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      Transient Pulmonary Atelectasis after Ketamine Sedation during Cardiac Catheterization in Spontaneously Breathing Children with Congenital Heart Disease

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            Abstract

            Background: Ketamine is applied widely for sedation during cardiac catheterization in spontaneously breathing children with congenital heart disease (CHD). However, a rare and unreported respiratory complication, transient and reversible atelectasis of lungs (TRAL), was identified.

            Purpose: The study was performed to investigate retrospectively the prevalence and clinical characteristics of TRAL after ketamine sedation in pediatric cardiac catheterization.

            Methods: Four thousand four hundred and seventy-four sick children were sedated with ketamine, and pediatric cardiac catheterization was carried out under spontaneous breathing. TRAL was detected in 33 children (17 M/16 F, age was 2.1±1.7 years) by retrospective analysis. The clinical and radiographic characteristics were recorded before, during and after TRAL.

            Results: In pediatric cardiac catheterization, the prevalence of TRAL was 0.74% after ketamine sedation. TRAL occurred in 23 children with cyanotic CHD, and 10 with acyanotic CHD. All TRALs had common clinical and radiographic features: the diffuse opacity of bilateral lungs developed rapidly (identified under X-ray fluoroscopy), associated with decrease in lung volume, and then the decrease in SpO2 (94.2±9.2% vs. 59.4±2.2%, P<0.05), and heart rates (143.5±14.3 bpm vs. 58.3±9.7 bpm, P<0.05) followed quickly. TRAL was relieved by supportive oxygen in 32 children (23 with face mask, and 9 with endotracheal intubation), and the duration of TRAL was 1.6±0.5 minutes. However, TRAL caused the death of one child.

            Conclusions: TRAL is a rare and urgent respiratory complication after ketamine sedation, and the mechanism is unclear. Rapid and diffuse opacity of bilateral lungs is the earliest sign of TRAL in pediatric cardiac catheterization, and the immediate supportive oxygen is crucial.

            Main article text

            Introduction

            In pediatric cardiac catheterization, ketamine has been applied widely for sedation in spontaneously breathing children and there was no report about the respiratory complication [1, 2]. However, a rare and unreported respiratory complication, transient and reversible atelectasis of lungs (TRAL), was identified in our institute. To our knowledge, TRAL constitutes a distinct subgroup, which was different from currently known complications in pediatric cardiac catheterization. In this study, we present data from 33 sick children with TRAL.

            Materials and Methods

            Patients

            From January 2004 to July 2015, 4474 sick children (1643 cyanotic CHD and 2831 acyanotic CHD) were sedated with ketamine, and pediatric cardiac catheterization was carried out under spontaneous breathing. Thirty three patients (17 males, 16 females) had onset of TRAL in cardiac catheterization. All patients underwent detailed evaluation of electrocardiogram (ECG), chest X-ray, and echocardiography. Patients requiring ventilatory treatment or intravenous inotropic support were excluded. The study was approved by our hospital research ethics committee, and informed consent was obtained from the parents of each child. Consent for the anaesthetic was obtained independently by the anaesthetist who was involved with the procedure.

            Procedure

            The patients were admitted to the catheterization laboratory and an intravenous cannula was placed and an infusion of one-third saline solution was started. Ketamine was applied for general anaesthesia (1 mg/kg at induction followed by an infusion of 3–5 mg/kg/h) in spontaneously breathing children. Concurrently, atropine was administered intravenously (0.01 mg/kg) or intramuscularly (0.02 mg/kg). In all patients, local anaesthesia with 1% lidocaine was administered before percutanous puncture of femoral artery and/or vein. The power injector (Medrad100, Pittsburgh, PA, USA) was used for angiocardiography. Nonionic contrast medium was applied in this study (Iopromide, Ultravist, Schering, Germany; Iohexol, Omnipaque, Nycomed, Norway; Iopamidol, Bracco Diagnostics, Plainsboro, NJ, USA).

            The first sign of TRAL was defined as the occurrence of opacity lungs. Once TRAL attacked in the examination, supportive 100% oxygen was administrated by bag and mask via a clear airway (Endotracheal intubation was not the routine procedure in the general anaesthesia). If adequate oxygenation failed to be maintained, endotracheal intubation (volume-limited ventilator) followed immediately after muscular relaxation. The images of chest fluoroscopy were recorded promptly to evaluate the radiographic features of TRAL before, during and after the onset. Standard guidelines for monitoring during delivery of general anesthesia and cardiac catheterization were carried out, including 3-lead surface ECG, pulse oximetry and so on. SpO2 was determined by means of pulse oximetry. The clinical manifestation, radiological findings and treatment were also recorded.

            Among the 33 sick children, 13 patients had exact records of SpO2 and heart rates before and during the onset of TRAL. Their approximate durations of TRAL, which ranged from the emergence to the disappearance of opacity lungs, were recorded too. When the left cardiac catheterization was performed, systolic aortic pressure was recorded by catheter.

            Statistical Analysis

            The data in the study were expressed as mean value±SD. The results were compared between before and during onset of TRAL using paired-samples T test, and P<0.05 was considered significant. Statistical software used in this study was SPSS 12.0.

            Results

            Thirty three sick children (17 males, 16 females) presented with TRAL in cardiac catheterization. Cyanotic CHD were 23 (Table 1), and acyanotic CHD were 10 (Table 2). The age were 2.1±1.7 years, weight were 11.5±4.9 kg and height were 80.6±17.3 cm. Angiocardiography was performed in 30 patients, and right cardiac catheterization in 3 children. The ages of patients with cyanotic CHD was younger than those with acyanotic CHD, 1.5±1.6 years vs. 3.4±1.2 years (P<0.05). Except for one child, abnormalities of ECG can be found in the other patients, including right ventricular hypertrophy (29 patients), left ventricular hypertrophy (one patient), supraventricular tachycardia (one patient) and atrioventricular block (one patient). The fluoroscopy time was 20±10.2 minutes.

            Table 1

            Clinical and Radiographic Characteristics of TRAL in Cyanotic CHD (n=23).

            NoAge (year)SexHeight (cm)Weight (kg)ECGDiagnosisPossible trigger factorMeans of supportive O2 therapyFrequenceSpO2 (%)
            Approximate duration of TRAL (min)
            Before TRALDuring TRAL
            15M11224RVHTOFVGET1NNN
            24.9F9619RVHPAA VSD PDASICAET175472
            30.3M626RVHTGA VSD PHVGET1100642
            42F8512RVHPAA VSDSICABM1NNN
            51.9M8011AVBCTGA VSD PSNET195602
            60.5M677.5SVTSV PS PDASICABM1NNN
            71M729.5RVHTOFVGBM192601.5
            81F7710RVHPAA VSDSICAET1NNDeath
            90.6M667.7RVHTOFNET187452
            100.9F6810RVHPAA VSDNBM1NNN
            115F10515RVHPAA VSDSICABM3NNN
            120.3M546RVHTOFSICABM1NNN
            130.8M666.7RVHTOFVGBM1NNN
            140.8M967.8RVHPAA VSD ASDSICABM1NNN
            154F11214RVHPAA PDASICABM276542.5
            161.2F719.1RVHDORV VSD PSSICABM1NNN
            170.8F718RVHTOFVGBM1NNN
            180.2M595RVHTOFESABM2NNN
            191M729.4RVHTOFVGBM1100661.5
            200.3F534.2RVHTOF PDAVGBM1NNN
            210.3M616.5RVHPAA VSDSICABM1NNN
            220.9F687.3RVHPAA VSDVGBM1NNN
            230.8M719.5RVHDORV TECD PSNBM1100542

            M, male; F, female; RVH, right ventricular hypertrophy; AVB, atrioventricular block; SVT, supraventricular tachycardia; TOF, tetralogy of fallot; PAA, pulmonary arterial atresia; DORV, double outlet of right ventricle; TECD, total endocardial cushion defect; TGA, complete transposition of the great arteries; CTGA, corrected transposition of the great arteries; SV, single ventricle; PS, pulmonary stenosis; VSD, ventricular septal defect; PH, pulmonary arterial hypertension; SICA, selective injection into collateral arteries; VG, ventriculogram; ET, with endotracheal intubation; BM, with bag and mask; ESA, excessive secretion of airway; N, not available; The first duration was recorded if TRAL occurred twice or more.

            Table 2

            Clinical and Radiographic Characteristics of TRAL in Acyanotic CHD (n=10).

            NoAge (year)SexHeight (cm)Weight (kg)ECGDiagnosisPossible trigger factorMeans of supportive O2 therapyFrequenceSpO2 (%)
            Approximate duration of TRAL (min)
            Before TRALDuring TRAL
            13M8415RVHPS PDAPBPVET1100671.5
            25M10520LVHPDAESABM1100551
            33F9116RVHPSPBPVBM1NNN
            42F7614RVHPSPBPVBM1NNN
            53F9916RVHPSPBPVBM1NNN
            61.3F719.5RVHASD PHESAET1100701
            75F10115RVHTA VSD PHNBM1NNN
            84.5M9318RVHASDNBM1100621
            93M10513.8RVHASDNET2NNN
            104F9217NormalPDANBM1100681

            M, male; F, female; RVH, right ventricular hypertrophy; AVB, atrioventricular block; SVT, supraventricular tachycardia; TOF, tetralogy of fallot; PAA, pulmonary arterial atresia; DORV, double outlet of right ventricle; TECD, total endocardial cushion defect; TGA, complete transposition of the great arteries; CTGA, corrected transposition of the great arteries; SV, single ventricle; PS, pulmonary stenosis; VSD, ventricular septal defect; PH, pulmonary arterial hypertension; SICA, selective injection into collateral arteries; VG, ventriculogram; ET, with endotracheal intubation; BM, with bag and mask; ESA, excessive secretion of airway; N, not available; The first duration was recorded if TRAL occurred twice or more, LVH, left ventricular hypertrophy; TA, truncus arteriosus.

            TRAL was precipitated by selective injection of collateral vessels in ten patients (Figure 1A–C), PBPV in four patients (Figure 2A–C), ventriculogram in eight patients (Figure 3A–D), and excessive secretion of airway in three patients. In the other eight cases, however, no obvious stimulus was apparent. Interventional therapy was performed in nine patients, including PBPV (four patients), transcatheter closure of PDA (two patients) and transcatheter closure of ASD (three patients). TRAL occurred twice or more in four patients.

            Figure 1

            The Child was Diagnosed as PAA with VSD.

            Selective injection into collateral artery was performed (A), and precipitated the onset of TRAL (B). Supportive 100% oxygen therapy with bag and face mask was started immediately, and the lungs were fully aerated again in 2.5 minutes (C). The onset of TRAL was characterized by the marked opacity lung associated with decrease of lung volume.

            Figure 2

            TRAL Occurred Immediately After PBPV.

            The X ray was taken before (A), during (B) and after TRAL (C). The lung opacity was accompanied with decrease in lung volume. After mechanical ventilation with the placement of the endotracheal tube, TRAL resolved quickly and the duration was about 1.5 minutes (C).

            Figure 3

            Before (A, B) and During (C, D) the Onset of TRAL, the Images of Pulmonary Arterial Phase (A, C) and Venous Phase (B, D) were Recorded.

            The branches of pulmonary arteries crowed, the lung volume decreased and the venous phase was obviously delayed (C, D).

            After TRAL occurred, SpO2 decreased quickly from 94.2±9.2% to 59.4±2.2% (P<0.05) and heart rates fell from 143.5±14.3 bpm to 58.3±9.7 bpm (P<0.05). The duration of TRAL was 1.6±0.5 minutes (the duration of diffuse pulmonary opacity under X-ray fluoroscopy). Systolic aortic pressure recorded by catheter was 115.3±17.5 mmHg. TRAL was relieved by supportive oxygen with face mask in 24 patients, and by mechanical ventilation with endotracheal intubation in nine patients. Except for one child, all patients were relieved completely by the administration of 100% oxygen.

            Common Clinical Course

            TRAL had common clinical and radiographic features in all patients: the diffuse opacity of bilateral lungs developed rapidly, associated with decrease in lung volume. And then the decrease in SpO2 and heart rates followed quickly. The sequence of opacity lungs was from center to peripheral area, and the opacity of the upper lung zone was often earlier and more apparent than that of lower lung. There was no evidence of cardiac enlargement. In particular, the opacity of lungs developed within one minute. During the onset of TRAL, there was no reflex increase in heart rates and breath sounds were inaudible. With progression, there was the occurrence or deterioration of cyanosis. If supportive or mechanical ventilation was given, the duration was short and the lungs were fully aerated again within 1–2.5 minutes, followed by the recovery of hypoxia and bradycardia sequentially. No sequelae can be found in the 3 months following up.

            Discussion

            TRAL is a rare but risk complication after ketamine sedation during cardiac catheterization in spontaneously breathing children. However, the mechanism is still unclear. As a previously unreported complication, TRAL shared distinct clinical and radiographic pictures. The hallmark of TRAL was the rapid and diffuse opacity change of bilateral lungs, which was the earliest sign of under X-ray fluoroscopy. It developed rapidly within 1 minute and lasted less than 2.5 minutes if supplemental oxygen was given. In this study, fluoroscopy allowed real time visualization of lungs in cardiac catheterization. Therefore, the detailed clinical course of TRAL became available. Accompanied by decrease in lung volume, TRAL manifested a picture characteristic of atelectasis rather than pulmonary edema/inflammation. The latter presented in POPE and ARDS [36].

            Because no evidence of severe upper airway obstruction was identified in most children, it was possible that diffuse atelectasis of TRAL was peripheral and not the result of central obstruction. Considering very short duration, we speculated that TRAL might result from the spasm of peripheral airway and diffuse spasmic closure of distal airway can lead to widespread atelectasis and lowers lung volume. Many factors, as presented in this study, might have potential to precipitate the spasmic obstruction of peripheral airway, followed by the onset of TRAL. If it is true, the rapid opacity change of lungs becomes explainable. Further research is required to evaluate the mechanism.

            Another distinct feature of TRAL is that it responds well to oxygen therapy. Whatever the etiology, most patients can be relieved quickly by 100% oxygen administered with bag and mask. If the mask fails to maintain adequate oxygenation, endotracheal intubation should follow immediately. Though most TRALs settled rapidly after the supportive oxygen therapy, one sick child died of TRAL in this study (despite the fact that mechanical ventilation was supported with the placement of the endotracheal tube). No consent was obtained to carry out the autopsy, and the cause remained unclear. The other 32 children recovered well and no sequelae were left. In our opinion, the earlier the diagnosis was made and supportive oxygen was given, the better the TRAL recovered. Because the earliest sign of TRAL was the rapid increase in opacity of lungs under X-ray fluoroscopy, it was important to recognize the phenomenon.

            Several factors probably precipitated the onset of TRAL in this study. Acute reduction in pulmonary blood flow may play an important role in the onset of TRAL, which was triggered by selective injection into major aortopulmonary collateral arteries in ten children, and by PBPV in four patients. There is a direct anatomical and physiological relation between the lung vasculature and the airways, and small peribronchiolar vessels serve an erectile function and maintain airway patency [7, 8]. The cessation of pulmonary blood flow had a major impact on lung mechanics. It has been confirmed that there was an abrupt and important increase in airway resistance, a fall in lung compliance, and a decrease in tidal volume during pulmonary valvuloplasty [9]. In addition, the similar decrease of pulmonary blood flow may result from selective injection of contrast medium into collateral arteries in PAA or TOF, especially when stenosis occurred in the proximal segment of collateral arteries. It also should be responsible for the only death of the child with PAA whose oxygenation failed to be maintained though the mechanical ventilation with endotracheal intubation was given.

            Angiocardiography was performed in 91% of patients in the study. It has been recognized that there were increases in airways and pulmonary vascular resistance after intravascular injection of contrast medium, though the mechanisms responsible for the effect remained unclear [10]. Other pulmonary adverse effects include pulmonary edema, bronchospasm and so on [11, 12]. It is still unclear whether contrast medium plays a role in the attack of TRAL. The same was to the excessive secretion of airway in three children. In addition, one fourth of patients had no obvious trigger factors, and it is unclear that TRAL of these patients occurred spontaneously or related with other unknown factors.

            It was during general anaesthesia with ketamine that TRAL occurred in the study. Though atelectasis can develop as a side effect of most anaesthetics during general anaesthesia, ketamine was considered an exception [13]. In addition, not conventional chest radiography but computed tomography could show the atelectasis resulting from general anaesthesia. Ketamine is a dissociative anesthetic agent and provides adequate anesthesia for most catheterization procedures [14, 15]. It was the only anaesthetic so far tested that has not produced atelectasis unless the patients were paralysed. The major side effect of ketamine is airway secretion, which can result in aspiration and laryngospasm. To offset the increase in airway secretions, atropine was administered in this study. Nevertheless, excessive secretion of airway still occurred in three patients. However, no severe upper respiratory obstruction was identified in these children. It is unknown whether there are direct relation between TRAL and the side effect of ketamine.

            Cyanotic CHD, mainly TOF and PAA, account for 70% in this study. Some clinical similarities present in both TRAL and paroxysmal hypoxemic spell, as seen in TOF and PAA. However, the differences are also obvious between them. TRAL responds well to supportive oxygen therapy and can also occur in acyanotic CHD, such as ASD and PDA. In addition, it is unclear about the radiographic features of hypoxemic spell. The mechanism of hypoxemic spell is still obscure [16, 17]. Though the most widely accepted explanation is that the hypoxemic spell probably results from the spasm of right ventricular infundibulum, it fails to explain the spells that occur in patients with TOF and PAA where pulmonary blood flow does not cross the right ventricular outflow tract [14, 15].

            Study Limitations

            The research was a retrospective study and many measurements were not set before the study. The SpO2 monitored by pulse oximetry may be inaccurate in cyanotic patients, and the duration of TRAL was only an approximate value. In addition, no detailed data were recorded about hemodynamics and lung mechanics in the attack, because TRAL was a life threatening event and all attentions were paid to the maintenance of adequate oxygenation.

            Conclusions

            TRAL is a distinct and risk respiratory complication characterized by transient and reversible pulmonary collapse in pediatric cardiac catheterization. Rapid and diffuse opacity of bilateral lungs is the earliest sign of TRAL, and the immediate supportive oxygen is crucial. However, further research is required to evaluate the mechanism.

            Sources of Funding

            This work was supported by Beijing Natural Science Foundation 7162160 and National Natural Science Foundation of China (81130029, 81341045).

            Conflict of Interest

            The authors declare no conflict of interest.

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            Author and article information

            Journal
            CVIA
            Cardiovascular Innovations and Applications
            CVIA
            Compuscript (Ireland )
            2009-8618
            2009-8618
            May 2016
            July 2016
            : 1
            : 3
            : 351-359
            Affiliations
            [1] 1Interventional Radiology, National Center for Cardiovascular Diseases, Cardiovascular Institute and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, China
            [2] 2Radiology Imaging Center, National Center for Cardiovascular Diseases, Cardiovascular Institute and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, China
            Author notes
            Correspondence: Zhao Shihua, PhD, MD, FESC, Radiology Imaging Center, National Center for Cardiovascular Diseases, Cardiovascular Institute and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 167 Beilishi Road, Beijing 100037, China, Tel.: +8610-88398158, Fax: +8610-68313012, E-mail: cjr.zhaoshihua@ 123456vip.163.com
            Article
            cvia20160019
            10.15212/CVIA.2016.0019
            014f0285-cb54-4796-9952-f113c4cedde2
            Copyright © 2016 Cardiovascular Innovations and Applications

            This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 Unported License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See https://creativecommons.org/licenses/by/4.0/.

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            ORIGINAL ARTICLE

            General medicine,Medicine,Geriatric medicine,Transplantation,Cardiovascular Medicine,Anesthesiology & Pain management
            lung physiology,lung injury,pediatric interventional cardiology,complication

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