Antonio Javier Rodríguez-Hernández1, Carlos Sevcik2. 1. Hospital La Fuenfría, Carretera de Las Dehesas, Madrid, Spain. 2. Centro de Biofísica y Bioquímica, Instituto Venezolano de Investigaciones Científicas, Caracas, Venezuela.
Abstract
Operative parameters of La Fuenfría Hospital such as: hospitalized patients; daily admissions and discharges were studies for the hospital as a whole, and for each hospital's service unit (henceforth called 'services'). Conventional statistical analyzes and fractal dimension analyzes were performed on daily In-Patient series. The sequence of daily admissions and patients staying on each service were found to be a kind of random series known as random walks (Rw), sequences where what happens next, depends on what happens now plus a random variable. Rw analyzed with parametric or nonparametric statistics may simulate cycles and drifts which resemble seasonal variations or fake trends which reduce the Hospital's efficiency. Globally, inpatients Rw s in LFH, were found to be determined by the time elapsed between daily discharges and admissions. The factors determining LFH R were found to be the difference between daily admissions and discharges. The discharges are replaced by admissions with some random delay and the random difference determines LFH Rw s. These findings show that if the daily difference between admissions and discharges is minimized, the number of inpatients would fluctuate less and the number of unoccupied beds would be reduced, thus optimizing the Hospital service.
Operative parameters of La Fuenfría Hospital such as: hospitalized patients; daily admissions and discharges were studies for the hospital as a whole, and for each hospital's service unit (henceforth called 'services'). Conventional statistical analyzes and fractal dimension analyzes were performed on daily In-Patient series. The sequence of daily admissions and patients staying on each service were found to be a kind of random series known as random walks (Rw), sequences where what happens next, depends on what happens now plus a random variable. Rw analyzed with parametric or nonparametric statistics may simulate cycles and drifts which resemble seasonal variations or fake trends which reduce the Hospital's efficiency. Globally, inpatients Rw s in LFH, were found to be determined by the time elapsed between daily discharges and admissions. The factors determining LFH R were found to be the difference between daily admissions and discharges. The discharges are replaced by admissions with some random delay and the random difference determines LFH Rw s. These findings show that if the daily difference between admissions and discharges is minimized, the number of inpatients would fluctuate less and the number of unoccupied beds would be reduced, thus optimizing the Hospital service.
Daily in-patients (InP) at La Fuenfría Hospital from May 1 2014 and December 19 2017.
Panels are: Panel A- Number of inpatients (InP) at La Fuenfría Hospital per day during the study duration; Panel B- Daily variations of inpatients (DInP) at the Hospital’s [Δy in Eq (2)]; Panel C- Hospital’s daily stays (Panel A) probability density function (pdf, the probability of observing a given mensurable or enumerable random event) for any number of inpatients (InP) staying at the Hospital observed during the study period (•) [28], a Gauss line () with the same mean and variance (s[y]2) as the set of 1329 data points making the series in Panel A (, s[y] = 24.4); Panel D- Daily difference between admissions (Fig 2A) and discharges (Fig 2C) in the Hospital (DDiAd). Panel E- Random walk Ξ built for DDiAd (Panel D) using Eq (5), please note the extreme resemblance to the sequence of InP in Panel A. In all cases abscissa is the number of days after May 1 2014. The largest negative or positive peaks are off scale outliers.
Daily in-patients (InP) at La Fuenfría Hospital from May 1 2014 and December 19 2017.
Panels are: Panel A- Number of inpatients (InP) at La Fuenfría Hospital per day during the study duration; Panel B- Daily variations of inpatients (DInP) at the Hospital’s [Δy in Eq (2)]; Panel C- Hospital’s daily stays (Panel A) probability density function (pdf, the probability of observing a given mensurable or enumerable random event) for any number of inpatients (InP) staying at the Hospital observed during the study period (•) [28], a Gauss line () with the same mean and variance (s[y]2) as the set of 1329 data points making the series in Panel A (, s[y] = 24.4); Panel D- Daily difference between admissions (Fig 2A) and discharges (Fig 2C) in the Hospital (DDiAd). Panel E- Random walk Ξ built for DDiAd (Panel D) using Eq (5), please note the extreme resemblance to the sequence of InP in Panel A. In all cases abscissa is the number of days after May 1 2014. The largest negative or positive peaks are off scale outliers.
Fig 2
Sequences of daily admissions and daily discharges from La Fuenfría Hospital.
Panels are: A- Daily admissions (Adm) sequence; B- Same as panel A, but scale modified to only to show data ⩾ 0; C- Daily discharge (Dis) sequence; D- Same as panel C, but the scale is modified to only show data ⩾ 0. In all cases abscissa is days elapsed since May 1 2014, Ordinate is number of daily admissions or discharges determined as indicated in Building the time series in Methods. Negative peak represent transcription errors of the data made available for this study, perhaps positive outliers could have the same origin, however this is harder to demonstrate.
Here we use fractal analysis, Fourier transforms, spectral analysis, and conventional statistics, to show that small hidden factors may indeed have a dramatic impact in reducing the hospital’s operative efficiency. The purpose of this paper is to show that factors that are not usually considered in hospital performance analysis may have a huge impact on hospital efficacy.
Methods
Statistical methods and spectral density (SD) calculation
Statistical methods
Medians and their 95% confidence interval (CI) were calculated using the nonparametric Hodges and Lehman method [26]. Random distribution about the median () was analyzed with the above and below runs (one or more data appearing as a sequence above or below the median), following the methods of Mood [27] and Wilks [28, 29]. Gaussianity (also known as normality) was verified with the Jarque-Bera [30], the robustified Jarque-Bera-Gel [31] and the Shapiro Wilk [32] tests. Linear regressions were carried out using the Theil nonparametric method [26] and correlations were estimated using the Spearman rank correlation coefficient [26]. Sequences were compared with the nonparametric Smirnov [33] test based on Kolmogorov statistics [34]. The procedures to generate random sequences to verify the differences between their fractal dimension which were described elsewhere [11, 35–37]
Fast Fourier Transforms (FFT) and calculating spectral density
FFT were calculated with a C++ (using g++ version 5.4.0 20160609 with C++14 standards, www.gnu.org) implementing the Cooley and Tukey algorithm [38], with Hamm windowed data [39]. Spectral densities were then obtained from the real and imaginary components of the FFT [39].
Sequences of daily admissions and daily discharges from La Fuenfría Hospital.
Panels are: A- Daily admissions (Adm) sequence; B- Same as panel A, but scale modified to only to show data ⩾ 0; C- Daily discharge (Dis) sequence; D- Same as panel C, but the scale is modified to only show data ⩾ 0. In all cases abscissa is days elapsed since May 1 2014, Ordinate is number of daily admissions or discharges determined as indicated in Building the time series in Methods. Negative peak represent transcription errors of the data made available for this study, perhaps positive outliers could have the same origin, however this is harder to demonstrate.
Ethics statement, author’s conflicts of interests and privacy of the information used in the study
No human or animal subjects were used in this study. Thus no animals were sacrificed. Neither personal nor animal pain or discomfort were induced at any point of the study.In compliance with the European Data Protection Law [41] no patient’s personal or clinical information is revealed in this paper. La Fuenfría Hospital Ethics Committee approved this study as indicated in a letter submitted to PLoS One.Though it is the author’s interest always to improve the efficiency of LFH. The authors state that they have no conflicts of interest or competing interests in the subject of this study.Excluding personal or clinical patient information, everything stored in the SELENE system, including the La Fuenfría Hospital “Cuadros de Mando” which we translated here as “Command panels”, are public information according to Spanish Law. All the original La Fuenfría Hospital “Cuadros de Mando” which we translate “Command panels” spreadsheets cis be provided with this revised manuscript. There is also a short Readme text file explaining some issues of the LFH data file. The Command panels, and a short Readme text file, used here are provided to PLoS One, and are freely available to anyone interested in them.
Data availability and privacy of the information used in the study
All relevant data are within the manuscript and its S1 Data files. The Command panels data used in this study are provided as S1 Data and are freely available. A short Readme text file is also included, which explains the LFH data file.Excluding personal or clinical patient information, everything stored in the SELENE system, including the La Fuenfría Hospital “Cuadros de Mando” which we translated here as “Command panels”, are public information according to Spanish Law. All the original La Fuenfría Hospital “Cuadros de Mando” which we translate “Command panels” spreadsheets cis be provided with this revised manuscript. The translated Command panels are provided to PLoS One, and are freely available to anyone interested in them.LFH Command Panels also include names and ID codes of Hospital personnel for administrative purposes. Since these are also protected by Spanish and EU laws on personal information privacy they were remove prom data posted in PLoS ONE.
Ethics statement and author’s conflicts of interests
No human or animal subjects were used in this study. Thus no animals were sacrificed. Neither personal nor animal pain or discomfort were induced at any point of the study.In compliance with the European Data Protection Law [41] no patient’s personal or clinical information is revealed in this paper. La Fuenfría Hospital Ethics Committee approved this study as indicated in a letter submitted to PLoS ONE.Though it is the author’s interest always to improve the efficiency of LFH. The authors state that they have no conflicts of interest or competing interests in the subject of this study.
Results
Analysis of runs above and below the median
During the period studied, the number of hospital in–patients were 150 (149–151) (median, , and 95% CI, n = 1329 days) ranging (102 –- 187) patients, meaning that Hospital’s is 0.77 (0.53–0.77) (median, , and 95% CI). Let us consider a random variable y = f(t) such that f(t) is independent from f(t − Δt) or from f(t + Δt) (where Δt is a short time lapse, ideally Δt → 0). This is, a variable for which its present is independent from its past, and whose present does not determine its future. Such variable produces a sequence of data which are uniformly distributed around their median . We say that a run occurs when one or more sequence points fall above or below the median, this is easily grasped by looking at Fig 3. In Fig 3C there are 5 runs, and in Fig 3D there are 9 runs. Points that are equal to are not considered in the analysis. Fig 3 presents four sets of monthly averages from the Function Recovery Uunit (FRU). Fig 3A, results from the total of inpatients (Adm) sequence (n = 22, n = 11,
P is ≈ 0.15); Fig 3B, Total discharged patients’ (Dis) sequence (n = 22, n = 8, P ≈ 0.04); Fig 3C, is the sum of lengths of stay (LoS) for all in–patients (InP) in the Unit during each month (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4); Fig 3D, is a sequence of the average stay duration (Mean LoS) of each in–patient at the Unit (n = 23, n = 10, P ≈ 0.13); Fig 3E, during de observation period the Function Recovery Unit gained relevance and the number of beds were increased, panel shows the changes in beds at the beginning in several months, as expected, the analysis of this sequence was found to be non random (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4), actually n may be just 3 in this case, but the algorithm probably found tiny decimal differences between data Fig 3 an in one segment; if n = 3, should n runs be 3 then P ≪ 4.5 ⋅ 10−4. Ps are probabilities (obtained with the Wald–Wolfovitz test) that the sequences are not randomly distributed about their medians. In all cases abscissa is the month number during the study period (January 2016 = 1, November 2017 = 23). Out of these P values the only one indicating a statistically significant non zero number of runs, occurs for InP sequence in Fig 3C [42, 43]. The sequence non-randomness the Fig 3C could have several reasons, one of them could be some kind of ‘periodicity’ (which would be odd, since its period would be longer that 2 years), but it could also stem from some kind of random walk. During the period studied, the Hospital’s in–patients were 150 (149–151) (median, , and 95% CI) ranging (102–187) patients. If we consider a random variable y = f(t) such that f(t) is independent from f(t − Δ t) or from f(t + Δt) (where Δt is a short time lapse, ideally Δt → 0). In other words, a variable for which its present is independent from its past, and whose present does not determines its future. Such variable produces a sequence of data which are uniformly distributed about their median . We say that run occurs when one or more sequence points fall above or below the median, this is easily grasped by looking at Fig 3. In Fig 3C there are 5 runs, and in Fig 3D are 9 runs. Points that are equal to are not taken into account in the analysis. Fig 3 presents four sets of monthly averages from the Function Recovery Uunit (FRU). Fig 3A, results from the total of inpatients (Adm) sequence (n = 22, n = 11,
P is ≈ 0.15); Fig 3B, Total discharged patients’ (Dis) sequence (n = 22, n = 8, P ≈ 0.04); Fig 3C, is the sum of lengths of stay (LoS) for all in–patients (InP) in the Unit during each month (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4); Fig 3D, is a sequence of the average stay duration (Mean LoS) of each in–patient at the Unit (n = 23, n = 10, P ≈ 0.13); Fig 3E, along de observation period the Function Recovery Unit gained relevance and the number of beds were increased, panel shows the changes in beds at the benign in several months, as expected, the analysis of this sequence was found to be non random (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4), actually n may be just 3 in this case, the algorithm probably found very minor decimal differences between data Fig 3 an in one segment; if n = 3, should n runs be 3 then P ≪ 4.5 ⋅ 10−4. Ps are probabilities (obtained with the Wald–Wolfovitz test) that the sequences are not randomly distributed about their medians. Fluctuations in Fig 3E, resulted from administrative decisions, thus a low P, indicative of non randomness, was to be expected. In all cases abscissa is month number in the study period (January 2016 = 1, November 2017 = 23). Out of these P values the only one indicating a statistically significant non zero number of runs, occurs for InP sequence in Fig 3C [42, 43]. The non-randomness of sequence Fig 3C could have several reasons, one of them is some kind of ‘periodicity’ (a strange one, since its period would be longer that 2 years), but it could also stem from some kind of random walk determined by the uncertainties in n and , [11, 37, 44]. It is difficult to prove, but the apparent ‘seasonality’ was probably determined by the increase in Unit’s bed capacity depicted in panel Fig 3E. The figure illustrates that relatively simple sequences of random variables having unknown pdfs such as n and , may interact in strange manners to produce apparently less random “simi-periodic” sequences such as Fig 3C. determined by the uncertainties in n and , [11, 37, 44]. It is difficult to prove, but the apparent ‘seasonality’ was probably determined by the increase in Unit’s bed capacity depicted in panel Fig 3E. The figure illustrates that relatively simple sequences of random variables having unknown pdfs such as n and , may interact in strange manners to produce apparently less random “semi periodic” sequences such as Fig 3C.
Fig 3
Four examples of runs around the median () from La Fuenfría’s Function Recovery Uunit.
(FRU). A: Total admissions (Adm) sequence (n = 22, n = 11, P ≈ 0.15); B, Total discharges (Dis) sequence (n = 22, n = 8, P ≈ 0.04); C, is the sum of lengths of stay (LoS) for all in–patients (InP) in the Unit during each month (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4); D, is a sequence of the average stay duration (Mean LoS) of each in–patient at the Unit (n = 23, n = 10, P ≈ 0.13); E, throughout the observation period the Function Recovery Unit gained relevance and the number of beds were increased, the panel shows the changes in beds at the behind ib several months, as expenses, the analysis of this senescence was found to be non random (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4, actually n runs may be just in this case, the algorithm probably found very minor decimal differences between data an in one segment; if n runs = 3, should n runs be 3 than P 4.5 ⋅ 10−4. P s are probabilities (obtained with the Wald–Wolfovitz test) that the sequences are randomly distributed about their medians. As indicated in the text of this communication P stands for probability of random distribution about the median. Fluctuations in E resulted from administrative decisions, thus a low P was to be expected. In all cases abscissa is time expressed as month number in the sequence, (January 2016 = 1, November 2017 = 23).
Four examples of runs around the median () from La Fuenfría’s Function Recovery Uunit.
(FRU). A: Total admissions (Adm) sequence (n = 22, n = 11, P ≈ 0.15); B, Total discharges (Dis) sequence (n = 22, n = 8, P ≈ 0.04); C, is the sum of lengths of stay (LoS) for all in–patients (InP) in the Unit during each month (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4); D, is a sequence of the average stay duration (Mean LoS) of each in–patient at the Unit (n = 23, n = 10, P ≈ 0.13); E, throughout the observation period the Function Recovery Unit gained relevance and the number of beds were increased, the panel shows the changes in beds at the behind ib several months, as expenses, the analysis of this senescence was found to be non random (n = 23, n = 5, P ≈ 4.5 ⋅ 10−4, actually n runs may be just in this case, the algorithm probably found very minor decimal differences between data an in one segment; if n runs = 3, should n runs be 3 than P 4.5 ⋅ 10−4. P s are probabilities (obtained with the Wald–Wolfovitz test) that the sequences are randomly distributed about their medians. As indicated in the text of this communication P stands for probability of random distribution about the median. Fluctuations in E resulted from administrative decisions, thus a low P was to be expected. In all cases abscissa is time expressed as month number in the sequence, (January 2016 = 1, November 2017 = 23).
LaN Fuenfría Hospital data statistical characteristics
Fig 2 presents sequences built in the preceding Building the time series Subsection. Panels Fig 2A (Adm) and Fig 2C (Dis) are sequences with a few negative, artefactual (see Building the time series Subsection, outliers. Panels Fig 2B and 2D are the same data with the scale magnified to see the positive part and better appreciate data detail when y ⩾ 0.Testing with the Jarque-Bera [30], the robustified Jarque-Bera-Gel [31] and the Shapiro-Wilk [32] tests, we found that none of the data sequences collected during the study period from La Fuenfría Hospital, were Gaussian (also called normal) variables, (Probability of Gaussianity, P ≪ 10−6). InP sequences contained a large number of ties (points with same value). In ti InP sequence every value is repeatedIn the expression: , is InP’s maximum values; , is InP’s minimum values and n, is total number of points in the sequences. Given the narrow range there are only 187 − 102 = 85 possible different values among 1329 integer data in the series, they are not all equally likely. Please notice that the number of ties increases as → 0, that is the more uniform bed occupation gets, the larger the number of ties, in the InP sequence, will get. This is to be expected when integers are sampled in a narrow range, under these conditions any statistical test, parametric or not, must be taken with caution, since test power decreases wit ties. Tie corrections were used for the nonparametric statistical procedures employed here [26]. Since the Hospital has 192 beds, data indicate that the Hospital operates with some leeway, having an occupancy ranging from 53.1 to 97.3%, with a 78.1% median.With the data in the sequence of InP (shown in Fig 2A) and Eq (2) a curve of DInP at the Hospital was built, this is shown in Fig 1B. The sequence in Fig 1D was obtained by subtracting to each Adm the same day Dis. Fig 1D presents a sequence obtained by subtracting Dis—Adm (DDiAd) to the Hospital.A direct visual comparison between sequences in Fig 1B (DInP) and Fig 1D (DDiAd) shows, that in spite of some differences, they are similar, and very different from the series in Fig 1A (InP). Sequences in Fig 1B (DInP) and Fig 1D (DDiAd) compared with the Smirnov test had the same distribution, that is, their distributions are statistically indistinguishable (Probability of identity P ⪅ 1, n = 1329, two tails). Yet, when Smirnov test was used to compare sequences Fig 2A and 2C, admission (Adm) and discharges (Dis) sequences were found to be highly statistically significantly different (Probability of identity P ≪ 10−6, n = 1329, two tails).Empirical Hospital occupancy Probability Distribution Functions (PDF) [28] calculated from these data is shown in Fig 4. Daily hospital occupancy data set was found to be not Gaussian when tested with the Jarque-Bera [30], and subsequently with the robustified Jarque-Bera-Gel [31] and the Shapiro Wilk [32] tests (P ≪ 10−6, in the three cases). The perception of data lacking Gaussianity becomes intuitive when very disperse data (dots) are observed around a Gauss pdf line in the same panel. The Gauss pdf line (shown also as pdf, in Fig 1C) with the same mean () and variance [s2(y)] as the set of 1329 data points forming the sequence in Fig 1A (, s[y] = 24.4).
Fig 4
Empirical Probability Distribution Functions (PDF) [28] of daily admissions and stays at La Fuenfría Hospital from May 12014 to December 19 017.
Panel A: Blue ine with ■ PDF of LFH in-patients (InP in Fig 1A); Red line with ⧫, PDFs for daily differences in admissions (Adm) and discharges (Dis), called DDiAd in Fig 1D. Panel B: Red line with ⧫ PDF of LFH daily Admissions in LFH (called Adm in Fig 2A); Red line with ■ PDF for LFH daily Discharged Dis in Fig 2C). Panel C: Same as Paanel B, but with abscissa expanded to exclude outliers. In all cases abscissa is the value ve aare interested in, and ordinate is the estimated accumulated probability from −∞ up to the abscissa value.
Empirical Probability Distribution Functions (PDF) [28] of daily admissions and stays at La Fuenfría Hospital from May 12014 to December 19 017.
Panel A: Blue ine with ■ PDF of LFH in-patients (InP in Fig 1A); Red line with ⧫, PDFs for daily differences in admissions (Adm) and discharges (Dis), called DDiAd in Fig 1D. Panel B: Red line with ⧫ PDF of LFH daily Admissions in LFH (called Adm in Fig 2A); Red line with ■ PDF for LFH daily Discharged Dis in Fig 2C). Panel C: Same as Paanel B, but with abscissa expanded to exclude outliers. In all cases abscissa is the value ve aare interested in, and ordinate is the estimated accumulated probability from −∞ up to the abscissa value.
La Fuenfría Hospital daily admissions and discharge variations sequences
Fig 4 contains empirical PDF [45] calculated for inpatients (InP), admissions (Adn), discharges (Dis) and difference between Adm and Dis: (DAdDis). It is important to note that Adm and Dis were were logged daily as separated entries in Hospital’s Command Panels. Data in Fig 4 (especially the expansion presented in Fig 4C) indicates that daily DInP is distributed following the same PDF as
, however Adm and Dis have different PDFs. The largest difference is observed for probabilities of no admissions (blue line in Fig 4C) and no discharges occur (red line in Fig 4C) in a given day (at zero value in the abscissa in Fig 4C), it is a day without admissions 30% likely but a day without discharges is only 20% likely. When the abscissa is > 0, the probability of daily admissions is surpassed by daily discharges. The largest difference between the curve predicted determines the significance of the difference between two PDFs by using the Smirnov test [33, 46] (based on Kolmogorov statistics [34]). Yet when analyzing at Fig 4C, it is evident that this is not the only difference between the curves.
Daily fluctuations in stay duration and average stay duration in operative units at La Fuenfría Hospital
Random fractals
Two curves are particularly relevant for the analysis of sequences in Figs 1 and 2, these are the, so called, white and Brownian noises [44]. In white noise every point in the sequence is independent from the past, and does not determine the future of the system. In brown noise, every point is dependent on the past and determines the future, although in in unpredictable manners.White noise properties. White noise is a sequence of independent random variables, no value is predictable nor dependent on on any prior or posterior value in the sequence. White noises have a fractal dimension D = 2 [11, 37, 44]. White noise curve looks very similar to sequences in Fig 1B and 1D, the random variable producing each point may have diverse PDFs, white noises are randomly distributed about 0, when N → ∞ white noise variables in a sequence produce runs [47]. When subject to Fourier transformation [48] white noises have a constant spectrum for all frequencies between 0 and ∞, reminding white light which contains all visible electromagnetic frequencies, leading to call this noise white.Brownian noise properties. Brownian noise is also called Brown noise [49, 50], red noise or random walk (Rw) [44]. For Brownian it noise always holds that
where υ(μ = 0, σ2) is a random variable with mean μ = 0 and variance σ2. Variable υ may be a uniform U[-1, 1] pdf, like
Yet, very often the variable is a Gaussian (also called normal) of the kind N(0, σ2) having mean μ = 0 and variance σ2 [11, 44]. Brown noise is a particular case of Markov chains [51], specially important in the waiting time theory witch studies situations with repressed queues waiting to receive some service [52, 53]. In layman’s terms, Brownian variables strictly depend on their past, yet they are random, it is impossible to predict their future or estimate their past values. Nonetheless, their current value depends on their past, and their future value depends on the present.Brown noise in hospital parameters is not unexpected, the admission of a patient depends on bed availability, the number of beds depends on many criteria related to the public health system. Availability also depends on demand, the disease suffered by patient occupying a bed, the efficiency of doctors in the hospital, treatment availability and so on. Brownian noise is characterized by wide and slow meandering, and has fractal dimension D = 1.5 [Eq (11)] and so does D [Eq (14)] when N → ∞ [11, 44]. Brownian noise distributes around its median (which is not necessarily 0) producing a variable number of runs .
Fractal analysis theory of sequences studied
As shown in Methods and in Results, in contrast with other methods to estimate the fractal dimension D, Eq (14) is extremely easy to calculate and certainly converges towards D as N → ∞, although nobody knows how far infinity is for certain [54], we all belie it is far away. Fractal series studied here have an extent which is hard to classify. An N = 1329 points may be long or short depending on persons’s point of view, it seems large for conventional statistics, yet is short when considered in the context of fractal analysis [37]. A D value deduced from a 1329 points series underestimates sequence D significantly. There is four-step solution for this:Generate a significant number of sequences with the characteristics of interest using Monte Carlo [55] simulation.Calculate their D and var(D) [Eqs (14) and (15)] [11].Calculate the set of traces’ mean D and its variance including variance between simulated traces as indicated in [11, 35–37].Compare real and simulated sequences parameters using the Vysochanskij–Petunin inequality (details Theorem 1 and in [35, 37]).
Fractal analysis of sequences from Hospital
Ruling out sources of errors in sequences
To analyze data in Table 2 we must consider the transcription errors in the SELENE® data base and how were they corrected for this study, as indicated in Methods and the problem of ties mentioned in the La Fuenfría Hospital data statistical characteristics Sub-Subsection, also the narrow data rage determines further underestimations of D.A case random noises in seen in [37] where much longer sequences needed for D to converge towards D, these sequences contain only decimal digits , not real numbers . Empiric data on Tables 1 and 2, may differ from D of a calibration white noise from a longer sequences.
Table 1
Fractal dimension D estimated for La Fuenfría Hospital sequences.
Sequence
Ds
var[Ds]
Admissions (Adm
1.49725
0.00356
Discharges (DisDs)
1.41904
0.00400
In Patients (InP
1.33806
0.00320
InP variation (DInP
1.56432
0.00302
Adm-Dis (DDiAd)
1.43369
0.00401
ΞiRw
1.33922
0.00382
Brownian noise§
1.28855
0.03837
White noise§
1.59825
0.01039
Dimension calculated with Eq (14); calculated with Eq, (15), for all sequences N = 1329. Labels mean: InP, in patients at La Fuenfría Hospital (Fig 1A); Adm, admissions to the Hospital (Fig 2A); Dis, discharges from La Fuenfría Hospital (Fig 2D); InP, daily sequence of inpatients (Fig 1A); DInP, InP daily variation (Fig 1B); DDiAd, Adm-Dis (Fig 1D); Ξ, Rw built for DDiAd curve in Fig 1E using Eq (5); Brownian noise, Brownian noise calculated as indicated in the Results’ Random fractals Sub-Section and Eq (7). White noise, White noise calculated as indicated under Random Fractals Subsubsection.
§ superscript, indicates that D is the average of M = 100 sequences with N = 1329 evaluated with Eq (9), total variance was calculated with Eq (18).
Table 2
Statistical comparison between fractal dimensions (D) estimated for the sequences appearing in Table 1.
Dis
Adm
DInP
Ξi
Bro§
Whi§
InP
2 ⋅ 10−3
4 ⋅ 10−4
2 ⋅ 10−4
16⩽P⩽1†
0.269
7 ⋅ 10−4
Dis
…
2 ⋅ 10−3
5 ⋅ 10−4
2 ⋅ 10−4
0.039‡
2 ⋅ 10−3
Adm
…
…
2 ⋅ 10−3
5 ⋅ 10−4
0.015‡
0.0053‡
DInP
…
…
…
2 ⋅ 10−4
9 ⋅ 10−3‡
0.045‡
Ξi
…
…
…
…
0.257
8 ⋅ 10−4
Bro§
…
…
…
…
…
7 ⋅ 10−4
Statistic significances: calculated using Eq (29). Labels mean: InP, in patients at La Fuenfría Hospital (Fig 1A); Adm, admissions to La Fuenfría Hospital (Fig 2A); Dis, discharges from La Fuenfría Hospital (Fig 2D); InP, daily sequence of inpatients (Fig 1A); DInP, InP daily variation (Fig 1B); Ξ
Rw (Fig 1E) built using Eq (5); Bro, Brownian noise calculated as indicated in the Random fractals Sub-subsection and Eq (7). Whi, White noise calculated as indicated in Sub-subsection the Random fractals.
§: D is the average of M = 100 sequences with N = 1329 evaluated with Eq (14), total variance was calculated [11, 37];
‡, are values having borderline significance, but that could more significant if the pdf of data would have been known and the Vysochanskij–Petunin inequality use would had not been necessary, we call them ‘undecided significance’.
†: Referred to Corollary 1 for Theorem 1.
Dimension calculated with Eq (14); calculated with Eq, (15), for all sequences N = 1329. Labels mean: InP, in patients at La Fuenfría Hospital (Fig 1A); Adm, admissions to the Hospital (Fig 2A); Dis, discharges from La Fuenfría Hospital (Fig 2D); InP, daily sequence of inpatients (Fig 1A); DInP, InP daily variation (Fig 1B); DDiAd, Adm-Dis (Fig 1D); Ξ, Rw built for DDiAd curve in Fig 1E using Eq (5); Brownian noise, Brownian noise calculated as indicated in the Results’ Random fractals Sub-Section and Eq (7). White noise, White noise calculated as indicated under Random Fractals Subsubsection.§ superscript, indicates that D is the average of M = 100 sequences with N = 1329 evaluated with Eq (9), total variance was calculated with Eq (18).Statistic significances: calculated using Eq (29). Labels mean: InP, in patients at La Fuenfría Hospital (Fig 1A); Adm, admissions to La Fuenfría Hospital (Fig 2A); Dis, discharges from La Fuenfría Hospital (Fig 2D); InP, daily sequence of inpatients (Fig 1A); DInP, InP daily variation (Fig 1B); Ξ
Rw (Fig 1E) built using Eq (5); Bro, Brownian noise calculated as indicated in the Random fractals Sub-subsection and Eq (7). Whi, White noise calculated as indicated in Sub-subsection the Random fractals.§: D is the average of M = 100 sequences with N = 1329 evaluated with Eq (14), total variance was calculated [11, 37];‡, are values having borderline significance, but that could more significant if the pdf of data would have been known and the Vysochanskij–Petunin inequality use would had not been necessary, we call them ‘undecided significance’.†: Referred to Corollary 1 for Theorem 1.
Estimates of the fractal dimension
D values estimated for Hospital sequences in Figs 1 and 2 are given in Table 1. White noise standard set of 100 series with 1329 point s had an estimated D = 1.5983 ± 0.0104 ; whereas the Brown noise standard set of 100 series with 1329 points had D = 1.2885 ± 0.0384 .
Statistical comparison of D values appearing in Table 1
D values calculated or several white and Brown noises, as well as for La Fuenfría Hospital parameters discussed previously, are summarized in Table 1, and P values to test statistical significance of differences between them appear in Table 2. An asterisk indicates marginally significant P which could have been more significant if we knew D’s and the Vysochanskij–Petunin inequality would not have been necessary to test for significance [56, 57], we consider these cases of undecided significance.In–patients sequence D (, Tables 1 and 2, and Fig 1A) is not statistically different from from Brownian (P > 0.13). An asterisk indicates marginally significant P which could perhaps have been more significant if the Vysochanskij–Petunin inequality use would not have been necessary [56, 57] due to the, we consider this cases as of undecided significance.An interesting case is the Rw
Ξ (Fig 1E) built for DDiAd (Fig 1D) using a recursive relation
Please note the resemblance of sequence Ξ (Fig 1D) and sequence in Fig 1A. Eyeball inspection of these two series shows tiny differences, yet estimates of their fractal dimension presented in Table 1 are not identical, D for InP sequences is 1.33806 ± 0.0032 calculated with Eqs (14) and (15), respectively, and is 1.33922 ± 0.00382 for the Ξ sequence (N = 1329 in both cases).Fig 1A and 1E are not identical, but yet their D values are statistically indistinguishable using Vysochanskij–Petunin [See Eq (31). We have
which indicates that Theorem 1 does not hold to this case, and that Vysochanskij–Petunin inequality, strictly, cannot be used to asses P(ΔD). Yet by virtue of Corollary 1 Eq (32) indeed for Δ(D) = 0 occurs per chance: i.e., it is not statistically significant [42, 43, 58].∴ The .
Monte Carlo simulated sequences
White Gaussian noise in Fig 5A is a sequence of and Fig 5C of . Brownian noise in Fig 5B is the result of
where b is the ith point in Fig 5B and g is the (i − 1)th point in Fig 5A. The required random normal variates of type N[0, 1] were generated as indicated in thin the Mathematical Appendix. In contrast with the Gaussian white noise (Fig 5A and 5C), Brownian noise sequences have slow and fast meanders and relatively long periods with trends to increase and/or to decrease which are just local tendencies in the segment, generated as an example (Fig 5B and 5E), the segment did not indicate any periodicity. Segments such as the one in Fig 5B for 7 ⋅ 103 ⩽ x ⩽ 104 look very much like the InP curve at La Fuenfría Hospital in Fig 1A which also produces a false sensation of periodicity with a slight tendency to decrease, yet they are just chaotic trends, in spite of the fact that the underlying random processes (Figs 1A and 5A and 5C) have no periodicities at all. A Rw expresses a system that is out of control, just like epidemics [5, 11, 44], storms [2, 61–64] or earthquakes [65], which if described with statistical parameters based on a (short) periods of time leads to wrong conclusions.
Fig 5
Two sequences generated with Monte Carlo simulation using Eq (23) as described by Box and Muller [59, 60].
Panels are: Panel A, Gaussian white noise and; B: Gaussian Rw, a Rw generated using Eq (7) from data on pane A; Panel C, Gaussian white noise and ; D: Gaussian Rw, a Rw generated using Eq (7) from data on pane C Abscissa and ordinate are arbitrary, Please notice [D ± s(D)] estimated with Eqs (14) and (15) are: Panel A, 1.66122 ± 7.60191 ⋅ 10−4; Panel B, 1.32692 ± 7.6926 ⋅ 10−4; Panel C, 1.6692 ± 7.64176 ⋅ 10−4; Panel D, 1.31723 ± 7.72806 ⋅ 10−4. Rw stands for random walk, more details in the communication text.
Two sequences generated with Monte Carlo simulation using Eq (23) as described by Box and Muller [59, 60].
Panels are: Panel A, Gaussian white noise and; B: Gaussian Rw, a Rw generated using Eq (7) from data on pane A; Panel C, Gaussian white noise and ; D: Gaussian Rw, a Rw generated using Eq (7) from data on pane C Abscissa and ordinate are arbitrary, Please notice [D ± s(D)] estimated with Eqs (14) and (15) are: Panel A, 1.66122 ± 7.60191 ⋅ 10−4; Panel B, 1.32692 ± 7.6926 ⋅ 10−4; Panel C, 1.6692 ± 7.64176 ⋅ 10−4; Panel D, 1.31723 ± 7.72806 ⋅ 10−4. Rw stands for random walk, more details in the communication text.
Power spectrum analyzes
A classic form to show function periodicities in time domain, is to transform this them into frequency domain function, which is a sum of sines and cosines, using a fast Fourier transform (FFT) [39, 48]. Transformed values for each frequency (f) are ‘complex numbers’ (), c comprised of two parts or components: one is sometimes referred to just the ‘real component a’ () and a, so called, ‘imaginary’ () component (). A complex number (c) is of the form
where parentheses indicate sets of numbers, and ∈ reads as “belongs to”. The ‘energy’, expressed as either a steady curve’s nonzero curve values, or sharp increases or variations in amplitude (such a as the peak in Fig 6B, something we could informally call its ‘weight’), contributed by each frequency component to total signal energy in a fluctuating complex process is given by
plotting against f id called a spectral density plot, and it is areal number.
Fig 6
False periodicity analysis in Rws. Use of spectral density ().
Panels are: Panel A- A perfectly periodic signal, the sine trigonometric function ; Panel B- of the sine function shown in panel A; Panel C- of Gaussian white noise shown at Fig 5A; Panel D- of Brown Rw shown in Fig 5B; Panel E- pf daily inpatients () sequence which in appears in Fig 1A. Ordinate of panels B through E, is power dissipated at each frequency. The sine function depicted dissipates all its energy at a single frequency observed at a single neat peak in its ψ (panel B). sequence for the number of hospitalized patientsSDf. All SD plots were filtered using a Hann window [39, 66]. The rapid oscillations observed at right of signals in panel B to D are an artefact due to sampling discrete points in the signal for the Fourier transformation. Rw stands for random walk, further details in the text.
False periodicity analysis in Rws. Use of spectral density ().
Panels are: Panel A- A perfectly periodic signal, the sine trigonometric function ; Panel B- of the sine function shown in panel A; Panel C- of Gaussian white noise shown at Fig 5A; Panel D- of Brown Rw shown in Fig 5B; Panel E- pf daily inpatients () sequence which in appears in Fig 1A. Ordinate of panels B through E, is power dissipated at each frequency. The sine function depicted dissipates all its energy at a single frequency observed at a single neat peak in its ψ (panel B). sequence for the number of hospitalized patientsSDf. All SD plots were filtered using a Hann window [39, 66]. The rapid oscillations observed at right of signals in panel B to D are an artefact due to sampling discrete points in the signal for the Fourier transformation. Rw stands for random walk, further details in the text.An intuitive manner to understand this, is to consider a perfect periodic signal such as a trigonometric sine function like where π = 3.1415926… and T is a constant (called the waveform’s period) with same units (meters, seconds, grams, volts, or else) as x. The example is show in Fig 6A. Fig 6B, presents Fig 6A’s power spectrum consisting of a single peak frequency. Please notice that to calculate the actual signal is sampled in Δx intervals (equivalent to multiplying by something called a Dirac comb and the FFT also contains the frequency components of the Dirac comb producing a burst of rapid vibrations in the right half of each trace [39].Fig 6C is a spectrum of the Gaussian white noise shown in Fig 5A; ordinates of panels B through E, in arbitrary units. In Fig 6C it is seen that all frequencies have the same ‘weight’, i.e., all frequencies contributions are equal. Fig 6D is a Brown Rw
spectrum,; in double logarithmic coordinates, the spectral density is a straight line which decays with a slope of . Fig 6E is of daily inpatients () sequence shown in Fig 1A.Although the simulated sequences in Fig 6 are 10000 points long and Hospital data are only 1329 points long, there is an evident similarity between the Brownian noise (Fig 6D), and from the sequence of Hospital inpatients () between May 1 2013 and December 19 2017 (Fig 6E). In both cases are characteristic of a Brown Rw and none of these s has a peak which could indicate a predominant periodic component which could suggest for any periodicity, despite of short lapses in the Brown Rws that could give this impression.Fig 6C is Gaussian white noise calculated for the signal in Fig 5A. In Fig 6C all frequencies have the same ‘weights’, the contributions of al frequencies are equal, which leads to the ‘white’ name of this kind of noise. Fig 6D shows of the Brownian Rw in Fig 5B, one may observe that in double logarithmic coordinates the spectral density follows a straight line which decays with a slope of . Finally, also in Fig 6E, we show corresponding to daily hospitalized patients sequence shown in Fig 1A. Except for that simulated sequences in Fig 6 are 104 points long and Hospital data are only 1329 points long, there is an evident similarity between the Brownian noise , and that from the sequence of Hospital discharges between May 1 2013 and December 19 2017. In both cases are characteristic of a Rw and none of these .The Hospital is divided into the following Clinical Operative Units (COU): RCPU, Relapsing Chronic Patients Unit, this unit operated until May 2016 when its beds were transferred to the CCU; Chronic Care Unit; PCU, Palliative Care Unit; FRU, Function Recovery Unit; TU, Tuberculosis Unit and NTU, Neurorehabilitation Treatment Unit. Fig 7A presents data on daily number of in–patients (InP) at each unit, and their average stay duration on Panel Fig 7B). Daily fluctuations of in–patients and average length of stays (LoS) for each COU calculated every day from January 1 2015 uo to December 12 201. Abscissas are days from January 1 2014, ordinates are in decimal logarithmic scale to better visualize some of sequence large outliers, which are particularly evident in Panel Fig 7B. Traces in Fig 7 seem to be a kind of Rw. All have some outlying peaks, particularly RCPU and UTB, however, less prominent peaks, occur in other COU too. It it is important to note that in this paper we sometimes refer to products or quotients between random variables, this is the case of averages including number of patients and stay duration in each COU in Fig 7B. We know that our data are not Gaussian, however even in the case of Gaussian values these averages, may be quotients of random variables following a a “pathological” statistical distribution such as the Cauchy pdf (See the Mathematical Appendix Subsection On Cauchy distributed variables).
Fig 7
Daily fluctuations of in-patients and average duration of stays for each Clinical Operative Unit recalculated every day from January 1 2015 until December 12 2017.
A- Number of in–patients (InP) at each Operative Unit. B- Average stay duration at each Operating Unit [Υ defined as in Eq (10)]. Abscissas are days elapsed from January 1 2014, ordinates are in logarithmic scale to better visualize some of sequence features. Unit initials mean: RCPU, Relapsing Chronic Patients Unit, this unit was suppressed on May 2016 and its beds were transferred to CCU; CCU, Chronic Care Unit; PCU, Palliative Care Unit; FRU, Function Recovery Unit; TU, Tuberculosis Unit; NTU, Neurrehabilitation Treatment Unit.
Daily fluctuations of in-patients and average duration of stays for each Clinical Operative Unit recalculated every day from January 1 2015 until December 12 2017.
A- Number of in–patients (InP) at each Operative Unit. B- Average stay duration at each Operating Unit [Υ defined as in Eq (10)]. Abscissas are days elapsed from January 1 2014, ordinates are in logarithmic scale to better visualize some of sequence features. Unit initials mean: RCPU, Relapsing Chronic Patients Unit, this unit was suppressed on May 2016 and its beds were transferred to CCU; CCU, Chronic Care Unit; PCU, Palliative Care Unit; FRU, Function Recovery Unit; TU, Tuberculosis Unit; NTU, Neurrehabilitation Treatment Unit.“If a sample is too small you can’t show that anything is statistically significant,whereas if sample is too big, everything is statistically significant.”… “you are doomed to significance.”Norman and Steiner [72, pg. 24].
Nonparametric statistical analysis of Hospital’s operative units sequences shown in Fig 7
As said in Section sequences in Fig 7B include data such InP average patients’ stay duration in each operative unit (Υ). This number calculated as:
where d represent a given period and j is the jh patient in the service, and N is the number of patients in each service at day d. Thus, Υ are quotients unknown distribution random variables. As mentioned in the Mathematical Appendix, those quotients of random variables have uncertain distributions, which in the case of Gaussian variables is the Cauchy pdf Eq (24) discussed in the Mathematical Appendix. These quotients follow unknown pdfs when terms in the ratio obey unknown pdfs. For these distributions sample mean () n and sample variance [s2(x)] are meaningless. Statistical sampling theory is based on the fact that and s2(x) converge towards the population mean (μ), and population variance [σ2]. Yet, μ and σ2 do not exist for Cauchy and other, so called, “pathological distributions” for which and s2(x) have nowhere towards to converge to. Cauchy sample experimental estimates of and s2(x) vary wildly, specially when sample sizes grow and large outlier values become very likely [73, 74]. Due to these only nonparametric descriptive analysis provides meaningful information on sample localization and dispersion.Caveat emptor: data samples from La Fuenfría Hospital, except for those in Fig 3, are rather large (986 ⩽ N ⩽ 1434). Under these circumstances small, but statistically significant changes, which lack relevance or meaning in practice, may be detected, [70, 75, 76]. Table 3 contains results where sequences in Fig 3 are subjects o a nonparametric Theil regression analysis [77]. As seen in Table 3, many of the hospital units sequences in Fig 6 seem to produce a small, but highly statistically significant, correlation between the sequence under study and time. All the time series in this figures are Rws (not shown), as was confirmed by their spectral density, characteristic of Brownian noise, without any evidence of periodicity, and resembling those in Fig 7D and 7E. As stated, in connection with the sequence in Fig 5B and 5D, Rws may some times exhibit rather long, trends to increase or decrease, that are independent from any variation in factors determining the Rw. The pdf of did not change in those periods. Due to these meanderings of time sequences, descriptive statistical parameters, even if optimally chosen, like in Table 3 fail to provide meaningful information on Rws like Fig 6B and some of the preceding figures.
Table 3
Nonparametric linear Theil [67–70] regression parameters of LFH clinical units’ time sequences expressed for each unit as in Fig 7.
Sequences
α
100 ⋅ β
ρS
P
N
InP
RCPU
12.8 (12.5, 13.0)
−1.0 (−1.1, −0.9)
−0.618
<10−6
986
CCU
67.9 (67.4, 68.4)
−2.9 (−2.1, −1.9)
−0.695
<10−6
1434
RCPU
18.3 (18.1, 18.4)
−0.5 (−0.6, −0.5)
−0.540
<10−6
1434
RFU
37.7 (37.1, 38.2)
1.9 (1.8, 2.1)
0.558
<10−6
1434
TB
6.6 (6.5, 6.8)
−0.3 (−0.33, −0.26)
−0.447
<10−6
1331
TNU
18.8 (18.5, 19.1)
0.5 (0.4, 0.6)
0.4231
<10−6
1434
ϒd¯
RCPU
16.1 (15.2, 16.9)
1.8 (1.5, 2.1)
0.343
<10−6
985
CCU
67.9 (67.4, 68.4)
0.1 (−0.09, 0.30)
0.002
0.96
1434
CPU
54.4 (53.5, 55.4)
0.6 (0.4, 0.9)
0.123
2⋅10−6
1434
RFU
59.6 (59.0, 60.2)
−0.3 (−0.5, −0.2)
−0.107
4⋅10−5
1434
TB
53.8 (51.6, 56.1)
−0.9 (−1.3, −0.4)
−0.181
<10−6
1331
TNU
84.1 (83.0, 85.3)
−1.7 (−2.0, −1.4)
−0.312
<10−6
1434
Sequence of InP: number of in-patients in the Unit. sequences are average stay duration at each Operating Unit [defined as in Fig 7 by Eq (10)]. Data presented as medians and their 95% Confidence Interval (in parentheses), regression line value when x = 0 (intercept), 100 ⋅ straight line regression coefficient (slope, multiplied by 100 to reduce Table width), nonparametric Spearman’s [71] crenelation coefficient, P is the probability that each sequence comes from a population with ρ = 0, usually called the probability that the correlation is not statistically significant, and N is the number of data pairs used for the linear regression analysis. HLF unit initials mean: RCPU, Relapsing Chronic Patients Unit, this unit was suppressed on May 2016 and its beds were transferred to CCU; CCU, Chronic Care Unit; PCU, Palliative Care Unit; FRU, Function Recovery Unit; TU, Tuberculosis Unit; NTU, Neurorehabilitation Treatment Unit.
Sequence of InP: number of in-patients in the Unit. sequences are average stay duration at each Operating Unit [defined as in Fig 7 by Eq (10)]. Data presented as medians and their 95% Confidence Interval (in parentheses), regression line value when x = 0 (intercept), 100 ⋅ straight line regression coefficient (slope, multiplied by 100 to reduce Table width), nonparametric Spearman’s [71] crenelation coefficient, P is the probability that each sequence comes from a population with ρ = 0, usually called the probability that the correlation is not statistically significant, and N is the number of data pairs used for the linear regression analysis. HLF unit initials mean: RCPU, Relapsing Chronic Patients Unit, this unit was suppressed on May 2016 and its beds were transferred to CCU; CCU, Chronic Care Unit; PCU, Palliative Care Unit; FRU, Function Recovery Unit; TU, Tuberculosis Unit; NTU, Neurorehabilitation Treatment Unit.
Discussion and conclusions
Study purpose an empirical finding
At least during the study period, the La Fuenfría Hospital operated, in median, at 76.8% of its total capacity and fluctuated in what could be interpreted as slow periodic meanders (Fig 1A). Yet, the daily admissions (Fig 1B) or discharges from LFH (Fig 1D) are random sequences which show no periodicities whatsoever. Daily differences (Fig 1D) between patients admitted (Fig 2B) and discharged (Fig 2D) from the Hospital were also random non periodic sequences. It was somewhat surprising to find that the operating Hospital’s curve (Fig 1A)) could be almost perfectly (Fig 1E) reproduced when daily differences between admitted and discharged patients (Fig 1D) were added sequentially as indicated in the Random fractals Section’s Eq (3).
Meaning of lack of control of a process
Data on Figs 1A and 6E reflect that Hospital bed occupancy is described by a random fractal function, the so called Brownian Rw. Just like Brownian Rw, bed occupancy fluctuates with important periods of low occupancy.The main characteristic of Brownian Rw. is that its complexity (reflected in its D) does not change if the number of daily inpatients (DInP) increases or decreases, this is called self affinity of the process [5, 44], it does not change with scaling DInP. This is shown by the Monte Carlo simulated traces of Fig 5 where the Gaussian white noise in panel Fig 5A looks very similar to the white noise in panel Fig 5C, exp of course for the ordinate scale; Something similar happens with the associated Brownian noises in panels Fig 5B and 5D, which have similar complexities, but the fluctuations in Panel Fig 5B are approximately 10 times wider in than in Panel Fig 5D.Still, from a production efficiency view point if the differences (in
Fig 5
) are very important since the fluctuation range of the Brownian Rw diminishes when g → 0 and production of goods or services increases as the system becomes more predictable (controlled), uniformly productive and efficient.At La Fuenfría Hospital InP would fluctuate less if the lag between Adm and Dis → 0. Identifying a problem is the first step to be able to solve it. This means, making the Hospital more efficient requires analyzing the factors that keep Adm and Dis out of synchrony.
Characteristics of La Fuenfría Hospital [78]
Hospital La Fuenfría (https://bit.ly/32FVmyf) is one of three medium and long stay SERMAS hospitals in Madrid’s Autonomous Region (MAC) together with Virgen de la Poveda Hospital and Guadarrama Hospital, under the Sanitary Chancellery (Consejería de Sanidad), LFH is in Cercedilla Municipality at the north of Madrid Region, at 60 km from Madrid city. The MAC comprises an area of of 8021.8 km2 and a population of 6.6 M.The long stay duration are related to local norms and procedures to handle patients, it is likely that in Spain the public health system has more leeway to tolerate longer stays than perhaps other EU nations, especially when dealing with needy patients. Concurrently, LFH manages many chronic cases, and it most important unit is FRU, responsible for recovering patients with disabilities stemming from bone surgery (prothesis, fractures, etc.) and motor deficiencies following cerebrovascular accidents (CVA or strokes). Thus perhaps it is to be expected that stays at LFHa may be longer than at hospitals dealing under ambulatory treatment.LFH is located in a pleasant rural area, Madrid’s Sierra de Guadarrama, convenient for its goals, but distant from Madrid (population 3.3 M) city and MAC, in general. Patients are referred from other SERMAS hospitals, thus, delays between LFH discharges and new patients arrivals, are not surprising. The analyst of data in this paper (CS) was completely unaware of this factors, but they popped out sharply from data analysis discussed here.
Classical statistical analysis of institutional efficiency
The most surprising finding in this study, is that curves representing in-patients, InP, and ΔInP are random Markovian processes [51]. In a Markovian processes the past determines what happens now, and what occurs now decides the future. If there were no random components in the sequence, known the present would allow to know past and future of the system. Yet, since uncertainty separates one instant from the next, the whole system becomes unpredictable. It dt drifts over time in ways that a naive observer can realize, one is driven to believe that the system is predictable and determined.If a present drift trend pleases us, we tend to believe that whatever we are doing is “correct”, in the opposite case we would tend to believe that we are doing something “wrong”, even if in reality we have no “merit” in the first case nor are we “guilty” in the second case. An examples of this is seen at times from 0 to 6000 in Fig 5B. But after that time the Rw in Fig 5B which produces a false appearance of relative “stability”, even when at all those times it is exactly the same system under the same Gaussian conditions as shown by the plot in Fig 5A.
Caveats and recommendations
The contribution of our work
We know (both authors are trained MDs) that hospitals and medicine are complex systems, yet our study shows that the waveform meandering between full and insufficient occupancy at LFH may be perfectly, explained considering a single factor: admission and discharges are systematically and randomly out of phase. These random differences, small as they may be, constitute the de determining factor at LFH: To the best of our knowledge nobody has previously singled this small but important hidden factor. We know (both authors are trained Mds) that hospitals and medicine are complex systems, yet our study shows that the waveform meandering between full and insufficient occupancy at LFH may be, exactly, explained considering a single factor: admission and discharges are systematically and randomly out of phase. This random difference, is the determining factor at LFH: To the best of our knowledge nobody has previously singled out this small but important hidden factor.
Detecting problem indicators
Descriptive statistics and common Command panels, are not enough to detect hidden administration problems with impact on hospital efficiency. Descriptive statistics limitations mentioned in in the prior Subsection operation curves open a question on how to evaluate and optimize the operation and administration of La Fuenfría Hospital whose operation curves are Markovian random walks.Random walk curve meanders reduce system efficiency. In a hospital performance case, low occupation equals inefficient periods, for the following reasons:The population demanding service, does not receive such service..The cost of operating the hospital operation costs (infrastructure, salaries, etc.) are wasted during periods of low occupancyAt la Fuenfría Hospital occupation was as low as 45% (Fig 1A) of its capacity. As discussed in the La Fuenfría Hospital data statistical characteristics Sub-section oscillations between full and partial occupation seem related to a daily lag between Admissions and Discharges. If this lag is eliminated, fluctuations in occupancy would disappear should this lag be eliminated fluctuations in occupancy would disappear.During the study period, the mean number of LFH in-patients was almost identical to its median , and ranged (102, 187). Since the hospital had 192 patient’s beds, thus the bed occupancy during the study period was and a median of ranging (53.1, 97.4)%. Thus over the observation period, on average 22% ranging (3, 47)% La Fuendría Hospital beds were vacant, which means that a similar proportion of the resources assigned to LFH was lost, and therefore this does not generate a lack of demand.
Can the problem be solved?
Our study indicates that LFH vacancies could be eliminated or greatly reduced if the daily difference - is nullified (see Meaning of Sub-section) of a process, Figs 2 and 5). Efficient service characterized by a Rw in time which may be increased by reducing broad meanders of the walk (Fig 5). In the case of La Fuenfría Hospital this study suggests that the key factor for reducing efficiency is the daily difference between admissions and discharges.Nonetheless, the solution probably transcends the realms of La Fuenfría Hospital. We have no information on other SERMAS hospitals, yet the description, La Fuenfría Hospital realms. We have no information on other SERMAS hospitals, yet the description of LFH provided in Introduction Section illustrates that LFH is interwoven in the SERMAS network, seems necessary to consider current communications and required modifications within the network. The easy aspect may be to improve communications between admission and discharge departments within LFH, although this may imply some changes to the internal computer network. Thus, if the admissions department were to be given notice prior to the actual discharges, this would enable the possibility to notify the SERMAS network that LFH will have space for a new patient and ensure that the hospital is ready to occupy the space immediately when it actually becomes available.However, this immediate availability is also hindered by the large area that SERMAS covers, the fact that there is a distance of 60 km from the city of Madrid (the largest set of SERMAS patients), and even more from other areas in Madrid’s Autonomous Region. Factors such as means and speed of transportation may be critical, institutional transportation within the SERMAS network is probably faster and easier to program, than solely relying on the patient’s and its family’s resources and efficiency, for example. However, if the efficiency of SERMAS hospitals is affected to the same extent as La Fuenfría Hospital’s, it may be worthwhile to study the system and to implement solutions between admission and discharges in SERMAS hospitals to improve the system’s efficiency.
Appendices
Mathematical appendix
Calculating D, approximated fractal dimension of sequences
Classical (Euclidean) geometry is useful to describe relatively simple forms such as straight lines, squares, circles, cones, pyramids, etc. All these forms may be represented as a linear combination of an integer number of orthogonal components called Euclidean dimensions. One- or two-dimensional Euclidean spaces are subsets of our sensory tri-dimensional space. Yet, almost all natural forms cannot be represented in terms of Euclidean geometry.According to Mandelbrot [5, pg. 15 and Ch. 39]:“A fractal is by definition a set for which the Hausdorff– Besicovitch dimension strictly exceeds the topological dimension. Every set with a non-integer D is a fractal.”The Hausdorff–Besicovitch dimension of a set in a metric space may be expressed as [5]:
where N(ϵ) is the number of open balls or radius ϵ required to cover the set. In a metric space given any point X, an open ball centered on X with radius ϵ, is the set of all points x for which distance between X and x is < ϵ.The term waveform is applied to the shape of a set, usually drawn as instant values of a periodic quantity in time. Besides classical methods such as moment statistics and regression analysis, properties like Kolmogorov y Sinai entropy [84], apparent entropy [7, 85, 86] and fractal [11] have been proposed to analyze waveforms. Fractal analysis may provide information on spacial extent (tortuosity or capacity to extend in space) and on self-similarity (the property of staying unchanged when measure scale changes) and self affinity [87]. In bidimensional spaces waveforms are planar curves, which may have coordinates of different units or dimensions.There is a simple algorithm to approximate fractal dimension of a curve [11]. To achieve this, fractal dimension D is estimated for a set of N points from a set{x, y} values were the abscissa x increases by a constant factor (Δx). The curve is transformed into a unit square (a square with side length equal to 1) [11] as follows. A first transformation normalizes every abscissa point as:
where xs are the original abscissa values, x is the largest x. A second transform normalizes the ordinate as:
where y are the original ordinate values, and y and y are minimum and maximum y, respectively. The unit square may be seen as covered with a N ⋅ N grid of cells. N containing a transformed curve point. A length L line may be divided into N(ϵ) = L/(2 ⋅ ϵ) segments of mean length 2 ⋅ ϵ, and covered with N radius ϵ open balls. Fractal dimension is the approximated as D [11, Ecuation (6a)] as
where D is again the Hausdorff–Besicovitch dimension, N′ = N − 1, and L is the curve length after embedding in the unit square. It is important to observe that D = D
only at the limit when N′ → ∞, for all other N′ values, D > D. Thus Ds obtained with same N′s are the only fit to be compared. D uncertainty may be estimated through its variance [11]:
where Δy is segment i length, distance between points (x, y) and (x, y) of the transform and is those segments’ mean. D means and variances may be used to compare empiric D values [35, Sections 5.2.1 and 5.2.4] [37] based on Vysochanskij–Petunin inequality [56, 57].
Generation of random sequences for calibration purposes
Monte Carlo simulation was used to generate M = 100 traces of N = 1329 points each of white noise (see Random Fractals Subsection) of white noise. White noises simulated were sequences of Gaussian variables of type N(0, 1) [Eq (23)]. Estimated fractal dimension D was calculated for each simulated trace as indicated in Subsection, D [Eq (14)] and var(D) [Eq (15)]. Eq (15) intra sequence D variance, due to unit square–embedded waveform Δy in each jth sequence. Each sequence is a (short?) segment from an infinite sequence with same properties. Every sequence of length N < ∞ generated as indicated may be used to produce a different approximation to D depending on where each is sample taken. To estimate D and its uncertainty means were calculated for M simulated traces as
The variance od D
curves (which may be visualized as random sets N points sampled from an infinitely curve) for the M waveforms sets was determined as
Then, total variance, , was determined as
where is the average variance within traces and var(D) calculated with Eq (15).and were used to compare the difference in D from the empiric sequences with Monte Carlo simulated sequences with known properties. In this manner it was possible to decide if empiric sequences were white, brow, or other kind noise, spite of N < ∞ [11, 37]. Statistical significance of the differences was established using the Vysochanskij and Petunin inequality (V-P, details in Theorem 1). V-P inequality allows comparing means of samples coming from a population with unknown pdf as long as it is unimodal, and has a definite variance [56, 57, 88]. Due to the unknown pdf, the comparison using V-P inequality tends to declare as not different to means that are weakly statistically significantly distinct (statistical error of type II [28]), but is % less likelier to produce type II errors than classical Tchebichev inequality [89], of which V-P inequality is a particular case. This means that parameter differences declared significant with the V-P inequality, are more significant than they appear. To compare the statistical significance of a difference between two D means [35, Adaptwd from Eqs. (34) and (35)] it is required only that
where the subindex t indicates total variance, and
where α is the largest probability we accept to declare a difference statistically significant. If D’s pdf is known and Gaussian Eq (20) constant would not be as specified by the V-P inequality, but ξ = 1.959…. This is true for any case where the pdf is known, thus we should write Eq (20) somewhat like within the parentheses, but this is unnecessary due to the demonstrated inequality [56, 57, 88].Eqs (16) to (18) were also calculated for sets of M = 100 Brownian sequences with N = 1329 like
and were used as standards to calculate the probability of significance between their estimated versus D calculates for and empirical distribution of interest. Their fractal dimension D, when N → ∞ is 1.5. An example may be found in [37]. The N[0, 1] variable was generated as indicated in Eq (23).
Generating uniform (rectangular) random variables
Uniform random variables of U[0, 1] type were generated. Fundamental to all Monte Carlo simulations [90] is a good uniform (pseudo) random (PRNG) number generator. Data for all numerical simulations carried out in this work were produced using random numbers (r) with continuous rectangular (uniform) distribution in the closed interval [0, 1] or U[0, 1]. All U[0, 1] [Eq (22)] were generated using the 2002/2/10 initialization-improved 623-dimensionally evenly distributed [91] uniform pseudo random number generator MT19937 algorithm [92, 93]. The procedure used makes exceedingly unlikely (P = 2−64 ≈ 5.4 · 10−20) that the same sequence, {r}, of U[0, 1] is used twice. Calculations were programmed in C++ using g++ version 5.4.0 20160609 with C++14 standards, under Ubuntu GNU Linux version 18.4. For further details on random number generator initializing see Sevcik [37].Rectangular random variables fulfill the following property
with mean , x, k may be a real number [11] or an integer [11, 37].
Generating random normal deviates
Random normal variables of the ding N[μ, σ] = N[0, 1] were generated with the Box and Muller [59, 94] algorithm
where r1 and r2 are two uniformly distributed random variates of the kind U[0, 1.].
On Cauchy distributed variables
The Cauchy distribution is symmetric about its median (location factor, ) and has a width (dispersion) factor (λ) and its pdf is
and also has a PDF like
where arctan refers to the arc tangent trigonometric function. Cauchy pdf has no central moments [28, 81], and thus has no defined mean, variance, skewedness or kurtosis [75, 81, 95]. If conventional equations for sample or s2(y) values are calculated, they will be seen to vary wildly and wild variability increases with sample size. Cauchy–type data can be described and compared only with nonparametric statistics. From Eq (25) it is possible to prove that a 95% CI of a Cauchyan variable is equivalent to ≈ μ ± 12.706λ which gives a ≈ 25.412λ span to the 95% CI. A Cauchy random variable is prone to assume values very far away from its median, outliers are very commonly observed as sample size increases [75, 81, 95].
The Vysochanskij-Petunin inequality [56, 57]
Theorem 1 (Vysochanskij-Petunin). : Let X be a random variable with unimodal distribution, mean μ and finite, non-zero variance
σ2. Then, for any
Using the inequality to calculate significance when
Theorem 1 holds even with heavily skewed distributions and puts bounds on how much of the data is, or is not “in the middle”. Setting ϵ = 0.05 then , for a two tailed test. By virtue of Eq (26) no matter which unimodal distribution, no matter how skewed, there will be <2.5% chance that a datum will belong to a population with mean μ and variance σ2 if it lays farther than ±2.981σ from μ. Please note that if the probability distribution function of data is Gaussian ±1.96σ suffices to reach the same confidence level. We introduced the ϵ variable in Eq (26) for the statistical argumentation that follows.Let and s2(D) be the mean and variance estimated for the random variable D, and and s2(D) be the mean and variance estimated for the random variable D (linearly independent from D), then
and the estimated variance of is
By virtue of the V-P inequality [Eq (26)]
which means Eq (26) thatTherefore, there is ≤ ϵ probability that due to random sampling variation, and with a confidence level P ≤ ϵ. Thus:
for a test with only one tail, since in this case we are only interested with one alternative, that . Again, when the probability distribution function is Gaussian, the value of λ for the one tailed case, would be ≈ 1.65 instead of the ≈ 2.108 demanded by Eq (26).Theorem 1 does not hold, but you can still get an answer using Eq (26) as shown in the following Corollary 1 of the V-P inequality. We know propose and prove a corollary of Theorem 1:Corollary 1. : If
then P is not known but is bound as
Proof. As indicated by Eq (26), then if
then ϵ is the value of ϵ at the threshold required for Theorem 1 to hold. When the predicted value of ϵ ⩾ ϵ, and since there is no limit to this inequality, it may happen that the estimated ϵ > 1, but there is no probability P > 1, by definition. Thus when it follows that ϵ does not express a probability. But since if
Eq (33) gives the highest P value which may be estimated with the V-P inequality is , P is undetermined but bound in the interval:(XLSX)Click here for additional data file.16 Oct 2021
PONE-D-21-14891
Hidden chaos factors inducing random walks which
reduce hospital operative efficiency
PLOS ONE
Dear Dr. Sevcik,Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.Please submit your revised manuscript by Nov 28 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.Please include the following items when submitting your revised manuscript:
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15 Dec 2021Journal Requirements.When submitting your revision, we need you to address these additional requirements.1. Please ensure that your manuscript meets PLoS ONE's style r ..... .Reply: We did our best to comply. We used a published PLoS article to reproduce its forminformation fields an and style. Not all the features were available in tha LaTeX remplate, butwe hope that any shortcomings will be easily solved for your typesetters. Also, most journaluse and require authos supplied Key Words, we added a small section with keywords to themanuscript, if this is unsuitable it will be trivial for your typesetters to comment or erase theKey Words section which is all in one line.2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1:YesReviewer #2: YesReply: No reply seems necessary.3. Please update your submission to use the PLoS LaTeX template. ... ,Reply: Done as suggested. This implied a long time modifying each of the entries of ourdatabase to conform to PloS ONE uses on doi numbers and url links. It took a long time sincethe BibTeX dbase contains 3315 entries and it most conform to the ABS book format we use fora book citif 847 references, thus far.It was a lot of work. Perhaps the most important of ourreferences (Sevcik, 1998) appeared in an on line journal , Complexity International, which isno longer available. Ten years ago we deposited a copy of Sevcik 1998 in arXiv, in a mannerthat complies with the extinct Complexity International Journal copyrights. The link to thearXiv file MUST be on the citation of this work, thus we had to tweak the citation to make thearXiv ling visible even using PLoS One bibliography style.4.Thank you for stating the following in the Acknowledgments Section of your manuscript:Reply: The information was set in the LaTeX template. It was divided into sections as done, forexample in https://doi.org/10.1371/journal.pone.0258052 which we use as styling example.5. Please review your reference list to ensure that it is complete and correct. ...Reply: Our references are stored in an extense BibTeX formatted data base used in all ourpublications. However, we have to modify the fields thr references in our BiBTrX dbase toaccommodate to PloS One bibliography style without destroying the references format for otheruses.Reviewer's Responses to QuestionsComments to the Author1. Is the manuscript technically sound, and do the data support the conclusions?The manuscript must describe a technically sound piece of scientific research with data that supportsthe conclusions. Experiments must have been conducted rigorously, with appropriate controls,replication, and sample sizes. The conclusions must be drawn appropriately based on the datapresented.Reviewer #1: YesReviewer #2: YesReply: No reply seems necessary.2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1:YesReviewer #2: YesReply: No reply seems necessary.3. Have the authors made all data underlying the findings in their manuscript fully available?Reply: We are unsure about the meaning of the YES choice by the reviewerss. It could mean inthe context of the question that we did it right in the manuscript, or that we should includemore. In any case we are including two MS Exel-formatted files with the original La FuenfríaHospital data. The manuscript, we feel, it is clear on how was the data used and corrected fora short breech of missing data. In any event, we are open to any questions from the readers.The original HLF spreadsheets provided have Spanish labels and headings, but each of thesemay be easily translated to any language using Google Translate ® for example.Reviewer #1: YesReviewer #2: Yes4. Is the manuscript presented in an intelligible fashion and written in standard English?Reply: As pointed out by Reviewer 2, there were some typos in the paper. We revisedonce more, but since our capacity to detect mistakes in our papers decreases as we re-read them, we hired a professional proofreader. We hope that now the issues arefixed.Reviewer #1: YesReviewer #2: No5. Review Comments to the Author.Please use the space provided to explain your answers to the questions above.Reviewer #1:The paper is very interesting and well structured. The analysis conducted is appropriate andwell communicated. The implications of the findings are also clearly outlined. However,the paper needs proof reading due to typos or missing punctuation; e.g. page 8 line 18 -These shows; page 8 line 20 and page 7 line 7 missing commas; page 9 line 40 - ''such asdescribed'' should read ''such as those described..''Reply: Thanks for your kind opinion. The revised version will be proof read by acertified professional English proofreader. Prior to this, we re-read the manuscriptand corrected the typos we were able to see.Reviewer #2:The aim of the authors is to show that factors not usually considered in hospitalperformance analysis may have a huge impact on hospital efficacy - by delving into thecase of La Fuenfría Hospital. The methodology is explained in a way that enablesreplication and the discussion and conclusions triangulate with the rest of the paper.However, the paper has many typos and grammatical mistakes, which makes it a difficultread and sometimes understand. Even the abstract seems like a literal translation from theoriginal language and does not flow well. I suggest an complete proof read and edit of thearticle by a native English speaking person.6. PLoS authors have the option to publish the peer review history of their article (whatdoes this mean?). If published, this will include your full peer review and any attachedfiles.If you choose “no”, your identity will remain anonymous but your review may still bemade public.Do you want your identity to be public for this peer review? For informationabout this choice, including consent withdrawal, please see our Privacy Policy .Reply: We appreciate Prof. Grima openness.Reviewer #1: NoReviewer #2: Yes: Prof. Simon GrimaSubmitted filename: Reply to reviewers comments.docxClick here for additional data file.6 Jan 2022Hidden chaos factors inducing random walks whichreduce hospital operative efficiencyPONE-D-21-14891R1Dear Dr. Sevcik,We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.Within one week, you’ll receive an e-mail detailing the required amendments. 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Authors: Daniel J Benjamin; James O Berger; Magnus Johannesson; Brian A Nosek; E-J Wagenmakers; Richard Berk; Kenneth A Bollen; Björn Brembs; Lawrence Brown; Colin Camerer; David Cesarini; Christopher D Chambers; Merlise Clyde; Thomas D Cook; Paul De Boeck; Zoltan Dienes; Anna Dreber; Kenny Easwaran; Charles Efferson; Ernst Fehr; Fiona Fidler; Andy P Field; Malcolm Forster; Edward I George; Richard Gonzalez; Steven Goodman; Edwin Green; Donald P Green; Anthony G Greenwald; Jarrod D Hadfield; Larry V Hedges; Leonhard Held; Teck Hua Ho; Herbert Hoijtink; Daniel J Hruschka; Kosuke Imai; Guido Imbens; John P A Ioannidis; Minjeong Jeon; James Holland Jones; Michael Kirchler; David Laibson; John List; Roderick Little; Arthur Lupia; Edouard Machery; Scott E Maxwell; Michael McCarthy; Don A Moore; Stephen L Morgan; Marcus Munafó; Shinichi Nakagawa; Brendan Nyhan; Timothy H Parker; Luis Pericchi; Marco Perugini; Jeff Rouder; Judith Rousseau; Victoria Savalei; Felix D Schönbrodt; Thomas Sellke; Betsy Sinclair; Dustin Tingley; Trisha Van Zandt; Simine Vazire; Duncan J Watts; Christopher Winship; Robert L Wolpert; Yu Xie; Cristobal Young; Jonathan Zinman; Valen E Johnson Journal: Nat Hum Behav Date: 2018-01