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JPH06311979A - Functional residual capacity measurement method - Google Patents

Functional residual capacity measurement method

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Publication number
JPH06311979A
JPH06311979A JP5138844A JP13884493A JPH06311979A JP H06311979 A JPH06311979 A JP H06311979A JP 5138844 A JP5138844 A JP 5138844A JP 13884493 A JP13884493 A JP 13884493A JP H06311979 A JPH06311979 A JP H06311979A
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JP
Japan
Prior art keywords
nitrogen
patient
flow rate
gas
measurement
Prior art date
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.)
Pending
Application number
JP5138844A
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Japanese (ja)
Inventor
Tetsuo Adachi
哲夫 安達
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I VISION KK
Original Assignee
I VISION KK
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Filing date
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Application filed by I VISION KK filed Critical I VISION KK
Priority to JP5138844A priority Critical patent/JPH06311979A/en
Publication of JPH06311979A publication Critical patent/JPH06311979A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】 【目的】公知になっている窒素洗いだし法を改良して,
患者の治療に必要な呼吸モードのままで患者の負担を少
なく測定誤差を少なくかつ容易に患者の機能的残気量を
測定する方法を実現する。 【樽成】吸気ガスを純酸素に切り替えた後の患者の呼気
ガスをすべて捕捉して一方向の変動のある流れとして,
そこに流量測定部6と窒素濃度計7を配置して両信号の
積の時間積分量から機能的残気量を算出する。
(57) [Summary] [Purpose] By improving the known nitrogen flushing method,
(EN) A method for easily measuring a functional residual capacity of a patient while reducing the burden on the patient while reducing the measurement error while maintaining the breathing mode necessary for treating the patient. [Taru-nari] All the exhaled gas of the patient after switching the inspiratory gas to pure oxygen is captured and as a flow with one-way fluctuation,
The flow rate measuring unit 6 and the nitrogen concentration meter 7 are arranged there, and the functional residual air amount is calculated from the time integrated amount of the product of both signals.

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】この発明は呼吸疾患患者の呼吸機
能の診断に有力な数値の一つである機能的残気量の測定
法の改善に関するものである。 【0002】 【従来の技術】機能的残値量(Functional
Residual Capacity以下FRCと略す
る)は肺胞が至適に開いて換気が行われているかを示す
数値として呼吸疾患患者の呼吸機能の診断に有効な数値
として有効であることは周知であるが,,測定がさほど
簡単ではなくいまだ患者が検査室に赴き高価で大型の機
械で専門の検査技師のみによってしか出来ない検査であ
った。まして乳幼児の場合は測定量が微少で患者の協力
が得られない事から殆ど不可能に近かった。しかし近年
乳幼児の呼吸不全にたいする治療技術が向上して乳幼児
でより客観的な呼吸機能データが必要とされるようにな
り,FRCの必要性が高まりつつある。FRCを測定す
る代表的な方法としてはヘリウムガスを用いる閉鎖回路
法,空気に含まれる窒素を純酸素によって洗い出す方
法,密封したボックスに患者を置いて呼吸による圧力と
流量の変化から求めるプレチスモグラフ法がある。乳幼
児でFRCを測定する場合,ヘリウムによる閉鎖回路法
はリークがあるため使用しにくく,窒素洗いだし法は呼
吸毎の窒素の排出量を算出する場合,測定量が小さくま
た死腔の補正も困難でこれも実用的精度は得られない。
プレチスモグラフ法は測定設備が大がかりで簡単に実行
できるものではない。窒素洗いだし法の原理を用いて乳
幼児のFRCを容易に測定する方法がGerhardt
氏等によって発表されている。(参考文献A simp
le Method for Mesuring fu
nctional residual Capacit
y by N2 washout in Small
Animals and Newborn lnfan
ts 邦訳:小動物および新生児における窒素洗いだしによる
機能的残気量測定のための簡易法 ペデアトリック リ
サーチ vol.19,No.11 19851165
〜1169頁)この方法を要約すると,窒素を含む吸気
ガスを自発呼吸している患者を呼気の終末タイミングで
既知の流量の純酸素吸気ガスの流れる閉鎖管の一点で呼
吸させるように切り替え,患者の下流に呼吸にともなう
流量の変動を抑制し濃度を均一にするための容量のある
室を設け,その出口に高感度の窒素濃度計をおいて切替
後から濃度信号をゼロになるまで積分する。流量が既知
かつ一定であるからその積分値に適切な係数を乗ずれば
総窒素排出量が求められ従って患者の呼気終末での肺気
量即ちFRCが求められる。この方法は窒素濃度計の測
定点での流量が一定または平均として一定とみなされれ
ば簡単な構成で容易に測定できる優れた方法である。し
かし実際には患者の呼吸による下流での流量変動は充分
に抑制することが意外に困難でまた現実の窒素濃度計時
間遅れがありまた応答時間も無視できず,流量変動との
整合は困難で,ごく限られた呼吸回数や呼吸量の条件で
のみしか正確な測定が期待できない。またこの方法は自
発呼吸でしか測定が出来ず,よりクリティカルな人工呼
吸を必要としている患者で測定が出来ない。 【0003】 【発明が解決しようとする課題】本発明は上記の簡易窒
素洗いだし法の特に乳幼児のFRC測定精度を向上し,
自発呼吸でも人工呼吸でも精度よくかつ容易にFRCを
測定できる方法を提供しようとするものである。 【0004】 【発明の構成例】第一図は本発明の構成例を示してい
る。人工呼吸器部1は空気など既知の濃度の窒素を含ん
だ吸気ガスを供給出来るもので,一方人工呼吸器部2は
純酸素の吸気ガスを供給するものである。具体的にはそ
れぞれを単独の市販の人工呼吸器を2台準備してもよ
い。ただ人工呼吸器部2は後に述べるように測定時に用
いるもので,純酸素または高い酸素濃度が既知で安定で
供給できること及び呼気側で排出されるガスをすべて捕
捉して閉鎖した管系に送り込めることが必要である。そ
れぞれの患者口は回路切替器3の入力3−1及び3−2
に接続されている。患者4はマスクまたは気管内挿管を
へて回路切替器3の出力口3−3に接続されて回路切替
器3の動作状態により当初3−1と3−3が接続され人
工呼吸器部1から窒素を含む吸気ガスを呼吸している。
一般に人工呼吸器は定常流を出して自発呼吸をさせた
り、陽圧間欠工呼吸を与えたりその混合モード(いわゆ
るIMV)を与えることが出来るので,この場合も患者
の状態と必要に応じて後に述べるようにいずれのモード
にでも人工呼吸器部1から呼吸させて測定を開始でき
る。一方人工呼吸器部2はできるだけ人工呼吸器部1と
吸気ガス以外は同じ条件で呼吸モードを設定しておく
が,その送気は回路切替器3の入口3−2で行き止まり
になった状態になってその呼気ガスは次に述べる測定系
を通じて排出されている。人工呼吸器部2の呼気弁を含
む呼気側回路5には患者4の呼気ガスを含むすべてのガ
ス流を回収出来るような構造として,回収したガスはそ
の下流にゴム製のバッグなど柔らかく弾力性のあるリザ
ーバ部8を通過させ,その更に下流に流量測定部6と窒
素濃度計7を配置する。窒素濃度計7としては真空グロ
ー放電光輝のの窒素濃度依存性を用いたものが広く用い
られており,所要サンプルガス量が数mL/分と少なく
0.1秒程度の遅れと応答性を持っている。実際の機器
構成においては,計測制御部9にはマイクロコンピュー
タを用いる。測定の前には流量測定部6の校正,窒素濃
度計7の校正等をおこなわせその結果を記憶しておけ
る。さらに患者4の口元にも患者呼吸を監視する目的で
ニューモタコグラフ等を用いる流量測定部10をおいて
おけばマイクロコンピュータはその信号を監視してい
て,呼気終末の認識をして測定時の切替器3の操作を自
動的に行わせる事が出来る。 【0005】 【測定動作の説明】測定は患者4の呼気終了のタイミン
グで回路切替器3を操作して次の吸気から人工呼吸器部
2からの送気つまり純酸素で患者を呼吸させることで開
始する。患者4のFRCに相当する部分に含まれる窒素
ガスが純酸素呼吸により呼気側回路5に向かって呼気と
混合して流出していく。流出ガスは一方向の変動する流
量となりその流量は流量測定部6でニューモタコグラフ
など圧力損失の小さい流量センサを用いて測定されまた
流れているガスの窒素濃度は窒素濃度計7によって測定
され計測制御部9に送られる。流出ガスの瞬時流量は患
者の自発呼吸かまたは人工呼吸モードならばその吸気呼
気の相によって増減変化する。しかしリザーバ部8があ
るので例え陽圧間欠人工呼吸であっても流皿がゼロにな
るような事はなく平滑化されて流量測定部7に与えられ
る。測定開始後は流量信号と窒素濃度信号を計測制御部
9では掛け合わせて瞬時の窒素ガス量を得てこれを濃度
信号がゼロになるまで積分する。その積分量は患者4か
ら洗い出された窒素の総量を表しており,測定開始前の
吸気ガスの窒素濃度で除すことによりFRCが求められ
る。種々の呼吸条件下で精度を保つためには窒素ガス濃
度信号の遅れ時間を考慮することが望ましい。遅れの補
正を行うには別途遅れ時間を正確に求めておき,その値
を計測制御部9に与えておき,その時間だけ古い流量信
号を用いて積分を行うとよい。なお濃度信号がゼロにな
ったらすばやく元の人工呼吸器部1に患者4を回路切替
器3を操作して戻すべきである。検査という観点からは
人工呼吸器部1は本来患者4を治療するために使用して
いる人工呼吸器であってよい。 【0006】 【発明の効果】計測開始後に於いて呼気側回路5の下流
での洗いだし流は変動しているがその流量を瞬間瞬間に
計測してその瞬間の濃度と掛け合わせる。従って患者の
呼吸モードが定常流下の自発呼吸でも陽圧間欠呼吸で吸
気の時間下流の流量がゼロになってもその状態に対応で
きる効果がある。説明例ではリザーバ8を呼気下流に設
けているがこの理由で必ずしもリザーバ8を用いる必要
はない。ただ流量信号として陽圧間欠人工呼吸の場合の
ように断続のある波形であるより前に引用した簡易法と
同様にリザーバのようなフィルタ素子で流量信号を平滑
しておいたほうが,流量測定部6や窒素濃度計7の応答
性が矩形波状の速い変化に対してアーチファクトによる
誤差を生じ易いことからそれを避ける意味で望ましい。
本発明では測定開始前流量計測部6と窒素濃度計7には
純酸素のみが流れている。もし人工呼吸器部2が純酸素
を用いていなく窒素が幾らか含まれていても開始前にお
いてこの濃度で計測制御部9の窒素濃度信号のゼロをバ
イアスしておけば計測開始後において患者からの追加の
窒素がなくなったとき入力濃度信号はゼロになるのでF
RCの算出は可能である。この点は患者4の状況により
例え短時間でも純酸素を吸入させたくない時など有効で
ある。また前述のように人工呼吸器部1の吸気ガスの酸
素濃度即ち(100−窒素濃度)は必ずしも空気の2
0.6%である必要がなく正確な数字が既知であればよ
い。実際にはあまり窒素濃度が低くなると測定誤差が大
きく実用的でないが,この点も患者4の治療上酸素濃度
が余り下げられない場合有効である。これまでに述べた
本発明による窒素洗いだし法は乳幼児を想定して説明し
たが,この方法は成人でも使用する各構成部品のサイズ
が異なるだけでそのまま適用でき,その効果を活用でき
る。コンピュータを測定システムに用いることにより測
定中のデータの計算処理はもちろん,窒素濃度のゼロの
監視を行い測定の終了を感知して自動的に元の治療用の
人工呼吸器部1に患者4をすばやく戻して測定に伴う純
酸素呼吸を必要最小限度にどどめることが可能になり患
者を安全に保つことが可能になる。また全体として測定
操作の簡易になり且つ精度の高い結果が得られるように
なる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in the method for measuring functional residual capacity, which is one of the influential numerical values for diagnosing respiratory function in patients with respiratory diseases. is there. 2. Description of the Related Art Functional residual value (Functional)
It is well known that the Residual Capacity (hereinafter abbreviated as FRC) is effective as a numerical value indicating whether the alveoli are optimally opened and ventilation is effective as a numerical value effective for diagnosing respiratory function in patients with respiratory diseases. , Measurement was not so easy, and the patient went to the laboratory and it was an expensive and large machine that could only be performed by a specialized technician. In the case of infants, it was almost impossible because the amount of measurement was so small that the patient could not cooperate. However, in recent years, the treatment technology for respiratory failure in infants has improved, and more objective respiratory function data have been required for infants, and the need for FRC is increasing. Typical methods for measuring FRC include a closed circuit method using helium gas, a method in which nitrogen contained in air is washed out with pure oxygen, and a plethysmograph method in which a patient is placed in a sealed box and the change in pressure and flow rate due to breathing is performed. is there. When measuring FRC in infants, the closed circuit method using helium is difficult to use because of leaks, and the nitrogen flushing method is small in measuring the amount of nitrogen discharged per breath and it is also difficult to correct dead space. Therefore, this is also not practically accurate.
The plethysmograph method requires large measuring equipment and cannot be easily implemented. Gerhardt is a method to easily measure the FRC of infants using the principle of the nitrogen flushing method.
It has been announced by Mr. (Reference A Simp
le Method for Measuring fu
nctional residual Capacit
y by N2 washout in Small
Animals and Newborn Infan
ts: A simple method for measuring functional residual capacity by nitrogen flushing in small animals and newborns Pedeatrick Research vol. 19, No. 11 19851165
To summarize this method, patients who spontaneously breathe inspiratory gas containing nitrogen are switched to breathe at a single point in a closed tube through which a known flow of pure oxygen inspiratory gas is breathed at the end timing of expiration, and the patient is breathed. A chamber with a capacity for suppressing fluctuations in flow rate due to respiration and making the concentration uniform is provided downstream of, and a highly sensitive nitrogen concentration meter is placed at its outlet, and the concentration signal is integrated until it becomes zero after switching. . Since the flow rate is known and constant, the integral value is multiplied by an appropriate coefficient to determine the total nitrogen excretion, and thus the end-expiratory lung volume or FRC of the patient. This method is an excellent method that can be easily measured with a simple configuration if the flow rate at the measurement point of the nitrogen concentration meter is considered to be constant or average. However, in reality, it is surprisingly difficult to sufficiently suppress the flow rate fluctuation in the downstream due to the patient's respiration, and there is an actual nitrogen concentration meter time delay, and the response time cannot be ignored, and matching with the flow rate fluctuation is difficult. , Accuracy can be expected only under the condition of very limited respiratory rate and volume. In addition, this method can measure only spontaneous breathing, and not in patients who require more critical artificial respiration. SUMMARY OF THE INVENTION The present invention improves the FRC measurement accuracy of the above-mentioned simple nitrogen flushing method, especially for infants,
It is intended to provide a method capable of accurately and easily measuring FRC in both spontaneous and artificial respiration. Configuration Example of the Invention FIG. 1 shows a configuration example of the present invention. The ventilator part 1 is capable of supplying inspiratory gas containing a known concentration of nitrogen such as air, while the ventilator part 2 is capable of supplying inspiratory gas of pure oxygen. Specifically, two commercial ventilators, each of which may be used alone, may be prepared. However, the ventilator part 2 is used at the time of measurement, as will be described later, and it is known that pure oxygen or high oxygen concentration can be stably supplied and that all gas discharged on the expiratory side can be captured and sent to the closed pipe system. It is necessary. The respective patient mouths are inputs 3-1 and 3-2 of the circuit switching device 3.
It is connected to the. The patient 4 is connected to the output port 3-3 of the circuit switching device 3 through a mask or endotracheal intubation, and initially 3-1 and 3-3 are connected depending on the operating state of the circuit switching device 3 and the ventilator part 1 Breathing inspiratory gas containing nitrogen.
In general, a ventilator can generate a steady flow for spontaneous breathing, positive pressure intermittent breathing, or mixed mode (so-called IMV), so in this case as well, the patient's condition and later As described below, the measurement can be started by breathing from the ventilator unit 1 in any mode. On the other hand, the ventilator part 2 sets the breathing mode under the same conditions as the ventilator part 1 except the inspiratory gas as much as possible. Then, the exhaled gas is discharged through the measurement system described below. The expiratory side circuit 5 including the expiratory valve of the ventilator unit 2 has a structure capable of collecting all gas flows including the exhaled gas of the patient 4, and the collected gas is soft and elastic such as a rubber bag downstream thereof. The flow rate measuring unit 6 and the nitrogen concentration meter 7 are arranged further downstream of the reservoir unit 8 having the above. As the nitrogen concentration meter 7, the one using the nitrogen concentration dependence of the vacuum glow discharge brightness is widely used, and the required sample gas amount is as small as several mL / min, and it has a delay and response of about 0.1 seconds. ing. In the actual device configuration, the measurement control unit 9 uses a microcomputer. Before the measurement, the flow rate measuring unit 6 and the nitrogen concentration meter 7 can be calibrated and the results can be stored. Further, if a flow rate measuring unit 10 using a pneumotachogram or the like is placed at the mouth of the patient 4 for the purpose of monitoring the patient's breathing, the microcomputer monitors the signal and switches the time of measurement by recognizing the end-expiration. The operation of the vessel 3 can be automatically performed. [Measurement of Measurement Operation] The measurement is performed by operating the circuit switching device 3 at the timing of the expiration of the patient 4 and breathing the patient from the next inspiration to the insufflation from the ventilator unit 2, that is, pure oxygen. Start. The nitrogen gas contained in the portion corresponding to the FRC of the patient 4 is mixed with the exhaled air toward the expiratory side circuit 5 by pure oxygen breathing and flows out. The outflow gas has a unidirectional fluctuating flow rate, and the flow rate is measured by a flow rate measuring unit 6 using a flow sensor with a small pressure loss such as a pneumotachography graph, and the nitrogen concentration of the flowing gas is measured by a nitrogen concentration meter 7 and measurement control is performed. Sent to department 9. The instantaneous flow rate of the outflow gas increases or decreases depending on the phase of the inspiratory expiration in the patient's spontaneous breathing or artificial respiration mode. However, since the reservoir 8 is provided, the flow tray does not become zero even if positive pressure intermittent artificial respiration is performed, and the flow is smoothed and supplied to the flow measuring unit 7. After the start of measurement, the measurement control unit 9 multiplies the flow rate signal and the nitrogen concentration signal to obtain an instantaneous nitrogen gas amount, and integrates this until the concentration signal becomes zero. The integrated amount represents the total amount of nitrogen washed out from the patient 4, and the FRC is obtained by dividing by the nitrogen concentration of the inspiratory gas before the start of measurement. In order to maintain the accuracy under various respiratory conditions, it is desirable to consider the delay time of the nitrogen gas concentration signal. In order to correct the delay, the delay time may be accurately obtained separately, the value may be given to the measurement control unit 9, and integration may be performed using the flow rate signal that is old by that time. When the concentration signal becomes zero, the patient 4 should be quickly returned to the original ventilator unit 1 by operating the circuit switch 3. From the viewpoint of examination, the ventilator unit 1 may be the ventilator originally used to treat the patient 4. After the start of measurement, the washout flow downstream of the expiratory circuit 5 varies, but its flow rate is measured at an instant and multiplied by the concentration at that instant. Therefore, even if the breathing mode of the patient is spontaneous breathing under a steady flow, even if the flow rate at the time downstream of inspiration becomes zero due to positive pressure intermittent breathing, there is an effect that it is possible to cope with the state. In the illustrated example, the reservoir 8 is provided downstream of the exhalation, but for this reason, the reservoir 8 does not necessarily have to be used. However, as in the case of the positive pressure intermittent respiration, the flow signal has an intermittent waveform. It is better to smooth the flow signal with a filter element such as a reservoir as in the simple method cited above. Since the responsiveness of 6 and the nitrogen concentration meter 7 easily causes an error due to an artifact with respect to a rapid change in a rectangular wave shape, it is desirable in the sense of avoiding it.
In the present invention, pure oxygen only flows through the flow rate measuring unit 6 before the start of measurement and the nitrogen concentration meter 7. Even if the ventilator unit 2 does not use pure oxygen and contains some nitrogen, if the nitrogen concentration signal of the measurement control unit 9 is biased to zero at this concentration before the start, the patient will start measuring after the start of measurement. Since the input concentration signal becomes zero when the additional nitrogen in the
RC can be calculated. This point is effective when it is not desired to inhale pure oxygen even for a short time depending on the condition of the patient 4. Further, as described above, the oxygen concentration of the inspiratory gas of the ventilator unit 1, that is, (100-nitrogen concentration) is not always equal to that of air.
It need not be 0.6% as long as an accurate number is known. Actually, if the nitrogen concentration is too low, the measurement error is large and it is not practical, but this point is also effective when the oxygen concentration cannot be lowered so much in the treatment of the patient 4. The nitrogen flushing method according to the present invention described so far has been described on the assumption of an infant, but this method can be applied to an adult as it is, only by changing the size of each component used, and the effect can be utilized. By using the computer for the measurement system, not only the calculation process of the data during the measurement but also the monitoring of the nitrogen concentration zero and the detection of the end of the measurement are detected and the patient 4 is automatically placed in the original therapeutic ventilator unit 1. The patient can be kept safe by quickly returning the device so that the amount of pure oxygen breathing accompanying the measurement can be minimized. Also, the measurement operation as a whole is simplified and a highly accurate result can be obtained.

【図面の簡単な説明】 【図 1】本発明によるFRC測定法の構成例である 【符号の説明】 1は人工呼吸器部1,2は人工呼吸器部2,3は回路切
替器,4は患者,5は人工呼吸器部2の呼気側回路,6
は流量測定部,7は窒素濃度計,8はリザーバ,9は計
測制御部そして10は流量測定部。
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a structural example of an FRC measurement method according to the present invention. [Description of reference numerals] 1 is a ventilator part 1, 2 is a ventilator part 2, 3 is a circuit switch, 4 Is the patient, 5 is the expiratory circuit of the ventilator 2, and 6
Is a flow rate measurement unit, 7 is a nitrogen concentration meter, 8 is a reservoir, 9 is a measurement control unit, and 10 is a flow rate measurement unit.

Claims (1)

【特許請求の範囲】 【請求項1】窒素を含んだ吸氣ガスを供給する人工呼吸
器部1及び純酸素濃度の吸氣ガスを供給する人工呼吸器
部2を有し,そのいずれでも瞬時に切り替えて使用でき
る回路切替器3を経て患者4を呼吸させておき,人工呼
吸器部2の呼氣側回路5で呼氣ガスをすべての回収した
ガス流の下流に流量測定部6と窒素濃度計7を配置した
窒素洗い出し法による機能的残気量の測定方法。 【請求項2】窒素を含んだ吸氣ガスを供給する人工呼吸
器部1及び純酸素濃度の吸氣ガスを供給する人工呼吸器
部2を有し,そのいずれでも瞬時に切り替えて使用でき
る切替器3を経て患者4を呼吸させておき,人工呼吸器
部2の呼氣側回路5で呼氣ガスをすべての回収したガス
流の下流にコンブライアントなリザーバ8を挿入してそ
の更に下流に流量測定部6と窒素濃度計7を配置した窒
素洗い出し法による機能的残気量の測定方法。 【請求項3】 【請求項1】または 【請求項2】の方法において,切替器3を患者4の呼氣
の終末に人工呼吸部1から2に切り替えると同時に流量
測定部6の信号と窒素濃度計7から得られる2つの信号
を乗じ時間と共に積分することを開始して窒素濃度計7
の信号がゼロになるとき迄に得た積分値から機能的残気
量を算出する測定方法。
Claims: 1. An artificial respirator part (1) for supplying an aspirate gas containing nitrogen and an artificial respirator part (2) for supplying an aspirate gas having a pure oxygen concentration, both of which are instantaneous. The patient 4 is made to breathe through the circuit switching device 3 which can be switched to and used, and the expiratory gas in the expiratory side circuit 5 of the artificial respirator unit 2 is connected to the flow rate measuring unit 6 and nitrogen downstream of all the collected gas flow. A method for measuring functional residual air amount by a nitrogen flushing method in which a densitometer 7 is arranged. 2. A switching device which has an artificial respirator part 1 for supplying an aspirate gas containing nitrogen and an artificial respirator part 2 for supplying an aspirate gas having a pure oxygen concentration, any of which can be instantly switched for use. The patient 4 is made to breathe through the ventilator 3, and the expiratory side circuit 5 of the ventilator part 2 inserts a conservative reservoir 8 downstream of all the collected gas flow and further downstream thereof. A method for measuring a functional residual air amount by a nitrogen flushing method in which a flow rate measuring unit 6 and a nitrogen concentration meter 7 are arranged. 3. The method according to claim 1 or 2, wherein the switching device 3 is switched from the artificial respiration unit 1 to 2 at the end of the expiration of the patient 4 and at the same time the signal of the flow rate measurement unit 6 and nitrogen. Start the integration of the two signals obtained from the densitometer 7 with time and start the nitrogen densitometer 7
Measurement method to calculate the functional residual capacity from the integrated value obtained until the signal of becomes zero.
JP5138844A 1993-04-30 1993-04-30 Functional residual capacity measurement method Pending JPH06311979A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5138844A JPH06311979A (en) 1993-04-30 1993-04-30 Functional residual capacity measurement method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5138844A JPH06311979A (en) 1993-04-30 1993-04-30 Functional residual capacity measurement method

Publications (1)

Publication Number Publication Date
JPH06311979A true JPH06311979A (en) 1994-11-08

Family

ID=15231511

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5138844A Pending JPH06311979A (en) 1993-04-30 1993-04-30 Functional residual capacity measurement method

Country Status (1)

Country Link
JP (1) JPH06311979A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007083031A (en) * 2005-09-21 2007-04-05 General Electric Co <Ge> Device and method for specifying frc and peep characteristic
JP2007083032A (en) * 2005-09-21 2007-04-05 General Electric Co <Ge> Device and method for determining and displaying functional residual capacity data and related parameter on patient to be ventilated
CN101310678B (en) 2008-05-07 2010-06-02 上海力申科学仪器有限公司 Measuring method of tidal volume in anesthesia machine

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007083031A (en) * 2005-09-21 2007-04-05 General Electric Co <Ge> Device and method for specifying frc and peep characteristic
JP2007083032A (en) * 2005-09-21 2007-04-05 General Electric Co <Ge> Device and method for determining and displaying functional residual capacity data and related parameter on patient to be ventilated
CN101310678B (en) 2008-05-07 2010-06-02 上海力申科学仪器有限公司 Measuring method of tidal volume in anesthesia machine

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