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Research article

Modeling the effect of time delay in the increment of number of hospital beds to control an infectious disease


  • One of the key factors to control the spread of any infectious disease is the health care facilities, especially the number of hospital beds. To assess the impact of number of hospital beds and control of an emerged infectious disease, we have formulated a mathematical model by considering population (susceptible, infected, hospitalized) and newly created hospital beds as dynamic variables. In formulating the model, we have assumed that the number of hospital beds increases proportionally to the number of infected individuals. It is shown that on a slight change in parameter values, the model enters to different kinds of bifurcations, e.g., saddle-node, transcritical (backward and forward), and Hopf bifurcation. Also, the explicit conditions for these bifurcations are obtained. We have also shown the occurrence of Bogdanov-Takens (BT) bifurcation using the Normal form. To set up a new hospital bed takes time, and so we have also analyzed our proposed model by incorporating time delay in the increment of newly created hospital beds. It is observed that the incorporation of time delay destabilizes the system, and multiple stability switches arise through Hopf-bifurcation. To validate the results of the analytical analysis, we have carried out some numerical simulations.

    Citation: A. K. Misra, Jyoti Maurya, Mohammad Sajid. Modeling the effect of time delay in the increment of number of hospital beds to control an infectious disease[J]. Mathematical Biosciences and Engineering, 2022, 19(11): 11628-11656. doi: 10.3934/mbe.2022541

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  • One of the key factors to control the spread of any infectious disease is the health care facilities, especially the number of hospital beds. To assess the impact of number of hospital beds and control of an emerged infectious disease, we have formulated a mathematical model by considering population (susceptible, infected, hospitalized) and newly created hospital beds as dynamic variables. In formulating the model, we have assumed that the number of hospital beds increases proportionally to the number of infected individuals. It is shown that on a slight change in parameter values, the model enters to different kinds of bifurcations, e.g., saddle-node, transcritical (backward and forward), and Hopf bifurcation. Also, the explicit conditions for these bifurcations are obtained. We have also shown the occurrence of Bogdanov-Takens (BT) bifurcation using the Normal form. To set up a new hospital bed takes time, and so we have also analyzed our proposed model by incorporating time delay in the increment of newly created hospital beds. It is observed that the incorporation of time delay destabilizes the system, and multiple stability switches arise through Hopf-bifurcation. To validate the results of the analytical analysis, we have carried out some numerical simulations.



    For a continuous risk outcome 0<y<1, a model with a random effect has potentially a wide application in portfolio risk management, especially, for stress testing [1,2,7,16,19], capital allocation, conditional expected shortfall estimation [3,11,17].

    Given fixed effects x=(x1,x2,,xk), two widely used regression models to estimate the expected value E(y|x) are: the fraction response model [10] and Beta regression model [4,6,8]. There are cases, however, where tail behaviours or severity levels of the risk outcome are relevant. In those cases, a regression model may no longer fit in for the requirements. In addition, a fraction response model of the form E(y|x)=Φ(a0+a1x1++akxk) may not be adequate when data exhibits significant heteroscedasticity, where Φ is a map from R1 to the open interval (0,1).

    In this paper, we assume that the risk outcome y is driven by a model:

    y=Φ(a0+a1x1++akxk+bs), (1.1)

    where s is a random continuous variable following a known distribution, independent of fixed effects (x1,x2,,xk). Parameters a0,a1,,ak are constant, while parameter b can be chosen to be dependent on (x1,x2,,xk) when required, for example, for addressing data heteroscedasticity.

    Given random effect model (1.1), the expected value E(y|x) can be deduced accordingly. It is given by the integral ΩΦ(a0+a1x1++akxk+bs)f(s)ds over the domain Ω of s, where f is the probability density of s. Given the routine QUAD implemented in SAS and Python, this integral can be evaluated as quickly as other function calls. Relative error tolerance for QUAD is 1.49e-8 in Python and is 1e-7 in SAS. But one can rescale the default tolerance to a desired level when necessary. This leads to an alternative regression tool to the fraction response model and Beta regression model.

    We introduce a family of interval distributions based on variable transformations. Probability densities for these distributions are provided (Proposition 2.1). Parameters of model (1.1) can then be estimated by maximum likelihood approaches assuming an interval distribution. In some cases, these parameters get an analytical solution without the needs for a model fitting (Proposition 4.1). We call a model with a random effect, where parameters are estimated by maximum likelihood assuming an interval distribution, an interval distribution model.

    In its simplest form, the interval distribution model y=Φ(a+bs), where a and b, are constant, can be used to model the loss rate as a random distribution for a homogeneous portfolio. Let yα and sα denote the α -quantiles for y and s at level α, 0<α<1. Then yα=Φ(a+bsα). The conditional expected shortfall for loss rate y, at level α, can then be estimated as the integral 11α[sα,+)Φ(a+bs)f(s)ds, where f is the density of s. Meanwhile, a stress testing loss estimate, derived from a model on a specific scenario, can be compared in loss rate to severity yα(=Φ(a+bsα)), to position its level of severity. A loss estimate may not have reached the desired, for example, 99% level yet, if it is far below y0.99, and far below the maximum historical loss rate. In which case, further recalibrations for the model may be required.

    The paper is organized as follows: in section 2, we introduce a family of interval distributions. A measure for tail fatness is defined. In section 3, we show examples of interval distributions and investigate their tail behaviours. We propose in section 4 an algorithm for estimating the parameters in model (1.1).

    Interval distributions introduced in this section are defined for a risk outcome over a finite open interval (c0,c1), where c0< c1 are finite numbers. These interval distributions can potentially be used for modeling a risk outcome over an arbitrary finite interval, including interval (0, 1), by maximum likelihood approaches.

    Let D=(d0,d1), d0<d1, be an open interval, where d0 can be finite or and d1 can be finite or +.

    Let

    Φ:D(c0,c1) (2.1)

    be a transformation with continuous and positive derivatives Φ(x)=ϕ(x). A special example is (c0,c1)=(0,1), and Φ:D(0,1) is the cumulative distribution function (CDF) of a random variable with a continuous and positive density.

    Given a continuous random variable s, let f and F be respectively its density and CDF. For constants a and b>0, let

    y=Φ(a+bs), (2.2)

    where we assume that the range of variable (a+bs) is in the domain D of Φ. Let g(y,a,b) and G(y,a,b) denote respectively the density and CDF of y in (2.2).

    Proposition 2.1. Given Φ1(y), functions g(y,a,b) and G(y,a,b) are given as:

    g(y,a,b)=U1/(bU2) (2.3)
    G(y,a,b)=F[Φ1(y)ab]. (2.4)

    where

    U1=f{[Φ1(y)a]/b},U2=ϕ[Φ1(y)] (2.5)

    Proof. A proof for the case when (c0,c1)=(0,1) can be found in [18]. The proof here is similar. Since G(y,a,b) is the CDF of y, it follows:

    G(y,a,b)=P[Φ(a+bs)y]
    =P{s[Φ1(y)a]/b}
    =F{[Φ1(y)a]/b}.

    By chain rule and the relationship Φ[Φ1(y)]=y, the derivative of Φ1(y) with respect to y is

    Φ1(y)y=1ϕ[Φ1(y)]. (2.6)

    Taking the derivative of G(y,a,b) with respect to y, we have

    G(y,a,b)y=f{[Φ1(y)a]/b}bϕ[Φ1(y)]=U1bU2.

    One can explore into these interval distributions for their shapes, including skewness and modality. For stress testing purposes, we are more interested in tail risk behaviours for these distributions.

    Recall that, for a variable X over (− ,+), we say that the distribution of X has a fat right tail if there is a positive exponent α>0, called tailed index, such that P(X>x)xα. The relation refers to the asymptotic equivalence of functions, meaning that their ratio tends to a positive constant. Note that, when the density is a continuous function, it tends to 0 when x+. Hence, by L’Hospital’s rule, the existence of tailed index is equivalent to saying that the density decays like a power law, whenever the density is a continuous function.

    For a risk outcome over a finite interval (c0,c1), c0,<c1, however, its density can be + when approaching boundaries c0 and c1. Let y0 be the largest lower bound for all values of y under (2.2), and y1 the smallest upper bound. We assume y0=c0 and y1=c1.

    We say that an interval distribution has a fat right tail if the limit limyy1  g(y,a,b)=+, and a fat left tail if limyy+0  g(y,a,b)=+, where yy+0 and yy1 denote respectively y approaching y0 from the right-hand-side, and y1 from the left-hand-side. For simplicity, we write yy0 for yy+0, and yy1 for yy1.

    Given α>0, we say that an interval distribution has a fat right tail with tailed index α if limyy1  g(y,a,b)(y1y)β=+ whenever 0<β<α, and limyy1  g(y,a,b)(y1y)β=0 for β>α. Similarly, an interval distribution has a fat left tail with tailed index α if limyy0  g(y,a,b)(yy0)β=+ whenever 0<β<α, and limyy0  g(y,a,b)(yy0)β=0 for β>α. Here the status at β=α is left open. There are examples (Remark 3.4), where an interval distribution has a fat right tail with tailed index α, but the limit limyy1  g(y,a,b)(y1y)α can either be + or 0. Under this definition, a tailed index of an interval distribution with a continuous density is always larger than 0 and less or equal to 1, if it exists.

    Recall that, for a Beta distribution with parameters α>0 and β>0, its density is given by f(x)=xα1(1x)β1B(α,β), where B(α,β) is the Beta function . Under the above definition, Beta distribution has a fat right tail with tailed index (1β) when 0<β<1, and a fat left tail with tailed index (1α) when 0<α<1.

    Next, because the derivative of Φ is assumed to be continuous and positive, it is strictly monotonic. Hence Φ1(y) is defined. Let

    z=Φ1(y) (2.7)

    Then limyy0z exists (can be ), and the same for limyy1z (can be +). Let limyy0  z=z0, and limyy1  z=z1. Rewrite g(y,a,b) as g(Φ(z),a,b) by (2.7). Let [g(Φ(z),a,b)]1β/z denote the derivative of [g(Φ(z),a,b)]1/β with respect to z.

    Lemma 2.2. Given β>0, the following statements hold:

    (ⅰ) limyy0  g(y,a,b)(yy0)β=limzz0  g(Φ(z),a,b)(Φ(z)y0)β and limyy1  g(y,a,b)(y1y)β=limzz1  g(Φ(z),a,b)(y1Φ(z))β.

    (ⅱ) If limyy0  g(y,a,b)=+ and limzz0{[g(Φ(z),a,b)]1β/z}/ϕ(z) is 0 (resp. +), then limyy0  g(y,a,b)(yy0)β=+ (resp. 0).

    (ⅲ) If limyy1  g(y,a,b)=+ and limzz1{[g(Φ(z),a,b)]1β/z}/ϕ(z)) is 0 (resp. +), then limyy1  g(y,a,b)(y1y)β=+ (resp. 0).

    Proof. The first statement follows from the relationship y=Φ(z). For statements (ⅱ) and (ⅲ), we show only (ⅲ). The proof for (ⅱ) is similar. Notice that

    [g(y,a,b)(y1y)β]1/β=[g(y,a,b)]1/βy1y=[g(Φ(z),a,b)]1/βy1Φ(z). (2.8)

    By L’Hospital’s rule and taking the derivatives of the numerator and the denominator of (2.8) with respect to z, we have limyy1[g(y,a,b)(y1y)β]1/β=0 (resp. +) if limzz0{[g(Φ(z),a,b)]1/β/z}/ϕ(z) is 0 (resp. +). Hence limyy1  g(y,a,b)(y1y)β=+ (resp. 0).

    For tail convexity, we say that the right tail of an interval distribution is convex if g(y,a,b) is convex for y1є<y<y1 for sufficiently small є>0. Similarly, the left tail is convex if g(y,a,b) is convex for y0<y<y0+є for sufficiently small є>0. One sufficient condition for convexity for the right (resp. left) tail is gyy(y,a,b)0 when y is sufficiently close to y1 (resp. y0).

    Again, write g(y,a,b)=g(Φ(z),a,b). Let

    h(z,a,b)=log[g(Φ(z),a,b)], (2.9)

    where log(x) denotes the natural logarithmic function. Then

    g(y,a,b)=exp[h(z,a,b)]. (2.10)

    By (2.9), (2.10), using (2.6) and the relationship z=Φ1(y), we have

    gy=[hz(z)/ϕ(z)]exp[h(Φ1(y),a,b)],gyy=[hzz(z)ϕ2(z)hz(z)ϕz(z)ϕ3(z)+hz(z)hz(z)ϕ2(z)]exp[h(Φ1(y),a,b)]. (2.11)

    The following lemma is useful for checking tail convexity, it follows from (2.11).

    Lemma 2.3. Suppose ϕ(z)>0, and derivatives hz(z),hz(z), and ϕz(z), with respect to z, all exist. If hzz(z)0 and hz(z)ϕz(z)0, then gyy(y,a,b)0.

    In this section, we focus on the case where (c0,c1)=(0,1), and Φ:D(0,1) in (2.2) is the CDF of a continuous distribution . This includes, for example, the CDFs for standard normal and standard logistic distributions.

    One can explore into a wide list of densities with different choices for Φ and s under (2.2). We consider here only the following four interval distributions:

    A. sN(0,1) and Φ is the CDF for the standard normal distribution.

    B. s follows the standard logistic distribution and Φ is the CDF for the standard normal distribution.

    C. s follows the standard logistic distribution and Φ is its CDF.

    D.D. sN(0,1) and Φ is the CDF for standard logistic distribution.

    Densities for cases A, B, C, and D are given respectively in (3.3) (section 3.1), (A.1), (A.3), and (A5) (Appendix A). Tail behaviour study is summarized in Propositions 3.3, 3.5, and Remark 3.6. Sketches of density plots are provided in Appendix B for distributions A, B, and C.

    Using the notations of section 2, we have ϕ=f and Φ=F. We claim that y=Φ(a+bs) under (2.2) follows the Vasicek distribution [13,14].

    By (2.5), we have

    log(U1U2)=z2+2aza2+b2z22b2 (3.1)
    =(1b2)(za1b2)2+b21b2a22b2. (3.2)

    Therefore, we have

    g(y,a,b)=1bexp{(1b2)(za1b2)2+b21b2a22b2}. (3.3)

    Again, using the notations of section 2, we have y0=0 and y1=1. With z=Φ1(y), we have limy0  z= and limy1  z=+. Recall that a variable 0<y<1 follows a Vasicek distribution [13,14] if its density has the form:

    g(y,p,ρ)=1ρρexp{12ρ[1ρΦ1(y)Φ1(p)]2+12[Φ1(y)]2} (3.4)

    where p is the mean of y , and ρ is a parameter called asset correlation.

    Proposition 3.1. Density (3.3) is equivalent to (3.4) under the relationships:

    a=Φ1(p)1ρ  and  b=ρ1ρ. (3.5)

    Proof. A similar proof can be found in [19]. By (3.4), we have

    g(y,p,ρ)=1ρρexp{1ρ2ρ[Φ1(y)Φ1(p)/1ρ]2+12[Φ1(y)]2}
    =1bexp{12[Φ1(y)ab]2}exp{12[Φ1(y)]2}
    =U1/(bU2)=g(y,a,b).

    The following relationships are implied by (3.5):

    ρ=b21+b2, (3.6)
    a=Φ1(p)1+b2. (3.7)

    Remark 3.2. The mode of g(y,p,ρ) in (3.4) is given in [14] as Φ(1ρ12ρΦ1(p)). We claim this is the same as Φ(a1b2). By (3.6), 12ρ=1b21+b2 and 1ρ=11+b2. Therefore, we have

    1ρ12ρΦ1(p)=1+b21b2Φ1(p)=a1b2.

    This means Φ(1ρ12ρΦ1(p))=Φ(a1b2).

    Proposition 3.3. The following statements hold for g(y,a,b) given in (3.3):

    (ⅰ) g(y,a,b) is unimodal if 0<b<1 with mode given by Φ(a1b2), and is in U-shape if b>1.

    (ⅱ) If b>1,then  g(y,a,b) has a fat left tail and a fat right tail with tailed index (11/b2).

    (ⅲ) If b>1, both tails of g(y,a,b) are convex , and is globally convex if in addition a=0.

    Proof. For statement (ⅰ), we have (1b2)<0 when 0<b<1. Therefore by (3.2) function log(U1U2) reaches its unique maximum at z=a1b2, resulting in a value for the mode at Φ(a1b2). If b>1, then (1b2)>0, thus by (3.2), g(y,a,b) is first decreasing and then increasing when y varying from 0 to 1. This means (y,a,b) is in U-shape.

    Consider statement (ⅱ). First by (3.3), if b>1, then limy1  g(y,a,b)=+ and limy0  g(y,a,b)=+. Thus g(y,a,b) has a fat right and a fat left tail. Next for tailed index, we use Lemma 2.2 (ⅱ) and (ⅲ). By (3.1),

    [g(Φ(z),a,b)]1/β=b1/βexp((b21)z2+2aza22βb2) (3.8)

    By taking the derivative of (3.8) with respect to z and noting that ϕ(z)=12πexp(z22), we have

    {[g(Φ(z),a,b)]1β/z}/ϕ(z)=2πb1β(b21)z+aβb2exp((b21)z2+2aza22βb2+z22). (3.9)

    Thus limz+{[g(Φ(z),a,b)]1β/z}/ϕ(z) is 0 if b21βb2>1, and is + if b21βb2<1. Hence by Lemma 2.2 (ⅲ), g(y,a,b) has a fat right tail with tailed index (11/b2). Similarly, for the left tail, we have by (3.9)

    {[g(Φ(z),a,b)]1β/z}/ϕ(z)=2πb1β(b21)z+aβb2exp((b21)z2+2aza22βb2+z22). (3.10)

    Thus limz{[g(Φ(z),a,b)]1β/z}/ϕ(z) is 0 if b21βb2>1, and is + if b21βb2<1. Hence g(y,a,b) has a fat left tail with tailed index (11/b2) by Lemma 2.2 (ⅱ).

    For statement (ⅲ), we use Lemma 2.3. By (2.9) and using (3.2), we have

    h(z,a,b)=log(U1bU2)=(1b2)(za1b2)2+b21b2a22b2log(b).

    When b>1, it is not difficult to check out that hzz(z)0 and hz(z)ϕz(z)0 when z± or when a=0.

    Remark 3.4. Assume β=(11/b2) and b>1. By (3.9), we see

    limz+{[g(Φ(z),a,b)]1β/z}/ϕ(z)

    is + for a=0, and is 0 for a>0. Hence for this β, the limit limy1  g(y,a,b)(1y)β can be either 0 or +, depending on the value of a.

    For these distributions, we again focus on their tail behaviours. A proof for the next proposition can be found in Appendix A.

    Proposition 3.5. The following statements hold:

    (a) Density g(y,a,b) has a fat left tail and a fat right tail for case B for all b>0, and for case C if b>1. For case D, it does not have a fat right tail nor a fat left tail for any b>0.

    (b) The tailed index of g(y,a,b) for both right and left tails is 1 for case B for all b>0, and is (11b) for case C for B for b>1.

    Remark 3.6. Among distributions A, B, C, and Beta distribution, distribution B gets the highest tailed index of 1, independent of the choices of b>0.

    In this section, we assume that Φ in (2.2) is a function from R1 to (0,1) with positive continuous derivatives. We focus on parameter estimation algorithms for model (1.1).

    First, we consider a simple case, where risk outcome y is driven by a model:

    y=Φ(v+bs), (4.1)

    where b>0 is a constant, v=a0+a1x1++akxk, and sN(0,1), independent of fixed effects x=(x1,x2,,xk). The function Φ does not have to be the standard normal CDF. But when Φ is the standard normal CDF, the expected value E(y|x) can be evaluated by the formula ES[Φ(a+bs)]=Φ(a1+b2) [12].

    Given a sample {(x1i,x2i,,xki,yi)}ni=1, where (x1i,x2i,,xki,yi) denotes the ith data point of the sample, let zi=Φ1(yi). and vi=a0+a1x1i++akxki. By (2.3), the log-likelihood function for model (4.1) is:

    LL=ni=1{logf(zivib)logϕ(zi)logb} (4.2)

    where f is the density of s. The part of ni=1logϕ(zi) is constant, which can be dropped off from the maximization.

    Recall that the least squares estimators of a0,a1,,ak, as a row vector, that minimize the sum squares

    SS=ni=1(zivi)2 (4.3)

    has a closed form solution given by the transpose of (XTX)1XTZ [5,9] whenever the design matrix X has a rank of k, where

    X=1x11xk11x12xk21x1nxkn,Z=z1z2zn.

    The next proposition shows there exists an analytical solution for the parameters of model (4.1).

    Proposition 4.1. Given a sample {\left\{({x}_{1i}, {x}_{2i}, \dots , {x}_{ki}, {y}_{i})\right\}}_{i = 1}^{n} , assume that the design matrix has a rank of k. If s \sim N(0, 1), then the maximum likelihood estimates of parameters {(a}_{0}, {a}_{1}, \dots , a) , as a row vector, and parameter b are respectively given by the transpose of {\left({\mathrm{X}}^{T}\mathrm{X}\right)}^{-1}{\mathrm{X}}^{\mathrm{T}}\mathrm{Z}, and {b}^{2} = \frac{1}{n}\sum _{i = 1}^{n}{({z}_{i}-{v}_{i})}^{2}. In absence of fixed effects {\{x}_{1}, {x}_{2}, \dots , {x}_{k}\} , parameters {a}_{0} and {b}^{2} degenerate respectively to the sample mean and variance of {z}_{1} , {z}_{2}, \dots , {z}_{n}.

    Proof. Dropping off the constant term from (4.2) and noting f\left(z\right) = \frac{1}{\sqrt{2\pi }}\mathrm{exp}\left(-\frac{{z}^{2}}{2}\right) , we have

    LL = -\frac{1}{2{b}^{2}}\sum _{i = 1}^{n}{({z}_{i}-{v}_{i})}^{2}-nlogb, (4.4)

    Hence the maximum likelihood estimates ({a}_{0}, {a}_{1}, \dots , {a}_{k}) are the same as least squares estimators of (4.3), which are given by the transpose of {\left({\mathrm{X}}^{T}\mathrm{X}\right)}^{-1}{\mathrm{X}}^{\mathrm{T}}\mathrm{Z}. By taking the derivative of (4.4) with respect to b and setting it to zero, we have {b}^{2} = \frac{1}{n}\sum _{i = 1}^{n}{({z}_{i}-{v}_{i})}^{2}.

    Next, we consider the general case of model (1.1), where the risk outcome y is driven by a model:

    y = \mathrm{\Phi }[v+ws], (4.5)

    where parameter w is formulated as w = \mathrm{exp}\left(u\right), and u = {b}_{0}+{b}_{1}{x}_{1}+ \dots +{b}_{k}{x}_{k}. We focus on the following two cases:

    (a) s \sim N\left(0, 1\right),

    (b) s is standard logistic.

    Given a sample {\left\{({x}_{1i}, {x}_{2i}, \dots , {x}_{ki}, {y}_{i})\right\}}_{i = 1}^{n}, let {w}_{i} = \mathrm{e}\mathrm{x}\mathrm{p}({b}_{0}+{b}_{1}{x}_{1i}+ \dots +{b}_{k}{x}_{ki}) and {{u}_{i} = b}_{0}+{b}_{1}{x}_{1i}+ \dots +{b}_{k}{x}_{ki}. The log-likelihood functions for model (4.5), dropping off the constant part \mathrm{log}\left({U}_{2}\right), for cases (a) and (b) are given respectively by (4.6) and (4.7):

    LL = \sum _{i = 1}^{n}-{\frac{1}{2}[\left({z}_{i}-{v}_{i}\right)}^{2}/{w}_{i}^{2}-{u}_{i}], (4.6)
    LL = \sum _{i = 1}^{n}\{-\left({z}_{i}-{v}_{i}\right)/{w}_{\mathrm{i}}-2\mathrm{log}[1+\mathrm{e}\mathrm{x}\mathrm{p}[-({z}_{i}-{v}_{i})/{w}_{i}]-{u}_{i}\}, (4.7)

    Recall that a function is log-concave if its logarithm is concave. If a function is concave, a local maximum is a global maximum, and the function is unimodal. This property is useful for searching maximum likelihood estimates.

    Proposition 4.2. The functions (4.6) and (4.7) are concave as a function of {(a}_{0}, {a}_{1}, \dots , {a}_{k}) . As a function of {(b}_{0}, {b}_{1}, \dots , {b}_{k}), (4.6) is concave.

    Proof. It is well-known that, if f(x) is log-concave, then so is f(Az + b), where Az + b : {R^m} \to {R^1} is any affine transformation from the m-dimensional Euclidean space to the 1-dimensional Euclidean space. For (4.6), the function f\left(x\right) = -({z-v)}^{2}\mathrm{exp}(-2u) is concave as a function of v, thus function (4.6) is concave as a function of {(a}_{0}, {a}_{1}, \dots , {a}_{k}) . Similarly, this function f\left(x\right) is concave as a function of u, so (4.6) is concave as a function of {(b}_{0}, {b}_{1}, \dots , {b}_{k}).

    For (4.7), the linear part -\left({z}_{i}-{v}_{i}\right)\mathrm{e}\mathrm{x}\mathrm{p}(-{u}_{i}) , as a function of {(a}_{0}, {a}_{1}, \dots , {a}_{k}) , in (4.7) is ignored. For the second part in (4.7), we know -\mathrm{log}\{1+\mathrm{e}\mathrm{x}\mathrm{p}[-(z-v)/\mathrm{e}\mathrm{x}\mathrm{p}\left(u\right)\left]\right\} , as a function of v , is the logarithm of the CDF of a logistic distribution. It is well-known that the CDF for a logistic distribution is log-concave. Thus (4.7) is concave with respect to {(a}_{0}, {a}_{1}, \dots , {a}_{k}) .

    In general, parameters {(a}_{0}, {a}_{1}, \dots , {a}_{k}) and {(b}_{0}, {b}_{1}, \dots , {b}_{k}) in model (4.5) can be estimated by the algorithm below.

    Algorithm 4.3. Follow the steps below to estimate parameters of model (4.5):

    (a) Given {(b}_{0}, {b}_{1}, \dots , {b}_{k}) , estimate {(a}_{0}, {a}_{1}, \dots , {a}_{k}) by maximizing the log-likelihood function;

    (b) Given {(a}_{0}, {a}_{1}, \dots , {a}_{k}) , estimate {(b}_{0}, {b}_{1}, \dots , {b}_{k}) by maximizing the log-likelihood function;

    (c) Iterate (a) and (b) until a convergence is reached.

    With the interval distributions introduced in this paper, models with a random effect can be fitted for a continuous risk outcome by maximum likelihood approaches assuming an interval distribution. These models provide an alternative regression tool to the Beta regression model and fraction response model, and a tool for tail risk assessment as well.

    Authors are very grateful to the third reviewer for many constructive comments. The first author is grateful to Biao Wu for many valuable conversations. Thanks also go to Clovis Sukam for his critical reading for the manuscript.

    We would like to thank you for following the instructions above very closely in advance. It will definitely save us lot of time and expedite the process of your paper's publication.

    The views expressed in this article are not necessarily those of Royal Bank of Canada and Scotiabank or any of their affiliates. Please direct any comments to Bill Huajian Yang at h_y02@yahoo.ca.



    [1] Hospital Bed Population Ratio (HBPR), OECD Data, Available from: https://data.oecd.org/healtheqt/hospital-beds.htm.
    [2] Hospital Bed Population Ratio (HBPR) in Saudi Arabia, The World Bank Data, Available from: https://data.worldbank.org/indicator/SH.MED.BEDS.ZS?locations=SA.
    [3] World Health Organization, World Health Statistics, 2005–2015.
    [4] P. Das, R. K. Upadhyay, A. K. Misra, F. A. Rihan, P. Das, D. Ghosh, Mathematical model of COVID-19 with comorbidity and controlling using non-pharmaceutical interventions and vaccination, Nonlinear Dyn., 106 (2021), 1213–1227. https://doi.org/10.1007/s11071-021-06517-w doi: 10.1007/s11071-021-06517-w
    [5] A. K. Misra, R. K. Rai, P. K. Tiwari, M. Martcheva, Delay in budget allocation for vaccination and awareness induces chaos in an infectious disease model, J. Biol. Dyn., 15 (2021), 395–429. https://doi.org/10.1080/17513758.2021.1952322 doi: 10.1080/17513758.2021.1952322
    [6] J. A. T. Machado, J. Ma, Nonlinear dynamics of COVID-19 pandemic: modeling, control, and future perspectives, Nonlinear Dyn., 101 (2020), 1525–1526. https://doi.org/10.1007/s11071-020-05919-6 doi: 10.1007/s11071-020-05919-6
    [7] R. Naresh, S. Pandey, A. K. Misra, Analysis of a vaccination model for carrier dependent infectious diseases with environmental effects, Nonlinear Anal. Modell. Control, 13 (2008), 331–350. https://doi.org/10.15388/NA.2008.13.3.14561 doi: 10.15388/NA.2008.13.3.14561
    [8] P. K. Tiwari, R. K. Rai, S. Khajanchi, R. K. Gupta, A. K. Misra, Dynamics of coronavirus pandemic: effects of community awareness and global information campaigns, Eur. Phys. J. Plus, 136 (2021), 994. https://doi.org/10.1140/epjp/s13360-021-01997-6 doi: 10.1140/epjp/s13360-021-01997-6
    [9] J. Pang, J. A. Cui, J. Hui, Rich dynamics of epidemic model with sub-optimal immunity and nonlinear recovery rate, Math. Comput. Modell., 54 (2011), 440–448. https://doi.org/10.1016/j.mcm.2011.02.033 doi: 10.1016/j.mcm.2011.02.033
    [10] C. T. Codeco, Endemic and epidemic dynamics of cholera: the role of the aquatic reservoir, BMC Infect. Dis., 1 (2001), 1–14. https://doi.org/10.1186/1471-2334-1-1 doi: 10.1186/1471-2334-1-1
    [11] M. E. Alexander, S. M. Moghadas, Periodicity in an epidemic model with a generalized non-linear incidence, Math. Biosci., 189 (2004), 75–96. https://doi.org/10.1016/j.mbs.2004.01.003 doi: 10.1016/j.mbs.2004.01.003
    [12] J. K. Ghosh, S. K. Biswas, S. Sarkar, U. Ghosh, Mathematical modelling of COVID-19: A case study of Italy, Math. Comput. Simul., 194 (2022), 1–18. https://doi.org/10.1016/j.matcom.2021.11.008 doi: 10.1016/j.matcom.2021.11.008
    [13] H. W. Hethcote, The mathematics of infectious diseases, SIAM Rev., 42 (2000), 599–653. https://doi.org/10.1137/S0036144500371907 doi: 10.1137/S0036144500371907
    [14] X. Meng, S. Zhao, T. Feng, T. Zhang, Dynamics of a novel nonlinear stochastic SIS epidemic model with double epidemic hypothesis, J. Math. Anal. Appl., 433 (2016), 227–242. https://doi.org/10.1016/j.jmaa.2015.07.056 doi: 10.1016/j.jmaa.2015.07.056
    [15] A. Rajput, M. Sajid, Tanvi, C. Shekhar, R. Aggarwal, Optimal control strategies on COVID-19 infection to bolster the efficacy of vaccination in India, Sci. Rep., 11 (2021), 1–18. https://doi.org/10.1038/s41598-021-99088-0 doi: 10.1038/s41598-021-99088-0
    [16] B. Dhar, P. K. Gupta, M. Sajid, Solution of a dynamical memory effect COVID-19 infection system with leaky vaccination efficacy by non-singular kernel fractional derivatives, Math. Biosci. Eng, 19 (2022), 4341–4367. https://doi.org/10.3934/mbe.2022201 doi: 10.3934/mbe.2022201
    [17] F. Bozkurt, A. Yousef, T. Abdeljawad, A. Kalinli, Q. Al Mdallal, A fractional-order model of COVID-19 considering the fear effect of the media and social networks on the community, Chaos, Solitons Fractals, 152 (2021), 111403. https://doi.org/10.1016/j.chaos.2021.111403 doi: 10.1016/j.chaos.2021.111403
    [18] M. Asif, Z. A. Khan, N. Haider, Q. Al-Mdallal, Numerical simulation for solution of SEIR models by meshless and finite difference methods, Chaos, Solitons Fractals, 141 (2020), 110340. https://doi.org/10.1016/j.chaos.2020.110340 doi: 10.1016/j.chaos.2020.110340
    [19] M. Umar, Kusen, M. A. Z. Raja, Z. Sabir, Q. Al-Mdallal, A computational framework to solve the nonlinear dengue fever SIR system, Comput. Methods Biomech. Biomed. Eng., 2022 (2022), 1–14. https://doi.org/10.1080/10255842.2022.2039640 doi: 10.1080/10255842.2022.2039640
    [20] A. Abdelrazec, J. Bélair, C. Shan, H. Zhu, Modeling the spread and control of dengue with limited public health resources, Math. Biosci., 271 (2016), 136–145. https://doi.org/10.1016/j.mbs.2015.11.004 doi: 10.1016/j.mbs.2015.11.004
    [21] R. Boaden, N. Proudlove, M. Wilson, An exploratory study of bed management, J. Manage. Med., 13 (1999), 234–250. https://doi.org/10.1108/02689239910292945 doi: 10.1108/02689239910292945
    [22] R. D. Booton, L. MacGregor, L. Vass, K. J. Looker, C. Hyams, P. D. Bright, et al., Estimating the COVID-19 epidemic trajectory and hospital capacity requirements in South West England: a mathematical modelling framework, BMJ Open, 11 (2021), e041536. https://doi.org/10.1136/bmjopen-2020-041536 doi: 10.1136/bmjopen-2020-041536
    [23] I. Area, X. H. Vidal, J. J. Nieto, M. J. P. Hermida, Determination in Galicia of the required beds at Intensive Care Units, Alex. Eng. J., 60 (2021), 559–564. https://doi.org/10.1016/j.aej.2020.09.034 doi: 10.1016/j.aej.2020.09.034
    [24] S. D. D. Njankou, F. Nyabadza, Modelling the potential impact of limited hospital beds on Ebola virus disease dynamics, Math. Methods Appl. Sci., 41 (2018), 8528–8544. https://doi.org/10.1002/mma.4789 doi: 10.1002/mma.4789
    [25] B. Dubey, A. Patra, P. K. Srivastava, U. S. Dubey, Modeling and analysis of an SEIR model with different types of nonlinear treatment rates, J. Biol. Syst., 21 (2013), 1350023. https://doi.org/10.1142/S021833901350023X doi: 10.1142/S021833901350023X
    [26] L. V. Green, How many hospital beds, INQUIRY: J. Health Care Organ. Provis. Financing, 39 (2002), 400–412. https://doi.org/10.5034/inquiryjrnl_39.4.400 doi: 10.5034/inquiryjrnl_39.4.400
    [27] J. Karnon, M. Mackay, T. M. Mills, Mathematical modelling in health care, in 18th World IMACS/MODSIM Congress, (2009), 44–56. https://doi.org/10.1.1.552.4422
    [28] A. Kumar, P. K. Srivastava, R. P. Gupta, Nonlinear dynamics of infectious diseases via information-induced vaccination and saturated treatment, Math. Comput. Simul., 157 (2019), 77–99. https://doi.org/10.1016/j.matcom.2018.09.024 doi: 10.1016/j.matcom.2018.09.024
    [29] A. K. Misra, J. Maurya, Modeling the importance of temporary hospital beds on the dynamics of emerged infectious disease, Chaos Interdiscip. J. Nonlinear Sci., 31 (2021), 103125. https://doi.org/10.1063/5.0064732 doi: 10.1063/5.0064732
    [30] W. Qin, S. Tang, C. Xiang, Y. Yang, Effects of limited medical resource on a Filippov infectious disease model induced by selection pressure, Appl. Math. Comput., 283 (2016), 339–354. https://doi.org/10.1016/j.amc.2016.02.042 doi: 10.1016/j.amc.2016.02.042
    [31] P. Saha, U. Ghosh, Global dynamics and control strategies of an epidemic model having logistic growth, non-monotone incidence with the impact of limited hospital beds, Nonlinear Dyn., 105 (2021), 971–996. https://doi.org/10.1007/s11071-021-06607-9 doi: 10.1007/s11071-021-06607-9
    [32] C. Shan, H. Zhu, Bifurcations and complex dynamics of an SIR model with the impact of the number of hospital beds, J. Differ. Equations, 257 (2014), 1662–1688. https://doi.org/10.1016/j.jde.2014.05.030 doi: 10.1016/j.jde.2014.05.030
    [33] C. Shan, Y. Yi, H. Zhu, Nilpotent singularities and dynamics in an SIR type of compartmental model with hospital resources, J. Differ. Equations, 260 (2016), 4339–4365. https://doi.org/10.1016/j.jde.2015.11.009 doi: 10.1016/j.jde.2015.11.009
    [34] A. Wang, Y. Xiao, H. Zhu, Dynamics of a Filippov epidemic model with limited hospital beds, Math. Biosci. Eng., 15 (2018), 739. https://doi.org/10.3934/mbe.2018033 doi: 10.3934/mbe.2018033
    [35] M. Zhang, J. Ge, Z. Lin, The impact of the number of hospital beds and spatial heterogeneity on an SIS epidemic model, Acta Appl. Math., 167 (2020), 59–73. https://doi.org/10.1007/s10440-019-00268-y doi: 10.1007/s10440-019-00268-y
    [36] X. Zhang, X. Liu, Backward bifurcation and global dynamics of an SIS epidemic model with general incidence rate and treatment, Nonlinear Anal. Real World Appl., 10 (2009), 565–575. https://doi.org/10.1016/j.nonrwa.2007.10.011 doi: 10.1016/j.nonrwa.2007.10.011
    [37] H. Zhao, L. Wang, S. M. Oliva, H. Zhu, Modeling and dynamics analysis of Zika transmission with limited medical resources, Bull. Math. Biol., 82 (2020), 1–50. https://doi.org/10.1007/s11538-020-00776-1 doi: 10.1007/s11538-020-00776-1
    [38] M. Zhu, Z. Lin, Modeling the transmission of dengue fever with limited medical resources and self-protection, Discrete Contin. Dyn. Syst. B, 23 (2018), 957. https://doi.org/10.3934/dcdsb.2018050 doi: 10.3934/dcdsb.2018050
    [39] C. Castillo-Chavez, B. Song, Dynamical models of tuberculosis and their applications, Math. Biosci. Eng., 1 (2004), 361. https://10.3934/mbe.2004.1.361 doi: 10.3934/mbe.2004.1.361
    [40] B. Dubey, A. Kumar, Stability switching and chaos in a multiple delayed prey–predator model with fear effect and anti-predator behavior, Math. Comput. Simul., 188 (2021), 164–192. https://doi.org/10.1016/j.matcom.2021.03.037 doi: 10.1016/j.matcom.2021.03.037
    [41] H. L. Freedman, V. S. H. Rao, The trade-off between mutual interference and time lags in predator-prey systems, Bull. Math. Biol., 45 (1983), 991–1004. https://doi.org/10.1016/S0092-8240(83)80073-1 doi: 10.1016/S0092-8240(83)80073-1
    [42] K. Gopalsamy, Stability and Oscillations in Delay Differential Equations of Population Dynamics, Springer Science & Business Media, 2013.
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