we generate a bivariate (correlated) sample, (Yi1,Yi2), where Yijlog-BS(α,xijβ,2), with i=1,,n and j=1,2, with based on the algorithm presented in [23]. As a result, we have the following algorithm:

4.1.

To investigate the capacity of the K-residuals to highlight specific problems of model goodness-of-fit, we will perform a simulation study similar to [4] using the following summary measure of fit:

S=1ni=1nKˆ(i)in+12,i=1,,n. (8)

In the presence of right censoring, we consider the adapted summary measure of fit, given by:

Sadap=1ni=1nKˆ(i)adapin+12,i=1,,n. (9)

4.2. A misspecified systematic component

Firstly, we consider a misspecified systematic component. In this case, we investigated if the presented residuals were able to detect the omission of important explanatory variables in the systematic part of the model. In order to do so, we consider the model:

Yij=β0+s=13βsxij(s)+Wij, (10)

where WijlogBS(α,0,2) and xij(s)N(0,1), with i=1,,n and j = 1, 2.

The sample sizes and true values of the parameters considered are n=50,100,200 and β0=0, β1=3, β2=1.5, β3=2 and α=0.5. The values assigned to the frailty parameter κ are determined in function to the values assigned to the Kendall's tau, which in this case we consider 0.1, 0.3, 0.5 and 0.7. The number of Monte Carlo replications used was 5000, for each value assigned to the Kendall's tau. In addition, we use the gamma frailty distribution. Subsequently, we use the generated samples and fit the model to the data through four distinct scenarios:

  • Scenario 1: We fitted the model (10), i.e. the model with all covariates.

  • Scenario 2: We fitted the model Yij=β0+s=12βsxij(s)+Wij, i.e. we omitted the covariate xij(3).

  • Scenario 3: We fitted the model Yij=β0+β1xij(1)+Wij, i.e. we omitted the covariates xij(2) and xij(3).

  • Scenario 4: We omitted all covariates from the model.

Then, we obtained the ST and SW measurements, which correspond to the fitted model with all covariates and with omitting covariates, respectively. In Table 1, we present the mean values of the measurements mentioned above for a sample size n = 100 (results for samples size n = 50 and n = 200 were omitted for presenting similar results) in each scenario considered.

Table 1.

Measures ST and SW according to the scenarios considered.

τ Scenario 1 Scenario 2 Scenario3 Scenario 4
0.1 0.000591 0.002411 0.004547 0.028376
0.3 0.000734 0.002160 0.007190 0.024706
0.5 0.001128 0.001993 0.003238 0.028080
0.7 0.001870 0.004271 0.006253 0.009526

Based on Table 1, we can see that, in general, for fixed Kendall's tau values, the mean values of the measures considered increase according to we omitted more covariates from the model. Moreover, we can see that the average values of ST increasing when we increase Kendall's tau values. Hence, we can conclude that the simulation study showed that the K-residuals were able to evidence the misspecification in the systematic component of the model.

In Figure 1 we present the Q-Q plots of the ordered K-residuals for a sample size n = 100 and τ=0.3 in each scenario considered. We can see that the Q-Q plot for Scenario 1 is very near to the reference diagonal, this means that the assumption where K-residuals have uniform distribution in the range [0,1] is verified. Along with, we can also note that Q-Q plots gradually move away from the reference diagonal as we omitted more model explanatory variables. Therefore, the residuals are sensitive to misspecification in the systematic component of the model.

Figure 1.

Figure 1.

Q-Q plots of ordered K-residuals considering misspecification in the systematic component of the model: (a) scenario 1, (b) scenario 2, (c) scenario 3 and (d) scenario 4.

4.3. Presence of outlier

Likewise, we will also investigate whether K-residuals can detect the existence of outliers that may generate some influence on the parameter estimates that may cause inferential changes. To do so, we generated 5000 bivariate samples (Yi1,Yi2), i=1,,n, with sizes n = 50, 100 and 200, in which we used gamma frailty and considered as true parameters β0=1.5, β1=3 and α=0.5. Again, we assigned the values 0.1, 0.3, 0.5 and 0.7 to Kendall's tau and thus obtained the true values for the parameter κ. To sample contamination, consider (yi1,yi2)=((7/5)yargmax(yi1)1i,yi2), where argmax(yi1)i returns the ith value such that yi1 is maximum, with i=1,,n. Thereby, we obtained the respective measurements, ST and SW, corresponding to the model adjustments to the case in which we did not contaminate the sample and to the case in which there was contamination. We present the mean values of ST and SW in Table 2.

Table 2.

Measures ST and SW – Presence of Outlier.

  n = 50 n = 100 n = 200
τ ST SW ST SW ST SW
0.1 0.001246 0.009017 0.000613 0.007489 0.000302 0.026853
0.3 0.001320 0.008143 0.000955 0.007715 0.000437 0.032681
0.5 0.001699 0.012168 0.001123 0.016090 0.000852 0.014765
0.7 0.002579 0.009703 0.001917 0.018154 0.001660 0.019405

Through Table 2 we can see that the average values of measure SW exceed the average values of measure ST for all sample sizes considered, i.e. the K-residuals detect the presence of outlier.

4.4. A misspecified stochastic component

Now, we consider misspecification in the stochastic component of the model. To produce this misspecification, we generate the data by considering a frailty distribution, called true frailty, and adjust it by considering others frailty distributions. The values assigned to the parameters were β0=0, β1=3 and α=0.5. Again we assign the values 0.1, 0.3, 0.5 and 0.7 to Kendall's tau.

We generated 5000 samples of sizes 50, 100 and 200. Subsequently, we obtained the ST and SW measurements which correspond to the fitted model through the use of the true frailty and to the fitted model with distinct frailty distributions from the frailty distribution true, respectively. Table 3 shows the mean values of the ST and SW measurements for a sample size 100 (we omitted the results for sizes 50 and 100, as they were analogous).

Table 3.

Measures ST and SW – misspecification on stochastic component.

    Fitted frailty model
True frailty τ Gamma Positive stable Logarithmic series
Gamma 0.1 0.000590 0.000670 0.000601
  0.3 0.000721 0.000807 0.000744
  0.5 0.001126 0.000968 0.000870
  0.7 0.001871 0.001404 0.001875
Positive stable 0.1 0.000724 0.000608 0.000667
  0.3 0.001341 0.000634 0.001576
  0.5 0.002213 0.000764 0.005018
  0.7 0.002773 0.001588 0.016349
Logarithmic series 0.1 0.001184 0.000672 0.000766
  0.3 0.001270 0.000682 0.000819
  0.5 0.001428 0.000699 0.000926
  0.7 0.001745 0.000762 0.001231

As we can notice by Table 3, in general, the measures values remained near, regardless of the true frailty distribution considered. Thus, the K-residuals was not able to capture the misspecification in the stochastic component of the model.

4.5. Presence of right censoring

Now, we will study the behavior of adapted K-residuals and to achieve this we will make a comparison between the K-residuals and the adapted K-residuals in the presence of right censoring.

In this case, we use the same scenario considered in the misspecification of the stochastic component of the model. And to introduce it to the right censoring of the sample, we simulate these values of the lognormal distribution with variance 1 and with means 1.5, 1.0 and 0.5 obtain 10%, 20% and 40% censoring.

We did this for one of the response variables of the generated bivariate sample and considered the other response variable of the pair as uncensored. Later, we adjusted the model and obtained the respective S and Sadap measures given in (8) and (9). Then, in Table 4 we present the averages of the S and Sadap measures for a sample size n = 100.

Table 4.

Measures S e Sadap – Presence of right censoring.

    10% 20% 40%
Frailty τ S Sadap S Sadap S Sadap
G 0.1 0.001218 0.000585 0.003123 0.000732 0.016263 0.007855
  0.3 0.003177 0.001565 0.003313 0.000666 0.020950 0.005465
  0.5 0.001651 0.000802 0.010454 0.003744 0.017202 0.005806
  0.7 0.002048 0.001370 0.011765 0.005711 0.020369 0.003375
PS 0.1 0.001156 0.000616 0.004232 0.002456 0.020873 0.017740
  0.3 0.002175 0.001839 0.005035 0.002246 0.014630 0.010150
  0.5 0.004207 0.003529 0.010284 0.009289 0.020428 0.012375
  0.7 0.001591 0.001227 0.003620 0.002616 0.014710 0.004962
LS 0.1 0.000844 0.000654 0.002086 0.000791 0.006873 0.001318
  0.3 0.000991 0.000734 0.061754 0.044018 0.010035 0.004237
  0.5 0.000827 0.000824 0.001572 0.000892 0.005856 0.001788
  0.7 0.000861 0.001067 0.008665 0.004325 0.023288 0.011020

Hence, based on Table 4 we can see that, in general, when we fix the frailty distribution, the average values of the S and Sadap measures increase as we increase the percentage of censoring. Furthermore, we also noticed that the values attributed to Kendall's tau did not affect the magnitude of the measures considered. Finally, we found that for all censoring percentages considered, the average values of the Sadap measure were lower than the corresponding average values of the S measure. Thus, we conclude that the adapted K-residual is better than the K-residual for working with data involving the presence of right censoring.

5. Application

In this section, we consider a real data set corresponding to the recurrence times of infections of kidney patients using a portable dialysis machine. Initially, we present a brief description of the data. Next, we conduct an exploratory analysis, which suggests a positive asymmetric distribution to model the times of infection. Based on this, we compare independent BS and bivariate BSAL models and, finally, we perform local influence study for fitted bivariate BSAL model.

5.1. Description of the data

We consider the data set given in [13] which are related to the recurrence times of infections of 38 kidney patients using a portable dialysis machine. The data considered here has been analyzed by means of Cox proportional hazard model with a multiplicative frailty parameter for each patient [22], by means of a scale-location model for bivariate survival times, using the FGM copula [1], through of the Weibull/gamma shared frailty models [9] and through of the shared frailty models: inverse Gaussian, compound Poisson and compound negative binomial [10]. The aim of this study is to estimate the times of the first and second recurrence of renal infection for each individual, using the bivariate BSAL model, as given in (1) and (2), considering as explanatory variable the variable sex ( 0=male, 1=female). And the percentages of censored observations for the first and second infection time were 16% and 32%, respectively.

5.2. Exploratory data analysis

Table 5 provides a descriptive summary of the data considered that include standard deviation (SD), coefficients of variation (CV), skewness (CS) and kurtosis (CK). Figure 2 shows plots of the marginal fit of the events with BS distribution and also the non-parametric estimates are displayed. Through Table 5, observing the values of CS and CK, it is reasonable to admit that the times have a positively skewed distribution. Therefore, based on these observations and by Figure 2, we notice a BS distribution could be can be suitable for modeling marginal the data considered.

Table 5.

Descriptive statistics for the data.

Variable Median Mean SD CV CS CK Min Max
Time 1 46.00 111.70 1444.01 128.91% 1.69 1.92 2.00 536.00
Time 2 39.00 91.55 117.44 128.28% 2.10 4.82 4.00 562.00

Figure 2.

Figure 2.

Marginal survival estimates by Kaplan–Meier and BS distribution: (a) Time 1 and (b) Time 2.

5.3. Modeling

Next, we will compare independent BS and BSAL models. We present in Table 6 the maximum likelihood estimates (standard errors in parentheses and p-values in []) of the model parameters considering independence within of the pairs observed and of the bivariate BSAL model and the statistics: Sadap, AIC and BIC. We observed that all parameters are significant at 10% for both fitted models and that all selection criteria indicate that the bivariate BSAL model is more suitable for analyzing these data.

Table 6.

Maximum likelihood estimates of the parameters (standard errors in parentheses and p-values in []) and the Sadap, AIC and BIC measures.

  Model
Parameter Independent Bivariate BSAL
  2.3242 1.8447
β0 (0.0573) (0.1012)
  [<0.05] [<0.05]
  1.0906 1.2833
β1 (0.0333) (0.0540)
  [<0.05] [<0.05]
  5.6126
κ (0.8267)
  [0.093]
  1.3967 1.2389
α (0.0147) (0.0252)
 
Sadap 0.1501 0.1245
AIC 204.0576 202.3188
BIC 211.0498 207.2316

To detect possible departures from the initial assumptions of the models, we present in Figure 3 the normal probability plots for the K-residuals with simulated envelope (for the independent case and for the bivariate BSAL model, respectively). Figure 3(a) shows an unusual behavior with points outside of the envelope. While Figure 3(b) shows an usual behavior that does not indicate serious deviation from assumption model.

Figure 3.

Figure 3.

Normal probability plots with envelope – considering independence within pairs (a) and considering the bivariate BSAL model (b).

We performed local influence study for fitted bivariate BSAL model.

In Figures 47 we present the index plots of Mr(θ), Mr(β), Mr(κ) and Mr(α) under the some perturbation schemes for the fitted bivariate BSAL model, where Mr()=Cr()/i=1nCr(). From these figures, were detected as potentially influential the following observations: #4, #8, #10, #11, #15, #20, #21, #22, #23, #29 and #35. The observations #8, #11, #15, #20, #22 and #35 correspond to a female patients that has the a pair of a long and a short periods of time until the occurence of failure or censoring. The observation #4 refers to a female patient that has the a pair of the longs periods of time until the occurence of the failure. The observations #23 and #29 have a pair of short periods of time until failure occurs, where observation #23 refers to a female patient and observation #29 refers to a male patient. Finally, the observations #10 and #21 correspond to a male patients, where observation #10 shows one of the lowest times until the first infection occurs, and observation #21 refers to the longest time until the second infection occurs.

Figure 5.

Figure 5.

Index plots of Mr() for: (a) θ, (b) β, (c) κ and (d) α, under joint perturbation in the response variable.

Figure 6.

Figure 6.

Index plots of Mr() for: (a) θ, (b) β, (c) κ and (d) α, under perturbation in the response variable (first coordinate).

Figure 4.

Figure 4.

Index plots of Mr() for: (a) θ, (b) β, (c) κ and (d) α, under the case-weights perturbation.

Figure 7.

Figure 7.

Index plots of Mr() for: (a) θ, (b) β, (c) κ and (d) α, under perturbation in the response variable (second coordinate).

6. Discussion

In this paper, we proposed the bivariate BSAL model with dependence structure modeled using frailty. We presented some residuals and obtained the appropriate matrices for assessing the local influence under different perturbation schemes. A simulation study for the residuals was performed to verify if the considered residuals were able to identify misspecifications. We observed that such residuals were not sensitive only to evidence misspecifications in the stochastic component of the model. As showed in the application we compared the proposed model with structure of dependence through the frailty with the model assuming independence within the pairs. We also highlighted the importance of the local influence methodology in detecting points that exercise disproportionate impacts on model parameter estimates and the importance of including dependence on statistical analysis.

Acknowledgements

This work was supported by FACEPE and CNPq, Brazil. The authors are grateful to the Associate Editor and reviewers for their constructive comments on an earlier version of this manuscript.

Appendix.

A.1. Score vector

The expressions used in the definition of the score vector are given by D(aj)=diag{a1j(w1,θ),,anj(wn,θ)}, D(b)=diag{b1(w1,θ),,bn(wn,θ)} and D(c)=diag{c1(w1,θ),,cn(wn,θ)}, where

aijwi,θ=δi1δi21f(wi1,wi2)f(wi1,wi2)wij+δi1(1δi2)2S(wi1,wi2)wijwi1S(wi1,wi2)wi1+(1δi1)δi22S(wi1,wi2)wijwi2S(wi1,wi2)wi2+(1δi1)(1δi2)1S(wi1,wi2)×S(wi1,wi2)wij, (A1)
biwi,θ=δi1δi21f(wi1,wi2)f(wi1,wi2)κ+δi1(1δi2)2S(wi1,wi2)κwi1S(wi1,wi2)wi1+(1δi1)δi22S(wi1,wi2)κwi2S(wi1,wi2)wi2+(1δi1)(1δi2)1S(wi1,wi2)×S(wi1,wi2)κ,

and

ciwi,θ=δi1δi21f(wi1,wi2)f(wi1,wi2)α+δi1(1δi2)2S(wi1,wi2)αwi1S(wi1,wi2)wi1+(1δi1)δi22S(wi1,wi2)αwi2S(wi1,wi2)wi2+(1δi1)(1δi2)1S(wi1,wi2)×S(wi1,wi2)α, (A2)

with wi=(wi1,wi2), for i=1,,n and j = 1, 2. The expressions used in Equations (A1) and (A2) are defined below.

f(wi1,wi2)wi1=Llog1Φξ21log1Φξ22ξ12K(ξ22)ξ112×K2(ξ21)+Llog1Φξ21log1Φξ22K(ξ22)×ξ12K2(ξ21)ξ112+ξ21(1ξ112)K(ξ21)2,f(wi1,wi2)wi2=Llog1Φξ21log1Φξ22ξ11K(ξ21)ξ122×K2(ξ22)+Llog1Φξ21log1Φξ22K(ξ21)×ξ11K2(ξ22)ξ122+ξ22(1ξ122)K(ξ22)2,2S(wi1,wi2)wij2=Llog1Φξ21log1Φξ22ξ1jK(ξ2j)2+Llog1Φξ21log1Φξ22ξ2j(1ξ1j2)K(ξ2j)2ξ1jK(ξ2j)2+ξ2j(1ξ1j2)K(ξ2j)2,2S(wi1,wi2)wi1wi2=2S(wi1,wi2)wi2wi1=Llog1Φξ21log1Φξ22×ξ11ξ12K(ξ21)K(ξ22),f(wi1,wi2)α=2ξ11ξ12αLlog1Φξ21log1Φξ22K(ξ22)×ξ21K2(ξ21)+ξ22K(ξ21)K2(ξ22)+Llog1Φξ21log1Φξ22ξ11(ξ2121)K(ξ21)2ξ11ξ21K2(ξ21)×1αξ12K(ξ22)+1αξ11K(ξ21)ξ12(ξ2221)K(ξ22)2ξ12ξ22×K2(ξ22),2S(wi1,wi2)αwij=2αLlog1Φξ21log1Φξ22ξ1jK(ξ2j)×ξ21K(ξ21)+ξ22K(ξ22)+1αLlog1Φξ21log1Φξ22ξ1jK(ξ2j)(ξ2j212ξ2jK(ξ2j)).

A.2. Observed information matrix

The observed information matrix is given by

L¨θθ1=L¨ββL¨βκL¨βαL¨κβL¨κκL¨καL¨αβL¨ακL¨αα,

being

L¨ββ=X1D(A11)+X2D(A12)X1+X1D(A21)+X2D(A22)X2,L¨βκ=L¨κβ=X1D(d1)+X2D(d2)Z,L¨βα=L¨αβ=X1D(e1)+X2D(e2)Z,L¨κκ=tr(D(f)),L¨κα=L¨ακ=tr(D(g))L¨αα=tr(D(h)),

where D(A1j)=diag{A11j,,An1j}, D(A2j)=diag{A12j,,An2j}, D(dj)=diag {/κ[a1j(w1,θ)],,/κ[anj(wn,θ)]}, D(ej)=diag{/α[a1j(w1,θ)],,/α[anj(wn,θ)]}, D(f)=diag {/κ[b1(w1,θ)],,/κ[bn(wn,θ)]}, D(g)= diag{/κ[c1(w1,θ)],,/κ[cn(wn,θ)]} and D(h)=diag{/α[c1(w1,θ)],,/α[cn(wn,θ)]}, with

Aijj=aijwi,θwij=δi1δi2f(wi1,wi2)wijf(wi1,wi2)2+1f(wi1,wi2)2f(wi1,wi2)wij2+δi1(1δi2)1S(wi1,wi2)wi1wij2S(wi1,wi2)wijwi12S(wi1,wi2)wijwi1S(wi1,wi2)wi12+δi2(1δi1)2S(wi1,wi2)wijwi2S(wi1,wi2)wi22+1S(wi1,wi2)wi2wij2S(wi1,wi2)wijwi2+(1δi1)(1δi2)×S(wi1,wi2)wijS(wi1,wi2)2+1S(wi1,wi2)2S(wi1,wi2)wij2

and

Aijj=aijwi,θwij=δi1f(wi1,wi2)wijf(wi1,wi2)wijf2(wi1,wi2)+1f(wi1,wi2)2f(wi1,wi2)wijwij×δi2+(1δi2)δi12S(wi1,wi2)wijwi12S(wi1,wi2)wijwi1S(wi1,wi2)wi12+1S(wi1,wi2)wi1×1S(wi1,wi2)wi1wij2S(wi1,wi2)wijwi1+δi2(1δi1)1S(wi1,wi2)wi2×wij2S(wi1,wi2)wijwi22S(wi1,wi2)wijwi22S(wi1,wi2)wijwi2S(wi1,wi2)wi22+(1δi1)(1δi2)S(wi1,wi2)wijS(wi1,wi2)wijS2(wi1,wi2)+1S(wi1,wi2)×S(wi1,wi2)wijS(wi1,wi2)wijS2(wi1,wi2)2S(wi1,wi2)wijwij,

where jj. Furthermore,

aijwi,θα=δi1δi2f(wi1,wi2)αf(wi1,wi2)wijf2(wi1,wi2)+1f(wi1,wi2)2f(wi1,wi2)αwij+δi1(1δi2)2S(wi1,wi2)αwi12S(wi1,wi2)wijwi1S(wi1,wi2)wi12+α2S(wi1,wi2)wijwi1×1S(wi1,wi2)wi1+(1δi1)δi21S(wi1,wi2)wi2α2S(wi1,wi2)wijwi22S(wi1,wi2)αwi22S(wi1,wi2)wijwi2S(wi1,wi2)wi22+(1δi1)(1δi2)1S(wi1,wi2)×2S(wi1,wi2)αwijS(wi1,wi2)αS(wi1,wi2)wijS2(wi1,wi2)

and

ciwi,θα=δi1δi2f(wi1,wi2)αf(wi1,wi2)2+1f(wi1,wi2)2f(wi1,wi2)α2×(1δi2)2S(wi1,wi2)αwi1S(wi1,wi2)wi12+α2S(wi1,wi2)αwi1×1S(wi1,wi2)wi1+(1δi1)δi21S(wi1,wi2)wi2α2S(wi1,wi2)αwi22S(wi1,wi2)αwi2S(wi1,wi2)wi22+(1δi1)(1δi2)S(wi1,wi2)αS(wi1,wi2)2S(wi1,wi2)αS(wi1,wi2)2+1S(wi1,wi2)2S(wi1,wi2)α2,

with

2f(wi1,wi2)wij2=ξ11ξ12K(ξ21)K(ξ22)Liv{log1Φ(ξ21)log1Φ(ξ22)}×ξ1jK(ξ2j)2+L{log1Φ(ξ21)log1Φ(ξ22)}12ξ2j+ξ1j2K(ξ2j)12ξ2j2K(ξ2j)+ξ1jK(ξ2j)2+12ξ2j(1ξ1j2)×K(ξ2j)+Llog1Φ(ξ21)log1Φ(ξ22)2K(ξ2j)×12ξ2j+ξ1j2K(ξ2j)12ξ2j+141ξ1j22ξ2j2+(1ξ1j2)×2ξ2jK(ξ2j)12ξ2j,
wi22S(wi1,wi2)wi2wi1=ξ11K(ξ21)Llog1Φ(ξ21)log1Φ(ξ22)×ξ12K(ξ22)2+L{log1Φ(ξ21)log1Φ(ξ22)}×K(ξ22)12ξ22+ξ122K(ξ22)12ξ22,wi12S(wi1,wi2)wi1wi2=ξ12K(ξ22)Llog1Φ(ξ21)log1Φ(ξ22)×ξ11K(ξ21)2+12ξ21+ξ112K(ξ21)12ξ21×K(ξ21)L{log1Φ(ξ21)log1Φ(ξ22)},3S(wi1,wi2)wij3=ξ1jK(ξ2j)L{log1Φ(ξ21)log1Φ(ξ22)}ξ1j2K2(ξ2j)+32ξ2jK(ξ2j)(1ξ1j2)+3ξ1jK(ξ2j)2Llog1Φ(ξ21)log1Φ(ξ22)+L{log1Φ(ξ21)log1Φ(ξ22)}×ξ2jK(ξ2j)+K(ξ2j)12ξ2j2ξ1j2K(ξ2j)+12ξ2j(1ξ1j2)+141ξ1j22ξ2j2,
2f(wi1,wi2)αwij=ξ1jK(ξ2j)αLiv{log1Φ(ξ21)log1Φ(ξ22)}ξ1j2×K2(ξ2j)2ξ21K(ξ21)+ξ22K(ξ22)+Llog1Φ(ξ21)log1Φ(ξ22)ξ1jK(ξ2j)2ξ2j(ξ2j2K(ξ2j))1+2×ξ2j(ξ2j2K(ξ2j))12ξ2jK(ξ2j)+ξ2jK(ξ2j)×Llog1Φ(ξ21)log1Φ(ξ22)ξ1jK(ξ2j)2+12×ξ2j(1ξ1j2)K(ξ2j)+Llog1Φ(ξ21)log1Φ(ξ22)ξ2j(ξ2j2K(ξ2j))1ξ1jK(ξ2j)2+12ξ2j(1ξ1j2)K(ξ2j)+2ξ1jK(ξ2j)2ξ2j(ξ2jK(ξ2j))1+12ξ2j(3ξ1j22)K(ξ2j)+ξ2j2(1ξ1j2)K(ξ2j)(ξ2j2K(ξ2j)),
α2S(wi1,wi2)wij2=2αξ1jK(ξ2j)2L{log1Φ(ξ21)log1Φ(ξ22)}×ξ21K(ξ21)+ξ22K(ξ22)ξ2j(ξ2j2K(ξ2j))1×L{log1Φ(ξ21)log1Φ(ξ22)}2α×L{log1Φ(ξ21)log1Φ(ξ22)}ξ21K(ξ21)+ξ22K(ξ22)(ξ1jK(ξ2j))2+12ξ2j(1ξ1j2)K(ξ2j)+1α×L{log1Φ(ξ21)log1Φ(ξ22)}2(K2(ξ2j))×ξ1j2ξ2j(ξ2j2K(ξ2j))1+12K(ξ2j)ξ2j(3ξ1j21)+ξ2j(1ξ1j2)(ξ2j2K(ξ2j)),
α2S(wi1,wi2)wi1wi2=α2S(wi1,wi2)wi2wi1=1αξ11ξ12K(ξ21)K(ξ22)2ξ21K(ξ21)+ξ22K(ξ22)Llog1Φ(ξ21)log1Φ(ξ22)}+ξ21(ξ212K(ξ21))+ξ22(ξ222K(ξ22))2,
2f(wi1,wi2)α2=1α2ξ11ξ12K(ξ21)K(ξ22)ξ21(ξ212K(ξ21))+ξ22(ξ222K(ξ22))2×2L{log1Φ(ξ21)log1Φ(ξ22)}(ξ21K(ξ21)+ξ22K(ξ22))+L{log1Φ(ξ21)log1Φ(ξ22)}ξ21(ξ212K(ξ21))+ξ22ξ222K(ξ22)2+4(ξ21K(ξ21)+ξ22K(ξ22))2Livlog1Φ(ξ21)log1Φ(ξ22)2L{log1Φ(ξ21)log1Φ(ξ22)}K(ξ21)×ξ21ξ21(ξ212K(ξ21))1+ξ22K(ξ22)ξ22(ξ222K(ξ22))12L{log1Φ(ξ21)log1Φ(ξ22)}(ξ21K(ξ21)+ξ22K(ξ22))×ξ21(ξ212K(ξ21))+ξ22(ξ222K(ξ22))2+Llog1Φ(ξ21)log1Φ(ξ22)2ξ21(K(ξ21)(ξ212K(ξ21)1)+ξ21)2ξ22×(K(ξ22)(ξ222K(ξ22)1)+ξ22),
3S(wi1,wi2)α2wij=1α2ξ1jK(ξ2j)ξ2j(ξ2j2K(ξ2j))22(ξ21K(ξ21)+ξ22K(ξ22))×L{log1Φ(ξ21)log1Φ(ξ22)}+(ξ2j212ξ2jK(ξ2j))×L{log1Φ(ξ21)log1Φ(ξ22)}+4Llog1Φ(ξ21)log1Φ(ξ22)(ξ21K(ξ21)+ξ22K(ξ22))22Llog1Φ(ξ21)log1Φ(ξ22)ξ21K(ξ21)(ξ21(ξ212K(ξ21))1)+ξ22K(ξ22)ξ22×(ξ222K(ξ22))12(ξ21K(ξ21)+ξ22K(ξ22))ξ2j22K(ξ2j)×ξ2j1L{log1Φ(ξ21)log1Φ(ξ22)}+ξ2j2+K(ξ2j)ξ2j×(ξ2j(ξ2j2K(ξ2j))1)L{log1Φ(ξ21)log1Φ(ξ22)}.

In addition, we have

wi22S(wi1,wi2)wi2wi1=wi22S(wi1,wi2)wi1wi2=wi12S(wi1,wi2)wi22

and

wi12S(wi1,wi2)wi1wi2=wi12S(wi1,wi2)wi2wi1=wi22S(wi1,wi2)wi12.

Funding Statement

This work was supported by the FACEPE (Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco) [grant number IBPG-0872-1.02/17]; and Conselho Nacional de Desenvolvimento Científico e Tecnológico [grant numbers 310359/2017-1, 302767/2018-5], Brazil.

Disclosure statement

No potential conflict of interest was reported by the author(s).

References

  • 1.Barriga G.D., Louzada-Neto F., Ortega E.M., and Cancho V.G., A bivariate regression model for matched paired survival data: local influence and residual analysis, Stat. Methods. Appt. 19 (2010), pp. 477–495. [Google Scholar]
  • 2.Birnbaum Z.W. and Saunders S.C., A new family of life distributions, J. Appl. Probab. 6 (1969), pp. 319–327. [Google Scholar]
  • 3.Choi Y.H. and Matthews D.E., Accelerated life regression modelling of dependent bivariate time-to-event data, Can. J. Statist. 33 (2005), pp. 449–464. [Google Scholar]
  • 4.Choi Y.-H. and Matthews D.E., Diagnostic tools for bivariate accelerated life regression models, Lifetime. Data. Anal. 21 (2015), pp. 434–456. [DOI] [PubMed] [Google Scholar]
  • 5.Cook R.D., Assessment of local influence, J. R. Stat. Soc: Ser. B (Methodological) 48 (1986), pp. 133–155. [Google Scholar]
  • 6.Cox D.R. and Hinkley D.V., Theoretical Statistics, Chapman and Hall/CRC, London, 1979. [Google Scholar]
  • 7.Genest C. and Rivest L.-P., Statistical inference procedures for bivariate archimedean copulas, J. Am. Stat. Assoc. 88 (1993), pp. 1034–1043. [Google Scholar]
  • 8.Giussani A. and Bonetti M., Marshall–Olkin frailty survival models for bivariate right-censored failure time data, J. Appl. Statist. 46 (2019), pp. 2945–2961. [Google Scholar]
  • 9.Gutierrez R.G., Parametric frailty and shared frailty survival models, Stata J. 2 (2002), pp. 22–44. [Google Scholar]
  • 10.Hanagal D.D. and Dabade A.D., A comparative study of shared frailty models for kidney infection data with generalized exponential baseline distribution, J. Data Sci. 11 (2013), pp. 109–142. [Google Scholar]
  • 11.Hofert M., Mächler M., and McNeil A.J., Estimators for archimedean copulas in high dimensions, preprint (2012), pp. 1207–1708.
  • 12.Hougaard P., Frailty models for survival data, Lifetime. Data. Anal. 1 (1995), pp. 255–273. [DOI] [PubMed] [Google Scholar]
  • 13.Klein J.P and Moeschberger M.L., Survival Analysis: Techniques for Censored and Truncated Data, Springer, New York, 2006. [Google Scholar]
  • 14.Kundu D., Narayanaswamy B., and Ahad J., Bivariate Birnbaum–Saunders distribution and associated inference, J. Multivar. Anal. 101 (2010), pp. 113–125. [Google Scholar]
  • 15.Kundu D., Bivariate log birnbaum–saunders distribution, Statistics 49 (2015), pp. 900–917. [Google Scholar]
  • 16.Leão J., Leiva V., Saulo H., and Tomazella V., Birnbaum–Saunders frailty regression models: Diagnostics and application to medical data, Biom. J. 59 (2017), pp. 291–314. [DOI] [PubMed] [Google Scholar]
  • 17.Leão J., Leiva V., Saulo H., and Tomazella V., A survival model with Birnbaum–Saunders frailty for uncensored and censored cancer data, Braz. J. Probab. Statist. 32 (2018), pp. 707–729. [Google Scholar]
  • 18.Leiva V., Aykroyd R.G., and Marchant C., Discussion of “Birnbaum–Saunders distribution: A review of models, analysis, and applications” and a novel multivariate data analytics for an economics example in the textile industry, Appl. Stochastic. Models Bus. Ind. 35 (2019), pp. 112–117. [Google Scholar]
  • 19.Liu L., Wolfe R.A., and Huang X., Shared frailty models for recurrent events and a terminal event, Biometrics 60 (2004), pp. 747–756. [DOI] [PubMed] [Google Scholar]
  • 20.Marchant C., Leiva V., and Cysneiros F.J.A., A multivariate log-linear model for Birnbaum-Saunders distributions, IEEE Trans. Reliab. 65 (2015), pp. 816–827. [Google Scholar]
  • 21.Marchant C., Leiva V., Cysneiros F.J.A., and Vivanco J.F., Diagnostics in multivariate generalized Birnbaum-Saunders regression models, J. Appl. Statist. 43 (2016), pp. 2829–2849. [Google Scholar]
  • 22.McGilchrist C. and Aisbett C., Regression with frailty in survival analysis, Biometrics 47 (1991), pp. 461–466. [PubMed] [Google Scholar]
  • 23.Nelsen R.B., An Introduction to Copulas, Springer, New York, 2007. Biometrics. [Google Scholar]
  • 24.Oakes D., Bivariate survival models induced by frailties, J. Am. Stat. Assoc. 84 (1989), pp. 487–493. [Google Scholar]
  • 25.Rieck J.R and Nedelman J.R., A log-linear model for the Birnbaum–Saunders distribution, Technometrics 33 (1997), pp. 51–60. [Google Scholar]
  • 26.Sahu S.K., Dey D.K., Aslanidou H., and Sinha D., A weibull regression model with gamma frailties for multivariate survival data, Lifetime. Data. Anal. 3 (1997), pp. 123–137. [DOI] [PubMed] [Google Scholar]
  • 27.Sankaran P.G. and Anisha P., Shared frailty model for recurrent event data with multiple causes, J. Appl. Stat. 38 (2011), pp. 2859–2868. [Google Scholar]
  • 28.Santos-Neto M., Cysneiros F.J.A., Leiva V., and Ahmed S.E., On new parameterizations of the Birnbaum-Saunders distribution, Pakistan J. Statist. 28 (2012), pp. 1–26. [Google Scholar]
  • 29.Saulo H., Leão J., Vila R., Leiva V., and Tomazella V., On mean-based bivariate Birnbaum-Saunders distributions: properties, inference and application, Commun. Statist-Theory Methods 49 (2019), pp. 1–25. [Google Scholar]
  • 30.Tsuyuguchi A.B., Paula G.A., and Barros M., Analysis of correlated Birnbaum–Saunders data based on estimating equations, TEST 29 (2020), pp. 661–681. [Google Scholar]
  • 31.Vilca F., Narayanaswamy B., and Camila B.Z., A robust extension of the bivariate Birnbaum–Saunders distribution and associated inference, J. Multivar. Anal. 124 (2014), pp. 418–435. [Google Scholar]
  • 32.Vilca F., Narayanaswamy B., and Camila B.Z., The bivariate Sinh-Elliptical distribution with applications to Birnbaum–Saunders distribution and associated regression and measurement error models, Comput. Stat. Data. Anal. 80 (2014), pp. 1–16. [Google Scholar]
  • 33.Vilca F., Romeiro R.G., and Balakrishnan N., A bivariate Birnbaum–Saunders regression model, Comput. Stat. Data. Anal. 97 (2016), pp. 169–183. [Google Scholar]

Articles from Journal of Applied Statistics are provided here courtesy of Taylor & Francis

RESOURCES