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beaucoup d'autres causes d'une IC à fraction d'éjection du ventricule gauche (FEVG) 10-20 x2. Lisinopril. 2.5/5 x1. 20-40. Perindopril.



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De 20 % à 40 % des patients atteints d'insuffisance à. FEVG préservée souffriront de fibrillation auriculaire34 qui peut être particulièrement mal tolérée



Combined spinal-epidural anesthesia for Cesarean section in a

Clinical features: A morbidly obese parturient with a potentially difficult airway suffering from idiopathic peripartum cardiomyopathy. (ejection fraction 20%) 



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INSUFFISANCE CARDIAQUE CHRONIQUE

beaucoup d'autres causes d'une IC à fraction d'éjection du ventricule gauche (FEVG) 10-20 x2. Lisinopril. 2.5/5 x1. 20-40. Perindopril.



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De 20 à 40 des patients atteints d'insuffisance à FEVG préservée souffriront de fibrillation auriculaire34 qui peut être particulièrement mal tolérée 



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8 déc 2020 · T Christiaens - Nekkersberglaan 31 - 9000 Gent ejection fraction N Engl J Med 2019;381:1609-20 doi: 

De 20 % à 40 % des patients atteints d'insuffisance à. FEVG préservée souffriront de fibrillation auriculaire3,4 qui peut être particulièrement mal tolérée, 
  • Quand le cœur fonctionne à 20% ?

    Dans les cas d'insuffisance cardiaque sévère, elle peut chuter autour de 20 %. La distinction systolique/diastolique est plutôt faite lors d'une insuffisance cardiaque gauche. Les insuffisances systoliques représentent 60 % des insuffisances cardiaques gauches.
  • Comment augmenter la fraction d'éjection du cœur ?

    Choix des traitements à sevrer Dans une métaanalyse sur l'amélioration de la fraction d'éjection ventriculaire gauche sous traitement pharmacologique et mécanique, les bêtabloquants améliorent la FEVG de 5 à 12 % alors que les modulateurs du système rénine angiotensine aldostérone améliorent la FEVG de 1 à 4 %(2).
  • Quels sont les quatre stades de l'insuffisance cardiaque ?

    Stade I : dyspnée pour des efforts inhabituels importants, aucune gêne dans la vie courante. Stade II : dyspnée pour des efforts importants de la vie courante. Stade III : dyspnée pour des efforts modestes de la vie courante. Stade IV : dyspnée permanente de repos.
  • Ensuite, sa paroi s'épaissit et ses cavités se dilatent : c'est l'hypertrophie cardiaque qui induit une fatigue du cœur menant à l'insuffisance cardiaque. Cette pathologie chronique est irréversible : une fois installée, elle s'aggrave, et l'espérance de vie à 5 ans est de 50%.
Purpose: To report a case of peripartum dilated cardiomyopathy associated with morbid obesity and possible difficult airway pre- senting for elective Cesarean section, which was successfully man- aged with combined spinal-epidural anesthesia. Clinical features: A morbidly obese parturient with a potentially difficult airway, suffering from idiopathic peripartum cardiomyopathy (ejection fraction 20%), was scheduled for an elective Cesarean section. A combined spinal epidural anesthesia was performed and 6 mg of bupivacaine were injected into the subarachnoid space. This was supplemented after 60 min with 25 mg of bupivacaine injected epidurally. The patient's hemodynamic status was monitored with direct intra-arterial blood pressure and central venous pressure

measurements. The patient's perioperative course was uneventful. Conclusion: In patients suffering from peripartum cardiomyopa-

thy, undergoing Cesarean section, combined spinal-epidural anes- thesia may be an acceptable anesthetic alternative. Objectif:Présenter un cas de cardiomyopathie du péripartum asso- ciée à de l'obésité morbide et à des difficultés d' intubation possibles chez une patiente qui a subi une césarienne réalisée avec succè s sous anesthésie rachidienne et péridurale combinée. Éléments cliniques:Une parturiente, présentant une obésité mor- bide et des difficultés d'intubation possibles, souffrait de cardi omyo- pathie idiopathique du péripartum (fraction d'éjection de 20 % ) au moment de subir la césarienne prévue. L'anesthésie rachidienne et péridurale combinée a été réalisée avec l'injection de 6 mg de bupivacaïne dans l'espace sous-arac hnoï- dien, complétée après 60 min, par l'injection péridurale de 25 mg de bupivacaïne. L'état hémodynamique de la patiente a été surveillé pardes mesures directes de la tension intra-artérielle et de la pression veineuse centrale. Aucun incident périopératoire n'a été observé.

Conclusion:

L'anesthésie rachidienne et péridurale combinée peut être un choix acceptable à envisager dans le cas de patientes atteintes de cardiomyopathie du péripartum qui subissent une césarienne.

ERIPARTUMcardiomyopathy occurs in

approximately 1/10,000 deliveries 1 and can result in severe ventricular dysfunction dur- ing late pregnancy or early puerperium. 2

We present a patient with peripartum cardiomyopa-

thy requiring Cesarean section (CS) who was ma n- aged with combined spinal-epidural (CSE) anesthesia.

Case report

A 25-yr-old, morbidly obese (weight 100 kg, height

1.58 m and body mass index 40) primigravida at 36

weeks gestation, with a Mallampati class IV airway, was scheduled for an elective CS. Two weeks before, she had complained of progressively worsening fatigue and dyspnea with minimal physical activity. A cardiol- ogy consultation obtained to evaluate progressively worsening fatigue led to the diagnosis of idiopathic dilated cardiomyopathy. Echocardiography revealed severe left ventricular dysfunction ejection fraction (EF) 20% with moderate pulmonary hypertension and moderate right ventricular dysfunction. Treatment with furosemide, digoxin, and potassium supplemen-OBSTETRICALANDPEDIATRICANESTHESIA681

Combined spinal-epidural anesthesia for Cesarean

section in a patient with peripartum dilated car- diomyopathy[L'anesthésie rachidienne et péridurale combinée pour la cé sarienne chez une patiente souffrant de cardiomyopathie du péripartum] Roman Shnaider MD, Tiberiu Ezri MD, Peter Szmuk MD, Stephen Larson DMD,

R. David Warters

MD, Jeffrey Katz MD

From the Department of Anesthesiology University of Texas Medical School at Houston, Houston, Texas, USA. Address correspondence to: Dr. Peter Szmuk, Assistant Professor, The University of Texas-Houston

Medical School, Department of

Anesthesiology, 6431 Fannin, MSB 5.020 Houston, Texas 77030, USA. Phone:

713-500-6184; Fax: 713-500-6201;

E-mail: Peter.Szmuk@uth.tmc.edu

Accepted for publication February 6, 2001.

Revision accepted April 11, 2001.

P tation was started and continued for ten days, and delivery via CS was planned.

On arrival in the operating room, the patient was

eupneic and was free of peripheral edema. Chest sounds were clear. Frequent (5·min -1 ) ventricular pre- mature beats were present on the electrocardiogram despite a normal potassium blood level and a serum digoxin level within the therapeutic range. The coag- ulation profile was normal. The patient's baseline blood pressure and heart rate were 102/70 mmHg (MAP 90) and 95 beats·min -1 respectively (Table).

A triple-lumen catheter and an arterial cannula

were inserted under local anesthesia into the right internal jugular vein and right radial artery respective- ly. Five hundred milliliters of lactated Ringer's solu- tion were infused over 15 min to increase the central venous pressure (CVP) from 10 to 15 mmHg.

A CSE was performed at the L3-L4 interspace in

the sitting position. Six milligrams of hyperbaric bupi- vacaine (0.8 mL of 0.75%) together with 15 µg of fen- tanyl were injected over 20 sec through a 27G, 120 mm Sprotte needle into the cerebrospinal fluid. No local anesthetic was given through the epidural catheter at this stage. A wedge was placed under the right hip to minimize aorto-caval compression. The upper levels of sensory block obtained were T8 at three minutes, T6 at five minutes and T5 at ten minutes. The operation proceeded uneventfully and a healthy baby was delivered eight minutes later (Apgar score 9/10 and umbilical cord pH 7.30). Supplementation of the subarachnoid block was necessary with bupivacaine 5 mL of 0.5% and 0.25% at 60 and 105 min respectively.

The patient remained stable hemodynamically

throughout the procedure. A total of 1300 mL of lac- tated Ringer's solution was administered (including the 500 mL which were administered before anesthe- sia). Echocardiography performed a week after delivery revealed an EF of 50%.

Discussion

Although the etiology of peripartum cardiomyopathy is uncertain, viral, autoimmune and idiopathic causes have been considered. 3

Cardiomyopathy is usually a

diagnosis of exclusion. Common misdiagnoses include other types of cardiomyopathy, valvulopathies, accel- erated hypertension, diastolic ventricular dysfunction, systemic infection, pulmonary embolism, etc. 4 There is an increased incidence with multiple gestation, preeclampsia, obesity, advanced maternal age, 1

African

descent and prolonged tocolysis. 4

Treatment includes

digitalis, diuretics, vasodilators, and anticoagulants. 4 If supportive treatment fails, cardiac transplantation may be indicated. 5 The prognosis is related to the recoveryof ventricular function. 4

The mortality rate of peripar-

tum cardiomyopathy is 30-60% and may be caused by severe pulmonary congestion, and/or thrombo- embolic events. 2,6

Survivors have a 50-80% risk of

developing cardiac failure during future pregnancies, with an associated mortality rate of 60%. 7 Cardiovascular status may benefit from prompt vagi- nal delivery or CS. 1 There is scant information in the literature regard- ing the anesthetic management of peripartum car- diomyopathy, although several anesthetic options for

CS have been reported. Malinow presented two

patients undergoing CS under spinal anesthesia and general anesthesia (GA) respectively. 8

Both had full

cardiac recovery within seven to eight days. Epidural lidocaine, titrated in small aliquots together with fen- tanyl, has been successfully employed in a patient with pulmonary hypertension and cardiomyopathy. 9

GA may be necessary for urgent CS.

6

However,

performing a rapid sequence induction on a patient with compromised cardiac function can be very chal- lenging. When time permits, a carefully administered regional anesthetic would seem to be advantageous. In addition to avoiding the stress of GA, the vasodi- latation produced by regional anesthesia is beneficial with isolated left ventricular dysfunction. 10

If time permits, hemodynamics should be optimized

by careful fluid replacement under the control of inva- sive monitoring prior to surgery. We chose to monitor CVP rather than pulmonary capillary wedge pressure for assessing the cardiac filling pressures primarily because the patient was asymptomatic and hemody- namically stable despite the low EF. Successful out- come using only non-invasive monitoring has been reported. 11

Intraoperative monitoring with trans-

esophageal echocardiography has been reported in obstetric patients with hypertrophic cardiomyopathy. 12

We preferred CSE to epidural anesthesia (EA) for

several reasons. First, CSE has a lower failure rate than EA. 13

Secondly, intra-operative patient satisfaction,

682CANADIANJOURNALOFANESTHESIA

TABLEHemodynamic parameters during surgery

Mean arterial Heart rateCentral venous

pressure (mmHg)(beats·min -1 )pressure (mmHg)

Preoperative909510

Postspinal859515

Post delivery8090 8

60 min 909214

from start

End of surgery879012

(85 min) anxiolysis, and post-operative pain scores have been superior with CSE. 14

Furthermore, some authors

report a lower incidence of hypotensive episodes with

CSE compared to EA.

13

Another advantage of CSE

includes a lower maternal and umbilical cord blood concentration of local anesthetics. 13 There are also disadvantages associated with using CSE. Local anesthetics should be injected into the epidural space in small increments to avoid severe hypotension 15 in case the catheter has accidentally migrated into the subarachnoid space. The epidural injection of opiates with the CSE technique may be dangerous because of the potential for accidental catheter migration and injection of a large dose of opi- oid into the subarachnoid space with the ensuing risk of respiratory arrest. 16

The incidence of meningitis after

CSE may be higher than after spinal or EA.

17

In our

case, careful fluid administration under the guidance of invasive monitoring and a well-tailored regional anes- thetic satisfied the anesthetic goals emphasized above. 9 To our knowledge this is the first report of the use of CSE anesthesia in a patient with peripartum dilated cardiomyopathy. Although a single case has no role in predicting anesthetic outcome, we believe this case demonstrates that CSE anesthesia is an acceptable option for patients with peripartum dilated cardiomy- opathy undergoing CS.

References

1Thornhill ML, Camann WR. Cardiovascular disease.

In: Chestnut DH (Ed.). Obstetric Anesthesia. St.

Louis: Mosby, 1994: 765.

2Homans DC. Current concepts. Peripartum cardiomy-

opathy. N Engl J Med 1985; 312: 1432-7.

3Heider AL, Kuller JA, Strauss RA, Wells SR.

Peripartum cardiomyopathy: a review of the literature.

Obstet Gynecol Surv 1999; 54: 526-31.

4Lampert MB, Lang RM. Peripartum cardiomyopathy.

Am Heart J 1995; 130: 860-70.

5Brown CS, Bertolet BD. Peripartum cardiomyopathy: a

comprehensive review. Am J Obstet Gynecol 1998;

178: 409-14.

6Chan F, Kee WDN. Idiopathic dilated cardiomyopathy

presenting in pregnancy. Can J Anesth 1999; 46:

1146-9.

7Veille J-C. Peripartum cardiomyopathies: a review. Am

J Obstet Gynecol 1984; 148: 805-18.

8Malinow AM, Butterworth JF, Johnson MD, et al.

Peripartum cardiomyopathy presenting at cesarean

delivery. Anesthesiology 1985; 63: 545-7.

9Breen TW, Janzen JA. Pulmonary hypertension and

cardiomyopathy: anaesthetic management for caesarean section. Can J Anaesth 1991; 38: 895-9. 10Sharrock NE, Bading B, Mineo R, Blumenfeld JD. Deliberate hypotensive epidural anesthesia for patients with normal and low cardiac output. Anesth Analg

1994; 79: 899-904.

11Gambling DR, Flanagan ML, Huckell VF, Lucas SB,

Kim JHK. Anaesthetic management and non-invasive

monitoring for caesarean section in a patient with car- diomyopathy. Can J Anaesth 1987; 34: 505-8.

12Nam E, Toque Y, Quintard JM, Barsam E, Besserve P,

Montravers P. Use of transesophageal echocardiogra- phy to guide the anesthetic management of cesarean section in a patient with hypertrophic cardiomyopathy.

J Cardiothorac Vasc Anesth 1999; 13: 72-4.

13Rawal N, Schollin J, Wesstrom G. Epidural versus com-

bined spinal epidural block for cesarean section. Acta

Anaesthesiol Scand 1988; 32: 61-6.

14Davies SJ, Paech MJ, Welch H, Evans SFG, Pavy TJ.

Maternal experience during epidural or combined

spinal-epidural anesthesia for cesarean section: a prospective, randomized trial. Anesth Analg 1997; 85:

607-13.

15D'Angelo R, Eisenach JC. Severe maternal hypotension

and fetal bradycardia after a combined spinal epidural anesthetic. Anesthesiology 1997; 87: 166-8.

16Myint Y, Bailey PW, Milne BR.Cardiorespiratory arrest

following combined spinal epidural anaesthesia for cae- sarean section. Anaesthesia 1993; 48: 684-6.

17Brown DL. Spinal, epidural and caudal anesthesia. In:

Chestnut DH (Ed.). Obstetric Anesthesia, 2nd ed. St.

Louis: Mosby, 1999: 201.

Shnaider et al.: CSEANDPERIPARTUMCARDIOMYOPATHY683quotesdbs_dbs42.pdfusesText_42
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