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A retrospective drug use evaluation of cabergoline for lactation inhibition at a tertiary care teaching hospital in Qatar

Authors AlSaad D, ElSalem S, Abdul Rouf P, Thomas B, Alsaad T, Ahmad A, Al Hail M

Received 13 September 2015

Accepted for publication 14 December 2015

Published 9 February 2016 Volume 2016:12 Pages 155—160

DOI https://doi.org/10.2147/TCRM.S96298

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Hoa Le

Peer reviewer comments 5

Editor who approved publication: Professor Garry Walsh


Doua AlSaad,1 Samah ElSalem,1 Palli Valapila Abdulrouf,1 Binny Thomas,1,2 Tayseer Alsaad,3 Afif Ahmed,1 Moza AlHail4

1Department of Pharmacy, Women’s Hospital, Hamad Medical Corporation, Doha, Qatar; 2Department of Pharmacy and Life Sciences, Robert Gordon University, Aberdeen, UK; 3Department of Pediatrics, Hamad General Hospital, 4Clinical Support Service Unit, Hamad Medical Corporation, Doha, Qatar

Background:
Breastfeeding is considered as gold standard for infant nutrition and should be interrupted only when a compelling indication exists. Certain medical conditions such as abortion, stillbirth, HIV infection, or infant galactosemia and certain medications such as chemotherapy necessitate lactation inhibition to protect the health of mother and infant. Drug use evaluation (DUE) studies are done to explore the current practice in a setting and help to identify areas in which further information and education may be needed by clinicians.
Objective: The aim of this study was to conduct a DUE of cabergoline to assess indications for lactation inhibition, dosage regimen, and its safety.
Method: A retrospective cross-sectional DUE study was conducted over a period of 4 months from September 1, 2013, till December 31, 2013, at the Women’s Hospital, Qatar. All cabergoline prescriptions written for lactation inhibition within 10 days of delivery or abortion were included in the study. A descriptive data analysis was undertaken.
Results: Of the 85 patients included, stillbirth (50.6%) was considered as the main reason for lactation inhibition, followed by abortion (27.1%) and neonatal death (12.9%). The remaining 9.4% of the patients had live baby, and the majority of them were prescribed cabergoline for lactation inhibition because their maternal medical conditions required the use of drugs with insufficient safety data (n=6). Seventy-four percent of patients received cabergoline at accurate time and dose. However, 14% of the patients had preexisting hypertensive disorder and 58.3% of them were diagnosed as uncontrolled hypertension.
Conclusion: The current DUE study found that cabergoline was mainly used to inhibit lactation for patients with stillbirth, abortion, and neonatal death. In mothers who use medications for other medical conditions, benefits and risks of breastfeeding should be carefully balanced before prescribing cabergoline. Current prescribing pattern can be further enhanced through informing health care providers regarding appropriate cabergoline dosage regimen and its safety in patients with uncontrolled hypertension.

Keywords: lactation inhibition, cabergoline, drug use evaluation, breastfeeding inhibition

Introduction

Human milk is the normative standard for infant feeding and nutrition. It provides short- and long-term nutritional, cognitive, emotional, and immunologic advantages. Medical contraindications to breastfeeding are few. These include infant galactosemia or mother’s HIV infection, untreated and active tuberculosis, or use of some chemotherapy agents. Furthermore, some mothers avoid breastfeeding on personal or social grounds. Regardless of the reason for not breastfeeding, this decision can be associated with complications including milk secretion, breast pain, engorgement, or mastitis.17

Various approaches are used to suppress lactation in women. Severe breast pain can be encountered in women who do not breastfeed and use analgesics or use nonpharmacological approaches to suppress lactation such as breast binder or ice packs.8 Furthermore, the use of pharmacological interventions such as estrogens alone, estrogen–androgen combination, pyridoxine, and dopamine agonists have been evaluated for efficacy in milk suppression and have shown variable results.5

Cabergoline is a dopamine agonist used to suppress lactation despite the lack of approval from the United States Food and Drug Administration for this indication. It exerts its effect through the inhibition of prolactin release from the anterior pituitary gland. Compared to bromocriptine, the older dopamine agonist, cabergoline is better tolerated with significantly less rebound breast activity and adverse effects and with more simple administration schedule.9,10

A number of studies have been conducted to examine the dose-dependent effect of cabergoline.1114 A range of oral doses between 0.4 mg and 1 mg was used, and the most effective dose for long-term suppression of lactation was found to be 1 mg.15 Accordingly, a single dose of 1 mg during the first 24–27 hours postpartum is recommended for lactation inhibition,10,16 while a dose of 0.25 mg every 12 hours for four doses is used for suppression of established lactation.16

Drug use evaluation (DUE) is a process of ongoing, systematic, criteria-based evaluation of drug use with the aim of ensuring that medications are used appropriately at the individual patient level.17 DUE studies are a powerful tool to explore the pattern of prescribing medications, promote optimal medication therapy, and prevent medication-related problems. In addition, DUE studies help to identify areas in which further education or information may be needed by health care providers.17

A valid indication is necessary for the use of cabergoline to inhibit lactation in nursing mothers. Physicians must be aware of the dose, indication, and frequency to prescribe cabergoline in nursing mothers. They also should review maternal medical conditions to ensure its safety. Therefore, we aimed to conduct a DUE of cabergoline to assess indications for lactation inhibition, dosage regimen, and its safety.

Method

Study setting and period

This DUE study was conducted at the Women’s Hospital, Qatar. This tertiary care facility has 234 beds including antenatal, postnatal, and high dependency units, an outpatient department followed by an emergency room, 16 labor rooms, and three operating theaters, as well as a level-3 neonatal intensive care unit. All cabergoline prescriptions for lactation inhibition written over a 4-month period between September 1, 2013, and December 31, 2013, were used in the study.

Study design

This retrospective cross-sectional study was conducted to evaluate the use of cabergoline in lactation inhibition. A literature review along with World Health Organization guidelines on conducting DUE studies was utilized for the DUE criteria selection.17 The primary outcomes for the study were

  1. Identify and assess indications for lactation inhibition.
  2. Evaluate the appropriateness of cabergoline dosage regimen.
  3. Evaluate the safe use of cabergoline in patients with existing medical comorbidities.

Eligibility criteria

Women who received a cabergoline prescription for lactation inhibition within 10 days of delivery or abortion were included in the study.

Data collection

A standardized data collection tool was developed utilizing the selected DUE criteria. Variables were designated to measure the prespecified outcomes. The tool was validated through piloting it on ten randomly selected files.

Outcome measures

The Centers of Disease Control and Prevention and American Academy of Pediatrics resources were utilized to identify the medical conditions that necessitate lactation inhibition.18,19 Drugs in Pregnancy and Lactation book and Drugs and Lactation Database (LactMed) by the US National Library of Medicine were used to identify the safety of medications with breastfeeding.15,20 A single dose of 1 mg of cabergoline within the first 24–27 hours of delivery/abortion is the recommended regimen for lactation inhibition.10,16 The main safety concerns for the use of cabergoline that were evaluated in this study were preexisting uncontrolled hypertension at the time of cabergoline administration and allergy with ergot alkaloid since the use of cabergoline in these populations could cause significant risk to patients.

Definitions

In this study, lactation inhibition refers to the prevention of milk formation within the first 27 hours postpartum before the mother starts breastfeeding, whereas lactation suppression pertains to suppression of established lactation. There is no clear definition and duration for controlled hypertension before cabergoline administration. So we defined controlled hypertension as having systolic blood pressure <150 mmHg and diastolic blood pressure <100 mmHg21 within the previous 24 hours before prescribing cabergoline without intravenous antihypertensive medications to control the blood pressure.

Data processing and analysis

Data collection was done using patients’ medical records, and the collected data were manually sorted and categorized. A descriptive data analysis was carried out and evaluated against the preset criteria.

Ethical consideration

Waiver of informed consent and ethical approval were obtained from the Medical Research Center, Hamad Medical Corporation (approval number 13393/13).

Results

A total of 232 patients were prescribed cabergoline, of which 85 patients were included in this study (Figure 1). Demographic characteristics of patients are shown in Table 1. Thirty-one percent of the patients were Qataris, and the majority of the patients had a singleton pregnancy (90.6%).

Figure 1 Patients selection for inclusion.

Table 1 Demographic characteristics
Notes: aOthers (n): Yemeni (5), Pakistani (5), Sudanese (4), Jordanian (4), Iranian (2), Palestinian (2), Lebanese (2), Bangladeshi (2), Indonesian (1), Moroccan (1), Nepalese (1), Mauritian (1), Syrian (1), and Senegalese (1). bData are missed for two patients.

Indications for lactation inhibition

Stillbirth was found to be the main reason to inhibit lactation (50.6%), followed by abortion (27.1%) and neonatal death (12.9%). Only 9.4% of the patients who received cabergoline for lactation inhibition had live baby (Table 2).

Table 2 Indication for lactation inhibition
Notes: aMedications used by each patient: Patient 1: prednisolone 5 mg daily, rosuvastatin 10 mg daily, tacrolimus 4 mg am and 3 mg pm, mycophenolate 1 g BID, kidney transplant. Patient 2: azathioprine 75 mg daily, tacrolimus 3 mg BID, prednisolone 5 mg daily, kidney transplant. Patient 3: amitriptyline 75 mg daily, fluphenazine 0.5 mg daily, nortriptyline 10 mg daily, depression. Patient 4: amitriptyline 25 mg daily, fluoxetine 20 daily, depression. Patient 5: oxcarbazepine 300 mg BID, levetiracetam 500 mg TID, epilepsy. Patient 6: carvedilol 12.5 mg BID, furosemide 40 daily, cardiomyopathy.
Abbreviations: BID, twice daily; TID, three times daily.

Appropriateness of indications for lactation inhibition

Following abortion, only one patient received cabergoline at gestational age <16 weeks as patient requested, whereas all the other patients received cabergoline at a higher gestational age.

In patients with live baby, no infant or maternal medical conditions that required lactation inhibition were encountered. One of the patients with severely inverted nipples requested cabergoline to suppress her lactation. Six patients who used medications for postkidney transplant, depression, epilepsy, and cardiomyopathy did not breastfeed their babies. All these patients were using combinations of medications (Table 2). Only one patient requested lactation inhibition with no clear reason.

Cabergoline dosage

The majority of the patients were prescribed cabergoline during hospital admission (83.5%), while the rest were prescribed cabergoline at discharge as home medication. Cabergoline was prescribed within the first 27 hours of delivery or abortion in >80% of the patients and was prescribed as a single dose of 1 mg in 71.8% of the patients. Appropriate prescribing pattern of both timing and dose was found in 74.1% of the patients (Table 3). It was noted that 50% of the patients with live baby received cabergoline after 27 hours of delivery.

Table 3 Dosage regimen of cabergoline
Note: aOthers (n): 1 mg for two doses 1 week apart (1), 0.5 mg single dose (2).

Safety of administration

Fourteen percent of the patients had hypertensive disorders during current pregnancy. Fifty-eight percent of these patients had uncontrolled blood pressure 24 hours prior to prescribing cabergoline (Figure 2). None of the patients who received cabergoline were allergic to ergot alkaloids (Table 1).

Figure 2 Cabergoline safety.
Note: Total patients n=85, patients with blood pressure disorder n=12.

Discussion

This DUE study explores the current clinical practice and provides an evidence for the use of cabergoline in lactation inhibition with an emphasis on the indications and safety. To the best of our knowledge, no DUE studies on cabergoline use for lactation inhibition were published elsewhere.

Lactogenesis starts at ~16 weeks of gestation.22,23 Most of the patients received cabergoline at late gestational ages. Only 9.4% of the patients who received cabergoline had live baby. The main reason for that was the use of other medications by the mothers for their existing maternal comorbidities. Not all the received medications contraindicate breastfeeding,15,20 but may be the use of combinations of these medications led to the decision of lactation inhibition. Generally, for many of the medications that possess a low risk to the nursing baby, breastfeeding can be continued with close monitoring of the baby and with proper timing between medication administration and breastfeeding if applicable or a safer alternative can be used when appropriate.

Many studies assessed the prolactin inhibitory effect of different cabergoline doses, and the 1 mg single dose was shown to be the most effective dose.13,14 In our study, the 1 mg single dose was prescribed in 71.8% of the patients. Cabergoline administration should take place within the first 24–27 hours of delivery.10,16 Delay beyond this time period was noted in 50% of the patients with live baby, which might reflect delay in making the decision of stopping breastfeeding until weighing benefits and risks.

Cabergoline should not be used in women with pregnancy-induced hypertension, for example, preeclampsia or postpartum hypertension, unless the potential benefit is judged to outweigh the possible risk.16 Hypertensive disorders were encountered in 12 patients, with 58.3% of them having uncontrolled blood pressure for the 24 hours prior to receiving cabergoline. Close monitoring of these patients would be required, especially for blood pressure.

One of the limitations of the study was its retrospective nature that does not provide information about all perspectives of the physicians and patients at the time of prescribing cabergoline. Moreover, unclear and incomplete documentation might reduce the amount of information that could be retrieved. Another limitation is that this DUE assesses the timing of writing the prescription, which might not reflect the exact time of administration, especially with patients who were planned to receive it at discharge as home medication.

Our study described different aspects of clinical practice regarding cabergoline use in lactation inhibition. Future work can be expanded to the evaluation of cabergoline in lactation suppression within the first 2–6 months postpartum, with a focus on patients with live nursing babies.

Conclusion

This DUE study found that cabergoline use in lactation inhibition was mainly for patients with stillbirth, abortion, and neonatal death. Maternal use of medications for other medical comorbidities requires careful evaluation of breastfeeding benefits and risks before prescribing cabergoline. To further enhance the current prescribing pattern, health care providers need to be informed regarding the appropriate dose, frequency, and safety concerns in patients with uncontrolled hypertension.

Funding

This work received a grant from the Medical Research Center, Hamad Medical Corporation, Qatar.

Disclosure

The authors report no conflicts of interest in this work.


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