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3 Poor 4, L5, M5の5誘 R Wave Progression例 に お け る 陳 旧性 前 壁 梗 塞 の 鑑 別 点 に お け る電 位 時 間積 分 値 の 平 均 値 を梗 塞 群, 導 点 を 用 い た 判 別 式Z=- 非 梗 塞 群 の 各 々 で 求 め 平 均 電 位 図 を作 成 した G5-9.0 G2+6.0 H L M5+0.4 (単 位:mV)で, ま た, QRS開 Z 0な 始 よ り20msecの ら ば 梗 塞 群, Z<0な ら ば 非 梗 塞 群 と診 断 す る と, 均 値 よ りIsopotential sensitivity specificity 図 を作 成 し た.梗 塞 群,非 racy 93.9%, 93.3%で,い 92.6%, accu ず れ の 判 別 式 も極 め て 高 い分 別 能 を 示 し た(表2).前 壁 梗 塞 の 心 電 図 変 化 は, 主 と して 左 前 胸 部 の 誘 導 を 中 心 に 現 わ れ る こ と は よ く知 ら れ て い る.そ 点(E I列)の し た.左 用 い て,同 こ で,左 前 胸 部32誘 導 み を用 い た 場 合 の 診 断 能 を検 討 前 胸 部32誘 447 導 点 のQRST 様 の 方 法 でG4, area F1の2誘 を 比 較 す る と, QRST 時点 の電位 の平 (Q 20) mapの 梗 塞 群 の平 均 電 位 図 area mapで 導 点 を選 は,梗 塞 群 は 非 梗 塞 群 に 比 べ て 左 前 胸 部 に 陰 性 域 が 張 り出 し,極 大,極 小 の 位 置 が 左 下 方 に 偏 位 し た.し か し, QRS area map, で は 梗 塞 群,非 Isopotential (Q 20) map 梗 塞 群 の2群 間 に 大 き なパ ター ン の 差 は 見 られ な か っ た(図2).そ mapを 平均 電位 パ ター ン に 差 の 見 られ たQRST こで両群 に area mapを 用 択 し,こ れ か ら 導 か れ た 判 別 式Z=-4.2 G4+ い て,左 前 胸 部 に-20μVS以 2.4 F1+0.2を め るか 否 か で 前 壁 梗 塞 の有 無 を診 断 す る と,sensi sensitivity 用 い て2群 87.9%, 間 の 判 別 を 行 う と, specificity 85.2%と87誘 導 点 か ら求 め た も の に 比 べ て 診 断 率 は や や 劣 っ て い た.尚,こ こ で い うsensitivityは(true tive)/(true positive+false negative)/(true false し て 算 出 し た. 4. 平 均 電 位 図 の2群 QRST 図1 area map, negative+ area 87.9%, 誘導 85.2%, area mapの accuracy パ ター ンか らで もあ る程 度 鑑 別 が 可 能 で あ っ た. 標 準12誘 導 心 電 図 を用 い た 診 断 基 準 次 にmapか ら得 ら れ た こ れ らの 情 報 を参 考 準12誘 導 心 電 図 を用 い て両 群 の判 別 を試 み た. QRST mapで,各 specificity あ り, QRST に し て,標 間 の比較 QRS 86.7%で 5. negative), specificityは(true positive)と posi tivity 上 の 陰 性 部 分 を認 mapに area mapお よびQRS area お い て,判 別 関 数 を作 成 す る際 にG4の PRWP例 の梗 塞 群 と非 梗 塞群 で有 意差 の あっ た誘 導部 位 いず れ のmapで も左 前 胸部 誘 導 で梗 塞群 の 値 が有 意 に低 か った. A線 は右 中腋 窩線, I線 は左 中 腋窩 線, E線 は胸部 正 中線 を示 す.黒 丸は 標 準12 誘 導心 電 図 の胸 部 誘 導 点 を示 す.
4 448 井 点 が 最 も判 別 に 寄 与 す る と考 え られ た.そ 標 準12誘 導 心 電 図 の 胸 部 誘 導 の う ち,最 に近 いV4誘 の 異 常Q波(幅 比>15%)6)が 表2 図2 導 を用 い て 検 討 し た.即 0.04sec,深 存 在 す るか,ま 判 別 関数 を用 い たPRWP例 PRWP例 こで もG4 ちV4で さ 2mm, た はT波 原 Q/R 敬 子 つ ま り 陰 性T波 ま た は 二 相 性T波 場 合 を 前 壁 梗 塞 とす る と,診 90.9%, specificity 66.7%, が 存在 す る 断 率 はsensitivity accuracy 80.0%で あ っ た. の 変 化, の診 断率Z 0な らば梗 塞群, Z<0な の梗 塞 群(左 側)と 非梗塞 群(右 側)の 平均 値 の電 位 図QRST らば 非梗 塞群 と診 断 した. area map(上 段)で は,梗 塞 群 で左 前 胸 部 に陰 性域 が張 り出 し,極 大,極 小 の位 置 が左 下 方 に偏位 してい る.陰 影 の部 分 は 陽性 電位 領 域,+は 極 大,-は 極小.
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8 2) Yamada K, Toyama J, Wada M, Sugiyama S, Sugenoya J, Toyoshima H, Mizuno Y, Kobayashi T, Okajima M: Body surfase isopotential mapping in Wolff-Parkinson-White syndrome: noninvasive method to determine the localization of the accessory atrioventricular pathway. Am Heart J (1975) 90, ) Toyama S, Suzuki K, Koyama M, Yosino K, Fujimoto K: The body surface isopotential mapping of the QRS wave in myocardial infarction. A comparative Electrocardiol (1982) 15, study of scintigram with Tallium 201. J 7) Young E, Cohr PF, Gorlin R, Levine HD, Herman MV: Vectorcardiographic diagnosis and electrocardiographic correlation in left ventricular asynergy due to coronary artery disease I: Severe asynergy of the anterior and apical segments. Circulation (1975) 51, ) Zema MJ, Klibfdeld P: Electrocardiographic poor R wave progression I: Correlation with the Frank vectorcardiogram. J Electrocardiol (1979) 12, ) DePace NL, Colby J, Hakki A, Manno B, Horowitz LN, Iskandrian AS: Poor R wave progression in the precordial leads: Clinical implications for the diagnosis of myocaridal infarction. JACC (1983) 2,
9 New York. 13) Grant RP: The relationship of unipolar chest leads to the electrical field of the heart. Circulation (1950) 1, ) Zema MJ, Kligfield P: Electrocardiographdic poor R wave progression III: The Normal Variant. J Electrocardiol (1980) 13, ) Zema MJ. Collins M, Alonso DR, Kligfield P: Electrocardiographic poor R wave progression: Correlation with post mortem findings. Chest (1981) 79, ) Wilson FN: The determination and significance of the areas of the ventricular deflections of the electrocardiogram. Am Heart J (1934) 10, ) Zema MJ, Kligfield P: Electrocardiographic poor R wave progression II: Correlation with angio graphy. J Electrocardiol (1979) 12, ) Zema MJ, Kligfield P: ECG Poor R wave progression: Review and synthesis. Arch Intern Med (1982) 142,
10 Usefulness of body surface maps for discriminating old myocardial infarction in cases with ECG findings of poor R wave progression Keiko IHARA First Department of Internal Medicine, Okayama University Medical School, Okayama 700, Japan (Director: Prof. T. Tsuji) The clinical usefulness of the body surface maps (maps) to discriminate old anterior myocardial infarction (OAMI) in patients whose ECG showed poor R wave progression (PRWP) was examined. The maps of 60 patients with PRWP, including 33 cases of OAMI and 27 without myocardial infarction (non-mi) were recorded. The multivariate stepwise discriminant analysis elucidated that 5 leads (G4, C3, J5, B3, A5) of the QRST area map would contribute to the discrimination of OAMI from non-mi, and the the formula z=-6.0 ~G ~C3+9.1 ~J ~B3-9.0 ~A5-1.1 (unit: 0.1mVS), using these parameters two groups were separated with a sensitivity of 90.9% and a specificity of 96.3%. The discriminating performance using 5 leads (G4, H2, H4, L6, M5) of the QRS area map and 5 leads (G5, G2, H4, L5, M5) of the Q20 map gave a sensitivity of 90.9%, and 93.9%, and specificity of 96.3%, and 92.6%, respectively. Furthermore, the formula was applied to 26 new consecutive patients with PRWP for evaluating this formula. The indicies obtained from the QRST area map gave the best results, and provided a sensitivity of 85.7% and a specificity of 100%. In the pattern of the QRST area map, the existence of the regions less than -20ƒÊVS can fairly identify the OAMI (sensitivity 87.9%, specificity 85.2%). These findings suggest that the mathematical models obtained from the result of map analysis, especially QRST area maps, are useful to discriminate OAMI among the cases with PRWP.
Electrophysiologic and vectorcardiologic studies in a patient with Wolff-Parkinson-White syndrome Type A associated with complete right bundle branch block Yasuki Sakamoto*, Shunpei Ohkubo*, Shutaro Satake*,
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