alexa Profound Hypotension during Kidney Transplantation for a Patient with a Depressive Disorder | Open Access Journals
ISSN: 2155-6148
Journal of Anesthesia & Clinical Research
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Profound Hypotension during Kidney Transplantation for a Patient with a Depressive Disorder

Maki Nabatame1*, Katsuaki Tanaka2 , Yuichi Nishi3, Kazutake Ikenaga2, Tadashi Matsuura2, Takashi Mori2and Kiyonobu Nishikawa2

1Department of Anesthesiology, Japan Community Health Care Organization, Hoshigaoka Medical Center, Hirakata City, Osaka, Japan

2Department of Anesthesiology, Osaka City University Graduate School of Medicine ,Osaka City, Japan

3Department of Anesthesiology, Japan Community Health Care Organization, Osaka Hospital Osaka City, Osaka, Japan

*Corresponding Author:
Maki Nabatame
Department of Anesthesiology
Japan Community Health Care Organization
Hoshigaoka Medical Center, 4-8-1 Hoshigaoka
Hirakata City, Osaka 5738511, Japan
Tel: +81-72-840-2611
Fax: +81-72-840-2286
E-mail: [email protected]

Received date: January 30, 2015; Accepted date: March 23, 2015; Published date: March 29, 2015

Citation: Nabatame M, Tanaka K, Nishi Y, Ikenaga K, Matsuura T, et al. (2015) Profound Hypotension during Kidney Transplantation for a Patient with a Depressive Disorder. J Anesth Clin Res 6:518. doi: 10.4172/2155-6148.1000518

Copyright: ©2015 Nabatame M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Anesthesia & Clinical Research

Introduction

The perioperative management of patients with depressive disorder is largely based on the individual’s clinical condition. Patients with long-term antipsychotic treatment are challenging for anesthesiologists because of its psychiatric condition, interactions of psychotropics and anesthetics, and the problems requiring surgery. Although antipsychotics and antidepressants are generally safe to continue perioperatively [1,2], evidence-based guidelines for the perioperative management of psychotropics are lacking [3]. We treated a patient taking chlorpromazine, phenobarbital, paroxetine and mianserin who experienced refractory hypotension during general anesthesia.

Case Report

A 63-year-old male (weight: 105 kg, height: 170 cm, body mass index (BMI): 36.3) presented to our hospital for elective living donor kidney transplantation for end-stage hyperuricemic nephropathy. He had a major depressive disorder which was treated with multiple medications, including benzodiazepines, a selective serotonin reuptake inhibitor (SSRI), and antipsychotics, for about ten years. He had an episode of temporary loss of consciousness eleven years before; epileptic seizure was suspected, and sodium valproate at a dose of 800 mg/day was prescribed. In preoperative evaluation, the psychiatrist determined that the patient’s mental condition was stable. He recommended to decrease the dose of benzodiazepines because of the potential danger of postoperative delirium. The patient was given haloperidol (3 mg/day) and mianserin (20 mg/day) for delirium prophylaxis three days before surgery. Immunosuppressive therapy was also started simultaneously. Although the patient took angiotensin-converting enzyme (ACE) inhibitor, it was discontinued six days before surgery. The list of preoperative medications is shown in Table 1.

Drug Dosage (mg/day)
Cyclosporine 600
Mycophenolate 1500
Alprazolam 0.4
Chlorpromazine 25
Cloxazolam 2
Estazolam 2
Etizolam 3
Haloperidol 3
Mianserin 10
Nitrazepam 10
Paroxetine 20
Phenobarbital 40
Promethazine 12.5
Cilnidipine 10
Furosemide 30

Table 1: Patient’s preoperative medications

Electrocardiography showed normal sinus rhythm and transthoracic echocardiography revealed normal left ventricular function. Chest radiography was unremarkable. Serum chemistry revealed elevated serum creatinine (5.13 mg/dL) and hyperkalemia (5.5 mmol/L) associated with chronic renal insufficiency. He had mild anemia (hemoglobin level of 10.4 g/dL). His preoperative blood pressure (BP) was 121/65 mmHg, and the heart rate (HR) was 75 beats/minute. On arrival, the patient was slightly drowsy. General anesthesia was induced with 200 µg of fentanyl and 180 mg of propofol, and the trachea was intubated with 80 mg of rocuronium. High peak airway pressure (30–40 mm H2O) was needed to obtain an adequate tidal volume during volume-controlled mechanical ventilation. A right radial arterial catheter and right internal jugular venous catheter were inserted. The anesthesia was maintained with 1.5% sevoflurane and continuous infusion of remifentanil at 0.2 µg/kg/min and rocuronium at 25 mg/h. Immediately after the beginning of the operation, the BP decreased to 60/30 mmHg, and HR increased to 100 beats/min. Arterial blood gas analysis revealed: FiO2 0.4 pH 7.303, PCO2 38.6, PO2 104, BE -6.7, HCO3 18.6, Hb 9.3, Ht 28.9. There was no rash and wheezing. Rapid infusion of 1000 ml of normal saline over 40 min was performed. The sevoflurane concentration was reduced to 1%, and the dose of remifentanil was reduced to 0.05 µg /kg/min. Although dopamine infusion was initiated at a rate of 3 µg/kg/min, which was subsequently increased to 12 µg/kg/min, the hypotension persisted (BP: 80/40 mmHg). A norepinephrine infusion (0.02 μg/kg/min) with incremental boluses of ephedrine (total dose: 15 mg) and norepinephrine (10-30 µg at a time, total dose: 180 µg) was also given. Additionally, vasopressin (0.96 units) and methylprednisolone (500 mg) were administered.

To evaluate the patient’s hemodynamic status, a transesophageal echocardiography (TEE) probe was inserted. TEE revealed decreased ventricular volumes with normal to hyperactive left ventricular contraction. After arterial anastomosis of the graft was completed, transfusion of 5% albumin and packed red blood cells were initiated to maintain adequate perfusion of the graft. Infusion of 20% mannitol (200 ml) was administered according to a standard protocol.

Hemodynamic stability was finally achieved after administration of vasopressors and massive volume expansion. The patient's systolic BP increased to 100 mmHg, and HR became 80 beats/min.The cardiac output measured with the Doppler method was 10–15 L/min, and the central venous pressure was 7–10 cm H2O.

Arterial blood gas analysis revealed mixed acidosis (pH 7.17, PCO2 55.1, BE -8.9, HCO3 19.3), which was corrected with 8.4% sodium bicarbonate. Intravenous carperitide infusion at 0.03–0.2 µg/kg/min was started with a bolus dose of furosemide (20 mg) for delayed diuresis. We administered fentanyl (total 300 µg) until the end of surgery for postoperative analgesia.

At the end of the surgery, the patient developed massive generalized edema especially noticeable in the face accompanied by palpebral edema (Figure1) and severe hypothermia with the pharyngeal temperature of 34.4 . Arterial blood gas analysis revealed: FiO2 1.0, pH 7.395, PCO2 38.6, PO283.6, BE -0.9, HCO3 23.2, Hb 11.8, Ht 36.5, Na138, K2.9, Glu 184. He remained unresponsive for >1 h after the discontinuation of the sevoflurane and remifentanil administration. The low bispectral index (BIS) value (<15) was obtained. He was also unresponsive to post-tetanic stimulation for >2 h after the cessation of rocuronium infusion. The chest radiogram was unremarkable. The duration of the anesthesia was 9 h, during which he received a total of 1680 ml of blood and 4700 ml of infusions including both crystalloid and colloid solutions. The estimated total urine volume was 230 ml, and the estimated blood loss was 650 ml.

anesthesia-clinical-research-Generalized-edema

Figure 1: Generalized edema especially noticeable in the face accompanied by palpebral edema.

The patient was transferred to the intensive care unit (ICU) where hypothermia was treated with forced air warming. He was given a continuous dopamine and carperitide infusion to maintain hemodynamic stability and urine output. About 2 h after arriving in the ICU, he gradually emerged from anesthesia and became agitated, with unstable respiratory condition.

Dexmedetomidine infusion was started at 0.1 μg/kg/h to achieve adequate sedation for mechanical ventilation. The generalized edema was improved after the overnight intensive treatment. The patient's trachea was extubated the next morning, and he was transferred to a general ward. He was discharged one month after the surgery with a well-functioning graft.

Discussion

This case report described a profound and sustained hypotension after induction of general anesthesia in a depressive patient who had been treated with multiple medications including a tetracyclic antidepressant, SSRI and antipsychotics (Table 1). Although there were many potential causes of the hypotension including hypovolemia and ACE inhibitor [4], we considered that α1-adrenoreceptor antagonism of psychoactive drugs are the main reason for the profound hypotension [5]. Antipsychotics are generally safe to continue in the perioperative period [1] and the incidence of intraoperative hypotension was low in patients on chronic antidepressant therapy [2], but in chronic kidney disease( CKD) patients the elimination half-lives of these agents could be prolonged , which could lead to accumulation of the drugs and their metabolites, causing unpredictably prolonged duration of action [6] . There is a report that haloperidol, which was added preoperatively for delirium prophylaxis [7] for our patient,could cause severe hypotension during anesthesia [8] .

If discontinuation of psychoactive drugs is planned, we should consider patient’s renal function and be aware of the risk of withdrawal symptoms and psychiatric recurrence or relapse [3]. Differential diagnosis of hypotension during general anesthesia includes cardiovascular depression, myocardial ischemia, anaphylaxis, hypovolemia, and deep anesthesia. In our case, intraoperative electrocardiography and TEE revealed no evidence of ischemic heart disease. Considering the severe hypotension and generalized edema, anaphylaxis was undeniable, although its typical signs were not present. We did not administer epinephrine for hypotension because epinephrine is contraindicated in our country for patients treated with phenothiazine-and buthyrophenon-containing antipsychotics owing to paradoxical hypotension [9]. Although estimated blood loss which reported by nursing staff was 650 ml, we suspected that it had been underestimated. Considering intraoperative hemoglobin value and hemodynamic instability, the measurement of intraoperative blood loss seemed inaccurate. In addition, obesity with BMI 36.3 may have contributed to the hypotension via compression of the vena cava and reduction of venous return in the supine position [10]. There was little possibility that ACE inhibitor caused this hypotension because of its discontinuation prior to the operation.

Donnelly et al. reported a case in which high-dose norepinephrine in conjunction with epinephrine and dopamine was successful in treating hypotension in a patient who was treated with clozapine [11]. There were several cases in which ephedrine and phenylephrine were not effective, but vasopressin was most beneficial to restore hemodynamic stability in patients receiving α-adrenergic antagonists [10,12]. The treatment of hypotension in patients receiving antipsychotics will vary based on the level of -adrenergic blockade and anesthesia [12]. In our case, the high-dose norepinephrine infusion and low-dose vasopressin were effective for treating the severe hypotension. If we had used more dose of vasopressin, we could have obtained hemodynamic stability more quickly.

Generally, intraoperative fluid management in kidney transplantation is intended to maintain an adequate intravascular volume and mean arterial pressure in order to maximize the graft function [6]. Traditional aggressive volume loading would cause volume overload, leading to pulmonary and systematic edema in patients with impaired cardiac function [6]. Although our patient’s cardiac function was normal and the intraoperative TEE findings suggested normal to hyperactive left ventricular contraction, massive fluid administration and blood transfusion with delayed diuresis could lead to volume overload and generalized edema. We should administer more vasopressor and less transfusion to avoid volume overload.

Delayed emergence from general anesthesia could be attributed to multiple clinical factors, including residual anesthetics, hypothermia, and brain edema [13]. In our case, hypothermia and the sedative effect of benzodiazepines and antipsychotics could be the main causes of the delayed emergence. Core temperature regulation during general anesthesia may be impaired by dopamine blockade of antipsychotic drugs [14]. Sedation is a common dose-related side effect of antipsychotics, which block the central histamine H1 receptors [5,15]. The additional haloperidol and mianserin could cause sedation and the delayed emergence in our patient.

In addition to that, the SSRIs have potential to cause delayed emergence through inhibition of cytochrome-P450 (CYP) isoforms, which metabolize many anesthetics [16]. We also consider prolonged duration of rocuronium contributed to delayed recovery. Rocuronium is not recommended for patients with renal failure [17], but benzylisoquinoline muscle relaxants are not available in our country. Neurotoxicity attributed to immunosuppressive drugs such as cyclosporine is known after organ transplantations [18]. Although our patient had history of suspected epileptic seizure, he had no seizure perioperatively.

To summarize, we presented a case of profound hypotension and generalized edema in a depressive patient with CKD. To minimize the perioperative adverse effects of the psychoactive drugs, dose reduction or discontinuation of these drugs are needed in CKD patient. Successful outcome in patients with psychiatric disorders and severe physical impairment can only be achieved with an appropriate preoperative assessment and cooperation between psychiatrists and anesthesiologists.

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Recommended Conferences

Article Usage

  • Total views: 11971
  • [From(publication date):
    April-2015 - Aug 23, 2017]
  • Breakdown by view type
  • HTML page views : 8200
  • PDF downloads :3771
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri, Food, Aqua and Veterinary Science Journals

Dr. Krish

[email protected]

1-702-714-7001 Extn: 9040

Clinical and Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals

Ronald

[email protected]

1-702-714-7001Extn: 9042

Chemical Engineering and Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001 Extn: 9040

Earth & Environmental Sciences

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

General Science and Health care Journals

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics and Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001 Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Informatics Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Material Sciences Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Mathematics and Physics Journals

Jim Willison

[email protected]

1-702-714-7001 Extn: 9042

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001 Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

John Behannon

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001 Extn: 9042

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords