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Paliperidone palmitate-induced facial angioedema: A case report

2020-04-08 01:28:12MaytineeSrifuengfungThanisornSukakulChanikaLiangcheepNateeViravan
World Journal of Clinical Cases 2020年20期

Maytinee Srifuengfung, Thanisorn Sukakul, Chanika Liangcheep, Natee Viravan

Maytinee Srifuengfung, Chanika Liangcheep, Natee Viravan, Department of Psychiatry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand

Thanisorn Sukakul, Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand

Abstract BACKGROUND Paliperidone palmitate is a once-monthly injectable, atypical antipsychotic. To our knowledge, there has been only one report of paliperidone palmitate-induced angioedema presenting with acute laryngeal edema with subsequent respiratory arrest. Here, we present a case report of paliperidone palmitate-induced angioedema with a relatively mild clinical presentation compared with the previously reported case, and the patient’s condition was not complicated by lifethreatening anaphylaxis.CASE SUMMARY A 79-year-old female, who had a major neurocognitive disorder due to Alzheimer’s disease with behavioral disturbances. Paliperidone palmitate was offlabel used to control her aggression, irritability, and psychosis. After induction doses (150 mg and 100 mg intramuscularly, given 1 wk apart), she developed intermittent swelling of the face, eyelids, and lips on day 17 after the initial dose,and the edema was explicitly seen on day 20. The diagnosis was paliperidone palmitate-induced angioedema. The monthly injection dose was discontinued on day 33 after the initial dose. The angioedema was subsequently alleviated, and it had completely resolved by day 40 after the initial dose.CONCLUSION Paliperidone palmitate-induced angioedema is a rare condition and can present with a mild, intermittent facial edema, which may be overlooked in clinical practice.

Key Words: Case report; Paliperidone palmitate; Paliperidone LAI; Long-acting paliperidone; Angioedema

INTRODUCTION

Paliperidone palmitate is a long-acting, atypical antipsychotic medication that is administeredviamonthly intramuscular (IM) injections. It is used to treat the psychotic symptoms of schizophrenia and delay the time to relapse[1,2]. In addition, the drug can be effectively used in patients with poor medication compliance to reduce recurrence and hospitalization rates[3]. Moreover, in patients with major neurocognitive disorders, it has been used off-label to control neuropsychiatric symptoms, including delusion, hallucination, agitation, and aggression. Paliperidone palmitate can also prevent relapse of schizophrenia as effective as fluphenazine decanoate while carrying a lower risk of tardive dyskinesia and anticholinergics use[4].

Angioedema refers to deep dermal, subcutaneous, and submucosal edemas of tissue caused by the release of vasoactive mediators. Medication-induced angioedema can lead to mortality if laryngeal edema occurs[5]. Angioedema has been reported to be associated with antipsychotics,e.g., chlorpromazine[6], haloperidol, iloperidone[7],risperidone[8], quetiapine, olanzapine, clozapine[9], and ziprasidone[10]. To our knowledge, there are only two previous reports of paliperidone-induced angioedema.The first case involved facial angioedema arising from dose-dependent oral paliperidone[11], while the second case concerned acute laryngeal edema with respiratory arrest resulting from a paliperidone palmitate injection[12]. The current report presents a rare case of paliperidone palmitate-induced angioedema that presented with intermittent facial edema. The previously reported cases of paliperidone-induced angioedema are also reviewed and discussed.

CASE PRESENTATION

Chief complaints

Intermittent facial edema at day 17 after an initial dose of paliperidone palmitate,administered by intramuscular injection.

History of present illness

A 79-year-old Thai woman was admitted to a psychiatric ward due to uncontrollable aggressive behaviors and psychotic symptoms. A retired teacher living with two daughters, she had started having memory problems and episodes of irritable mood two years prior to the admission. Moreover, she had been diagnosed with a major neurocognitive disorder due to Alzheimer’s disease one year before the admission,and she was treated with donepezil (5 mg/d). Two weeks before admission, she had developed progressive irritable mood, aggressive behaviors, nihilistic delusions, visual and auditory hallucinations, and agitation, which prompted her daughters to take her to the outpatient clinic. Her primary doctor believed that the patient’s psychiatric symptoms were explained by the progression of Alzheimer’s disease rather than donepezil-induced hallucination because donepezil had been constantly given at low dose (5 mg/d) for one year. Initially, oral risperidone, titrated to 2 mg/d, was administered for five days, but it was unable to control her behaviors. The medication was then switched to oral quetiapine, titrated to 400 mg/d, for five days;unfortunately, it too failed to control her aggressive behaviors and psychosis. She was therefore admitted.

During admission, oral quetiapine was titrated to 600 mg/d but was unable to control her violent behaviors. Quetiapine was switched to oral paliperidone and was titrated from 3 to 6 mg/d over four days. The patient responded well to paliperidone,and the psychotic and aggressive behaviors were markedly ameliorated. However, she still had a low tendency to comply with oral paliperidone; consequently, after nine days, the drug was switched to paliperidone palmitate. An induction dosage was given in the form of an initial dose of 150 mg IM, followed by 100 mg IM the next week. The patient was discharged from the hospital with no oral antipsychotic.

At home, 17 d after receiving the initial dose of paliperidone palmitate, the patient started to show mild facial swelling with symmetrical eyelids and lip edema without itchiness (Figure 1). The symptoms usually lasted two to three hours and disappeared with no treatment. A few days later, on day 20 after the initial dose, the edema became worse and prominent. There were no other manifestations that indicated anaphylaxis,such as breathlessness, signs of hypotension, nausea, and vomiting. No other specified rash was observed. The patient denied taking any other nonprescription medications,or new kinds of food or herbs.

History of past illness

The patient had an underlying, major neurocognitive disorder due to Alzheimer’s disease; type 2 diabetes mellitus; dyslipidemia; and hypertension. Her current medications were donepezil (5 mg/d), metformin (500 mg/d), simvastatin (500 mg/d), felodipine (5 mg/d), and atenolol (25 mg/d). All medications had been taken orally and regularly at a stable dose for more than a year preceding the edema.

Personal and family history

The patient had a history of aspirin allergy of unknown presentation since childhood.She had never had facial edema caused by food. The patient also had no relatives who had reported being allergic to medications or who had had angioedema.

Physical examination

The patient visited the outpatient clinic 33 d after receiving the initial dose of paliperidone palmitate. Her vital signs were stable: Body temperature, 37.0 °C; Heart rate, 68 bpm; Respiratory rate, 18 breaths per minute; Blood pressure, 122/60 mmHg;Oxygen saturation in room air, 98%. There was no edema of the face or extremities,nor rash or skin discoloration. Both lungs were clear on auscultation, and all other systems were normal.

Laboratory examinations

The patient’s serum renal, hepatic, and thyroid functions, including electrolytes, were normal. Naranjo’s algorithm score[13]was 6 (probable adverse drug reaction).

FINAL DIAGNOSIS

Based on the patient’s history and the Naranjo score, the final diagnosis was paliperidone palmitate-induced angioedema.

TREATMENT

On day 33 after the initial paliperidone palmitate dose had been given, the patient visited the outpatient clinic. Her scheduled monthly paliperidone palmitate dose was stopped and replaced with oral paliperidone (3 mg/d). Antihistamine, corticosteroid,and epinephrine were not given to the patient.

OUTCOME AND FOLLOW-UP

After the injectable paliperidone palmitate was stopped, the patient’s facial edema reduced and had completely resolved by day 40 after the initial dose of paliperidone palmitate. The oral paliperidone was titrated to 6 mg/d and was continued for two months before being tapered off due to clinical stability. No recurrent facial edema or other allergic symptoms were observed during subsequent, routine, follow-up visits.

Figure 1 Recurrent, asymptomatic, facial swelling. The pictures on the left demonstrate the eyelids (A: Baseline; B: Eyelids with edema). The pictures on the right demonstrate the lower face and lips (C: Baseline; D: Mildly swollen face and lip edema).

DISCUSSION

Paliperidone palmitate is a long-acting, injectable formula of the atypical antipsychotic, paliperidone. Approved by the Unites States Food and Drug Administration for the treatment of schizophrenia and schizoaffective disorders, it has been in use since 2009. It is given by intramuscular injection, with the first two induction doses (150 mg and 100 mg) being given one week apart, followed by a single, monthly, maintenance dose of 25–150 mg[14]. Its clinical effects can be seen on day 8 after the initial dose. Paliperidone palmitate reaches its peak plasma level on days 12-13, and its serum half-life is 25-49 d[15,16].

Angioedema refers to deep dermal, subcutaneous, and submucosal edemas of the tissue. The edema is non-pitting and tends to appear in the lax-skin area. Angioedema often involves the face, lips, and tongue, and it can be fatal if the larynx or pharynx is involved. The pathogenesis of medication-induced angioedema can be either an immunological reaction (such as an IgE-mediated, complement activation), or a nonimmunological reaction (for example, interference with arachidonic acid metabolism,kinin-dependent mechanisms, or direct mast cell degranulation)[5]. To date, the mechanism of antipsychotic-induced angioedema remains unclear; the available evidence indicates that it could involve either immunological[17]or non-immunological reactions[18].

To our knowledge, there is only one reported case of angioedema resulting from paliperidone palmitate injections. The case concerned a 30-year-old male with schizophrenia from Greece[12](Table 1). He developed acute laryngeal edema and respiratory arrest two months after first being injected with paliperidone palmitate(150 mg). The patient was intubated for two days; on the third day after extubation, he became delirious and was given haloperidol (10 mg IM). During the following hour,he developed an upper airway obstruction and was reintubated. His clinical condition was improved by intravenous methylprednisolone. There was also a case of oral paliperidone-induced angioedema. A 19-year-old female with schizophrenia from Turkey (Table 1) presented with facial edema two hours after her oral paliperidone dosage had been increased from 3 to 6 mg. The edema resolved within one week of the oral paliperidone dosage being reverted to 3 mg, but it re-emerged following rechallenge with 6 mg oral paliperidone[11].

This report presents a rare case of paliperidone palmitate-induced angioedema.Paliperidone palmitate was administered to a 79-year-old elderly patient who had amajor neurocognitive disorder due to Alzheimer’s disease with behavioral disturbances and psychotic symptoms. She developed intermittent facial edema 17 d after the first administration, and the symptoms lasted for another 23 d (to day 40 after the initial paliperidone palmitate dose). This might be explained by the long half-life of paliperidone palmitate, which ranges from 24 to 49 d[15].The duration of the symptoms of medication-induced allergic angioedema may vary among the few reported cases due to the unclear pathophysiological pathways of the drug and the possible influence of culprit medications. Although this patient received antihypertensive medications(such as calcium channel antagonists, which could induce angioedema), the duration of the oral antihypertensive administration was not compatible with the onset of the symptoms[19]. Of interest, the angioedema in this case report exhibited only with the paliperidone palmitate injection, not with the oral paliperidone. This phenomenon has also been noted in case reports of paliperidone[12]and risperidone[20]usage. The mechanism remains unclear. We hypothesized that increasing dose might be a key factor in developing angioedema in this patient because angioedema did not occur when oral paliperidone 6 mg (equivalent to paliperidone palmitate injection 75 mg)[14]or risperidone 2 mg (equivalent to paliperidone palmitate injection 50 mg)[21]were given, but developed at higher dose of paliperidone palmitate injection 150 mg and 100 mg.

Table 1 Review of paliperidone-induced angioedema case reports

Both immunological and non-immunological reactions could be suspected in this case. Although the complement level and serum tryptase were not investigated in this patient, a non-immunological reaction was more likely due to the delayed onset of angioedema and the absence of an urticarial rash. Paliperidone is the active metabolite of risperidone, and the mechanism of angioedema from paliperidone may resemble that of risperidone. Risperidone can suppress the activity of the C1-inhibitor, thereby increasing anaphylatoxin level, which in turn increases vasodilation and vascular permeability. Moreover, risperidone can also induce bradykinin aggregation and stimulate nitric oxide and prostacyclin, all of which increase vascular permeability[18].Should angioedema from paliperidone be caused by an immunological reaction, crossreactivity with other antipsychotics (clozapine-olanzapine[17], clozapine-olanzapinequetiapine[9], and haloperidol-iloperidone[7]) and paliperidone could occur. A decision to change to alternative drugs warrants careful consideration during treatment.

Discontinuation of the paliperidone palmitate proved to be adequate for the management of angioedema in this case. In concordance with previous reported cases,dose reduction[11,22]or discontinuation (with[9]or without[8,17]an antihistamine and corticosteroid) of the culprit antipsychotic is sufficient for the management of antipsychotic-induced angioedema. However, in more severe cases in which the respiratory tract could be involved, the administration of an additional corticosteroid,antihistamine, and/or epinephrine was warranted[7,20].

The present case report has some mentionable strengths. Firstly, unlike earlier reports, our pictures clearly show the presence of angioedema. Moreover, as the patient’s daughters, both with master’s degrees, were circumspect, the information obtained was highly accurate. A limitation of this case report was the lack of immunology testing; it is therefore difficult to provide the exact mechanism of angioedema.

CONCLUSION

Paliperidone palmitate-induced angioedema can present with intermittent facial edema which may be overlooked. The symptoms remit with medication discontinuation. The symptoms of angioedema in this case were relatively mild relative to those of the previously reported case[12], and the patient’s condition was not complicated by life-threatening anaphylaxis. However, there has been a report that the degree of symptoms of angioedema arising from paliperidone may be dosedependent[11]. Therefore, when introducing paliperidone or increasing its dosage,patients should be closely monitored for adverse reactions, especially psychiatric patients who are unable to detect their illness.

ACKNOWLEDGEMENTS

The authors gratefully acknowledge the patient’s daughters, who provided useful information regarding their beloved mother.

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