CA2062249A1 - Photoplethysmographics using component-amplitude division multiplexing - Google Patents

Photoplethysmographics using component-amplitude division multiplexing

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Publication number
CA2062249A1
CA2062249A1 CA002062249A CA2062249A CA2062249A1 CA 2062249 A1 CA2062249 A1 CA 2062249A1 CA 002062249 A CA002062249 A CA 002062249A CA 2062249 A CA2062249 A CA 2062249A CA 2062249 A1 CA2062249 A1 CA 2062249A1
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Canada
Prior art keywords
modulating
component
signals
amplitude
signal
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
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CA002062249A
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French (fr)
Inventor
Rex Mccarthy
Robert Smith
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Sensormedics Corp
Original Assignee
Rex Mccarthy
Robert Smith
Sensormedics Corporation
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Publication of CA2062249A1 publication Critical patent/CA2062249A1/en
Abandoned legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/41Detecting, measuring or recording for evaluating the immune or lymphatic systems
    • A61B5/414Evaluating particular organs or parts of the immune or lymphatic systems
    • A61B5/417Evaluating particular organs or parts of the immune or lymphatic systems the bone marrow
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1455Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters

Abstract

Photoplethysmographics Using Component-Amplitude-Division Multiplexing Abstract A plurality of carrier signals, distinguishable by amplitudes of signal components (e.g., frequency compo-nents), are respectively applied to a plurality of energy emitters (e.g., infrared and red light emitters). A
detector receives the sum of the energy after modulation at each emitter wavelength, e.g. by blood tissue of a patient. An output of the detector is then demultiplexed, whereby a component of modulation at each emitter wave-length may be determined. The carrier signals may com-prise time-varying periodic signals with identical fre-quency and frequency components, such as mixtures of identical sets of pure sine waves. When the number of signal components exceeds the number of emitter wave-lengths, sufficient information is provided during demul-tiplexing to detect and correct errors introduced by ambient light source and other interference.

Description

I~.lA~ 2 l9:33 LYON~ LYO~I P, 3/39 2~2249 ~h~

. a-~b Thi~ invention relatQ~ to ~hotoplethy~mographics.
Mor~ pe~ aally, thi5 lnv~nkion ~lates to a~mponent-ampl1tude-dlvl~lon mult~plex~g and ~omultipl~txlng o~
~ignale for ~n~rared and r~d ab~orp~ion o~ ~loo~

2.
It ~s w~l known in ~he a~t ~o aolleat photo~
ple~hy~ogr~phi~ d~A ~imult~neou~ly a~ a plurall~y of ~n~r~y waveleng~hs. For sxampla, blood ~xygon ~onoen-tration may be mea~u~ed by d~termlning abRorption by a patient'~ t~ues on infrar~d a~d r~ lightr the degree o~ ab~orp~ion i~ ~ypioally di~ren~ fo~ ~h~se two wave-lengthG. In~rare~ and rad llght ~re ~mi~ted in~o the - 15 patient'~ ~issu~6 (e.gO ~ by infr~re~ ~d red LED~) an~ th~
total energy re~e~ve~ to be de~octed ~y ~ slngl~ det~stor (e.g., a photodiod~. Howev~r, one probl~m ls th~t the signal produ~ed b~ th~ ~teo~or mus~ b~ proo~6~ed ~o ~parat2 ~h~ in~rar~d and red portiQn~ ~rom eaoh other.
zo One m~thod o~ th~ p~ior art i~ shown ~n U.~. Pat~n~
No~ 4,407,290. Tlm~-division ~ultlpl~xing i6 used to alterna~ly ~wi~ch on ~he in~r~r~3~ arld ~6~d ~ er~, a~c a ~: r~gu~n~y g~eat~r ~han th~ p~tionk ~ ~ puls~ r~ta . Th~
de~eotor si~nal ls then 6epar~t~d in~o in~rar2d and re~
~ortlon~ by ~ampling in ~yn~hro~y wi~h the on~o~ switch-ing o~ ~he ln~rared ~nd r~d emitters.
While ~hi3~ method ~ucc~ss~ully separates the infrar~d and rqd porti~ns, it ~n~rally r~quire~ that ~amplinq tho d~c~or signal must be ~ynohronize~ with th~ on/of~
30 ~wit¢hing of the in~rared and r~ ~mit~ers. It i~ al~o diffioult w~ a u~ing thl8 me~hod to obmp~nsate ~r n~ise - ;

~ `iP~, 3 92 19:34 LYON& LYOI\I p, ~/39 2~22~9 sources such as am~i~nt lis~h~ and eleatromagn~tia lnter~erenc~.
A ~ond method o~ the pr.~or A~t 1~ s~wn ~n U.~, Pat~nt No. 4,800 r 885. Th~ in~rar~d ~nd re~ em~t~ars are driven at two difPer~n~ ~eguenaie~. Th~ deteQtor sl~nal ~ s ~h~n s~p~rat~d into ln~r~d and ~ed porti~n6 ~y tering a~ ~hosQ ~wo di~f~rPn~ frequen~
While this me~hod suc~ u~Lly 60parate ~he in~rared ~nd red por~on~, the m~tho~ ribe~ in th~ patent lo re~uire~ d~ultiplexing ~ignal6 which ar~ pha~e-synahronized wi~h th~ multiplexing ~r~quencle~, and pro~
ducea a high~r power QU~pUt than ~hs timo-divielon multi-plexing ~et~od. Also, while this method may avoid noi6e soura~s at predetermlned and known ~r~qu~ncies, i~ is di~-ficul~ to oompensat~ ~or noi~ ~ou~c~6 which were notXnown b~f~re thc multiplexlng ~re~uancie~ wer~ 6hos~n.

The invention provld~ a method o~ multipl~xing and de~ultiplexing o~ sig~al~, oall~d ~componen~-amplitude-divi6ion" h~re~n, which m~y be Appll~d to moa~ring blood~i~sue ab~o~p~ion at infrar~d and rod wavalen~th6. A
plurallty of carrier signal~, di~tingui~hable by ~mpli~
tudes oX ~ighal component6 ~e.g., fre~u~ncy compon~nts), are reep~c~iv~ly applied to a plurall~y o~ en~rgy emitter~
(e.g., infra~d and red ~mit~er~ d~tector r~eivQ~
the sum o~ the ~nsrgy a~t~r mo~ulation at ~ach emitter wavel~gth, ~.~. by blood tl6~u~ ~ a pa~ient. An ou~pu~
o~ the d~teator is th~n de~ultiplexad, wh~r~by a ~omponent o~ modulatlon ~t ea~h ~mlt~r w~v~length m~y b2 d~termin~d.
In a pre~erred embodim~nt, ~h~ carrier ~iqnals may oomprise ~im~--varying perio~i~ signal~ with ld~ntlaal frequency an~ frequenay compon~n~ uc:h a~ mixtur0~ o~
id~ntical ~st~ o~ pure sino wav~s. For ex~mpl~, in a 35 pr~errad ~mbodiment, a first ~arrier ~ may compris~ a mixture o~ two sino wave~ al wl + ~ ~Y2, whil~ a oeaond ilA~, 3 ' 92 13:3d LYO~ LYOI~I P, 5/39 2~622~9 car~ier ,B rn~y c:ompri~e a ~i ~e~nt ~nix~ur~ o~ tha same two 5ine w~v~ wl ~ ~2 w~. ~lt~l~na~i~rely, ~ A~ay ~omprlse~
a mixture o~ thre~ sine wave~ ~1 wl i ~2 W2 ~ k3 w3, wh~le ~ may ~o~npri6~ a dif~rent miX'f:Ur~a 0~ ~h~ ~ame khre~ 6ine 5 wa~re ~1 wl + d2 wZ ~ ,/33 W3. When ~he numbe~ of signal compon~nt~ ~xceeda the number o~ ~nitter ~av~lan~th~, su:~-fioient ln~ormatlon is prov~ed during de~nul~iplexing to dete~ and ~orrea~ er~ors introdu~d by aml~ ~ ent 1 ight ~ouro~s ~nd other int~r~rena~.
10 ~ ~
Flgure 1 show~ a blo~k di~ram o~ ~ photopl~hy~mo-~raphlc ~ysl:em aomprising an ~m~odiment c~ ~hs ir,vention.
Flgur~ 2 ~hows a blocX diayram o~ ~h~ compone~t-ampl ~ t-lde-divi~ior; multlpl~x~r ~nd demul~ipleXer of an 15 em~odiment oS the invention.

An em~odl~en~ o~ this invention may b~ usQd together with lnv~ntlons which ara di~olo~ ln a cop~nding appli~
cation titled "P~OTOPLE~Y~MOGRAP~IC~ U~ING ENER~
~0 REDUCING WAVEFO~ 8HAP~NGIl, appli~a~ton Se~Al No. _ _, Lyon ~ ~yon ~ooke~ No~ 1~1/238, riled ~ a~ in th~
nama of ~h~ ~me i~vsnto~, hereby inoorporated by ra~er-~nG~ as 1~ ~ully ~e~ ~orth herein~

Figur~ ~ shows a bloc~ dia~ra~ o~ a photopl~thyemu-graphic 3yRtem ~omprising an ~mbo~lm~n~ o~ ~e l~ven~ion.
A plurallty of energy amltt~r~ 101 may ~ac~ be tuned to a ~pa~a~e wavel~ngth. In a p~er~ed embodiment ~o~
measur~ng blo4d ~xygen, one o~ ~he emit~or ~01 may com-pri-~ an ln~r~rc~ light e~itt~r ~nd may ~perate at a wav~length o~ abou~ 880 nanomet~r~; another one o~ th~
emitters 101 may aompri~e a r~d light emit~er a~d may opsrate at a wavelength of about 655 nan~meter~. ~As uged hs~ein, "light~ r~ers to eleotromagn~tia ~nergy of any IijhF~, 3 ' '~2 13:35 LY01`~ LYOI~ P, 6/~,~
.

~2~

wavel~ngth, ~he~hsr vi~ik71~a o~ nst. 3 ~Iow~er, it may oacur that otha~ wav~l~ng~h6 may be u~3~3rul, suc~ as for measuring blood ca~bon dioxide, blo~d t::arbo~ morlt:xide, other blood ga~ c:onc~3n~ratlons, bloocl gluct: E~a, OI' mor~
gen~rally, o~her chemloal and/or phy~L/::al Conaen~ration~.
In a p~ rred emloo~ t, ea~h o~ the emit~r~ 101 may comprise an LED (such ~ pa~t numbe~ OPC~B03 ma~ by Ma~ktQch In~ernational Corp~ ~r th~ in~r~d LE~ ~n~ part numb~r M~lS00-Pt~ made by ~axXtaah Irlterrl~tional Corp. ~or ~0 the re~ LE~), a~ i6 well known ln ~h~ ~r~, and may ~e collpl~d by m~an~; of an L~D driver 102, a~ 1~ w~ll knowrl in the art, to a carrier output 103 o~ a muxJdelnux circul~
104 ~ee ~igure 2).
En~rgy ~rom tha ~mi~t~r~ lOl i~ appli~d to a ti~ue 5 6~ctlon 105 o~ a patient. In A pxe~rxed em~odiment ~or Ineas~lring blood oxygen, the ti~u~ ~ect;lon 105 i~ prefer-ably cho~en ~uah ~ha~ ener~y ~ m ~la ~ t~r~ lol pa ~:eE;
~hrough the patien~'~ blo~d ve~sel~, ~ueh a~ an ~nd o~ th~
pati~nt'~ ~in~er~ th~a patient's aa~lob~, or ( or neonat~) 20 tha patient~ hand or ~oo~. The t~ua ~e~ion loS may mo~ulate t~e energy ~rom the o~i~te~6 101, as i8 well known ln th~ art , e . g ., by ab~orblng ~o~ o~ ~h~ ~ne~gy at ea~h wavel~ngth. Typically, energy may be modulated by transml 6?~ n 'chrough ~hl3 tl ~3~uo E;Qa~iOn 105, but it m~y ~5 oç-:ur ~hat ~nsrgy may b~ modulaLtad by r~lea~lon or by oth6~r maarl~, A detector lO~ r~a~i~re~ ~n~rgy al~t~r ~nodula~ion by ~he ti~U~ E;ec:~ion lOS and g~ne~ra~ An output signal whioh indicat~ th~ t4~al ene~gy r~o~ived. In a pr~f~rred 30 ~mbodlmen~, the d~tecto~ 106 may ~ompris~ a photo~iode ~uc:h as pa~. number OSI-1140 made~ by Opl:o 50n50~, Inc.), a~ i well knowrl in the art: . An ~ukpu - o~ the det~ct~r 106 is ampli~ll d by arl ampli~ r 107 and ~ouple!d by m~an~
o~ a ~llter 108 to a d~t~ctor i31put 109 o~ the mux/d~mux 35 circui~ 104.
The mux/d~mux cir~uit 104 y~norates a data outx)ul:
~iynal 110 3~ a ~ata ou~put 111~ fo~ each ~nex~sly wav~

MAR, 3'~2 19:~6 L`~OI~I~ LY~N P, 7/3~

2~22~

length, which i.ndloates the ~o~ulation ~hlah th~ tl66u~
s~ction 105 applied ~o that ~nqr~y w~velength. In a pre~err~d embodlment ~or ma~u~1ng blo~ oxy~n, in~orma-~ion ~ch as blood o~yg~n cona~ntr~ion may be calaula~Qd from ~h~ outpu~ ~ig~al, A~ 18 ~ell k~own in th~ art.

exl~
Componen~-ampli~ud~-divl~ion mul~iplexing (''c~DM~
a6 ueed herein, iB def$n~d a~ ~llow~. In CAD~, a plural-lty oP oArri~r elgnale are Qon~tru~to~, aaoh o~ which m~y oompri%e a ~ixtura of aarrier ~ompon~nt~. ~ach carrier signal m~y ~e separately mo~ula~ed, and the ~s~ltants summed. Th~rea ~er, th~ separa~e modulation~ may be recover~d ~rom the sum, a~ die~los~d ~er~in.
~huo, a ~ire~ oarrier may comprise a mixture o~ twa car~ier co~pon~nt~ ~1 wl ~ ~2 w2, while a s~aond carri~r ma~ oomprise a ~i~fer~n~ mixture o~ ~h~ sam~ t~o carri~r componants ~ wl ~ ~2 w2. ~l~er~a~ively, ~ may ~ompr~se a mixture of ~hxoe components ~1 wl + ~2 w~ + ~3 w3, wh~la may comprise a di~çrent mixturs o~ th~ sam~ thr~a ~om ~0 ponents ~1 Wl ~ ~2 w2 ~ ~3 w3.
~ he following r~latlon~ descr~e cons~ruction o~ ea~h carri~r when the num~er o~ aarr~er a~mpon~nt~ ~m) ~nd the number o~ oarrier ~lgnals (n) ~o~h e~ual 2, i.~.
m - n - 2:
2S [ ~1 ~2 ~ [ wl ] [ ~ ] ( ~1 ~2 w~
ar ~ 3) where ~ is a matrix o~ mixing ~actors ~1, a2, ~ 2:
R is a vector o~ ~arrie~ ~omponen~ wl, W2S and ~ i~
a vector o~ ~arrier si~nal~
Applying these relatlon~ to th~ a~e where m = n ~ 2 woul~ b~ cl~ar to one ~f ordinary gkill ln th~ art, a~er 3S peru~l o~ ~h~ speolfication, drawing snd ~lal~8 Aere~n.
Tha ~ollowing relation da~rlb~s ~epara~B modula~lon of ~ac~ ~arrier ~ig~als MAP, 3 92 19: 37 LYO~ L~'GI\I P, 8/39 20622~9 ml ~ * m~ ~ = a ( 114 l wh~re ml i~ a ~ir~t modula~tin~ aff~o~ ~e.y,, at an lnfrared wav~leng~h): ~a i~ a second mod~llatlng effac~ ~.g~, at a re~ wavQleng~h); an~ a is dQ~eated ~um of the modulat~d c:ar~i~r signal6 ~hq dete~d sum a may l; e d~compos~ lnto epar~
part~ ~or ~aoh c:arri~r ~om~onent: wl, w~:
a ~ l wl ~ ~2 wa) ~ ~a ~ wl ~ ~3a wa~ ~15) o~
lo ~ = ~1 wl + t2 w2 ~116) tl - ml al ~ m2 ,Bl ~117 ) ~2 = ml ~2 + m2 ,B2 ~118) or r ~1 a2 r ml ~ r tl 1 ~ t~
- ,~1 ,B2 ~ - m2 t2 or whe~e ~: ~6 the matrlx o~ mlxln~ tor~ 2, ~
,B2 7 ~1 is a vector o~ modula~ion ~f~ak~ ml, m2: and T ~ 8 a vea~or o~ modulated oarrl~r Gomponent par~
Separa~ omponerlts m~y be d~mul~ipl~xed by mul~i plying by tha ~ multipli¢~ e lnver~ o~ tha mixing 2~ matrix It:
( 12 1 ) or 2 2 ) Th~ mixin~ ma~rix ~ 6hould hav~ a lOr~ multiplicativi3 3 D invex~e . It would ~ alear to OIIO o~ ordinary ~kill in th6~ ar~, a~er perusal o~ the epec:i~ioation, drawin~ an~
claim~ h~r~in, that X - I, the id~ntity matrix, ~nd ~ven X ;~ S, woul~ be workable, an~ ar~ withln the ~ope an~
~pi~it o~ the invention. However, a~ u~ed h~rQi~, a 35 mixing matrix X ~ll f~e~e from ~. Al~o, it ie g~n~rally pre~rable that R dif~r~ ~ub~t~ntlally ~rom ~ .

~IIAP, 3'92 19:37 LYON~ L`,~ON P, 9/39 .

~224~

The ~ollowing rolation~ de~aribe ~on~tru~ion of ~ach carri~r wh~n the numbQr of ~a~ri~r ~omponer~ts (m) ~ the nurnb~r o~ carri~r ~ignals (n), whiGh ~ 2 , ~ . ~. m 5 n a 2:
2 ~3 - - Wl ~ - a~
,al ~2 ,~13 W2 ~ (123) lo zl Z2 z3 W~ Z
o~
X f~ 12d.~
where ~ 15 the matrix o~ mixirlg ~aator~ 2, a3, 2, ,~3, zl, z2, z3 ~ the t~ector o~ aarrier compon~nts wl, w2, w3~ an~l ~ is the vector ~ aarrier ~ignal6 ~, ,B, z An add~tlonal row zl, z2, ~3 haE: been ad~d to ~ to præE3erVB it~ inver~a~ility, and an addition~l elemsnt z has b~en added to C: a~ a r~sult . Be~ . u~e no ~arri~r 8ig-~O nal z i8 actually u~, the row zl, z2, 23 may he oho enarbitra~ily, ~o long as X rem~ inv~r~ibl~. O~ 04U~83/
the value ~ç x~l d~pends upon the sel~ot~on o~ the row zl, ~, z~-Bo~ause tlle ~ow zl, 82, z3 may be c~hoean arbitrarlly, 25 X 1 may be cc~mputed more ~h~r~ ono~, u~ g ~nore than on~ row zl, 22, z3~ Thu6, there will b~ Xa) u61n~ z~a, ~2a, Y~, with X'l~ , u~in~ zll~, z2b, æ3~, with ~ 1b, and l~c, uslrlg zlc, z2c:, z3c, wi~h X 1c. a~a, Rb and ~c may ~ach be u6e~1 to ~ompute ~. By ~omparing th~ ~eeultant element~ Qf ~5 3 o gena:rat~d usin~ ~, Rb, and lSo, int~r~r~nc~ in on~ or mor~ oarrl~r components wl, w2, w3 may b~ d~t~cted.
Error~ ~nay b~ ~oxr~cted by ma~ority v~tlng th~ r~sultant el~m~nte Or ~a.
Applyincl ~h~se relat.ion~ to ~h~ c;a~e whe:re m ~ n ~ 2 35 would be cl~ar to c:n~ o~ obdinary ~)cill in ~he a~t, a~t~r perl~al o~ ~h~ epec:l~ication, dr~wings and alaim~ hl3r~in.

lil~R, 3 92 1?:3& LYOII,~ LYON P. 10,'39 2~16~9 ~U~
Figure 2 show~ a blo~c dll~gram o th~ componen~-amplltude-divislon multiplex~r ~n~ ~multipl~X~r o~ an embodim~nt ~f th~ lnvention.
A ~rrier ~o~nponent genera~:c,r aOl gerlerate~ a plural-ity o~ carrier co~nponent~ 20~ wl, w~. ~n a pr~err~d ~mb~diment, par~ o~ eaoh aa~r~x c~ on~n~ 20a wl, w2 ~
allor-~t~d ~o ~aach emitt~ wav~l~n~h. ~lso, in a pre-~erred embodimsnt, ~Ach car~ler co~nponerlk 2 ~a wl, w2 may 10 comprio~ a ~ine wav~, a~ follow~
wl - aof3 ~r Pl t) t343 w2 = 008 121r f2 ~) (20~) wh~re ~1, f2 ar~ fre~uenr~.ie~
In a prefe~red ~mbodim~nt, fl and ~ are chossn such 15 that lnteff2renc~e ~r~m nois~ souro~3s, ~uch a~ ambisnt light and electroma~netla in~er~erenoe, i~ minimiz~d. In a pre:~erred embodiment, fl and ~2 ar~ ~1BO Gho!3~3n ~uah that a bandwidth o~ about 4 Hz ~o~ the modula~in~ e~ t~
ml, m2 is allowed. ~re~auencie~ in th~ ra~g~ o~ ab3ut lo-50 ~z a~a p~eferr~d, but i~ would ~e clear to on~ bl~ ordi-nary 6kill ln t:h~ ar~, a~er pe~u6sl of th~ spe~ifioation, drawing~ an~ im~ he~eln, that o~her Pro~u~noies would ba workable, and ~re wi~hin ~ cope and ~p~ rit o~ th~
invention .
It would also be cl~ar to one o~ o~din~ry sk~ll in the art, af~er p~rusal o~ the s~e;:i~icat~oll, drawing~ and claim~ h~rein, ~ha~ ~here i~ r~o r~quir~e3nt: tha~ wl, w2 mu~t b~ g ine wave~ . Other typ~ rri~r oompone;nt~;
2 02, ~uoh a~ squa~e wa~e~ or o~her wav~orm~, would b~
worlcabl~, and ar~ within th~ soop~ ~nd ~pirit o~ ~ha inv~n~ion.
I~ would al~o be ~laar to orle o~ ordinary æk~ 11 in the art, a~t~r p~aru~al of the ~p~cl~ tlon, drawing~ an~
c}aimæ h~reirl, tha~ th~ invention may be adapt~d ~ m~a-~urem~nt o~ o~h~r conA~ltuent~, ~uah a~ ~lood ~a~bon dioxide, blood caxbon monoxld.~, oth~r blood g~s ~:on~en~ra-MhR, 3 Q2 1~:3g LYGN& L`~GN P, 11i39 2~22~9 g tlvn~;, blood gluao~o, o~ mor~ ~on~3r311y, oth~ ch~mic~al and~or physlaal con~en~ation~.
It wo-lld al80 ba clea~ t~ ona of or~in~ry ~kil l in the art, a~ter perusal oi~ th~ ~peci~ioatlon, drawlng~ and cl~im~ herq~in, ~hat ~he ohoic~ m ~ n ~ 2 i~ particular t~ mea~uxement oP bloo~ oxygen, an~ tha~ other ~ho~oes of m, n would b~ worlcabl~, and ar~3 withl~ the ~cop~3 and ~p~it o the inv~rlt~on . For example, i~ may ocour that other ~hoices o~ m, n may ~e u~3eful, ~uoh a~ ~r meaeuring lo blvod ~ar~on dioxlde 0 blood ~arbon monoxide, othar blood gas ~oncentration~, blood glucose, or mox~ generally, oth2r ~hemlcal Eln~l/or phy~ al concentr~tions.
Ea~h carri~r compon~nt: ~02 wlt w2 i~ ~ouplesl ~y mean~s o~ ~ pha~2 d~lay 205 l:o a ~oefficient ampliier ~06 ~or lS multiplyi~g by a aoeffl~ien~ e~iE the miacing matrix IC, to produc:e ~L mixing produc:~ 207. ~he mlxing produs:ts 207 ar~
~umm~ by a plural i~y o~ mix~ng su~ming ~ix uits ao8 ~o produce a pl~ allty o carrier slgnal~ 20~ his t6 ~he mat~lx m~l~ipli~a~ion ~hown in a~ua~iOn 113, 120 ~ach carrier ~i~nal 20~ a, ~ i3 aoupl~d by means o~
a ~rightne6~ ampli~i2r 210, for ad~ue~ th~ bri~htn~ss o~ a co~reepondin~ bmit~r 101, to th~ corr~ponding o~-~ie~ outpu1: 103 of ~he mux/demux ~ir~ui~ 104.
The det~c:~or i nput lû9 ~ s het~o~yn~d, a~ i5 W6~
25 known in ~he a~$, wi~h the aomplex 6~ier componen~-s 202 wl, w2 ~o r~store eaoh of the mo~ulated ;:arri~r c~mpon~nt6 2g2 wl, w2 to baseband. ~he ~t~ctor input log is ~oupl~d to an iRpUt 0~ eaah of a ~lu~ality o~ h~l:ro~yne el~mant~
211. A seaond lnput o~ eaeh of ~h~ hstrodyn~ el~m~nt~ 211 30 i~ ooupled ~o one of th~ aarri~r compon~n~s 202 wl, w2, ~haæe-ehifte,~ :Eor ~ r~al or ~n imaglnary par~-, a~ i~ ~ell known in the aLrt . The E: haee-E~hlft~d carrier component~
20a w~, w~ are m~lltiplisd to pro~uoo a s~t o~ ~ompï~x ~real and imagin~ry) components 21~ o~ each of th~ a2rriex 35 aom~on~nte Z0~ wl, w2, a~ ie w~ll known in the ar~.
Th~ complax aomponents 21~ are c:o~pled to a ba~eband ~i~t~r al3, which romov~ all oo~npon~rlts exaopt c~m~leae ~1¦A~,3 ' ~2 19~ LYON~ LYOI`I P, 12/39 2~622~9 ba~band aompc~nents ~14. Thf3 co~npl~ax ba~aband c~mpona~t 214 are coupled to a veotor ma~nltud~ computt3r 215, whloh oomput~s a vs~or magnltud~ o~ the complex base~nd Gomponents 21~.
The v~a~or ma~nltu~Q 216 is coupl~d to an inver~e co~fiaient ampli~l~r ~17 i~or mul~iplying l~y aoe~f.i~ient~
of ~he inver~Q mixlng ma~r~ x iC~ o p~oduce an lnYsrse mlxlng p~oduat 2~8~ Th~ invar~e mix~ng produ~t~ 218 ar~
~un~m~d by a plurali~y o~ lm~er~ mixing 6ummin~ cir~uit~
219 to produc~ the data output ~i~nal~ 110 . ~h~ ~ is the mal:rix multlplioa~ion shown in equa~ior~
~he da~a output slgnals 110 e~ah ~n~i~ate the pr~uc:t o~ th~ modulation sff~ct for the cor~pond~ng carrier signal 209 wl, w2~ as multiplied by a corr~ction by 'ch~
corre~ponding brigh~ness amplifier 210. Ea~h da~a o~tpu~
signal llO i~ coupled ~o ~he oor~ ondin~ data output lll of the mux~demux cir~uit 104 .
~n a pr~Qrr~d ~ml~o~imsn~, sign~l gene~tion and 51~
nal manipulatis:~n as d~3 ori3~t~ horein ~r~ pr~f~ral~ly E~er-fo~ed by a digital m~o~pxD~e~or (~uch a~ p~rt number DBPS~iOOl ma~e by MotorDla) s:~pærating under ~o~twara aon-trolO I~ would }~e clear to one o~ ordlnarY ~kill in th~
art, af~r pe~tl6al o~ th~ sp~aiflc~tion, drawings and cl aim~ hersin, ~hat pi~ogxamming a e~anda~ diglt~l mioro -proce~or to p~r~o~m ~ignal ~en~ration and signal manipu-la~ n as de60rib~d h~arein woul~ be a ~t~aightforwaxd ~a6k and woul~ not require undu~ experim~ntat~ on.
It would ~e ol~ar t~ on~ o~ o~dinary 3kill in the art, a~ter perusal of the ~peoirlcalti~n, drawing~ and ~o clalms h~ar~in, that the inv~n~Glon may bq ~ombln~d wi~h known methodE~ o~ aompu~ing bloo~ oxy61erl Gonaentr~tion Ind other blood g~ values from thQ data output signal~ 110 whlch are produ~ed. Providing a ~ys~em which comblne~ ~he inventlon wit:h such known m~hode would b~ ~ ~traight~or-~5 ward task, a~ter p~ru~al of the ~p~cifiaation, drawing~
and clalms n~rein, and woul~ no~ r~quire undu~
experim~ntatiotl .

MAP, 3 '`~2 19:i:) Li'OI``I& LYON P, 13/39 2~62249 ~l~s~na~i~ Em~?QU imen"l;~
Whlle prc!~err~3tl embo~ aent~ are ~l~clo~d hersain, many v~riiatians ~re po~ whlc~h remain wlthin th~
czonoept and 5COpla o~E ~he lnven~,lorl, and the~ Y~riatlon~
5 would become cl~ar l:o on~ u~ or~ nary ekill in 'ch~ ~rt aft~r peru3~l of ~he ~peoi~i~æ~ion, drawing~ and ol~lms herein .

Claims (62)

1. A device for collecting photoplethysmographic data, comprising means for generating a first and a second sig-nal, each comprising a set of component signals, said first and second signals being distinguishable by ampli-tudes of said component signals;
means for applying said first and second signals to a modulating medium;
means for detecting a composite signal at an output of said modulating medium, said modulating medium having a first an a second modulating effect; and means for generating a first and a second output signal responsive to said composite signal, said first output signal indicating said first modulating effect and said second output signal indicating said second modulat-ing effect.
2. A device as in claim 1, wherein said first and second signals are periodic time-varying signals with identical periods.
3. A device as in claim 1, wherein said first and second signals have identical frequency components.
4. A device as in claim 1, wherein said means for detecting comprises a photodiode.
5. A device as in claim 1, wherein said composite signal comprises a sum of said
6. A device for collecting photoplethysmographic data, comprising means for generating a plurality of carrier signals, each comprising a set of component signals, said carrier signals being distinguishable by amplitudes of said component signals;
means for applying at least two of said carrier signals to a modulating medium;
means for detecting a composite signal at an output of said modulating medium, said modulating medium having a plurality of modulating effect; and means for generating a plurality of output signals responsive to said composite signal, each said output signal indicating one said modulating effect,
7. A device for collecting photoplethysmographic data, comprising means for multiplying a mixing matrix and a vector of component signals;
means for applying a plurality of modulating effects to a resultant of said means for multiplying; and means for multiplying an inverse of said mixing matrix and a resultant of said means for applying.
8. A device as in claim 1 or 7, wherein said photo-plethysmographic data comprises blood gas data.
9. A device as in claim 1 or 7, wherein said photo-plethysmographic data comprises at least one of the group:
blood oxygen, blood carbon dioxide, blood carbon monoxide.
10. A device as in claim 7, wherein said mixing matrix is a square matrix.
11. A device as in claim 1 or 7, wherein at least one of said component signals comprises a sum of at least one of the group: a sine wave, a square wave.
12. A device as in claim 1 or 7, wherein said means for applying comprises a plurality of light-emitters.
13. A device as in claim 1 or 7, wherein said means for applying comprises a plurality of light-emitters tuned to a plurality of wavelengths.
14. A device as in claim 7, wherein said means for applying comprises a modulating medium.
15. A device as in claim 1 or 14, wherein said modu-lating medium comprises animal tissue.
16. A device as in claim 1 or 14, wherein said modu-lating medium comprises at least one of the group: blood, blood vessels, bone marrow, ligament, muscle, skin.
17. A device as in claim 1 or 7, wherein at least one of said modulating effects comprises amplitude modulation.
18. A device as in claim 1 or 7, wherein said modu-lating effects comprise an amplitude modulation effect which varies with energy wavelength.
19. A device as in claim 1 or 7, wherein at least one of said modulating effects comprises a time-varying component.
20. A device as in claim 1 or 7, wherein at least one of said modulating effect comprises a time-varying component which is correlated with a biological process,
21. A device as in claim 1 or 7, wherein at least one of said modulating effects comprises at least one transmission response of a modulating medium.
22. A device as in claim 7, comprising means for detecting a composite resultant of said means for applying; and means for separating said composite resultant into a vector resultant.
23. A device as in claim 22, wherein said means for separating comprises at least one hetrodyning element.
24. A device as in claim 22, wherein said composite resultant comprises a sum of at least two elements of said vector resultant.
25. A device for collecting photplethysmographic data, comprising means for component-amplitude-division multi-plexing a plurality of modulating signals; and means for component-amplitude-division demulti-plexing said plurality of signals.
26. A device as in claim 25, wherein said plurality of modulating signals comprises an infrared wavelength modulating signal and a red wavelength modulating signal.
27. A device as in claim 25, wherein said means for component-amplitude-division multiplexing and said means for component-amplitude-division demultiplexing collec-tively comprise a plurality of carrier signals.
28. A device as in claim 25, wherein said means for component-amplitude-division multiplexing and said means for component-amplitude-division demultiplexing collec-tively comprise a plurality of carrier components.
29. A device as in claim 25, wherein said means for component-amplitude-division multiplexing and said means for component-amplitude-division demultiplexing collec-tively comprise a mixing matrix and an inverse of said mixing matrix.
30. A device as in claim 25, wherein said means for component-amplitude-division multiplexing and said means for component-amplitude-division demultiplexing collec-tively comprise means for error detection.
31. A device as in claim 30, wherein said means for error detection comprises a number of carrier components in excess of a number of carrier signals.
32. A device as in claim 30, wherein said means for error detection comprises a plurality of mixing matrices.
33. A device as in claim 25, wherein said means for component-amplitude-division multiplexing and said means for components-amplitude-division demultiplexing collec-tively comprise means for error correction.
34. A device as in claim 33, wherein said means for error correction comprises means for majority voting a resultant of component-amplitude-division multiplexing and demultiplexing with a plurality of mixing matrices.
35. A device for collecting photoplethysmographic data, comprising a plurality of n emitters disposed to emit energy into a modulating medium at a plurality of wave-length;
a multiplexer coupled to an input of said emit-ters, wherein each said emitter is coupled to a carrier signal comprising a sum of at least n carrier components;
a detector disposed to receive energy from said modulating medium; and a demultiplexer coupled to an output of said detector, wherein an output of said demutliplexer indi-cates absorption by the modulating medium at said plural-ity of wavelengths.
36. A device as in claim 35, wherein each said car-rier signal is a time-varying periodic signal with identi-cal period.
37. A method of collecting photoplethysmographic data, comprising the step of generating a first a second signal, each comprising a set of component signals, said first and second signals being distinguishable by amplitudes of said component signals;
applying said first and second signals to a modulating medium;
detecting a composite signal at an output of said modulating medium, said modulating medium having a first and a second modulating effect; and generating a first and a second output signal responsive to said composite signal, said first output signal indicating said first modulating effect and said second output signal indicating said second modulating effect.
38. A method as in claim 37, wherein said first and second signals are periodic time-varying signals with identical periods.
39. A method as in claim 37, wherein said first and second signals have identical frequency components.
40. A method as in claim 37, wherein said modulating medium comprises animal tissue.
41. A method as in claim 37, wherein said modulating medium comprises at least one of the group: blood, blood vessels, bone marrow, ligament, muscle, skin.
42. A method as in claim 37, wherein said composite signal comprises a sum of said first modulating effect applied to said first signal and said second modulating effect applied to said second signal.
43. A method of collecting photoplethysmographic data, comprising the steps of generating a plurality of carrier signals, each comprising a set of component signals, said carrier sig-nals being distinguishable by amplitudes of said component signals;
detecting a composite signal at an output of said modulating medium, said modulating medium having a plurality of modulating effect; and generating a plurality of output signals respon-sive to said composite signal, each said output signal indicating one said modulating effect.
44. A method of collecting photoplethysmographic data, comprising the steps of multiplying a mixing matrix and a vector of component signals;
applying a plurality of modulating effects to a resultant of said step of applying.
45. A method as in claim 37 or 44, wherein said photoplethysmographic data comprises blood gas data.
46. A method as in claim 37 or 44, wherein said photoplethysmographic data comprises at least one of the group: blood oxygen, blood carbon dioxide, blood carbon monoxide.
47. A method as in claim 44, wherein said mixing matrix is a square matrix.
48. A method as in claim 37 or 44, wherein at least one of said component signals comprises a sum of at least one of the group: a sine wave, a square wave.
49. A method as in claim 37 or 44, wherein at least one of said modulating effects comprises amplitude modulation.
50. A method as in claim 37 or 44, wherein said modulating effects comprise an amplitude modulation effect which varies with energy wavelength.
51. A method as in claim 37 or 44, wherein at least one of said modulating effects comprises a time-varying component.
52. A method as in claim 37 or 44, wherein at least one of said modulating effects comprises a time-varying component which is correlated with a biological process.
53. A method as in claim 37 or 44, wherein at least one of said modulating effects comprises at least one transmission response of a modulating medium.
54. A method as in claim 44, comprising the steps of detecting a composite resultant of said step of applying; and separating said composite resultant into a vec-tor resultant.
55. A method as in claim 54, wherein said step of separating comprises at least one hetrodyning step.
56. A method as in claim 54, wherein said composite resultant comprises a sum of at least two elements of said vector resultant.
57. A method of collecting photoplethysmographic data, comprising the steps of component-amplitude-division multiplexing a plurality of modulating signals; and component-amplitude-division demultiplexing said plurality of signals.
58. A method as in claim 57, wherein each said modu-lating signal comprises a modulating effect.
59. A method as in claim 57, wherein said plurality of modulating signals comprises an infrared wavelength modulating signal and a red wavelength modulating signal.
60. A method in claim 57, wherein said step of component-amplitude-division multiplexing and said step of component-amplitude-division demultiplexing collectively comprise a step of error detection.
61. A method as in claim 57, wherein said step of component-amplitude-division multiplexing and said step of component-amplitude-division demultiplexing collectively comprise a step of error correction.
62. A method as in claim 61, wherein said step of error correction comprises majority voting a resultant of component-amplitude-division multiplexing and demultiplex-ing with a plurality of mixing matrices.
CA002062249A 1991-03-05 1992-03-04 Photoplethysmographics using component-amplitude division multiplexing Abandoned CA2062249A1 (en)

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