scieee Science in your language
[en] (orig)

Detection of atrial fibrillation episodes in long-term heart rhythm signals using a support vector machine

Abstract

Atrial fibrillation (AF) is a serious heart arrhythmia leading to a significant increase of the risk for occurrence of ischemic stroke. Clinically, the AF episode is recognized in an electrocardiogram. However, detection of asymptomatic AF, which requires a long-term monitoring, is more efficient when based on irregularity of beat-to-beat intervals estimated by the heart rate (HR) features. Automated classification of heartbeats into AF and non-AF by means of the Lagrangian Support Vector Machine has been proposed. The classifier input vector consisted of sixteen features, including four coefficients very sensitive to beat-to-beat heart changes, taken from the fetal heart rate analysis in perinatal medicine. Effectiveness of the proposed classifier has been verified on the MIT-BIH Atrial Fibrillation Database. Designing of the LSVM classifier using very large number of feature vectors requires extreme computational efforts. Therefore, an original approach has been proposed to determine a training set of the smallest possible size that still would guarantee a high quality of AF detection. It enables to obtain satisfactory results using only 1.39% of all heartbeats as the training data. Post-processing stage based on aggregation of classified heartbeats into AF episodes has been applied to provide more reliable information on patient risk. Results obtained during the testing phase showed the sensitivity of 98.94%, positive predictive value of 98.39%, and classification accuracy of 98.86%.

Read accessible full text

Detection of atrial fibrillation episodes in long-term heart rhythm signals using a support vector machine

Author: Czabanski, Robert
Publisher: MDPI
Year: 2020
DOI: 10.3390/s20030765
Source: https://dspace.vsb.cz/bitstreams/73ca448c-d0f9-4197-9a40-65b5907954f0/download
senso s
A icle
De ec ion o A ial Fib illa ion Episodes in
Long-Te m Hea Rhy hm Signals Using a Suppo
Vec o Machine
Robe Czabanski 1, K zysz o Ho oba 2,*, Janusz W obel 2, Adam Ma onia 2,
Radek Ma inek 3, Tomasz Kupka 2, Michal Jezewski 1, Radana Kahanko a 3,
Janusz Jezewski 2and Jacek M. Leski 1
1Depa men o Cybe ne ics, Nano echnology and Da a P ocessing, Silesian Uni e si y o Technology,
PL44100 Gliwice, Poland; [email p o ec ed] (R.C.); [email p o ec ed] (M.J.);
[email p o ec ed] (J.L.)
2
Łukasiewicz Resea ch Ne wo k–Ins i u e o Medical Technology and Equipmen , PL 41800 Zab ze, Poland;
[email p o ec ed] (J.W.); [email p o ec ed] (A.M.); [email p o ec ed] (T.K.);
[email p o ec ed] (J.J.)
3Depa men o Cybe ne ics and Biomedical Enginee ing, VSB–Technical Uni e si y o Os a a,
708 00 Os a a-Po uba, Czech Republic; [email p o ec ed] (R.M.); [email p o ec ed] (R.K.)
*Co espondence: k zysz o .ho [email p o ec ed]
Recei ed: 19 Decembe 2019; Accep ed: 27 Janua y 2020; Published: 30 Janua y 2020


Abs ac :
A ial ib illa ion (AF) is a se ious hea a hy hmia leading o a signi ican inc ease o he
isk o occu ence o ischemic s oke. Clinically, he AF episode is ecognized in an elec oca diog am.
Howe e , de ec ion o asymp oma ic AF, which equi es a long- e m moni o ing, is mo e e icien
when based on i egula i y o bea - o-bea in e als es ima ed by he hea a e (HR) ea u es.
Au oma ed classi ica ion o hea bea s in o AF and non-AF by means o he Lag angian Suppo
Vec o Machine has been p oposed. The classi ie inpu ec o consis ed o six een ea u es, including
ou coe icien s e y sensi i e o bea - o-bea hea changes, aken om he e al hea a e analysis
in pe ina al medicine. E ec i eness o he p oposed classi ie has been e i ied on he MIT-BIH
A ial Fib illa ion Da abase. Designing o he LSVM classi ie using e y la ge numbe o ea u e
ec o s equi es ex eme compu a ional e o s. The e o e, an o iginal app oach has been p oposed
o de e mine a aining se o he smalles possible size ha s ill would gua an ee a high quali y
o AF de ec ion. I enables o ob ain sa is ac o y esul s using only 1.39% o all hea bea s as he
aining da a. Pos -p ocessing s age based on agg ega ion o classi ied hea bea s in o AF episodes
has been applied o p o ide mo e eliable in o ma ion on pa ien isk. Resul s ob ained du ing he
es ing phase showed he sensi i i y o 98.94%, posi i e p edic i e alue o 98.39%, and classi ica ion
accu acy o 98.86%.
Keywo ds:
suppo ec o machine (SVM); hea a e a iabili y (HRV); HRV ea u es; a ial
ib illa ion (AF); AF de ec ion
1. In oduc ion
A ial ib illa ion (AF) is he mos common hea a hy hmia, which occu s when he a ia con ac s
quickly and i egula ly a a es o 400 o 600 pe minu e. These con ac ions a e independen om
en icles, which hemsel es ope a e a much lowe a e. AF symp oms o en include palpi a ions,
i egula hea bea , sho ness o b ea h, ches pains and o he s, bu hey can be also asymp oma ic
and is hen called silen AF. The equency o AF occu ence is s ic ly co ela ed wi h he pa ien ’s
age [
1
,
2
]. The p ognosis indica es ha he AF occu ence wi hin he pe iod o he nex 20–30 yea s will
Senso s 2020,20, 765; doi:10.3390/s20030765 www.mdpi.com/jou nal/senso s
Senso s 2020,20, 765 2 o 24
double, mainly due o he longe li e span o he popula ion. The AF de ec ion is impo an , since his
hea a hy hmia is a well-known isk ac o o occu ence o ischemic s oke, e en six imes highe
han among pa ien s wi hou he a hy hmia [3].
Figu e 1p esen s he ECG signals om he MIT-BIH A ial Fib illa ion da abase (MIT-BIH AF)
published on PhysioNe [
4
–
6
], comp ising bo h segmen s wi h he AF episodes and non-AF segmen s.
AF episodes occu i egula ly and may las om a ew hea bea s o hou s, which signi ican ly
hinde he possibili y o diagnose he silen AF by means o occasionally pe o med ambula o y
ECG eco dings. I implies ha he longe he eco ding, he highe chance o de ec he silen AF
episodes [
7
,
8
]. The mos e icien echniques o long- e m moni o ing a e: Hol e moni o , con inuous
eleme y [
9
–
12
], o implemen able de ices wi h in e nal memo y [
13
–
15
]. Howe e , isual analysis
o long 24-h eco ding equi es a lo o ime and e o s om he ca diologis s, hus he me hods o
au oma ed de ec ion o a ial ib illa ion a e needed o imp o e he objec i i y o in e p e a ion. When
based on ECG, he e icien au oma ed AF de ec ion equi es a high quali y signal. I may no be
ensu ed by he long- e m moni o ing echniques which usually comp ise pe iods o daily physical
ac i i y o he pa ien which dis o he ECG signal.
Senso s 2020, 20, 765 2 o 24
is impo an , since his hea a hy hmia is a well-known isk ac o o occu ence o ischemic
s oke, e en six imes highe han among pa ien s wi hou he a hy hmia [3].
Figu e 1 p esen s he ECG signals om he MIT-BIH A ial Fib illa ion da abase (MIT-BIH AF)
published on PhysioNe [4–6], comp ising bo h segmen s wi h he AF episodes and non-AF
segmen s. AF episodes occu i egula ly and may las om a ew hea bea s o hou s, which
signi ican ly hinde he possibili y o diagnose he silen AF by means o occasionally pe o med
ambula o y ECG eco dings. I implies ha he longe he eco ding, he highe chance o de ec he
silen AF episodes [7,8]. The mos e icien echniques o long- e m moni o ing a e: Hol e moni o ,
con inuous eleme y [9–12], o implemen able de ices wi h in e nal memo y [13–15]. Howe e ,
isual analysis o long 24-h eco ding equi es a lo o ime and e o s om he ca diologis s, hus
he me hods o au oma ed de ec ion o a ial ib illa ion a e needed o imp o e he objec i i y o
in e p e a ion. When based on ECG, he e icien au oma ed AF de ec ion equi es a high quali y
signal. I may no be ensu ed by he long- e m moni o ing echniques which usually comp ise
pe iods o daily physical ac i i y o he pa ien which dis o he ECG signal.
Figu e 1. ECG signals (04043 and 04045) aken om he MIT-BIH AF da abase, wi h ecognized
segmen s o a ial ib illa ion and he non-AF ones.
The AF episode is mani es ed in ECG by signi ican changes o du a ion o he bea - o-bea (RR)
in e als [16–19], see Figu e 1. Howe e , he RR in e als i egula i y caused by AF occu ences is
much mo e easy o obse e a e con e ing RR in e als in o he ins an aneous hea a e (HR)
signal (Figu e 2). The p esen ed HR signals con i m ha AF episodes occu e y acciden ally, and
hey can las a ew seconds (signal 04048), bu also expand o long las ing episodes (signal 04936).
In he ligh o abo e ac s an e icien au oma ed me hod o AF de ec ion should be based on
es ima ion o RR i egula i y o equi alen i.e., HR i egula i y obse ed in long- e m eco ding
[20,21]. Mo eo e , such app oach enables o in ol e he a ious eco ding me hods which can
p o ide signals in which he hea bea s can be de ec ed. Beside elec oca diog am, such signals
include pho ople hysmog am [22–24] o seismoca diog am [25]. Using a pho oelec ic senso is
a ac i e in case o home eleca e as long- e m eco ding should be accomplished by
ins umen a ions being minimally oublesome and incon enien o he pa ien [26,27]. I may be a
sma moni o in a o m o a w is b acele wi h a specialized e lec i e op ical senso o pe o m he
hea a e moni o ing using he me hod p e iously de eloped by he au ho s [28].
The gene al concep o he me hods mos commonly used o au oma ed de ec ion o AF
episodes elies on de e mina ion o ea u es es ima ing he RR in e al changes, and hen applica ion
o he s a is ical analysis o mo e ad anced classi ie o di e en ia e be ween AF episode and no mal
sinus hy hm segmen s, basing on he in o ma ion on RR i egula i y. The ea u e se is composed
mos commonly o di e en s a is ical measu es (mean o median HR, oo mean squa e o
successi e RR di e ences, u ning poin a io). I can also include no malized RR in e als [29,30] o
no malized RR di e ences [31], Shannon en opy [19] o coe icien o sample en opy [15,32]. O he
Figu e 1.
ECG signals (04043 and 04045) aken om he MIT-BIH AF da abase, wi h ecognized
segmen s o a ial ib illa ion and he non-AF ones.
The AF episode is mani es ed in ECG by signi ican changes o du a ion o he bea - o-bea (RR)
in e als [
16
–
19
], see Figu e 1. Howe e , he RR in e als i egula i y caused by AF occu ences is
much mo e easy o obse e a e con e ing RR in e als in o he ins an aneous hea a e (HR) signal
(Figu e 2). The p esen ed HR signals con i m ha AF episodes occu e y acciden ally, and hey can
las a ew seconds (signal 04048), bu also expand o long las ing episodes (signal 04936).
In he ligh o abo e ac s an e icien au oma ed me hod o AF de ec ion should be based on
es ima ion o RR i egula i y o equi alen i.e., HR i egula i y obse ed in long- e m eco ding [
20
,
21
].
Mo eo e , such app oach enables o in ol e he a ious eco ding me hods which can p o ide
signals in which he hea bea s can be de ec ed. Beside elec oca diog am, such signals include
pho ople hysmog am [
22
–
24
] o seismoca diog am [
25
]. Using a pho oelec ic senso is a ac i e
in case o home eleca e as long- e m eco ding should be accomplished by ins umen a ions being
minimally oublesome and incon enien o he pa ien [
26
,
27
]. I may be a sma moni o in a o m o
a w is b acele wi h a specialized e lec i e op ical senso o pe o m he hea a e moni o ing using
he me hod p e iously de eloped by he au ho s [28].
The gene al concep o he me hods mos commonly used o au oma ed de ec ion o AF episodes
elies on de e mina ion o ea u es es ima ing he RR in e al changes, and hen applica ion o he
s a is ical analysis o mo e ad anced classi ie o di e en ia e be ween AF episode and no mal sinus
hy hm segmen s, basing on he in o ma ion on RR i egula i y. The ea u e se is composed mos
commonly o di e en s a is ical measu es (mean o median HR, oo mean squa e o successi e RR
Senso s 2020,20, 765 3 o 24
di e ences, u ning poin a io). I can also include no malized RR in e als [
29
,
30
] o no malized RR
di e ences [
31
], Shannon en opy [
19
] o coe icien o sample en opy [
15
,
32
]. O he o m o p esen
he RR i egula i y a e: he densi y his og am o he di e ence be ween successi e RR in e als [
33
,
34
],
map ha plo s RR in e als e sus change o RR in e als [
35
], mapping he RR-in e al ime se ies o
bina y symbolic sequences [36,37] o Ma ko sco e o RR in e al [16].
Senso s 2020, 20, 765 3 o 24
o m o p esen he RR i egula i y a e: he densi y his og am o he di e ence be ween successi e
RR in e als [33,34], map ha plo s RR in e als e sus change o RR in e als [35], mapping he
RR-in e al ime se ies o bina y symbolic sequences [36,37] o Ma ko sco e o RR in e al [16].
Figu e 2. Two HR signals exp essed in bea s pe minu e (bpm) wi h clinically ecognized AF
segmen s o di e en cha ac e is ics o HR changes in ela ion o no mal sinus hy hm (non-AF). The
AF segmen s a e ma ked using he expe s’ anno a ions p o ided o pa icula eco ds in he
MIT-BIH AF da abase.
In he simples app oach o AF classi ica ion he Recei e Ope a ing Cha ac e is ics (ROC)
cu e has been used o ind he op imal h eshold alues o he inpu ea u es p o iding he bes
classi ica ion pe o mance [30,35,36,38]. The s a is ical es (Kolmogo o -Smi no ) was used in [33]
o check i he densi y his og ams o he es da a di e om he s anda d densi y ones p epa ed as a
empla e o AF episodes. In o de o di e en ia e be ween AF and non-AF pa e ns he a ious
classi ica ion me hods ha e been applied: Neyman-Pea son de ec o [31], Random Fo es (RF)
model and k-nea es neighbo s classi ie [32], Suppo Vec o Machine (SVM) wi h p omising esul s
epo ed in [39–41], as well as a i icial neu al ne wo k [42], also wi h in e al ansi ion ma ices as
an inpu [43].
In [39] SVM app oach was used o classi ica ion o he 30-s segmen s o ECG and 300-bea
sequences o RR in e als. Two pa ame e s o S a iona y Wa ele T ans o m (peak- o-a e age
powe a io and log-ene gy en opy) we e used o aw ECG-based app oach, while i e ea u es
we e ex ac ed om HR signal. The e iciency o AF de ec ion achie ed by he ea u e-based
classi ica ion o he RR sequences was es ed agains he algo i hm based on aw ECG. Highe
sensi i i y was ensu ed by he HR-based app oach, while ECG-based algo i hm p o ided imp o ed
speci ici y and classi ica ion accu acy. The classi ie based on SVM wi h adial basis unc ion was
p oposed in [40], wi h wo ea u es as he inpu s: he a e age o RR di e ences and he s anda d
de ia ion o di e ences in a de ined du a ion. The same SVM classi ie was employed in [41]. The
inpu se comp ised mo e RR in e al ea u es: median hea a e, minimum RR in e al, mean RR
in e al, a ious en opy measu es, and di e ence i egula i y measu e.
The ea u es es ima ing he RR a iabili y a e calcula ed in a sliding window comp ising an
es ablished numbe o consecu i e RR in e als (o HR alues). Since he e is no s anda d o he
window leng h, many wo ks ha e aimed o ind he op imal leng h, p o iding he bes classi ica ion
pe o mance. Some wo ks assumed ha AF episodes o less han 30 s du a ion a e no clinically
signi ican , which led o highe op imal numbe o hea bea s: 100 [33], 128 [35] and 150 [37]. O he
au ho s claim ha longe windows end o miss sho AF episodes, and hus hey applied
signi ican ly sho e windows: 30 [32], 12 [15] o e en 8 bea s [44]. I is ob ious ha di e en
Figu e 2.
Two HR signals exp essed in bea s pe minu e (bpm) wi h clinically ecognized AF segmen s
o di e en cha ac e is ics o HR changes in ela ion o no mal sinus hy hm (non-AF). The AF segmen s
a e ma ked using he expe s’ anno a ions p o ided o pa icula eco ds in he MIT-BIH AF da abase.
In he simples app oach o AF classi ica ion he Recei e Ope a ing Cha ac e is ics (ROC) cu e
has been used o ind he op imal h eshold alues o he inpu ea u es p o iding he bes classi ica ion
pe o mance [
30
,
35
,
36
,
38
]. The s a is ical es (Kolmogo o -Smi no ) was used in [
33
] o check i he
densi y his og ams o he es da a di e om he s anda d densi y ones p epa ed as a empla e o AF
episodes. In o de o di e en ia e be ween AF and non-AF pa e ns he a ious classi ica ion me hods
ha e been applied: Neyman-Pea son de ec o [
31
], Random Fo es (RF) model and k-nea es neighbo s
classi ie [
32
], Suppo Vec o Machine (SVM) wi h p omising esul s epo ed in [
39
–
41
], as well as
a i icial neu al ne wo k [42], also wi h in e al ansi ion ma ices as an inpu [43].
In [
39
] SVM app oach was used o classi ica ion o he 30-s segmen s o ECG and 300-bea
sequences o RR in e als. Two pa ame e s o S a iona y Wa ele T ans o m (peak- o-a e age powe
a io and log-ene gy en opy) we e used o aw ECG-based app oach, while i e ea u es we e
ex ac ed om HR signal. The e iciency o AF de ec ion achie ed by he ea u e-based classi ica ion
o he RR sequences was es ed agains he algo i hm based on aw ECG. Highe sensi i i y was
ensu ed by he HR-based app oach, while ECG-based algo i hm p o ided imp o ed speci ici y and
classi ica ion accu acy. The classi ie based on SVM wi h adial basis unc ion was p oposed in [
40
],
wi h wo ea u es as he inpu s: he a e age o RR di e ences and he s anda d de ia ion o di e ences
in a de ined du a ion. The same SVM classi ie was employed in [
41
]. The inpu se comp ised mo e
RR in e al ea u es: median hea a e, minimum RR in e al, mean RR in e al, a ious en opy
measu es, and di e ence i egula i y measu e.
The ea u es es ima ing he RR a iabili y a e calcula ed in a sliding window comp ising an
es ablished numbe o consecu i e RR in e als (o HR alues). Since he e is no s anda d o he
window leng h, many wo ks ha e aimed o ind he op imal leng h, p o iding he bes classi ica ion
pe o mance. Some wo ks assumed ha AF episodes o less han 30 s du a ion a e no clinically
signi ican , which led o highe op imal numbe o hea bea s: 100 [
33
], 128 [
35
] and 150 [
37
]. O he
au ho s claim ha longe windows end o miss sho AF episodes, and hus hey applied signi ican ly
Senso s 2020,20, 765 4 o 24
sho e windows: 30 [
32
], 12 [
15
] o e en 8 bea s [
44
]. I is ob ious ha di e en window leng h
epo ed as he op imal alue depends on he me hod used o au oma ed AF de ec ion. Ano he
impo an aspec o using he sliding window o AF de ec ion is how many bea s i is shi ed. Shi ing
he window e e y hea bea esul s in one bea esolu ion o he AF classi ica ion. Then each hea bea
(RR in e al), usually co esponding o he middle o he window, is classi ied as AF o non-AF. In such
case, de e mina ion o classi ica ion pe o mance is e iden as each au oma ically classi ied bea can be
ela ed o he e e ence one, basing on he expe anno a ions. O he wise, addi ional condi ion has o
be applied— he window is labeled as AF episode only i he numbe o clinically anno a ed AF bea s
wi hin he window exceeds a p ede ined h eshold, usually 0.5 like in [
35
,
45
]. Howe e , i is ob ious
ha he h eshold alue a ec s he classi ica ion pe o mance. The h eshold has been included in o
he inpu ea u e se and uned o op imum sensi i i y and speci ici y in [
38
]. Howe e , i should be
no ed ha in such app oach, he e e ence in o ma ion is modi ied o achie e he bes classi ica ion
pe o mance o he au oma ed me hod es ed, which seems o be a he doub ul.
In o de o a oid sho alse posi i e AF episodes o sho a i ac o classi ied AF he
pos -p ocessing co ec ion was applied, like dedica ed mechanism called AF ala m enhance [
16
]. I is
he hys e esis coun e ha begins (o ends) an episode i es ablished numbe o consecu i e analyzed
RR segmen s ha e been classi ied as AF (o non-AF). O he pos -p ocessing me hod was based on
median il e ing [45].
In [
16
], a e combining R-R in e al Ma ko sco e wi h wo P-wa e measu emen s: he loca ion
exp essed by P-R in e al du a ion, and he mo phology de ined as simila i y be ween wo consecu i e
P-wa es, he sensi i i y did no change, whe eas speci ici y and posi i e p edic i e alues inc eased sligh ly.
A no el deep lea ning has been adop ed o au oma ed de ec ion o AF in he long- e m ECG
eco dings. This classi ie lea ns di ec ly om he RR in e als and he e o e he e is no need o ex ac
he ea u es. The model based on deep Recu en Neu al Ne wo k (RNN) wi h Long Sho -Te m
Memo y (LSTM) was used in [
46
], and combining wi h he Con olu ional- and Recu en -Neu al
Ne wo ks o ex ac high le el ea u es was p oposed in [
45
]. Al hough a high classi ica ion pe o mance
has been epo ed, he compu a ional complexi y o deep lea ning model is much highe han adi ional
ea u e-based classi ie . In his pape , we desc ibe he me hod o au oma ed AF de ec ion which
assigns he ec o o pa ame e s quan i a i ely desc ibing he HR signal in o wo classes ep esen ing
he absence o p esence o a ial ib illa ion. As es ima ion o HR a iabili y is also impo an pa o he
Fe al Hea Ra e (FHR) analysis [
47
–
49
], he indices widely used o FHR a iabili y desc ip ion ha e
been conside ed as po en ially use ul o AF de ec ion. The de ec ion me hod p esen ed in his pape
was de i ed om he machine lea ning p inciples. Ou classi ica ion ou ine was pe o med by means
o he Lag angian Suppo Vec o Machine (LSVM) [
50
]— he s a e-o - he-a classi ie based on he
linea ly con e gen lea ning algo i hm. The e icien LSVM lea ning p ocedu e was ob ained om he
e o mula ion o he Quad a ic P og aming (QP) op imiza ion p oblem o he Suppo Vec o Machine
(SVM) [
51
]. Addi ional agg ega ion s age has been applied o p o ide mo e eliable in o ma ion on
isk o he pa ien . The pe o mance o he p oposed AF de ec ion me hod was examined using he
MIT-BIH A ial Fib illa ion da abase, which includes 25 en-hou long ECG eco dings.
2. Ma e ials and Me hods
Au oma ed de ec ion o he a ial ib illa ion episodes p oposed in his wo k s a s wi h ex ac ion
o six een HR i egula i y ea u es composing he classi ie inpu ec o . Then he LSVM classi ie is
applied o ma k a gi en hea bea as AF o non-AF one. Final s ep is agg ega ion o he classi ied bea s
in o AF episodes.
2.1. HR I egula i y Fea u es
Conside ing on-line de ec ion o AF and limi ed compu a ional powe o he de eloped mobile
moni o , we applied a simple linea classi ie which ecognizes he AF hea bea s basing on easily
accessible in o ma ion abou hea hy hm and HR ea u es [
52
,
53
]. Apa om he HR alue, o he
Senso s 2020,20, 765 5 o 24
ou inpu ea u es ha e been selec ed in a se ies o p elimina y in es iga ions ca ied ou among
la ge ea u e se [
54
]. Ha ing he in o ma ion on hea bea s de ec ed, he ins an aneous hea a e
alues HRi(exp essed in bea s pe minu e) a e calcula ed acco ding o he o mula:
HRi[bpm]=60000
RRi[ms], (1)
whe e: RRiis he i- h in e al be ween wo consecu i e hea bea s exp essed in milliseconds.
Nex , he ea u es a e de e mined in symme ical mo ing window comp ising 21 o HRi alues:
•MEDi=median{HRi−k,. . . ,HRi+k};
•MADi=median{xi−k,. . . ,xi+k}, whe e xi= |HRi−MEDi|;
•QNTi— ep esen s he quan ile o o de 0.7 es ima ed o e 21 alues o hea a e;
•
PRP
i
—is he a io o numbe o HR alues be ween h esholds le el o 120 o 160 bpm, o
o al numbe .
whe e: iis he numbe o consecu i e hea bea s o be classi ied, and k=1. . . 10.
The alues o he addi ional pa ame e s: window wid h Nse o 21, quan ile o de se o 0.7 and
HR h esholds o 120 and 160 we e de e mined as a esul o p e iously pe o med expe imen s [54].
Fo he new classi ica ion me hod, he inpu ec o has been signi ican ly expanded. I addi ionally
comp ises se en measu es ob ained om classical analysis o HR a iabili y used in adul s’
elec oca diog aphy. This analysis includes exclusi ely sinus exci a ion, i.e., gene a ed by he
sinus-a ial node. Thus, i conce ns only sinus hy hm a iabili y, and any o he ypes o exci a ion a e
excluded and eplaced wi h a i icially gene a ed bea s. Co ec ed in his way he se ies o changes in he
subsequen RR in e als become he basis o he de e mina ion o hea a e a iabili y measu es. The
mos commonly used quan i a i e analysis me hods can be di ided in o ime, equency, ime- equency
and non-linea me hods. In he p esen ed wo k, he indices desc ibing he HR a iabili y we e used
in an unusual way as a se o ea u es allowing he de ec ion o a ial ib illa ion episodes. The ou
selec ed ea u es, ob ained in s a is ical analysis in ime domain wi hin he same mo ing window, a e
as ollows:
•The mean hea a e:
HR[bpm]=1
N
N
X
i=1
HRi. (2)
•S anda d de ia ion o ins an aneous hea a e alues:
STD_HR [bpm]=
u
1
N−1
N
X
i=1HR −HRi2. (3)
•
Roo Mean Squa e o Successi e Di e ences (RMSSD) which measu es he a iabili y wi hin a
da a se —RR in e als—acco ding o he ollowing equa ion:
RMSSD[ms]=
u
1
N−1
N−1
X
i=1
(RRi+1−RRi)2. (4)
•
Pe cen age o di e ences be ween he RR in e als ha exceed he alue o 50 ms, deno ed as
pNN50 [%]:
pNN50 =PN−1
i=1Ai
N−1∗100%, (5)

Senso s 2020,20, 765 6 o 24
whe e:
Ai=(1 when RRi+1−RRi>50
0 when RRi+1−RRi≤50 (6)
In addi ion, h ee non-linea ea u es o HRV analysis we e applied in he o m o :
•
Poinca e g aph, which is a g aphical ep esen a ion o he cu en in e al RR
i
plo ed agains
subsequen one RR
i+1
. Using he ellipse i ing echnique, in each mo ing window comp ising
21 hea bea s, wo s anda d de ia ions a e de e mined om he poin s: pe pendicula o he
eg ession line (SD1) and along he line (SD2). The SD1 desc ibes he sho - e m a iabili y o he
hea hy hm, while he SD2 e e s o he long- e m HR a iabili y.
•
Tu ning Poin s Ra io (TPR) measu es he andomness o luc ua ions wi hin a da a se , by
calcula ing he a io o he numbe o u ning poin s o he maximum numbe o possible u ning
poin s. Tu ning poin is ound i bo h he p eceding and succeeding poin s a e ei he g ea e o
lowe . I is expec ed in andom da a se o a bi a y leng h N, ha he numbe o possible u ning
poin s is (2N−4)/3, wi h a s anda d de ia ion o p(16N−29)/90.
A sepa a e g oup o ea u es used o he de ec ion o AF episodes a e pa ame e s commonly
used in e al hea a e analysis [
55
,
56
]. I u ns ou ha in pe ina al medicine qui e di e en ea u es
a e used o desc ibe he FHR a iabili y, mainly sho - e m (bea - o-bea ) [
57
]. Fo he de ec ion o
AF episodes, ou widely known sho - e m coe icien s (indices) ha e been selec ed [
58
,
59
]. They
a e cha ac e ized by high sensi i i y o changes in subsequen alues o RR in e als and hus hey
po en ially may be use ul o AF de ec ion [60–62]:
•
The Yeh’s index (DI_Yeh) whose de e mina ion s a s wi h calcula ion o he auxilia y alues d
i
ep esen ing he a io o he di e ence be ween wo successi e RR in e als o hei sum:
di=RRi−RRi+1
RRi+RRi+1
. (7)
Then, o he analyzed signal agmen , he DI_Yeh index is de ined as he s anda d de ia ion
om he ob ained coe icien s di:
DI_Yeh [ms]=
u
1
N−2
N−1
X
i=1di−d2, (8)
whe e: d =1
N−1
N−1
P
i=1
di,N—numbe o bea s se o 21.
•
The Zugaib’s a iabili y index (STV_Zug) has been de ined as an a e age o he absolu e alues
o he di e ences be ween successi e Di alues and hei median alue:
STV_Zug[ms]=1
N−1
N−1
X
i=1
|Di−Med|, (9)
whe e: Med—median alue o he D
i
se ies, N—numbe o bea s se o 21. The D
i
alue ep esen s
he a io o he absolu e alue o he di e ence be ween he hea in e als RR o hei sum:
Di=RRi+1−RRi
RRi+1+RRi
, (10)
Senso s 2020,20, 765 7 o 24
•
The Huey’s index (STV_Huey) was de ined as he sum o absolu e alues o di e ences o
subsequen ins an aneous HR alues o which he sign o di e ence was changed:
STV_Huey [bpm]=
N−1
X
i=2
k·HRi+1−HRi. (11)
whe e:
k=(1 o (HRi−1−HRi)·(HRi−HRi+1)<0
0 o (HRi−1−HRi)·(HRi−HRi+1)≥0. (12)
•
The de ini ion o de Haan’s index (STI_Haan) is based on a pola coo dina e sys em whose bo h
axes e e o RR in e als exp essed in milliseconds, and poin s ep esen he pai s o subsequen
in e als (RR
i−1
, RR
i
), as shown in Figu e 3. STI_Haan is de e mined as he in e qua ile ange o
he angles
ϕi
be ween he lines connec ing he poin wi h o igin o he coo dina e sys em, and he
X axis, designa ed o subsequen pe iods RRi:
STI_Haan =IQR(ϕi), (13)
whe e: i =1, 2 . . . N,N—numbe o bea s.
Senso s 2020, 20, 765 7 o 24
• The de ini ion o de Haan’s index (STI_Haan) is based on a pola coo dina e sys em whose bo h
axes e e o RR in e als exp essed in milliseconds, and poin s ep esen he pai s o
subsequen in e als (RRi-1, RRi), as shown in Figu e 3. STI_Haan is de e mined as he
in e qua ile ange o he angles ϕi be ween he lines connec ing he poin wi h o igin o he
coo dina e sys em, and he X axis, designa ed o subsequen pe iods RRi:
STI_Haan=IQR(), (13)
whe e: i = 1, 2…N,N – numbe o bea s.
Figu e 3. Dis ibu ion o successi e RRi in e als in he pola coo dina e sys em, illus a ing
he de ini ions o he de Haan’s index desc ibing he sho - e m HR a iabili y.
2.2. LSVM Classi ie
The p oposed me hod o au oma ed ecogni ion o AF episodes is based on a machine lea ning
app oach. To achie e high accu acy o AF de ec ion, we applied he classi ica ion ou ine ha
o igina es om he S a is ical Lea ning Theo y (SLT) [63]. The SLT is he base o he machine
lea ning me hods which a e cha ac e ized by a high gene aliza ion abili y, meaning he high
e iciency when e alua ing p e iously unknown da a i.e., da a ha ha e no been used when
designing he classi ie (also called as classi ie aining o lea ning). One o he majo achie emen s
o SLT is he S uc u al Risk Minimiza ion (SRM) p inciple, which s a es ha he quali y o machine
lea ning depends bo h on he empi ical da a and he complexi y o he model. The mos -known
p ac ical implemen a ion o he SRM is he Suppo Vec o Machine (SVM) me hodology [51,64,65].
The SVM allows o inding he hype plane in he inpu ea u e space which di ides he conside ed
classes wi h he wides ma gin o sepa a ion. The inpu da a ha a e used o de ine he ma gin a e
called he suppo ec o s. The o iginal SVM algo i hm was o mula ed as a linea ly cons ained
quad a ic op imiza ion p oblem. Consequen ly, he lea ning p ocedu e o high compu a ional
complexi y was ob ained [66–68]. As he low compu a ional cos o he de ec ion me hod is o ou
special in e es , in he p oposed solu ion he Lag angian Suppo Vec o Machine (LSVM) [50] was
applied. I s lea ning eplaces he quad a ic p og amming wi h he linea ly con e gen i e a i e
algo i hm which esul s in signi ican educ ion o he compu a ional complexi y and highe
e iciency when compa ed o he o iginal SVM [50].
Le us conside a aining se ℒ, which con ains NTRN ec o s (1),(2),⋯,()∈ℝ o
pa ame e s quan i a i ely desc ibing he HR signal, and he co esponding ou pu alue
(1),(2),⋯,()∈󰇝−1,1󰇞 de ining he absence (non-AF) ()=−1 o he p esence
()=1 o he AF episode. The linea SVM classi ica ion p oblem o ℒ can be o mula ed as he
cons ained minimiza ion: min
ℝ
×
ℝ


(,)=
2+, (14)
subjec o he condi ion: (−)+≥, (15)
Figu e 3.
Dis ibu ion o successi e RR
i
in e als in he pola coo dina e sys em, illus a ing he
de ini ions o he de Haan’s index desc ibing he sho - e m HR a iabili y.
2.2. LSVM Classi ie
The p oposed me hod o au oma ed ecogni ion o AF episodes is based on a machine lea ning
app oach. To achie e high accu acy o AF de ec ion, we applied he classi ica ion ou ine ha o igina es
om he S a is ical Lea ning Theo y (SLT) [
63
]. The SLT is he base o he machine lea ning me hods
which a e cha ac e ized by a high gene aliza ion abili y, meaning he high e iciency when e alua ing
p e iously unknown da a i.e., da a ha ha e no been used when designing he classi ie (also called as
classi ie aining o lea ning). One o he majo achie emen s o SLT is he S uc u al Risk Minimiza ion
(SRM) p inciple, which s a es ha he quali y o machine lea ning depends bo h on he empi ical da a
and he complexi y o he model. The mos -known p ac ical implemen a ion o he SRM is he Suppo
Vec o Machine (SVM) me hodology [
51
,
64
,
65
]. The SVM allows o inding he hype plane in he inpu
ea u e space which di ides he conside ed classes wi h he wides ma gin o sepa a ion. The inpu
da a ha a e used o de ine he ma gin a e called he suppo ec o s. The o iginal SVM algo i hm
was o mula ed as a linea ly cons ained quad a ic op imiza ion p oblem. Consequen ly, he lea ning
p ocedu e o high compu a ional complexi y was ob ained [
66
–
68
]. As he low compu a ional cos o
he de ec ion me hod is o ou special in e es , in he p oposed solu ion he Lag angian Suppo Vec o
Machine (LSVM) [
50
] was applied. I s lea ning eplaces he quad a ic p og amming wi h he linea ly
con e gen i e a i e algo i hm which esul s in signi ican educ ion o he compu a ional complexi y
and highe e iciency when compa ed o he o iginal SVM [50].
Senso s 2020,20, 765 8 o 24
Le us conside a aining se
L
, which con ains N
TRN
ec o s
x0(1)
,
x0(2)
,
· · ·
,
x0(NTRN)∈
R
o pa ame e s quan i a i ely desc ibing he HR signal, and he co esponding ou pu alue
y0(1)
,
y0(2)
,
· · ·
,
y0(NTRN)∈{−1, 1}
de ining he absence (non-AF)
y0(n)=−
1 o he p esence
y0(n)=
1 o he AF episode. The linea SVM classi ica ion p oblem o
L
can be o mula ed as he
cons ained minimiza ion:
min
RN×RN SVM(w,ξ)=wTw
2+γ1Tξ, (14)
subjec o he condi ion:
D(X0w−1w0)+ξ≥1, (15)
and:
ξ≥0, (16)
whe e w∈R and w0∈Ra e he pa ame e s o wo bounding planes:
(xTw−w0= +1,
xTw−w0=−1. (17)
sepa a ing he aining da a wi h he ma gin
2
kwk
,
γ≥
0 is a cons an ha con ols he ade-o be ween
model simplici y and model ma ching o he aining da a,
1∈RN
deno es he ec o wi h all en ies
equal o one,
ξ∈RN
is he ec o o he slack (e o ) a iables, ha allow he classes o be bounded
wi h he maximum “so ” ma gin i.e., wi h he minimum sum o de ia ions o aining e o s and
maximum ma gin o he co ec ly classi ied ec o s,
D=diag(y0(1),y0(2),· · · ,y0(N)) ∈RN×N
is
a diagonal ma ix wi h class labels along i s diagonal,
X0="xT
0(1).
.
.xT
0(2).
.
.· · · .
.
.xT
0(N)#T
∈RN×
is he
ma ix o aining inpu da a.
In con as o SVM, he Lag ange suppo ec o machine maximizes he ma gin be ween he
sepa a ing planes wi h espec o bo h o ien a ion (
w
) and loca ion o he planes (
w0
). Mo eo e , in he
LSVM c i e ion unc ion he sum o he slack a iables
1Tξ
(14) is eplaced wi h he sum o squa es
ξTξ
making he cons ain (16) edundan . Consequen ly, he linea LSVM is de ined as minimiza ion
p oblem o he unc ional:
min
R ×R×RN pLSVM(w,b,ξ)=1
2wTw+w2
0+γ
2ξTξ, (18)
subjec o he cons ain (17). Mo eo e , he dual p oblem o (20):
min
RN
+
dLSVM(λ)=1
2λTQλ−1Tλ, (19)
whe e:
Q=I
γ+HHT∈RN×N
,
H=D"X0
.
.
.−1#∈RN×( +1)
and
I∈RN×N
is he iden i y ma ix, has he
non-nega i i y cons ain only λ∈RN
+.
The solu ion can be de e mined based on he Ka ush-Kuhn-Tucke necessa y and su icien
op imali y condi ions [
50
]. This leads o a linea ly con e gen i e a i e scheme which cons i u es he
LSVM me hod:
λ(k+1)=Q−11+Qλ(k)−1−αλ(k)+, (20)
whe e: kis he i e a ion index and
Qλ(k)−1−αλ(k)+∈RN
is he ec o wi h all o i s nega i e
componen s se o ze o.
Senso s 2020,20, 765 9 o 24
The abo e algo i hm is con e gen o any s a ing poin i :
0<α< 2
γ. (21)
The pa ame e s o he bounding planes ha sepa a e he classes can be eco e ed om he solu ion
o he dual p oblem by using he ollowing o mulas:











w=X0TDλ,
w0=−1TDλ,
ξ=λ
γ.
(22)
The LSVM app oach educes signi ican ly he ime necessa y o pe o m calcula ions o he
op imal (w,w0)while p ese ing high classi ica ion e iciency o he o iginal SVM lea ning.
The basic LSVM is a linea classi ie , hus o handle he non-linea ly sepa able da a he so-called
“ke nel ick” is equi ed. I is based on he p emise ha he complex non-linea classi ica ion p oblem
will be linea ly sepa able in some ea u e space o highe dimensionali y and in ol es he non-linea
ans o ma ion o inpu da a in he high-dimensional space. The linea sepa a ing plane
xTw−w0=
0
is hen eplaced by he non-linea su ace:
KxT
e,XT
0eDλ=0, (23)
whe e: xe="xT.
.
.−1#T
,X0e="X0
.
.
.−1#, and Kis he ke nel unc ion. Rede ini ion o he dual p oblem
(19) by using:
Q=I
γ+DKX0e,XT
0eD, (24)
which makes he LSVM i e a i e schema (20) alid o any posi i e semide ini e ke nel
K
[
50
]. In he
p oposed app oach we used he adial (Gaussian) ke nel:
K(x,y)=exp−χkx−yk2, whe e χ > 0. (25)
2.3. Pe o mance E alua ion
The pe o mance (gene aliza ion abili y) o he AF classi ica ion was e alua ed by he classi ica ion
accu acy (CA), de ined as he pe cen age o co ec ly classi ied cases in he es ing se (da a which was
no used du ing classi ie aining). As he AF de ec ion p ocess is a kind o diagnos ic es gi ing
nega i e o posi i e esul s, we also measu ed he classi ica ion quali y using sensi i i y (Se), speci ici y
(Sp), posi i e (PPV) and nega i e (NPV) p edic i e alue, calcula ed o he es ing da a se using
a con usion ma ix. Since e alua ion o he classi ica ion e iciency is di icul when analyzing all he
p ognos ic measu es simul aneously, we calcula ed also he F-Sco e (FS), de ined as a ha monic mean
o Se and PPV:
FS [%]=2·Se·PPV
Se +PPV. (26)
2.4. Hea bea Agg ega ion
The agg ega ion o he classi ied hea bea s should lead o emo al o acciden al changes o
hea bea s a us, and hus o ob ain mo e eliable in o ma ion on AF episodes. This p ocess is con olled
by wo pa ame e s: he window wid h and pe cen age h eshold. Each hea bea s a us is alida ed
in symme ical window by checking i he numbe o he hea bea s wi h he same s a us exceeds
he pe cen age h eshold. We de ined he pe cen age h eshold o he AF s a us, as he numbe o
hea bea s classi ied as AF o he numbe o all bea s in he analyzed window. I he h eshold is
exceeded he AF s a us emains unchanged, o he wise is se o non-AF. The op imal alues o he
Senso s 2020,20, 765 16 o 24
o compa e ou esul s wi h hose epo ed ea lie . On his esea ch ma e ial he LSVM classi ie , ed wi h
six een ea u es desc ibing he hea a e a iabili y, ensu ed he sensi i i y 98.10%, speci ici y 97.50%,
posi i e p edic i e alue 96.67%, classi ica ion accu acy 97.75 and F-Sco e 97.38%. A e agg ega ion
s age hose pe o mance measu es inc eased o 98.94%, 98.80%, 98.39%, 98.86% and 98.66 espec i ely.
Especially, signi ican inc ease o he PPV alue was no ed a lowe numbe o alse AF de ec ions.
Ob ained pe o mance is highe han ha p o ided by p e iously de eloped classi ica ion me hod
based on linea classi ie , whe e Se =95.42% and PPV =94.97% [
53
]. Thus, he p oposed mo e ad anced
me hod has be e abili y o de ec he ue occu ences o AF and p o ides lowe numbe o alse
a hy hmias. I should be emphasized ha bo h in case o simple linea classi ie and ad anced LSVM
app oach he agg ega ion s age signi ican ly imp o es he e iciency o AF episodes de ec ion. Du ing
his s udy he HR ea u es ha e been de e mined in 21 bea s wide window [
54
]. Ne e heless, he
esul s ob ained so a by he au ho s a e be e han hose p o ided by o he au oma ed AF de ec ion
me hods epo ed ea lie , e alua ed using he MIT-BIH AF da abase (Table 6).
The mos ob ious ea u e o measu e he RR i egula i y seems o be he di e ence be ween
successi e in e als RR. In [
33
] he s anda d densi y his og am o RR di e ences was p epa ed as
a empla e—using he anno a ed AF episodes, and hen he simila i ies be ween he densi y his og ams
o he es da a and he s anda d densi y his og am we e es ima ed using he s anda d coe icien o
a ia ion (CV es ) and Kolmogo o -Smi no (K-S) s a is ical es . Fo he op imal h eshold o he es
ou pu ound by ROC, he K-S es showed Se =94.4%, Sp =97.2%, and PPV =96.1%, o he window
leng h o 100 in e als. De ec ion o AF episodes based on densi y his og am o RR di e ences was also
de eloped by Huang e al. [
74
]. The p oposed mo e ad anced analysis included wo s eps: AF e en
de ec ion using he del a RR in e al dis ibu ion di e ence cu e and AF e en classi ica ion. Using
he ROC cu es o de e mining he h eshold o he K-S es , he au ho s ha e achie ed he highe
Se and Sp (96.1% and 98.1%, espec i ely) o he MIT-BIH AF da abase. The algo i hm desc ibed
in [
34
] has been based on he ex ac ion o simple geome ic ea u es de e mined om he his og am o
RR p ema u i y, compu ed as he pe cen age a ia ion om he cu en hea a e and he di e ences
be ween wo successi e RR in e als. The ea u e se included: numbe o nonemp y bins, main
dis ibu ion wid h, di e ence be ween mean and median and geome ic es o bimodali y. The sco e
sys em was in oduced o inally classi y en-second segmen as non-AF o AF pe iod. Using he
MIT-BIH AF da abase, he RR p ema u i y algo i hm p o ided he sensi i i y o 91% and PPV o 92%,
while o he RR di e ences Se =92%, and PPV=78%. The map ha plo s RR in e als e sus RR
di e ences was p oposed in [
35
]. Fo e e ence, a window was labeled as ue AF episode i 1/2 o
in e als in he window we e anno a ed as AF. Th eshold alue o disc imina i e pa ame e —nonemp y
cell—was de e mined by ROC, and led o sensi i i y 95.8% and speci ici y 96.4% o he op imal
window leng h o 128 in e als.
Ano he linea ans o ma ion o RR in e als o di e en ia e be ween AF episodes and no mal
sinus hy hm was desc ibed in [
44
]. The p oposed algo i hm s a s wi h p ep ocessing (es ima ing
he RR end and il e ing he ec opic bea s), hen wo unc ions o measu e he RR i egula i y a e
calcula ed, and inally usion o hese signals is used o de ec ion o AF episodes elying on he ixed
h eshold. Based on he dis ibu ion o he usion signal ou pu o AF and non-AF bea s, he op imal
de ec ion h eshold wi h iden ical alues o sensi i i y and speci ici y was se . Using he MIT-BIH AF
he au ho s epo ed e y high alues o sensi i i y (97.1%) and speci ici y (98.3%). Fo ha app oach
a e y sho window o 8 bea s was ound as op imal. The au ho s unde line ha he p oposed me hod
can be ma ched o de ec e y sho episodes, bu i is a he expense o lowe speci ici y.
The nex app oach applying only RR in e al was based on he a iance o no malized RR in e als
o e en-second sliding window [
29
]. Acco ding o he au ho s, he no maliza ion imp o es he de ec ion
pe o mance. The au ho s used he mo phology independen QRS de ec o o compu e RR in e als and
a iance, and hen hey smoo hed he esul ing classi ica ions, using simple majo i y o ing scheme o e
600 bea windows, o u he obus ness. Howe e , he es s ca ied ou on he MIT-BIH AF da abase
showed ha he p oposed algo i hm has sensi i i y o 96% bu speci ici y only o 89%, which is su icien

Senso s 2020,20, 765 17 o 24
o AF sc eening only. The mo e ad anced no maliza ion o RR in e als by an a ine ans o ma ion
was p oposed in [
30
]. In e al i egula i y was ep esen ed by he spa seness o no malized in e al
p obabili y dis ibu ion which was measu ed by he no malized en opy calcula ed in he window.
The au ho s used h ee leng hs o he window (30, 50 and 70 bea s) o show hei in luence on he
no maliza ion. The ROC analysis enabled hem o ind he h eshold alue o he en opy classi ie
ou pu , ha ensu ed he ollowing alues o Se, Sp, PPV and CA: 96.39%, 96.38%, 95.19%, 96.38%.
Table 6.
An o e iew o published esul s o exis ing AF de ec ion me hods using he MIT-BIH A ial
Fib illa ion Da abase.
Me hod Fea u es Window Key Techniques Resul s
Se Sp PPV CA
Ta eno e al.
2001 [33]RR di e ence 100 bea s His og am, Kolmogo o -Smi no
es , ROC. 94.4 97.2 96.1 –
Huang e al.
2011 [74]RR di e ence 23 bea s His og am, SD analysis,
Kolmogo o -Smi no es . 96.1 98.1 – –
Pe ucci e al.
2005 [34]
RR di e ence, RR
p ema u i y 60 s Geome ic measu es o his og am,
Sco e sys em. 92 – 92 –
Lian e al.
2011 [35]
RR in e al, RR
di e ence 128 bea s Mapping RR in e als e sus RR
di e ences, h esholds. 95.8 96.4 – –
Pe enas e al.
2015 [44]RR in e al 8 bea s Th esholds 97.1 98.3 – –
Logan e al.
2005 [29]RR in e al 600 bea s Va iance o no malized RR in e al,
simple majo i y o ing. 96 89 – –
Islam e al.
2016 [30]RR in e al 70 bea s No maliza ion o RR in e als by an
a ine ans o ma ion. 96.39 96.38 95.19 96.38
Babaeizadeh.
e al. 2009 [16]
RR in e al P-wa e
measu emen s -S a iona y i s -o de Ma ko
p ocess, decision ee. 94 99 98 –
Zhou e al.
2014 [36]RR in e al 127 bea s
Mapping he RR sequence in o
symbolic one, Shannon en opy,
ROC.
96.89 98.25 97.62 97.67
Zhou e al.
2015 [75]RR in e al 127 bea s Online e sion o [36] 97.37 98.44 97.89 97.99
Cui e al. 2017
[37]RR in e al 150 bea s Mapping he RR sequence in o
symbolic one, dissimila i y index. 97.04 97.96 – 97.78
Dash e al.
2009 [38]RR di e ence 128 bea s Tu ning poin s, RMSSDD, Shannon
en opy, ROC. 94.4 95.1 – –
Lake e al.
2011 [15]RR di e ence 12 bea s Coe icien o sample en opy
(CoSEn), ROC. 91 94 – –
Kennedy e al.
2016 [32]RR di e ence 30 bea s Random o es , k-nea es neighbo . 97.6 98.3 92.1 –
Ande sen e al.
2017 [39]
RR in e al
ECG ea u es
300 bea s
30 s
Sample en opy, Shannon en opy,
CoSEn, SVM.
96.81
94.27
96.20
98.84 –96.45
96.68
Kuma e al.
2018 [76]ECG ea u es 1000
samples Wa ele ans o m, Random o es . 95.8 97.8 – 96.8
Nu yani e al.
2015 [40]RR di e ence SVM wi h adial basis unc ion. 95.81 98.44 – 97.50
Colloca e al.
2013 [41]
RR di e ence
Median HR 30 En opy, SVM wi h adial basis
unc ion 99.20 - 59.33 86.60
Faus e al.
2018 [46]- 100
Deep Recu en Neu al Ne wo k
(RNN) wi h Long Sho -Te m
Memo y (LSTM).
98.51 98.32 – 98.67
Ande sen e al.
2019 [45]- 31
Deep lea ning combining wi h he
con olu ional- and Recu en -Neu al
Ne wo ks.
98.98 96.95 95.76 97.80
W obel e al.
2018 [53]
HR i egula i y
ea u es 21 Linea classi ie 95.42 96.12 94.97 95.62
P oposed
me hod 2019
HR i egula i y
ea u es 21 LSVM 98.94 98.39 98.86 98.66
Senso s 2020,20, 765 18 o 24
The sequence o RR in e al is assumed o be con olled by a s a iona y i s -o de Ma ko p ocess
cha ac e ized by a ansi ion p obabili y ma ix as i was p oposed o he i s ime by Moody and
Ma k [
4
] o au oma ed de ec ion o he AF episodes. As Ma ko sco e e lec s he ela i e likelihood
o RR in e als sequence in AF episode e sus no-AF one, i can be compa ed o he ixed h eshold
applied o classi y he sequences [
16
]. In ha wo k he du a ion s a is ics wi h combining all eco ds
in o one p o ided he alues o Se, Sp, and PPV: 94%, 98% and 97%. Fu he mo e, a possibili y
o imp o emen o he AF episode de ec ion by addi ional in o ma ion on ECG mo phology was
in es iga ed. When he RR in e al Ma ko sco e was comple ed wi h he wo P-wa e measu emen s:
he loca ion (P-R in e al a ia ion) and he mo phology (simila i y be ween wo consecu i e P-wa es)
he Sp and PPV inc eased o 99%, while he Se emained unchanged. As he au ho concluded
educ ion o he alse posi i e cases is a esul o de ec ing alid P-wa es on he ECG eco ding wi h
i egula hy hm o he han AF. Ne e heless, he sensi i i y which de ines he abili y o de ec ue AF
occu ences was signi ican ly lowe han he alue achie ed by ou me hod.
In [
37
] he changes in RR du a ion du ing he sequence ha e been ep esen ed as he bina y
wo ds, whe e alue o 1 co esponds o inc ease o in e al du a ion, and 0 means no change o
a dec ease. Then, he es ing segmen is classi ied by compa ing i s in o ma ion-based dissimila i y
index wi h hose ob ained o he empla es o AF episode and no mal sinus hy hm. Pa ame e s
o he classi ica ion model: he numbe o bi s, window leng h and he shi o he dissimila i y
compa ison bounda y we e op imized o p o ide he bes pe o mance exp essed by sensi i i y o
97.04%, speci ici y o 97.96% and classi ica ion accu acy o 97.78%. Ano he app oach based on
mapping he RR sequence in o symbolic one was p oposed in [
36
]. The de ec ion p oceeds in h ee
s ages: he ini ial, whe e a RR in e al sequence is p e-p ocessed wi h nonlinea and in ege il e s,
he second, whe e he in o ma ion o he RR in e al changes is con e ed in o symbolic sequence, and
inal, whe e he Shannon en opy is calcula ed o disc imina e whe he o no he sequence ela es o
AF episode. Op imal disc imina ion h eshold o Shannon En opy was ob ained by ROC analysis.
The RR sequences o 127 bea s we e p ocessed. The ollowing alue o Se, Sp, PPV and CA we e:
96.89% 98.25% 97.62% 97.67%, while o he online e sion o he algo i hm: 97.37%, 98.44%, 97.89%
and 97.99% [75].
The en opy concep , e e ing o he diso de o unce ain y o a p ocess, was used in many
me hods o au oma ed de ec ion o AF episodes, usually being included in he ea u e se , bu also as
he only measu e o RR i egula i y. Th ee s a is ics desc ibing andomness, a iabili y and complexi y
o he RR in e al ime se ies we e p oposed in [
38
]. The u ning poin s a io, oo mean squa e o
successi e RR di e ences and Shannon en opy we e employed o cha ac e ize he a ial ib illa ion.
Using he h esholds and da a segmen o 128 bea s de e mined by ROC he sensi i i y o 94.4%
and speci ici y o 95.1% we e achie ed o he signals om he MIT-BIH A ial Fib illa ion Da abase.
The op imized sample en opy measu e, called coe icien o sample en opy (CoSEn), being able o
de ec e y sho AF episodes (e en 12 bea s) was p oposed by Lake and Moo man [
15
]. This ea u e
es ima ed he p obabili y ha sho empla es will ma ch wi h o he segmen s wi hin he analyzed
RR in e al ime se ies. Tha p ocess was con olled by wo pa ame e s: he empla e leng h and he
ole ance ma ching, whose op imal alues we e es ablished by ROC analysis. The au ho s ound he
cu o CoSEn alue, which di e en ia e be ween AF and no mal sinus hy hms, o p o ide a sensi i i y
o 91% and a speci ici y o 94%. In [
32
] he CoSEn was combined wi h h ee o he ea u es: he
coe icien o a iance, oo mean squa e o he successi e di e ences, and median absolu e de ia ion.
The de ec ion pe o mance o each i egula i y measu e was assessed indi idually by ROC analysis,
and CoSEn pe o med bes . The abo e pa ame e s we e also used as he inpu ea u es se o
wo classi ie s: andom o es (RF) and k-nea es neighbo . Bo h classi ica ion models signi ican ly
imp o ed he Sp and PPV alues o e CoSEn, bu wi h subs an ial d op in Se. The bes speci ici y o
98.3% and PPV o 92.1% we e p o ided by RF model, while he sensi i i y achie ed he bes alue
97.6% when using CoSEn as he only disc imina i e ea u e. Those esul s we e epo ed o he
combined da abase, wi h MIT-BIH AF among o he s. When only MIT-BIH AF da abase was employed,
Senso s 2020,20, 765 19 o 24
he au ho s no iced signi ican educ ion o de ec ion pe o mance o CoSEn and median absolu e
de ia ion, exp essed by smalle a ea unde he ROC cu e.
Th ee en opy ea u es: sample en opy, coe icien o sample en opy, Shannon en opy, oge he
wi h wo linea measu es: oo mean squa e and no malized oo mean squa e o successi e di e ences
cons i u ed he se o RR i egula i y measu es being es ed in [
39
]. Apa om ha HR app oach,
he au ho s in es iga ed he ECG-d i en app oach wi h wo ea u es: peak- o-a e age powe a io
and log-ene gy en opy, ex ac ed om 2-le el s a iona y wa ele ans o m coe icien s. The suppo
ec o machine was used o classi ica ion in bo h app oaches. Th ee di e en segmen leng hs we e
e alua ed: 60, 100, 300 bea s o HR and 10, 15, 30 s o ECG da a. Like in [
35
], any segmen con aining
a leas o 50% AF bea s was labeled as ue AF when p ocessing ECG. Fo HR app oach his le el was
educed o 30%. The longes windows p o ided he bes esul s o bo h HR (Se 96.81%, Sp 96.20%, CA
96.45%) and ECG (94.27%, 98.84%, 96.98%, espec i ely) app oaches.
The pe o mance o AF de ec ion using he ea u es ex ac ed exclusi ely om ECG signals was
assessed by Kuma [
76
]. As he da a was aken om MIT-BIH da abase, he ob ained esul s may
be ela ed o hose p o ided by he HR-based me hods desc ibed he e. The p oposed classi ica ion
me hod employed wo ea u es: he log-ene gy en opy and pe mu a ion en opy compu ed om he
sub-band signals ob ained using lexible analy ic wa ele ans o m. Using andom o es classi ie ,
he au ho s epo ed sensi i i y o 95.8%, speci ici y o 97.8% and accu acy o 96.8%.
Two ea u es: he a e age o RR di e ences in a de ined du a ion, and he s anda d de ia ion o
di e ences in a de ined du a ion, we e examined as he inpu s o he classi ie based on SVM wi h
adial basis unc ion in [
40
]. The p oposed me hod showed ollowing pe o mance on he MIT-BIH AF
da abase: Se =95.81%, Sp =98.44% and CA =97.50%. The same SVM classi ie was employed in [
41
].
The inpu se comp ised mo e RR in e al ea u es: median hea a e, minimum RR in e al, mean RR
in e al, a ious en opy measu es, and di e ence i egula i y measu e. The MIT-BIH AF da abase
was used in ha s udy, bu only du ing he aining s age, when e y good esul s ha e been achie ed
(sensi i i y =99.07%, PPV =98.27%, accu acy =98.84). When es ing on a se ies o 200 signals om he
MIT-BIH A hy hmia da abase, he bes accu acy was 86.60% o he window o 30 bea s, sensi i i y
eached 99.20%, bu PPV was only 59.33%.
The newes app oach o au oma ed AF de ec ion p oposed in [
46
] and [
45
] has been based on deep
lea ning algo i hm, which aims o de elop he classi ica ion model by using all a ailable in o ma ion
om he inpu . In case o AF de ec ion om he ECG signals i means no need o ex ac ion o he
ea u e nei he om aw ECG no om RR in e al ime se ies. In hose wo ks he RR da a om
MIT-BIH AF we e pa i ioned using sliding window o 100 bea s [
46
] o 31 bea s bu shi ed wi h
10 bea s [
45
], and hen ed o Recu en Neu al Ne wo k wi h Long Sho -Te m Memo y. In bo h
wo ks e y good esul s we e epo ed: Se =98.51%, Sp =98.32%, CA =98.67% in [
46
], and 98.98%,
96.95%, 97.80% wi h PPV o 95.76% in [
45
], when median il e ing was used as pos p ocessing o
imp o e he de ec ion pe o mance. I should be no ed, howe e ha de elopmen o he deep lea ning
algo i hm has been enabled by ecen ad ances in pa allel compu ing on G aphics P ocessing Uni s.
The compu a ional complexi y o deep lea ning model is much highe han adi ional ea u e-based
classi ie . This limi s i s applica ion in wea able de ices o long e m moni o ing wi h online AF
de ec ion, like w is band moni o in a o m o w is b acele .
5. Conclusions
Despi e se ious medical consequences, a ial ib illa ion is s ill an unde es ima ed clinical and
diagnos ic p oblem. Recogni ion o his o m o a hy hmia equi es a long- e m moni o ing o he
hea hy hm, since e y o en pa ien s a e asymp oma ic. Mo eo e , he AF episodes can occu
acciden ally and may las om minu es o hou s. The objec i i y and e iciency o he isual analysis
o long- e m eco dings can be imp o ed by au oma ed AF de ec ion.
The pape p oposed a LSVM-based app oach wi h an o iginal aining s age which ou pe o ms
o he au oma ed AF de ec ion me hods based on he in o ma ion on bea - o-bea i egula i y p oposed
Senso s 2020,20, 765 20 o 24
in he li e a u e. Ou me hod ensu es a e y high e iciency in de ec ion o ue AF episodes exp essed
by sensi i i y o 98.94%, and a he same ime low numbe o alse episodes, as he posi i e p edic i e
alue eached 98.36%. These esul s we e achie ed wi h pos -p ocessing agg ega ion s age, showing
a need o inal e i ica ion o he classi ied bea s. I also u ned ou ha ex ending he inpu ea u e
ec o o include pa ame e s desc ibing he hea i egula i y and being ypically used in he e al hea
a e analysis, had posi i e e ec on classi ica ion e iciency. Designing he LSVM-based classi ie o
deal wi h such la ge amoun o da a like om MIT-BIH AF Da abase led us o aluable conclusion.
No he size o he aining se is o c ucial impo ance, bu he occu ence o he inpu ec o s
con aining he quan i a i e pa ame e s o HR a iabili y desc ip ion which allow sepa a ing he AF
and non-AF hea bea s wi h he wides sepa a ion ma gin (suppo ec o s), hus gua an eeing he
bes classi ica ion quali y.
Au ho Con ibu ions:
Concep ualiza ion, R.C, K.H. and J.W.; Da a cu a ion, A.M., R.M and R.K.; Me hodology,
R.M., T.K., R.K. and J.J.; So wa e, R.C., J.W. and A.M.; Supe ision, K.H. and R.C.; Valida ion, J.W., T.K., M.J. and
J.M.L.; W i ing-o iginal d a , K.H. and R.C.; W i ing- e iew & edi ing, K.H., M.J., J.J. and J.M.L. All au ho s ha e
ead and ag eed o he published e sion o he manusc ip .
Funding: This esea ch ecei ed no ex e nal unding.
Acknowledgmen s:
This scien i ic esea ch wo k was suppo ed by he Na ional Science Cen e and
he Na ional Cen e o Resea ch and De elopmen in Poland unde he g an s 2017/27/B/ST6/01989 and
STRATEGMED2/269343/18/NCBR/2016, as well as om he Minis y o Science and Highe Educa ion unding o
s a u o y ac i i ies (BK-2019, BK-2020).
Con lic s o In e es : The au ho s decla e no con lic o in e es .
Re e ences
1.
Lau, J.K.; Low es, N.; Neubeck, L.; B iege , D.B.; Sy, R.W.; Galloway, C.D.; Albe , D.E.; F eedman, S.B. iPhone
ECG applica ion o communi y sc eening o de ec silen a ial ib illa ion: A no el echnology o p e en
s oke. In . J. Ca diol. 2013,165, 193–194. [C ossRe ]
2.
G ond, M.; Jauss, M.; Hamann, G.; S a k, E.; Vel kamp, R.; Naba i, D.; Ho n, M.; Weima , C.; Köh mann, M.;
Wach e , R.; e al. Imp o ed De ec ion o Silen A ial Fib illa ion Using 72-Hou Hol e ECG in Pa ien s Wi h
Ischemic S oke: A P ospec i e Mul icen e Coho S udy. S oke
2013
,44, 3357–3364. [C ossRe ] [PubMed]
3. Camm, A.J. A ial Fib illa ion and Risk. Clin. Ca diol. 2012,35, S1–S2. [C ossRe ] [PubMed]
4.
Moody, G. A new me hod o de ec ing a ial ib illa ion using RR in e als. Compu . Ca diol.
1983
, 227–230.
5.
Goldbe ge , A.L.; Ama al, L.A.; Glass, L.; Hausdo , J.M.; I ano , P.C.; Ma k, R.G.; Mie us, J.E.; Moody, G.B.;
Peng, C.K.; S anley, H.E. PhysioBank, PhysioToolki , and PhysioNe : componen s o a new esea ch esou ce
o complex physiologic signals. Ci cula ion 2000,101, e215–e220. [C ossRe ]
6.
The MIT-BIH A ial Fib illa ion Da abase–PhysioNe . A ailable online: h ps://physione .o g/physiobank/
da abase/a db/(accessed on 20 May 2018).
7.
Fi zmau ice, D.A.; Hobbs, F.R.; Jowe , S.; Man , J.; Mu ay, E.T.; Holde , R.; Ra e y, J.P.; B yan, S.; Da ies, M.;
Lip, G.Y. Sc eening e sus ou ine p ac ice in de ec ion o a ial ib illa ion in pa ien s aged 65 o o e :
Clus e andomised con olled ial. BMJ 2007,335, 383. [C ossRe ]
8.
Rawenwaaij-A s, C.; Kallee, L.; Hopman, J. Task Fo ce o he Eu opean Socie y o Ca diology and he
No h Ame ican Socie y o Pacing and Elec ophysiology. Hea a e a iabili y. S anda ds o measu emen ,
physiologic in e p e a ion, and clinical use. Ci cula ion
1996
; 93: 1043–1065. In e n. Med.
1993
,118, 436–447.
9.
Des eghe, L.; Raymaeke s, Z.; Lu in, M.; Vijgen, J.; Dilling-Boe , D.; Koopman, P.; Schu mans, J.;
Vanduynho en, P.; Dendale, P.; Heidbuchel, H. Pe o mance o handheld elec oca diog am de ices
o de ec a ial ib illa ion in a ca diology and ge ia ic wa d se ing. Ep Eu opace 2016,19, 29–39.
10.
Habe man, Z.C.; Jahn, R.T.; Bose, R.; Tun, H.; Shinbane, J.S.; Doshi, R.N.; Chang, P.M.; Saxon, L.A. Wi eless
Sma phone ECG Enables La ge-Scale Sc eening in Di e se Popula ions. J. Ca dio asc. Elec ophysiol.
2015
,
26, 520–526. [C ossRe ]
11.
Lee, J.; Reyes, B.A.; McManus, D.D.; Mai as, O.; Chon, K.H. A ial ib illa ion de ec ion using an iPhone 4S.
IEEE T ans. Biomed. Eng. 2012,60, 203–206. [C ossRe ]
Senso s 2020,20, 765 21 o 24
12.
Vaid, J.; Poh, M.Z.; Saleh, A.; Kalan a ian, S.; Poh, Y.K.C.; Ra ael, A.; Ruskin, J. Diagnos ic accu acy o a no el
mobile applica ion (Ca diio Rhy hm) o de ec ing a ial ib illa ion. J. Ame ican Coll. Ca diol.
2015
,65, A361.
[C ossRe ]
13.
Glo ze , T.V.; Hellkamp, A.S.; Zimme man, J.; Sweeney, M.O.; Yee, R.; Ma inchak, R.; Cook, J.; Pa aschos, A.;
Lo e, J.; Radosla ich, G.; e al. A ial high a e episodes de ec ed by pacemake diagnos ics p edic dea h
and s oke: epo o he A ial Diagnos ics Ancilla y S udy o he MOde Selec ion T ial (MOST). Ci cula ion
2003,107, 1614–1619. [C ossRe ] [PubMed]
14.
Hind icks, G.; Pokushalo , E.; U ban, L.; T
á
bo sk
ý
, M.; Kuck, K.-H.; Lebede , D.; Riege , G.; Pü e ellne , H.;
on behal o he XPECT T ial In es iga o s. Pe o mance o a New Leadless Implan able Ca diac Moni o in
De ec ing and Quan i ying A ial Fib illa ion Resul s o he XPECT T ial. Ci c. A hy hmia Elec ophysiol.
2010,3, 141–147. [C ossRe ]
15.
Lake, D.E.; Moo man, J.R. Accu a e es ima ion o en opy in e y sho physiological ime se ies: he p oblem
o a ial ib illa ion de ec ion in implan ed en icula de ices. Am. J. Physiol. Ci c. Physiol.
2011
,300,
H319–H325. [C ossRe ] [PubMed]
16.
Babaeizadeh, S.; G egg, R.E.; Hel enbein, E.D.; Lindaue , J.M.; Zhou, S.H. Imp o emen s in a ial ib illa ion
de ec ion o eal- ime moni o ing. J. Elec oca diol. 2009,42, 522–526. [C ossRe ] [PubMed]
17.
Ch is o , G.B.I. Au oma ic de ec ion o a ial ib illa ion and lu e by wa e ec i ica ion me hod. J. Med.
Eng. Technol. 2001,25, 217–221. [C ossRe ]
18.
Ch is o , I.; Bo olan, G.; Daskalo , I. Sequen ial analysis o au oma ic de ec ion o a ial ib illa ion and
lu e . Compu . Ca diol. 2001,28, 293–296.
19.
Hind icks, G.; Pio kowski, C. A ial ib illa ion moni o ing: ma hema ics mee s eal li e. Ci cula o y
2012
,
126, 791–802. [C ossRe ]
20.
Ha gi ai, S. Is i possible o de ec a ial ib illa ion by simply using RR in e als? Compu . Ca diol.
2014
,41,
897–900.
21.
Slocum, J.; Sahakian, A.; Swi yn, S. Diagnosis o a ial ib illa ion om su ace elec oca diog ams based on
compu e -de ec ed a ial ac i i y. J. Elec oca diol. 1992,25, 1–8. [C ossRe ]
22.
Bonomi, A.; Schippe , F.; Ee ikainen, L.; Ma ga i o, J.; Aa s, R.; Babaeizadeh, S.; De Mo ee, H.; Dekke , L.
A ial Fib illa ion De ec ion Using Pho o:ple hysmog aphy and Accele a ion Da a a he W is . In P oceedings
o he 2016 Compu ing in Ca diology Con e ence (CinC), Vancou e , BC, Canada, 11–14 Sep embe 2016;
pp. 081–339.
23.
Lu, S.; Zhao, H.; Ju, K.; Shin, K.; Lee, M.; Shelley, K.; Chon, K.H. Can pho ople hysmog aphy a iabili y
se e as an al e na i e app oach o ob ain hea a e a iabili y in o ma ion? J. Clin. Moni . Compu .
2008
,22,
23–29. [C ossRe ] [PubMed]
24.
Tamu a, T.; Maeda, Y.; Sekine, M.; Yoshida, M. Wea able Pho ople hysmog aphic Senso s—Pas and P esen .
Elec onics 2014,3, 282–302. [C ossRe ]
25.
Hu nanen, T.; Leh onen, E.; Tadi, M.J.; Kuusela, T.; Ki iniemi, T.; Sa as e, A.; Vasanka i, T.; Ai aksinen, J.;
Koi is o, T.; Pankaala, M. Au oma ed De ec ion o A ial Fib illa ion Based on Time–F equency Analysis o
Seismoca diog ams. IEEE J. Biomed. Heal. In o m. 2017,21, 1233–1241. [C ossRe ] [PubMed]
26.
W obel, J.; Jezewski, J.; Ho oba, K.; Pawlak, A.; Czabanski, R.; Jezewski, M.; Po wik, P. Medical Cybe -Physical
Sys em o Home Teleca e o High-Risk P egnancy: Design Challenges and Requi emen s. J. Med. Imaging
Heal. In o m. 2015,5, 1295–1301. [C ossRe ]
27.
Jezewski, J.; Pawlak, A.; Ho oba, K.; W obel, J.; Czabanski, R.; Jezewski, M. Selec ed design issues o he
medical cybe -physical sys em o elemoni o ing p egnancy a home. Mic op ocess. Mic osys .
2016
,46,
35–43. [C ossRe ]
28.
Roj, D.; Ma onia, A.; Sobo nicka, E.; W obel, J. Ha dwa e design issues and unc ional equi emen s o
sma w is band moni o o silen a ial ib illa ion. In P oceedings o he 2017 MIXDES—24 h In e na ional
Con e ence “Mixed Design o In eg a ed Ci cui s and Sys ems”, Bydgoszcz, Poland, 22–24 June 2017;
pp. 596–600.
29.
Logan, B.; Healey, J. Robus de ec ion o a ial ib illa ion o a long e m elemoni o ing sys em. Compu .
Ca diol. 2005,32, 619–622.
30.
Islam, S.; Ammou , N.; Alajlan, N.; Aboalsamh, H. Rhy hm-based hea bea du a ion no maliza ion o a ial
ib illa ion de ec ion. Compu . Boil. Med. 2016,72, 160–169. [C ossRe ]

Senso s 2020,20, 765 22 o 24
31.
Ghod a i, A.; Mu ay, B.; Ma inello, S. RR in e al analysis o de ec ion o A ial Fib illa ion in ECG moni o s.
In P oceedings o he 2008 30 h Annual In e na ional Con e ence o he IEEE Enginee ing in Medicine and
Biology Socie y, Vancou e , BC, Canada, 20–24 Augus 2008; pp. 601–604.
32.
Kennedy, A.; Finlay, D.D.; Gulden ing, D.; Bond, R.R.; Mo an, K.; McLaughlin, J. Au oma ed de ec ion o
a ial ib illa ion using R-R in e als and mul i a ia e-based classi ica ion. J. Elec oca diol.
2016
,49, 871–876.
[C ossRe ]
33.
Ta eno, K.; Glass, L. Au oma ic de ec ion o a ial ib illa ion using he coe icien o a ia ion and densi y
his og ams o RR and ∆RR in e als. Med. Boil. Eng. 2001,39, 664–671. [C ossRe ]
34.
Pe ucci, E.; Balian, V.; Filippini, G.; Maina di, L. A ial ib illa ion de ec ion algo i hms o e y long e m
ECG moni o ing. Compu . Ca diol. 2005,32, 623–626.
35.
Lian, J.; Wang, L.; Muessig, D. A Simple Me hod o De ec A ial Fib illa ion Using RR In e als. Am. J.
Ca diol. 2011,107, 1494–1497. [C ossRe ] [PubMed]
36.
Zhou, X.; Ding, H.; Ung, B.; Pickwell-MacPhe son, E.; Zhang, Y. Au oma ic online de ec ion o a ial
ib illa ion based on symbolic dynamics and Shannon en opy. Biomed. Eng. Online
2014
,13, 18. [C ossRe ]
[PubMed]
37.
Cui, X.; Chang, E.; Yang, W.-H.; Jiang, B.C.; Yang, A.C.; Peng, C.-K. Au oma ed De ec ion o Pa oxysmal
A ial Fib illa ion Using an In o ma ion-Based Simila i y App oach. En opy 2017,19, 677. [C ossRe ]
38.
Dash, S.; Chon, K.H.; Lu, S.; Raede , E.A. Au oma ic Real Time De ec ion o A ial Fib illa ion. Ann. Biomed.
Eng. 2009,37, 1701–1709. [C ossRe ] [PubMed]
39.
Ande sen, R.S.; Poulsen, E.S.; Pu husse ypady, S. A no el app oach o au oma ic de ec ion o A ial
Fib illa ion based on In e Bea In e als and Suppo Vec o Machine. In P oceedings o he 2017 39 h
Annual In e na ional Con e ence o he IEEE Enginee ing in Medicine and Biology Socie y (EMBC), Jeju
Island, Ko ea, 11–15 July 2017; pp. 2039–2042.
40.
Nu yani, N.; Ha ji o, B.; Yahya, I.; Les a i, A. A ial ib illa ion de ec ion using suppo ec o machine.
In P oceedings o he Join In e na ional Con e ence on Elec ic Vehicula Technology and Indus ial,
Mechanical, Elec ical and Chemical Enginee ing (ICEVT & IMECE), Su aka a, Indonesia, 4–5 No embe
2015; pp. 215–218.
41.
Colloca, R.; Johnson, A.E.; Maina di, L.; Cli o d, G.D. A suppo ec o machine app oach o eliable
de ec ion o a ial ib illa ion e en s. Compu . Ca diol. 2013, 1047–1050.
42.
Yang, T.-F.; De ine, B.; Mac a lane, P.W. A i icial neu al ne wo ks o he diagnosis o a ial ib illa ion.
Med. Boil. Eng. 1994,32, 615–619. [C ossRe ]
43.
A is, S.G.; Ma k, R.G.; Moody, G.B. De ec ion o a ial ib illa ion using a i icial neu al ne wo ks.
In P oceedings o he Compu e s in Ca diology, Venice, I aly, 23–26 Sep embe 1991; pp. 173–176.
44.
Pe
˙
enas, A.; Ma ozas, V.; Sö nmo, L. Low-complexi y de ec ion o a ial ib illa ion in con inuous long- e m
moni o ing. Compu . Boil. Med. 2015,65, 184–191. [C ossRe ]
45.
Ande sen, R.S.; Peimanka , A.; Pu husse ypady, S. A deep lea ning app oach o eal- ime de ec ion o a ial
ib illa ion. Expe Sys . Appl. 2019,115, 465–473. [C ossRe ]
46.
Faus , O.; Shen ield, A.; Ka eem, M.; San, T.R.; Fuji a, H.; Acha ya, U.R. Au oma ed de ec ion o a ial
ib illa ion using long sho - e m memo y ne wo k wi h RR in e al signals. Compu . Boil. Med.
2018
,102,
327–335. [C ossRe ]
47.
W obel, J.; Ma onia, A.; Ho oba, K.; Jezewski, J.; Czabanski, R.; Pawlak, A.; Po wik, P. P egnancy Telemoni o ing
wi h Sma Con ol o Algo i hms o Signal Analysis. J. Med. Imaging Heal. In o m.
2015
,5, 1302–1310. [C ossRe ]
48.
Jezewski, J.; Ho oba, K.; Roj, D.; W obel, J.; Kupka, T.; Ma onia, A. E alua ing he e al hea a e baseline
es ima ion algo i hms by hei in luence on de ec ion o clinically impo an pa e ns. Biocybe n. Biomed. Eng.
2016,36, 562–573. [C ossRe ]
49.
W obel, J.; Roj, D.; Jezewski, J.; Ho oba, K.; Kupka, T.; Jezewski, M. E alua ion o he Robus ness o Fe al Hea
Ra e Va iabili y Measu es o Low Signal Quali y. J. Med. Imaging Heal. In o m.
2015
,5, 1311–1318. [C ossRe ]
50.
Mangasa ian, O.L.; Musican , D.R. Lag angian suppo ec o machines. J. Mach. Lea n. Res.
2001
,1, 161–177.
51. Co es, C.; Vapnik, V. Suppo - ec o ne wo ks. Mach. Lea n. 1995,20, 273–297. [C ossRe ]
52.
Roj, D.; W obel, J.; Ma onia, A.; Ho oba, K.; Henzel, N. Con ol and signal p ocessing so wa e embedded in
sma w is band moni o o silen a ial ib illa ion. In P oceedings o he 2017 MIXDES—24 h In e na ional
Con e ence “Mixed Design o In eg a ed Ci cui s and Sys ems”, Bydgoszcz, Poland, 22–24 June 2017;
pp. 585–590.
Senso s 2020,20, 765 23 o 24
53.
W obel, J.; Ho oba, K.; Ma onia, A.; Kupka, T.; Henzel, N.; Sobo nicka, E. Op imizing he Au oma ed
De ec ion o A ial Fib illa ion Episodes in Long- e m Reco ding Ins umen a ion. In P oceedings o he
2018 25 h In e na ional Con e ence “Mixed Design o In eg a ed Ci cui s and Sys em” (MIXDES), Gdynia,
Poland, 21–23 June 2018; pp. 460–464.
54.
Henzel, N.; W obel, J.; Ho oba, K. A ial ib illa ion episodes de ec ion based on classi ica ion o hea a e
de i ed ea u es. In P oceedings o he 2017 MIXDES—24 h In e na ional Con e ence “Mixed Design o
In eg a ed Ci cui s and Sys ems”, Bydgoszcz, Poland, 22–24 June 2017; pp. 571–576.
55.
W
ó
bel, J.; Ho oba, K.; Pande , T.; Je˙zewski, J.; Czaba´nski, R. Imp o ing e al hea a e signal in e p e a ion
by applica ion o my iad il e ing. Biocybe n. Biomed. Eng. 2013,33, 211–221. [C ossRe ]
56.
Jezewski, M.; W obel, J.; Ho oba, K.; Gacek, A.; Henzel, N.; Leski, J. The P edic ion o Fe al Ou come by
Applying Neu al Ne wo k o E alua ion o CTG Reco ds. In Compu e Recogni ion Sys ems 2. Ad ances in
So Compu ing; Ku zynski, M., Puchala, E., Wozniak, M., Zolnie ek, A., Eds.; Sp inge : Be lin/Heidelbe g,
Ge many, 2007; Volume 45, pp. 532–541.
57.
Jezewski, J.; W obel, J.; Ma onia, A.; Ho oba, K.; Ma inek, R.; Kupka, T.; Jezewski, M. Is Abdominal Fe al
Elec oca diog aphy an Al e na i e o Dopple Ul asound o FHR Va iabili y E alua ion? F on . Physiol.
2017,8, 305. [C ossRe ] [PubMed]
58.
Czabanski, R.; Jezewski, M.; W obel, J.; Ho oba, K.; Jezewski, J. A Neu o-Fuzzy App oach o he
Classi ica ion o Fe al Ca dio ocog ams. In IFMBE P oceedings o he 14 h No dic Bal ic Con e ence
on Biomedical Enginee ing and Medical Physics, Riga, La ia, 16–20 June 2008; Volume 20, pp. 446–449,
ISBN 978-3-540-69366-6.
59.
Czaba´nski, R.; Je˙zewski, J.; Ho oba, K.; Je˙zewski, M. Fe al s a e assessmen using uzzy analysis o e al hea
a e signals—Ag eemen wi h he neona al ou come. Biocybe n. Biomed. Eng. 2013,33, 145–155. [C ossRe ]
60.
Ma onia, A.; Jezewski, J.; Kupka, T.; Ho oba, K.; W obel, J.; Gacek, A. The in luence o coincidence o e al
and ma e nal QRS complexes on e al hea a e eliabili y. Med. Boil. Eng. 2006,44, 393–403. [C ossRe ]
61.
Jezewski, J.; Ma onia, A.; Kupka, T.; Roj, D.; Czabanski, R. De e mina ion o e al hea a e om
abdominal signals: E alua ion o bea - o-bea accu acy in ela ion o he di ec e al elec oca diog am.
Biomed. Tech./Biomed. Eng. 2012,57, 383–394. [C ossRe ]
62.
Jezewski, M.; Czabanski, R.; Ho oba, K.; Leski, J. Clus e ing wi h Pai s o P o o ypes o Suppo Au oma ed
Assessmen o he Fe al S a e. Appl. A i . In ell. 2016,30, 572–589. [C ossRe ]
63. Vapnik, V. S a is ical Lea ning Theo y; John Wiley & Sons: New Yo k, NY, USA, 1998; ISBN 978-0471030034.
64.
Abe, S. Suppo Vec o Machines o Pa e n Classi ica ion; Sp inge Science and Business Media LLC: London,
UK, 2010; ISBN-13: 9781849960977.
65.
S einwa , I.; Ch is mann, A. Suppo Vec o Machines; Sp inge : New Yo k, NY, USA, 2008; ISBN 978-0-387-77242-4.
66.
Joachims, T. Lea ning o Classi y Tex Using Suppo Vec o Machines—Me hods, Theo y, and Algo i hms; Kluwe
Academic Publishe s: No ell, CA, USA, 2002; ISBN 079237679X.
67.
Suykens, J.; Vandewalle, J. Leas Squa es Suppo Vec o Machine Classi ie s. Neu al P ocess. Le .
1999
,9,
293–300. [C ossRe ]
68.
Tsang, I.W.; Kwok, J.T.; Cheung, P.M. Co e ec o machines: Fas SVM aining on e y la ge da a se s.
J. Mach. Lea n. Res. 2005,6, 363–392.
69.
Czabanski, R.; Jezewski, M.; Ho oba, K.; Jezewski, J.; Leski, J. Fuzzy Analysis o Deli e y Ou come A ibu es
o Imp o ing he Au oma ed Fe al S a e Assessmen . Appl. A i . In ell. 2016,30, 556–571. [C ossRe ]
70.
Jezewski, M.; Leski, J.; Czabanski, R. An A emp o Op imize he Ca dio ocog aphic Signal Fea u e Se o
Fe al S a e Assessmen . J. Med. Imaging Heal. In o m. 2015,5, 1364–1373. [C ossRe ]
71.
Jezewski, M.; Leski, J.M. Nonlinea Ex ension o he IRLS Classi ie Using Clus e ing wi h Pai s o P o o ypes.
In Ad ances in In elligen Sys ems and Compu ing; Bu duk, R., Jackowski, K., Ku zynski, M., Wozniak, M.,
Zolnie ek, A., Eds.; Sp inge : Cham, Swi ze land; Heidelbe g, Ge many; New Yo k, NY, USA, 2013; Volume
226, pp. 121–130. ISBN 978-3-319-00968-1.
72.
Dubi zky, W.; G anzow, M.; Be a , D. Fundamen als o Da a Mining in Genomics and P o eomics; Sp inge
Science & Business Media: New Yo k, NY, USA, 2007. [C ossRe ]
73.
Pica d, R.R.; Cook, R.D. C oss- alida ion o eg ession models. J. Am. S a . Assoc.
1984
,79, 575–583. [C ossRe ]
74.
Huang, C.; Ye, S.; Chen, H.; Li, D.; He, F.; Tu, Y. A no el me hod o de ec ion o he ansi ion be ween a ial
ib illa ion and sinus hy hm. IEEE T ans. Biomed. Eng. 2010,58, 1113–1119. [C ossRe ]
Senso s 2020,20, 765 24 o 24
75.
Zhou, X.; Ding, H.; Wu, W.; Zhang, Y. A Real-Time A ial Fib illa ion De ec ion Algo i hm Based on he
Ins an aneous S a e o Hea Ra e. PLoS ONE 2015,10, e0136544. [C ossRe ]
76.
Kuma , M.; Pacho i, R.B.; Acha ya, U.R. Au oma ed diagnosis o a ial ib illa ion ECG signals using en opy
ea u es ex ac ed om lexible analy ic wa ele ans o m. Biocybe n. Biomed. Eng.
2018
,38, 564–573. [C ossRe ]
©
2020 by he au ho s. Licensee MDPI, Basel, Swi ze land. This a icle is an open access
a icle dis ibu ed unde he e ms and condi ions o he C ea i e Commons A ibu ion
(CC BY) license (h p://c ea i ecommons.o g/licenses/by/4.0/).