Literature DB >> 32287500

Effects of limited medical resource on a Filippov infectious disease model induced by selection pressure.

Wenjie Qin1, Sanyi Tang2, Changcheng Xiang3, Yali Yang4.   

Abstract

In reality, the outbreak of emerging infectious diseases including SARS, A/H1N1 and Ebola are accompanied by the common cold and flu. The selective treatment measure for mitigating and controlling the emerging infectious diseases should be implemented due to limited medical resources. However, how to determine the threshold infected cases and when to implement the selective treatment tactics are crucial for disease control. To address this, we derive a non-smooth Filippov system induced by selective treatment measure. The dynamic behaviors of two subsystems have been discussed completely, and the existence conditions for sliding segment, sliding mode dynamics and different types of equilibria such as regular equilibrium, pseudo-equilibrium, boundary equilibrium and tangent point have been provided. Further, numerical sliding bifurcation analyses show that the proposed Filippov system has rich sliding bifurcations. Especially, the most interesting results are those for the fixed parameter set as the bifurcation parameter varies, the sliding bifurcations occur sequentially: crossing → buckling → real/virtual equilibrium → buckling → crossing. The key factors which affect the selective treatment measures and the threshold value of infected cases for emerging infectious disease have been discussed in more detail.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Filippov infectious disease model; Medical resources limitation; Selective strategy; Sliding bifurcation; Threshold policy

Year:  2016        PMID: 32287500      PMCID: PMC7126627          DOI: 10.1016/j.amc.2016.02.042

Source DB:  PubMed          Journal:  Appl Math Comput        ISSN: 0096-3003            Impact factor:   4.091


Introduction

In the last few years, frequent outbreaks and quick spread of the emerging infectious disease become a worldwide public healthy problem. It endangers not only people’s health but also the stability of the whole society. In 2003, SARS (Severe Acute Respiratory Syndrome) killed 774 people, infected more than 8000 globally and threatened to spread around the world [1], [2]. The A/H1N1 (Hemagglutinin 1, Neuraminidase 1) influenza virus, which caused the 2009 pandemic, continues to circulate in some parts of the world, causing variable levels of disease and outbreaks [3]. By September 14, 2014, a total of 4507 probable and confirmed cases, including 2296 deaths from Ebola virus disease (EVD) had been reported from five countries in West Africa-Guinea, Liberia, Nigeria, Senegal, and Sierra Leone [4]. In the early stages of the emerging infectious disease, it is deficient to recognize the emergence of these infectious systematically and comprehensively, the measures of disinfection and isolation are failed to protect and control infected people, so the patients have little resistance to infection of any kind and emerging infectious spread through the camps like wildfire. The emerging infectious disease including SARS, A/H1N1, Ebola, Dengue fever [5] etc. are often accompanied by other viral diseases such as common flu. Moreover, in the early stages of emerging infectious diseases (taking SARS as an example in the rest of paper) outbreak, there is only a very few number of individuals infected by SARS, and the medical resources are enough at this stage. Meanwhile, the early symptoms are very similar to flu and there is no effective way to identify the infected patients. Thus, patients infected with different viruses can be got treatment in different areas of the hospital at the same time. With the growing numbers of SARS infected cases, those pose a grave threat to public health. Meanwhile, various kinds of control strategies have constraints based on the limited medical resources such as doctors, vaccines, drugs, hospital beds, isolation places, medical devices, and so on, especially in rural areas in many developing countries [6], [7], [8], [9], [10]. The medical resource limitation seriously restricts the prevention and treatment for SARS. At this moment, the department of health or state has to cite the urgency of fighting SARS, adopts green passage policy that speeds for isolation and treatment for SARS, so the doctors have to focus their attentions on the SARS infected cases only. For the patients with common flu, the doctors can only prescribe medicines and advise them to go home for home treatment, which can significantly relieve the pressure of limited medical resources on hospital or doctors. In order to describe the effects of limited medical resource and selection strategy discussed above, the number of the patients infected by SARS in a compartment has been chosen as an index for hospital or doctors to use decisions. That is, if the number of the patients infected by SARS is below the threshold level which can be determined analytically (see main text for more details), there is no limited medical resource and selection pressure; above the threshold, due to the limited resource, and doctors treat SARS only. This type of control strategy is called as threshold control policy [11], [12], which can be described by Filippov systems [13], [14]. Recently, non-smooth Filippov infectious disease models have been investigated by many researchers [10], [15], [16], [17], [18]. In the present work, a non-smooth Filippov infectious disease model with threshold strategy induced by selective treatment measure is derived. The sliding mode dynamics and the existence of all types equilibria have been discussed. Numerical sliding bifurcation analyses show that the proposed Filippov system has rich sliding bifurcations. The key factors which affect the selective treatment measures and the threshold value of infected cases for emerging infectious disease have been discussed in more detail. Our main results show that reducing the threshold value to an appropriate level could contribute to the efficacy on prevention and treatment of emerging infectious disease, which indicates that the selection pressures can be beneficial to prevent the emerging infectious disease under medical resource limitation.

Models and threshold level

Let S(t), I 1(t), I 2(t) and R(t) denote the numbers of susceptible, the patients with SARS, common flu and recovered individuals at time t, respectively. For simplification, we assume that the people can only be infected either by SARS virus or by common flu virus. Further, based on the classical infectious disease model with limited capacity for treatment [9], [10], [19], [20], [21], [22], [23], [24], [25] we propose the following SI 1 I 2 R model as the basic model in this study The parameters of model (2.1) are summarized in Table 1 . Obviously, two probabilities p 1, p 2 ∈ [0, 1]. Note that some very special cases of model (2.1) have been studied in our previous work [10], and the main purpose in this work is to investigate the generalized cases and reveal the rich dynamics and important biological implications concerning emerging infectious disease control.
Table 1

Parameter and definition for model (2.1).

ParametersDefinitions for epidemic dynamics
ARecruitment rate of susceptible individuals
β1The basic transmission coefficient of SARS
β2Basic transmission coefficient of flu
μSNatural death rates of susceptible individuals
μRNatural death rates of recovered individuals
μ1Disease-related and natural death of the patients with SARS
μ2Disease-related and natural death of the patients with flu
ν1Natural recovery rate for SARS
ν2Natural recovery rate for flu
c1The maximal recovery rate per unit time for the patients with SARS
c2The maximal recovery rate per unit time for the patients with flu
b1Delayed effects on the treatment for the patients with SARS
b2Delayed effects on the treatment for the patients with flu
p1Probability that doctors treat the patients with SARS
p2Probability that doctors treat the patients with flu
Parameter and definition for model (2.1). It follows from model (2.1) that the total recovery rate is the major concern for the doctors once the emerging infectious disease outbreaks. Intuitively, how to choose the treatment proportions p 1 and p 2 for the patients infected by different virus such that the total recovery rate reaches its maximal value? To address this question, we discuss the selective strategies in the following. Conditional upon resource limitation, we first assume that medical treatment service for SARS is more than the patients infected by flu, that is Based on the total recovery rate defined by (2.2), we define the function with respect to p 1 and p 2 as follows Taking the derivatives of the function with respect to p 1 and p 2 respectively, one yields and it follows from inequality (2.3) that and consequently the function is monotonically increasing with respect to p 1. According to the sign of the function with respect to I 1, we address the following interesting results concerning the selection strategies. To show this, we define the threshold value for SARS patients as follows which decides whether the hospital carries out the selective strategy or not. Thus, there are two cases: If I 1 < I can obtain the maximum value at If I 1 > I can obtain the maximum value at Therefore, taking into account above facts, in the early stages of SARS outbreak (I 1 < I), the patients with flu can be treated simultaneously with SARS, i.e., . Then model (2.1) becomes With the increasing number of infected cases with SARS (I 1 > I), the doctors have to isolate and treat SARS patients only, i.e., . Thus model (2.1) becomes To simplify models (2.6) and (2.7), we assume that the number of the patients infected by flu each year is a constant, i.e., . Thus, models (2.6) and (2.7) can be rewritten as the following Filippov system [13], [14] with where and with vector . Model (2.8) with (2.9) is a description of the threshold control policy, which is referred to as an on-off control, see [11], [12] for more detailed discussion on Filippov system. Note that the special case (i.e. b 1 = 0) has been investigated recently [10]. Let Then model (2.8) with (2.9) can be rewritten as the following generalized Filippov system [13], [14] where Furthermore, the discontinuity boundary (or manifold) Σ separating two regions G 1 and G 2 is described as and H(Z) is a smooth scalar function with non-vanishing gradient H(Z) on Σ. The main characteristics of Filippov system (2.10) is that selective strategy is suppressed when the number of patients infected by SARS (i.e., I(t)) is below a previously chosen threshold policy I. With this number I(t) increases and exceeds the threshold I, the hospital will treat severe cases only since the shortage of medical resources, that is, the selective strategy is implemented. The following definitions on all types of equilibria of Filippov system (2.10) [26], [27] are necessary throughout the paper. A point Z * is called a real equilibrium of Filippov system (2.10) if or . Similarly, a point Z * is called a virtual equilibrium if or . Both the real and virtual equilibria are called regular equilibria. A point Z * is called a pseudo-equilibrium if it is an equilibrium of the sliding mode of system (2.10), i.e., and 0 < α(Z) < 1, and where ⟨·, ·⟩ denotes the standard scalar product. A point Z * is called a boundary equilibrium of Filippov system (2.10) if and (or ). A point Z * is called a tangency point of Filippov system (2.10) if Z * ∈ Σ and (or ), where is the Lie derivative [28] for .

Qualitative analysis of two subsystems

If I < I, then the following system plays a key role in analyzing the Filippov system (2.10) and the basic reproduction number of subsystem (3.1) reads It is obvious that subsystem (3.1) always has a unique disease-free equilibrium which is globally asymptotically stable if . The endemic equilibria of subsystem (3.1) are solutions of which yields where Noting that n 1 < 0 if and only if if and only if n 1 > 0 if and only if . For the simplicity and convenience of exposition, we denote For subsystem (3.1) , we have If there exists a unique endemic equilibrium ; If and m 1 < 0, there exists a unique endemic equilibrium ; If and m 1 ≥ 0, there exists no endemic equilibrium; If and Δ 1 > 0, there exists two endemic equilibria and ; If and two endemic equilibria and coalesce at a unique endemic equilibrium of multiplicity 2; If and Δ 1 < 0, there exists no endemic equilibrium; If and m 1 ≥ 0, there exists no endemic equilibrium. Next, we will study the stability of the endemic equilibria of subsystem (3.1). The characteristic equation about the endemic equilibrium is given by where We can obtain the following lemmas from (3.3). If then the endemic equilibrium of system (3.1) is a stable node or focus when ; is an unstable node or focus when and system (3.1) has at least one closed orbit in Ω; is a center of the linear system when . If and Δ 1 > 0 and A > A 1, then the endemic equilibrium of system (3.1) is a saddle; and is an unstable node or focus when ; is a center of linear system when . The methods of proving Lemmas 3.1–3.3 are similar to those in Refs. [23], [24], see these references for more details. If I > I, then the Filippov system (2.10) becomes and it has a unique disease-free equilibrium which is globally asymptotically stable if . Here, is the basic reproduction number of subsystem (3.5). For convenience, we denote where The characteristic equation about for is given by where Similar conclusions as Lemmas 3.1–3.3 for subsystem (3.5) can be obtained, and those are not described here.

Basic properties of Filippov system (2.10)

Existence of sliding domain

It follows from Filippov convex method [13], [14] that one can define the sliding vector field as a convex combination of the two vector fields with Noting that the control indicates that the flow is governed by alone, which must be tangent to the switching surface Σ. Analogously, shows a tangency of flow with Σ. Therefore, the sliding subset can be defined as The boundaries of the sliding subset are and where one of the vector fields is tangent to Σ at the boundaries or . In particular, we can use the signs of to define the sewing region, escaping region and sliding region, see Refs. [29], [30] for more details. By simple calculation, we have solving the inequality 0 ≤ α(Z) ≤ 1 with respect to S, one yields Therefore, the sliding segment of Filippov (2.10) can be defined as

Sliding mode dynamics

Here we employ Utkin’s equivalent control method introduced in [14] to obtain the differential equation for sliding dynamics defined in the region Σ. It follows from that and solving the above equation with respect to ε yields According to Utkin’s equivalent control method, we can obtain the dynamics defined in Σ which can be determined by the following scalar differential equation

Equilibria of Filippov system (2.10)

For the simplicity and convenience of exposition, we denote real equilibrium as E, virtual equilibrium as E, pseudo-equilibrium as E, boundary equilibrium as E and tangent point as E, respectively. Regular equilibrium: For convenience, we just consider the subsystem has two endemic equilibria. From Lemma 3.1, subsystem (3.1) has two endemic equilibria and provided that and Δ 1 > 0. If then both and are real equilibria for subsystem (3.1), denoted by and ; While if then both and become virtual equilibria for subsystem (3.1), denoted by and ; Else if then the equilibria and become the virtual and real equilibria, denoted by and , respectively. Analogously, subsystem (3.5) has two endemic equilibria for as and Δ 2 > 0. And could be a real or virtual equilibrium (denoted by or , respectively) which depends on the size of and I. Pseudo-equilibrium: For the existence of pseudo-equilibrium, we denote according to (4.4) the S component of the pseudo-equilibrium of sliding flow satisfies the following equation where and S is a unique positive steady state of (4.4). That is, if holds true, Filippov system (2.10) exists a unique pseudo-equilibrium E. For the stability of pseudo-equilibrium we rewrite sliding mode equation (4.4) as it follows from (4.5) that which indicates that the pseudo-equilibrium E is locally stable in Σ. Boundary equilibrium: The boundary equilibria of Filippov system (2.10) satisfy equations which indicates that if then we have boundary equilibrium . We denote or provided (4.6) as i.e., or (if or exists), and or provided (4.6) as i.e., or (if or exists). Tangent point: According to Definition 2.4, the tangent point E on sliding segment Σ satisfies equations and Hence, there may be two possible tangent points including and . The richness of equilibria of Filippov system (2.10) could result in a number of equilibrium bifurcations as the key parameter varies. Thus, in the coming section, we would like to investigate the local and global sliding bifurcations of system (2.10).

Sliding bifurcation analysis of Filippov system (2.10)

By employing numerical methods to investigate the qualitative behaviors of Filippov system (2.10), the sliding bifurcation analyses including local and global bifurcations of one parameter Filippov system (2.10) are provided in this section. Therefore, we fix all other parameters and choose the maximal recovery rate for the patients with flu (i.e., c 2) as a bifurcation parameter, noting that c 2 is directly related to the threshold value I.

Local sliding bifurcation

Throughout this section, we will investigate the local sliding bifurcation of Filippov system (2.10). Boundary equilibrium bifurcation, as a type of local sliding bifurcation in Filippov system, is characterized by the collision of pseudo-equilibrium, tangent point, and real equilibrium (or tangent point and real equilibrium) at the discontinuity surface when one parameter passes through a critical value, and includes boundary node, focus and saddle bifurcations which will be addressed in the following. Noting that the boundary equilibrium bifurcation occurs at E if is invertible (or equivalently the eigenvalues of have real part different from zero and . Here the symbol is the characteristic polynomial of subsystems (3.1) or (3.5) about the boundary equilibrium E). These bifurcations are classified as boundary saddle, boundary node and boundary focus in [31]. It follows from Section 4.2 that Filippov system (2.10) maybe have boundary equilibria and if and exist for . For the boundary equilibria and by simple calculations we have and from Lemma 3.3, we know that possesses complex eigenvalues with nonzero real part if is an saddle (a note, or a focus). Again, similar argument as above will yield for the boundary equilibria and . Hence, a boundary equilibrium bifurcation occurs at . Boundary-saddle bifurcation: This type of bifurcation may occur for Filippov system (2.10) if three types of equilibria E and E collide together simultaneously as parameter c 2 passes through a critical value [31]. For example, when the parameter c 2 passes through a critical value a saddle a tangent point and a pseudo-equilibrium E collide together, so the boundary-saddle bifurcation occurs at as shown in Fig. 1 (B). In this case, the critical value A saddle (an unstable real equilibrium), a stable pseudo-equilibrium E and an invisible tangent can coexist for as shown in Fig. 1(A) with . They collide together simultaneously as and are substituted by a virtual equilibrium an invisible tangent while the pseudo-equilibrium E is disappeared, when the parameter see Fig. 1(C) with for more details.
Fig. 1

Boundary-saddle bifurcation for Filippov system (2.10). Parameters are: and (A) (B) (C).

Boundary-saddle bifurcation for Filippov system (2.10). Parameters are: and (A) (B) (C). Boundary-node bifurcation: From Fig. 2 , we can see that the stable note and a tangent point collide together as the parameter c 2 passes through the critical value the boundary node bifurcation occurs at where the critical value is A stable note and a tangent point coexist, as shown in Fig. 2(A) with when . They collide at (see Fig. 2(B)) and are substituted by a pseudo-equilibrium E, a tangent point and a virtual equilibrium as see Fig. 2(C) with for more details.
Fig. 2

Boundary-node bifurcation for Filippov system (2.10). Parameters are: and (A) (B) (C).

Boundary-node bifurcation for Filippov system (2.10). Parameters are: and (A) (B) (C). Boundary-focus bifurcation: Similarly, a boundary focus bifurcation of Filippov system (2.10) occurs at as see Fig. 3 , and A stable focus and a tangent point coexist, as shown in Fig. 3(A) when c 2 < 0.635. They collide at (see Fig. 3(B) with ) and are substituted by a pseudo-equilibrium E, a tangent point and a virtual equilibrium when c 2 > 0.635, as shown in Fig. 3(C) with .
Fig. 3

Boundary-focus bifurcation for Filippov system (2.10). Parameters are: and (A) (B) (C).

Boundary-focus bifurcation for Filippov system (2.10). Parameters are: and (A) (B) (C).

Global sliding bifurcation

Filippov system (2.10) could have standard periodic solutions that lie entirely in regions G 1 or G 2 through a Hopf bifurcation, respectively [31], [32]. Meanwhile, as mentioned in Refs. [26], [31], Filippov system (2.10) may have additional two types of new periodic solutions: periodic solutions which have a sliding segment in sliding segment Σ (i.e., sliding periodic solutions) and those which have only isolated points in common with Σ (i.e., crossing periodic solutions). Noting that a crossing periodic solution can pass through the boundary of the sliding segment Σ. Accordingly, the orbits corresponding to periodic solutions will be called standard, sliding and crossing cycles. In this section, we focus on the global sliding bifurcations such as grazing bifurcation (i.e., touching bifurcation), buckling bifurcation and crossing bifurcation. Grazing (or touching) bifurcation: It follows from the Refs. [26], [31], a standard periodic solution can collide with the sliding segments, and this type of bifurcation is called grazing or touching bifurcation. Noting that Filippov system (2.10) has a stable periodic solution in the interior of region G 2, as shown in Fig. 4 (A) with . At this moment, Filippov system (2.10) has two tangent points and lying on the boundary of the sliding mode, subsystem (3.5) has an unstable real equilibrium while subsystem (3.1) has one unstable virtual equilibrium . As the parameter c 2 increases and passes through around 0.85, a grazing or touching bifurcation occurs, as shown in Fig. 4(B), which indicates that the standard period solution of Filippov system (2.10) collides with its tangent point . As c 2 continues to increase the cycle becomes a sliding cycle, where a piece of sliding segment belongs to the cycle, as shown in Fig. 4(C) with .
Fig. 4

Grazing (or touching) bifurcation for Filippov system (2.10). Parameters are: .

Grazing (or touching) bifurcation for Filippov system (2.10). Parameters are: . Especially, as the bifurcation parameter c 2 is increased to 1.6, the stable periodic cycle is disappeared, and pseudo-equilibrium E appears at . Meanwhile, for subsystem (3.5), the real equilibrium becomes a virtual equilibrium the real/virtual equilibrium bifurcation occurs at as shown in Fig. 4(D). Meanwhile, Fig. 4(D)also shows that pseudo-equilibrium of Filippov system cannot coexist with the real equilibria. Buckling bifurcation: This type of bifurcation is defined as a standard piece of the cycle starts to pass the invisible quadratic tangent point as the bifurcation parameter varies [31], as shown in Fig. 5 (C). Fig. 5(B) clearly shows that Filippov system (2.10) has a stable sliding periodic solution, an invisible quadratic tangent point an unstable regular equilibria and . As c 2 increases and exceeds 0.7 the piece of the cycle starts to pass the invisible quadratic tangent point and consequently the cycle passes through the whole piece of the sliding segment Σ, and the sliding cycle does exist in region G 2 and sliding segment Σ, see Fig. 5(C) for details. It follows from Fig. 5(B)–(D) that a buckling bifurcation occurs at . Similarly, Fig. 5(F)–(H) also shows there exists a buckling bifurcation as unlike 5(B)–(D), the sliding cycle as shown in Fig. 5(G) does exists in region G 1 and Σ.
Fig. 5

Buckling and crossing bifurcations for Filippov system (2.10). Parameters are:

Buckling and crossing bifurcations for Filippov system (2.10). Parameters are: Crossing bifurcation: Along with the variation of bifurcation parameter, a stable sliding periodic solution becomes a stable crossing periodic solution, this type bifurcation is called crossing bifurcation. It is interesting to note that a sliding cycle with a single sliding segment ending at does exists in both regions G 1, G 2 and sliding segment Σ, see Fig. 5(H). As c 2 increases and reaches 3.45 the sliding cycle only passes the tangent point on the sliding segment Σ. At this moment, the stable sliding periodic solution becomes a stable crossing periodic solution, as shown in Fig. 5(I) with . Fig. 5(J) shows that the sliding crossing cycle becomes a crossing cycle as c 2 continues to increase and reach 4. Noting that the sliding segment Σ is located within the crossing cycle which exists in both regions G 1 and G 2. It follows from Fig. 5(H)–(J) that a crossing bifurcation occurs at . Similarly, Filippov system (2.10) must exist one crossing bifurcation from Fig. 5(A) to (B). In summary, as bifurcation parameter c 2 increases from 0.5 to 4 and all other parameters are fixed as those in Fig. 5, Filippov system (2.10) has rich sliding bifurcations, the following local and global sliding bifurcations occur sequentially: crossing → buckling → real/virtual equilibrium → buckling → crossing. Especially, as the bifurcation parameter c 2 changes around 1.6, the stable periodic cycle is disappeared, and pseudo-equilibrium E appears at all the orbits tend to the pseudo-equilibrium E, which is locally asymptotically stable. There exists a real/virtual equilibrium bifurcation for Filippov system (2.10) in such case.

Key parameters and biological significance

Previous analysis indicates that limited medical resources, the basic reproduction numbers and threshold values I (or the selective strategy) are significant factors affecting the spread of the emerging infectious disease. In this section, we first investigate how the limited medical resources (i.e., b 1) affects the dynamic behaviors of Filippov system (2.10) or the spread of SARS. As the medical resource limitation (i.e., b 1 ≠ 0) is taken into account, then the dynamical behaviors of both subsystems (3.1) and (3.5) of Filippov system (2.10) become much more complex. Meanwhile, the dynamic behavior of the Filippov system (2.10) could be dramatically affected by the existence of medical resource limitation. In fact, the sliding mode could change as threshold value I changes, as shown in Fig. 6 (A), the length of sliding segment is increased with growing recovery rate c 1 from 0.6 to 1.5. Meanwhile, noting that Filippov system (2.10) does not have pseudo-equilibrium in this case . However, with the medical resource limitation (i.e., b 1 ≠ 0), there exists a pseudo-equilibrium E, which is globally stable with respect to the sliding segment Σ, as shown in Fig. 6(B). Those indicates that the emerging infectious disease will become endemic instead of elimination.
Fig. 6

The impacts of b1 on the existence of pseudo-equilibrium of Filippov system (2.10). Parameters are: and .

The impacts of b1 on the existence of pseudo-equilibrium of Filippov system (2.10). Parameters are: and . Meanwhile, as seen in Fig. 7 , the rate of growth in the number of the patients with SARS is far more quickly before than after controlling. By comparing the red line with the blue one in Fig. 7, the limited medical resource has been a great influence on the time when the peak of patients appears and how long does the spread of SARS last. In fact, the blue line (with sufficient medical resources, i.e., ) shows that there is a peak of patients in rapid and a sharp decline, the spread of SARS lasts only for a short time. The red line (with limited resources, i.e., ) shows there is a delay in appearance of the peak of patients, and the peak value increases obviously, which indicates that the limited medical resources does not facilitate the treatment of infectious disease.
Fig. 7

The time series of I with different parameter value b1. Parameters are: and initial value . (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

The time series of I with different parameter value b1. Parameters are: and initial value . (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.) Therefore, in order to prevent and control the spread of emerging infectious disease, it is crucial to implement the selective strategy timely to control the basic reproduction numbers . Then, the key parameters and threshold value I which affect the basic reproduction numbers and selective strategy are investigated, respectively. Obviously, it follows from the expressions of the basic reproduction numbers that they are monotonically decreasing functions with respect to c 1. Meanwhile, we can solve with respect to c 1 and derive that so provided as shown in Fig. 8 (A). An improved the maximum cure rate for SARS will help prevent and control the spread of SARS.
Fig. 8

The monotonicity of and with respect to c1 and I. Parameters are: .

The monotonicity of and with respect to c1 and I. Parameters are: . Furthermore, the threshold value I is a monotonically decreasing function with respect to c 1. Therefore, in order to control the spread of SARS, it is crucial to reduce the threshold value I to here That is, the smaller the threshold value I is, the more beneficial to prevent and control SARS, as shown in Fig. 8(B). Those indicate that it is best to timely selective treatment for SARS infected cases so as not to miss the best timing of treatment.

Concluding remarks

In order to understand the effect of the delayed treating (b 1 ≠ 0) for the patients with emerging infectious disease on control strategy, we have deduced a non-smooth infectious disease model induced by selection pressures. Analysis of this model reveals rich dynamics including local and global sliding bifurcations. Our main results show that reducing the threshold value to an appropriate level could contribute to the efficacy on prevention and treatment of emerging infectious disease, which indicates that the selection pressures can be beneficial to prevent the emerging infectious disease under medical resource limitation. Comparing the results for the model with we have studied in Ref. [10] with b 1 ≠ 0, we conclude that the term b 1 makes the dynamical behavior of the system change more interesting and complicated. By using theoretical techniques [26], [27], [31], the existence conditions for sliding segment, sliding mode dynamics and different types of equilibria such as regular equilibrium, pseudo-equilibrium, boundary equilibrium and tangent point have been provided. Further, numerical sliding bifurcation analyses show that the proposed Filippov system has more rich local and global sliding bifurcations than the case studied in Ref. [10], as shown in Figs. 1–5 for more details. Especially, the most interesting results are those for the fixed parameter set as the bifurcation parameter varies, the sliding bifurcations occur sequentially: crossing → buckling → real/virtual equilibrium → buckling → crossing. According to the analyses of key parameters and biological significance, the results indicate that the dynamic behavior of the Filippov system (2.10) could be dramatically affected by the existence of medical resource limitation (i.e., b 1 ≠ 0), see Fig. 6(B) for more detail, the existence and stability of pseudo-equilibrium shows that the emerging infectious disease will become endemic. That is, the case shown in Figs. 4(D) and 5(E), which reveals that there are several hidden factors that can adverse affect the control strategy under medical resource limitation. Therefore, it is very necessary to implement the selective strategy in the control and treatment of SARS, see Fig. 8. Meanwhile, this points to the urgent need for improvement in medical facilities, access to rapid diagnosis and treatment with more effective drugs for SARS.
  8 in total

1.  Backward bifurcation of an epidemic model with treatment.

Authors:  Wendi Wang
Journal:  Math Biosci       Date:  2006-02-08       Impact factor: 2.144

2.  Saturation recovery leads to multiple endemic equilibria and backward bifurcation.

Authors:  Jingan Cui; Xiaoxia Mu; Hui Wan
Journal:  J Theor Biol       Date:  2008-05-22       Impact factor: 2.691

3.  Extrapolating from sequence--the 2009 H1N1 'swine' influenza virus.

Authors:  Venkataramanan Soundararajan; Kannan Tharakaraman; Rahul Raman; S Raguram; Zachary Shriver; V Sasisekharan; Ram Sasisekharan
Journal:  Nat Biotechnol       Date:  2009-06       Impact factor: 54.908

4.  Dissolving polymer microneedle patches for influenza vaccination.

Authors:  Sean P Sullivan; Dimitrios G Koutsonanos; Maria Del Pilar Martin; Jeong Woo Lee; Vladimir Zarnitsyn; Seong-O Choi; Niren Murthy; Richard W Compans; Ioanna Skountzou; Mark R Prausnitz
Journal:  Nat Med       Date:  2010-07-18       Impact factor: 53.440

5.  Sliding mode control of outbreaks of emerging infectious diseases.

Authors:  Yanni Xiao; Xiaxia Xu; Sanyi Tang
Journal:  Bull Math Biol       Date:  2012-07-27       Impact factor: 1.758

Review 6.  Transmission of infectious diseases during commercial air travel.

Authors:  Alexandra Mangili; Mark A Gendreau
Journal:  Lancet       Date:  2005 Mar 12-18       Impact factor: 79.321

7.  Optimal vaccine allocation for the early mitigation of pandemic influenza.

Authors:  Laura Matrajt; M Elizabeth Halloran; Ira M Longini
Journal:  PLoS Comput Biol       Date:  2013-03-21       Impact factor: 4.475

8.  Ebola virus disease in West Africa--the first 9 months of the epidemic and forward projections.

Authors:  Bruce Aylward; Philippe Barboza; Luke Bawo; Eric Bertherat; Pepe Bilivogui; Isobel Blake; Rick Brennan; Sylvie Briand; Jethro Magwati Chakauya; Kennedy Chitala; Roland M Conteh; Anne Cori; Alice Croisier; Jean-Marie Dangou; Boubacar Diallo; Christl A Donnelly; Christopher Dye; Tim Eckmanns; Neil M Ferguson; Pierre Formenty; Caroline Fuhrer; Keiji Fukuda; Tini Garske; Alex Gasasira; Stephen Gbanyan; Peter Graaff; Emmanuel Heleze; Amara Jambai; Thibaut Jombart; Francis Kasolo; Albert Mbule Kadiobo; Sakoba Keita; Daniel Kertesz; Moussa Koné; Chris Lane; Jered Markoff; Moses Massaquoi; Harriet Mills; John Mike Mulba; Emmanuel Musa; Joel Myhre; Abdusalam Nasidi; Eric Nilles; Pierre Nouvellet; Deo Nshimirimana; Isabelle Nuttall; Tolbert Nyenswah; Olushayo Olu; Scott Pendergast; William Perea; Jonathan Polonsky; Steven Riley; Olivier Ronveaux; Keita Sakoba; Ravi Santhana Gopala Krishnan; Mikiko Senga; Faisal Shuaib; Maria D Van Kerkhove; Rui Vaz; Niluka Wijekoon Kannangarage; Zabulon Yoti
Journal:  N Engl J Med       Date:  2014-09-22       Impact factor: 91.245

  8 in total
  1 in total

1.  On the optimal control of SIR model with Erlang-distributed infectious period: isolation strategies.

Authors:  Luca Bolzoni; Rossella Della Marca; Maria Groppi
Journal:  J Math Biol       Date:  2021-09-22       Impact factor: 2.164

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.