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(1)

“5 A5 ‘H’

11L1

Ftc. 1. Schematic diagram of the conductivit unit.

(Submitted for 1)ublication September 25, 1962; accepted March 12, 1963.)

ADDRESS: 719 \Vest Water Street, Elmira, New York.

PEDIATRIcs, July 1963

89

A

Simple,

Home-assem

bled

Apparatus

William R. Phillips, M.D.

I

N THIS ARTICLE we d!escribe a metllOdl

of d!eterlllining the electrical

cond!uctiv-ity of sweat. Tile instrument described!

(Fig. 1) andl the technique used is basically

tile same as tilat used by Shwadllman et

a!. in the preceding artidle.l Tile

instru-ment silo\Vfl in Figure 2 differs only in

tluat the iontophoresis equipment is built

into the same cabinet with the

collductiv-ity unit.

The instrumeiut described! in this article

measures tile electrical cond!uctance of

cm-(!iluted sweat. Because tilere is no \Veiglling

and! dilution of the sample, and! because iuo

chemical analysis is done, several sources

of error are removed. The results of the test

are known immediately.

The method was conceived ill 1959 fol-lowing publication of Gibson and Cooke’s2

article on iontopluoresis of pilocarpule and

of Bloxam’s irticle descril)ing all

illstrfl-ment for measuring tile electrical

con-ductance of hod!y fluids. An electrical

iia-gram u5Cdl for the iontopiloresis of

pilo-carpme has alread!y been publislled.2 Our

only change in tins electrical circuit as

I)resentedl by Gibson and Cooke was tue

insertion of a 1/100-watt fuse in the skin

electrodle circuit. Tluis fuse blows at 16

milleamperes. We also use a small

22%-volt “B” battery andl omit the pilot ligiut. A built-in timing d!evice is addled! for

dOll-venience.

The electrical d!iagranl for tile

cOildiuc-tivity part of tiue instrument is Silown in

Figure 1. The wheatstone bridge is dlriven

with 6 volts alternating current. This avoids

significant polarization of tiue sample. An

“electric eye” is used instead of a meter.

The conductivity chamber for Ilolding tiuc

sample of sweat is a 5-cm section of a Kato

nhicro-sedlinlelltatioll rate IPettd’ The

chamber electrodes are two 5-inch lengths

of 30-gauge 14-carat wluite-gold ‘ire. These

wires are illserted! illtO the ends of tile

Kato pil)ette containing sweat, andi

ad!-vancedi until their tips are 2 cm apart. Tiue

other endis of tlleSe wires are collllected!

to tile bridige circuit by two bindling posts.

The instrument is caiibratec! by using

soltt-tions of SOd!iulll dilloridle of known strengtil

expressed in meq/i. Tile strength of the

various calibratillg solutiomis used is

mdi-cated OIl the conductivity mdlicatOr as shown in Figure 2. There are no

provi-SiOl1S for temperature conil)ellsatiOll. Tiue

instrument is sufficiently accurate at any

comfortable room temperature. No part of tile instrument is custom built. Each

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90 SWEAT CONDUCTIVITY

Fic. 2. 1, interval timer for iontophoresis; 2, con-eluctivity indicator; :3, switch for conductivity unit; 4, pilot light for the conductivity unit (there is no pilot light for the iontophoresis section of the

instrument); 5, “electric eye”; 6, conductivity

chamber; 7, combination switch and regulator for

the iontophoresis current; 8, jacks for the skin

electrodes; 9, Milleammeter for indicating the

ionto-phoresis current; and 10, 1/100 watt fuse in the

skin electrode circuit.

commercially. The total cost of parts is $40.

For construction of the conductivity unit

alone the cost of parts is $20.

TECHNIQUE

The iontophoresis is done with the

in-strument disconnected from the 115-volt

house current. A 0.1% solution of

pilo-carpine chloride is iontophoresed into a

3-by-6-cm area on the forearm at a current

flow of 4 milleamperes for a period of 6

minutes. In infants or emaciated children

whose forearms are too small, an area on

the back is used. After washing and

dry-ing, the iontophoresed area is covered

with a shallow plastic cup (Fig. 3). The

edges of the cup must effectively seal the

area to prevent escape of sweat, as well

as to prevent evaporation. The cup is

fastened to the skin with a small strip of

adhesive and then bandaged snugly but

comfortably against the arm or back with

several turns of elastic bandage. A 75-watt

lamp is placed 6 or 8 in. from the cup to

keep it warm during the collection period.

This heat prevents condensation of salt free

moisture on the walls of the cup. It also

increases the yield.

After a collection period of 25 minutes

the bandage and the cup are removed. The

sweat on the skin is immediately scooped

up with a sharp edged spoon (Fig. 4).

With a mouthpiece and rubber tube

suffi-cient sample is drawn into the Kato pipette

from the pool of sweat in the spoon. The

pipette is mounted into its mounting clip

on the instrument. The gold wires are

in-serted in each end of the pipette and

ad-vanced until their ends are 2 cm apart,

using the etchings on the pipette for exact

positioning. It is only necessary that tilere

be enough sweat in the pipette to allow

the tips of the wires to be embedded in

the sweat and their tips still be 2 cm

apart. There must be no intervening

bub-bles. As each wire is positioned its

corre-sponding binding post is tightened.

The instrument is now plugged into the

house current and the switch of the

con-ductivity unit is turned on. After the

“elec-tric eye” begins to glow green, the knob

of the conductivity indicator is adjusted to

that point wilich gives the widest opening of the “eye.” The pointer now indicates

that strength of sodium chloride solution

(in meq/l) wilose conductance equals tile

(3)

Normal’ Cy8tic Fibrosis*

Age Nv mber

(yr) !l.eadincjf

Age

Number (yr) Readingf

.lge

Number (yr) Iteadingt

12 ‘2 15)7 3 1)7 4 17 5 ‘2 6 ‘2 7 ‘2 8 3 9 5 10 6 11 6 12 8 13 10 14 15 15 15 16 15 17 ‘24 >150 135 >150 >150 150 125 135 125 >150 140 150 120 150 125 130 125 >150 57 60 40 70 30 35 25 40 30 20 30 28 30 25 50 22 50 70 30 50 30 30 25 33 35 50 30 30 50 40 30 30 50 60 45 65 45 60 35 35 32 30

C Normal range 20 to 80, average 44; cystic fibrosis range 120 to > 150.

t

The instrument reading indicates the strength of sodium chloride solution in meq/l that equals in conductance

the sample of sweat.

TABLE I

THE ELECTRICAL CONDUCTANCE OF SWEAT: NORMAL AND ABNORMAL (CYSTIC Fimcosts)

1 (1 wk)

‘2 3 4 5 6 7 547 8 9 5)7 11 5 i-I 11 1 5 13 557 14 15 16 17 18 517 19 ‘20 ‘21 15)7 ‘23 1557 ‘24 ‘25 ‘26 15)7 27 ‘28 15)7 ‘29 15)7 30 81 ‘2 ‘2 33 ‘2 34 ‘2 35 ‘2 36 ‘2 37 ‘2 38 ‘2 39 3 40 4 41 4 42 4

43 4 30

44 5 ‘25

45 5 35

46 5 65

47 5 40

48 6 25

49 6 50

50 6 50

51 6 40

52 6 70

53 6 40

54 7 50

55 7 35

56 8 75

57 8 45

58 8 30

59 9 30

60 9 50

61 9 35

62 10 40

63 10 40

64 11 50

65 11 30

66 11 50

67 11 30

68 11 43

69 15 60

70 18 48

71 25 55

72 28 55

73 30 50

74 36 65

75 36 70

76 37 80

77 38 40

78 38 55

79 40 40

80 46 65

81 50 60

82 54 55

(4)

92 SWEAT CONDUCTIViTY

emphasized that this reading is not the

level of tile sodium cilloride in the sweat. It is rather an indication of the total

elec-trolyte content as reflected by its ability to

conduct electricity. It is true that sodium

and chloride ions are the most influential

iOflS 011 this condluctance because of their

numerical superiority in sweat.

Accord-ingly sweat samples showing abnormally

high conductivity rates will also have

aT)-normally higlu sOdliunl andl chloridle

con-tent.

RESULTS

A large series of \vell-colltrOlled tests has

1)eefl presented in an earlier article.1 The

following results were obtained in a pedi-atric practice located in an area where

Cilemical analysis of sweat was not readily

available.

In 104 attempts we were unable to

oh-tam sufficient sweat for testing in four

subjects. Three of these failures were in

infants and OllC was in an adult. The yield

of sweat was usually between 0.2 and 0.5

ml. Only a fraction of this amount is

needed. Of tile 100 successfully completed

tests, 8:3 were made 011 normal subjects.

or n patients with illnesses other than

cystic fibrosis. In tilis nollcystic fibrosis

group tile lowest readhng was 20, while

the Ilighest was 80; the average was 44. Tile remaining 17 tests were done on 17

patiellts known to have cystic fibrosis. In

this group the lowest reading was 120,

while five of the group gave readings

higher than 150, whicil is beyond the

ac-curate range of the instrument

(

Table I).

SUMMARY AND CONCLUSIONS

All apparatus for determining the

elec-trical conductivity of undiluted sweat has

been described. The technique used and

the results obtained have been presented.

The results indicate that the instrument,

\vllen used with the technique described,

is of value in the diagnosis of cystic

fi-brosis ill children.

ADDENDUM

Since this ork \VdS completed the instrument

has l)eell improve(l l the’ addition of a control

for calibration. This is accomplished b simply

sui)stituting I variable 70K-ohm resistor for the

50K-ohm 6xei resistor in the wheatstone bridge

(Fig. 1). At the beginning of a test, a standard

solution containing 100 med1 of saline solution is

Plt1e(l in the conductivity pip:tte. The

conduc-tivitv indicator is set at 100. The calibration

con-trol is tlse’n adjusted until the eye is at its widest opening. This automatically compensate’s for

van-ations in ambient temperature, as well as other intrinsic variations from the original calibration.

REFERENCES

1. Shvachmin, H., Dunham, R., and Phillips, IV.

Fl. : Electrical conductivity of sveat : a simple

diagnostic test ill children. PEDIATHICS, 32:85,

1963.

2. Cil)SOl1, L. E., and Cooke, B. E. : A test for

concentration of electrolyte in swe’at in cystic

fll)rosis of tl#{236}epancreas utilizing pilocarpine

iOfltO1)horeSis. PEDIATRICs, 23:545, 1959.

:3. Bloxam, A. P.: A new instrument for the

measurement of electrical conductivity of

(5)

1963;32;89

Pediatrics

William R. Phillips

Apparatus

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(6)

1963;32;89

Pediatrics

William R. Phillips

Apparatus

ELECTRICAL CONDUCTIVITY OF SWEAT: A Simple, Home-assembled

http://pediatrics.aappublications.org/content/32/1/89

the World Wide Web at:

The online version of this article, along with updated information and services, is located on

American Academy of Pediatrics. All rights reserved. Print ISSN: 1073-0397.

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