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Türk Kardiyol Dem

Arş

/999; 27:156-158

Changes in QT Dispersion Magnitude During

Respiratory Phases: Role of Maximum Inspiration and Expiration

Ertan YETKiN, MD, Ahmet Y ANlK, MD, Makbule KUTLU, MD, Mehmet İLERi, MD, Sengül ÇEHRELİ, MD

Türkiye Yüksek ihtisas Hospital, Department ofCardiology, Ankara, Turkey

ÖZET

SOLUNUM FAZLARlNDA DiSPERSiYON DEGiŞiM_LERi: MAKSiMf!.M iNSPiRASYON VE EKSPIRASYONUN ROLU

QT interval dispersiyonunun

güvenilirliği

ve prognostik

değeri hakkında

gözlemciler

arası değişiklikten

kaynakla- nan

tartışmalar

mevcuttur.Bu

çalışma sağlıklı erişkinlerde

QT intervalinin ve QT dispersiyonunun

sol~ı­

nunı

fazlarmdan

etkilendiği

hipotezini öne

sürnıektedır.

Sağlık

personelinden

oluşan

60 gönüllü

erişkin

(38 erkek, 22

kadın,

ortalama

yaş=25) çalışma

grubunu

oluşturdu.

Elektrokardiyogranılar aynı

tekniker

tarafından

50

nını/s hızında

normal solunum, zorlu

inspiriyunı

ve zorlu ekspi-

riyunı sırasında

çekildi. QT interval 12 derivasyonda ölçülen maksimum ve minimum QT intervalleri arasmdaki fark olarak

tamnılandı. Düzeltilmiş

QT intervali (QTc) Bazzet formu/üne göre

hesaplandı.

Normal

solununıla karşılaştırıldığında

zorlu

inspiriyunı

ve ekspiriyum

sırasındaki

QTc maximum interval/eri arasmda

farklılık

yoktu

(sırasıyla

409±22ms vs 417±26

nıs,

P>0.05 ve 412±

18nıs

vs 417± 26ms, P>0.05). Zorlu

inspiriyunı

ve ekspiriyum

sırasmdaki

QTc dispersiyonu normal solu- numdakinden daha

düşüklü (sırasıyla

36±8 ms vs 44± 9 ms P<0.001 ve 32±7 vs 44±9 ms, P< 0.001 ). Zorlu ek-

spi;·iyunıdaki QTc dispersiyonu zorlu inspiriyumdakinden daha

düşüktü

(p<0.01 ).

Sağlıklı erişkinlerde

QT disper- siyonu solunum

fazlarından

etkilenmektedir ve normal

solununıla karşılaştırıldığında

hem zorlu

inspiriyunıda

hem d e zorlu

ekspiriyunıda

QT dispersiyonu

azalmaktadır.

Anahtar kelime/er: QT dispersiyonu, solunum

fazları

QT dispe rsion d efined as interlead QT variability in a I 2 lead electrocardiogram (ECG) was proposed by Day et aJ(1) asa simple m ethod to e valuate the repo-

larİzation

heterogenicity of the ventricular myocardi- um(2,3). Due to its great potential elinical usefull- ness(4-5) it has gained much importance during re- cent years. However there is stili controversy about the reliability and its prognostic value because of Recived· 20 Ekim 1998, revi sion

acccpıed

February 9 1999 Adress for correspondence: Dr. Ertan Yetkin, Hoşdere Caddesi 8/20

Ayrancı

, Ankara 1 Turkey

e-mail: eryetkin @

ıumeı.neı.ır

Phone: +90 31 2 466393

156

inter- and intraobserver variability(7). T he present study hypothesis that QT interval duration and QT dispersion are effected by the respiratory phases in healthy subjects.

PATIENTS and METHODS

Sixty healthy volunteers (38 men, 22 women, mean age

=25±3) from the medical staFf compriscd the study group.

All subjects had normal ECG tracing. 1 2 lead ECG wcre recorded by the same technician ata rate of 50 mm/s

du~­

ing normal respiration, maximum inspiration and

ın.axı­

muın

expiration. ECGs were coded and all

annotatıons

were masked. QT interval was

ıneasurcd

from the onset of the QRS complex to the end of the T wave,defined as its return to the T-P isoel ectric basel ine. QT interval

ıneasure­

ınent

in individual leads of a single heart beat were per- formed by a blinded observer us ing a standart electrocardi- ographic lineal. After complction of the measurements all ECGs were decoded. QT dispersion was defined as the diff erence between the maximal and

miniınal

QT interval measurements occuring among any of the 1 2 leads. Cor- rected QT interval (QTc) was calculated according to Ba- zett's form ula(8) as follows; QTc = QT/ square root of the R-R interval. QTc dispers ion was calculated in a simil iar manner used for QT dispersion. QTc dispersion for nor- mal breathing , maximum inspiration and maximum expi- ration were calculated. Results are expressed as mean ± SO. And for comparison Wilcoxon matched pairs test was used. A p value of p<0.05 was considered as significant.

RESULTS

Table 1 represents the maximum QTc interval and QT dispers ion measurement during normal breath- ing, maximum insp iration, and maximum expiration.

There were no s ignificant differences QTcmax inter-

val measurement during maximum inspiration and

expiration compared to that in normal breathing

(409±22 ms vs 417±26 ms, p>0.05 and 412±18 ms

vs 417±26 ms, p>0.05 respectively). QTc disper-

s ion magnitude during bo th maximum ins piration

and maximum expiration were s ig nificantly lower

(2)

E. Yetkin et al: Changes in QT Dispersion Magnitude During Respiratory Phases: Role of Maximum lnspiration and Expiration

Table 1. Maximum and minimum correcled QT intervals and QTc dispersion values during

Normal Respiration Maximum lnspiration Maximum Respiration

QTcmax (ms) 417±26 409±22 4 1 2±1 8

QTcmin (ms) 373±18 373±14 380±13

QTdc (ms) 44±9 36±8* # 32±7**

* P< 0.003 vs during normal respiration, ** P< 0.003 vs during normal respiration, If P< 0.01 vs maximum expiration., QTcmax =Maxi- mum corrected QT interval duration, QTcmin =Minimum corrected QT interval duration, QTdc = Corrected QT dispersion. All values are given as mean±SD.

than that during normal breathing(36±8ms vs 44±9 ms, p<O.OOl and 32±7 ms vs 44±9ms p<O.OOI).

There were also significant difference between the QTc dispersion during maximum inspiration and ex- piration ( p<O.O 1 ).

DISCUSSION

The present data demonstrated two main

fındings.

First the QTc dispersion during both maximum in- sp iration and maximum expiration are lower than that of normal breathing. Second, QTc dispersion during maximum expiration is lower than that dur- ing maximum inspiration. K.rautzner et al

(7)

has found significant intra- and interobserver variability regarding the QT dispersion in healthy individuals and has suggested that QT dispersion may be a con- sequence of inaccuracies of QT interval measure- ment or of a different orientation of individual leads to a si ngle repolarization vector. Commonly used electrocardiographic machines record simultaneous- ly 3 or 6 leads only ; thus QT interval used for QT dispersion measurement are evaluated in 2 or 4 heart beats possibly from different phases of respiratory cycle. In our study both maximum inspiration and maximum expiration decrease QT dispersion value by about 1 8% and 25% respectively. T he result o f this study may contribute to the intra- and interob- server variability documented by K.rautzner et al

(7).

Krupienicz et. al

(9)

has reported simili ar QT disper- sion decrease during both maximum inspiration and expiration . But there were not statistically signifi- cant difference between maximum inspiration and expiration. In our study we have also showed that the QT dispersion during maximum expiration is

signifıcantly

lower than that during maximum inspi- ration. The change in QT dispers ion magnitude may be rela ted to the anatomic location of the heart in the

c hest cage. Such a relation was found to be responsi- ble for the "P pulmonale" appearance in e lectrocar- diogram by Maeda et aJ (I O)_ Considering the heart in a more stationary position during maximum in- spiration and expiration than that during normal res- piration may be a n explanation of the lower QT dis- persion magnitude. According to this hypoth esis , lower QT dispersion value during maximum expira- tion may also be related to the close proximity of the heart to the chest wall. Neverthe less, it is hard to say that the change in QT d ispersion magnitude is completely due to the position of the heart during respiration. The partial a lveolar

a nd

COı

pres- sures, body habitus may also play a role in QT dis- persion. Kiely et.a)(I I) has found that hypercapnia sign ificantly increased both QTc interval and QTc dispersion . The documented phenomenon of the re- lation between QT disper sion magnitude and respir- atory phases adds an other question mark to the val- ue of QT dispersion as a marker of regional inhomo- geneity of ventricular repolarization in humans.

In conclusion, QT dispersion magnitude is effected by the respiratory phases in healthy s ubjects and decrease during both max imum inspiration and expi- ration compared to normal respiration. And the de- crease is more evident during maximum expiration.

REFERENCES

1. Day CP, McComb JM, Campbell RWF: QT disper- sion: an indication of arrhytmia risk in patient with long QT interval. Br Heart J 1 990; 63: 243-244.

2. Statters DJ, Malik M, Ward DE, Camm AJ: QT dis- persion: Problems of methodology and elinical signifi- cance. J Cardiovasc Electrophysiol 1 994; 5: 672-685.

3. Hii JTY, Wyse DG, Gillis AM, Duff HJ, Solylo MA, Mitchell LB: Precordial QT interval dispersion as a marker of torsade de pointes. Circul ation 1992; 86: 1376-

1382.

157

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Türk Kardiyol Dem

Arş

/999; 27: 156-158

4. Barr CS, Naas A, Freeman M, Struthers AD: QT dis- persion and sudden unexpected death in chronic heart failure. Lancet 1994; 343: 327-329.

S. Trusz-Giuza M, Wozniak-Skowerska I, Giec L, Szydlo K: Dispersion of the QT interval as predictor of cardiac death in patients with coronary heart disease.

PACE 1 996; 19:1900- 1904.

6. Leitch J, Basta M, Dobson A: QT dispersion doesn't

predicı

early venticular fibrillation after

acuıe

myocardial infarction. PACE

ı995;

1 8:45-58.

7. Krautzner J, Gang YI, Camm AJ, Malik M: Short and long

ıerm

reproducebility of QT, QTc and QT disper- sion measurement in healty subjects. PACE

ı994;

17:928:

937.

158

8. Ahnve S: Correction of the QT interval for heart rate : review of different

formuıas

and the use of Bazett's for- mula in myocardial infarction. Am Heart J 1985; 109:568- 74.

9. Krupienicz A, Czarnecki R, Adamus J: QT disper- sion magnitude is related to the respiratory phase in healty subjects. Am J Cardiol

ı

997; 80(9):

ı

232- 1 234.

10. Maeda S, Katsura H, C hida K, et al: Lack of corre-

ıation

between P pulmanale and right atrial overload in chronic obstructive airways disease. Br Heart J

199ı;

65:

ı326.

ll. Kiely DG, Cargill RI, Lipwort BJ: Effects of hyper- capnia on hemadynamic, inolropic, lusitropic and electro- physiologic indices in humans. Chest

ı

996; 1 09(5):

ı

215-

1221.

Referanslar

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