Hydroxychloroquine sulphate and plaquenil review

Before prescribing this drug, your doctor may perform tests, such as Vectra DA, to assess the severity of your disease and response to current medications. Before you take Plaquenil or generic hydroxychloroquine, tell your doctor if you've ever had an allergic reaction to this or similar drugs. The dosage of Plaquenil is weight-dependent.

That means the specific dosage you'll get depends on both your illness and how much you weigh. If you weigh less than pounds, you'll get a lower dosage than someone who weighs more than For rheumatoid arthritis , the usual starting dose of Plaquenil is mg twice a day or mg once a day in people weighing 80 kg or more.

For lupus , the typical dosage ranges from mg to mg per day, in one or two doses. The origin of antimalarials dates back to the s in Peru. In , chemists first purified the quinine from the bark. By , anecdotal evidence of improvement in lupus and rheumatoid arthritis came from WWII Allied troops taking a synthetic form of quinine to prevent malaria.

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Over time, other derivatives of quinine were approved by the FDA—chloroquine in and hydroxychloroquine in In rare cases, Plaquenil can cause a problem with blood flow in the eyes that leads to a condition called hydroxychloroquine retinopathy. If it's not caught early, it's often irreversible and can cause impaired vision or even blindness. If it's caught early and you go off the drug, the problem may be reversible.

While you're on this drug, be sure to tell you doctor about any vision changes you notice.

Doctors generally recommend regular eye exams, and depending on other risk factors, your doctor may require you to have yearly tests to check for early signs of this serious side effect. Anyone starting Plaquenil treatment should have a baseline eye exam within the first year.

An older DMARD for RA and other autoimmune diseases

If you're considered low risk, you may not need to be tested for another five years. Certain drugs may interact with Plaquenil, affecting how it works or causing it to be less effective. Tell your doctor about every medication and supplement you are taking. If you're pregnant or trying to get pregnant, discuss Plaquenil with your doctors. Though Plaquenil is generally regarded as safe during pregnancy, it's recommended that you use effective birth control while taking the drug and for up to six months after going off of it.

Dealing with chronic inflammation? An anti-inflammatory diet can help. Our free recipe guide shows you the best foods to fight inflammation. Get yours today! Hydroxychloroquine retinopathy. Eye Lond. Therapy and pharmacological properties of hydroxychloroquine and chloroquine in treatment of systemic lupus erythematosus, rheumatoid arthritis and related diseases.

However, anti-malarials are not a sufficient treatment for more severe lupus symptoms such as kidney disease and nervous system or blood vessel involvement. When lupus spreads to these organs, immunosuppressive medications are usually added to help minimize irreversible injury. Three anti-malarial drugs are prescribed for lupus symptoms. Hydroxychloroquine Plaquenil is the most commonly prescribed because it is generally believed to cause fewer side effects; chloroquine Aralen has a reputation for more serious side effects, but it may be prescribed in situations where hydroxychloroquine cannot be used.

Quinacrine Atabrine is another alternative, but it is prescribed less often because it can sometimes cause a yellow discoloration of the skin. It is sometimes given in addition to hydroxychloroquine if the patient does not respond to Plaquenil alone. Quinacrine tablets are no longer manufactured and can only be obtained through a compounding pharmacist. Your doctor will advise you on how to obtain quinacrine if this becomes your advised method of treatment.

Anti-malarial medications help to control lupus in several ways by modulating the immune system without predisposing you to infection. Anti-malarials can protect against UV light and sometimes even improve skin lesions that do not respond to treatment with topical therapy ointments. Anti-malarial medications may prevent activation of plasmacytoid dendritic cells, a component of the immune system that is responsible for making interferon.

Yes, anti-malarials can be taken with other lupus medications, including corticosteroids e. Anti-malarial drugs may be given in combination with prednisone to reduce the amount of steroid needed to control lupus symptoms and thus to alleviate some of the side effects of the steroid. In addition, since it usually takes about months for your anti-malarial medications to fully take effect, you may be given a steroid medication to act as a bridging medication and alleviate your symptoms during this interim.

Anti-malarials are safe to use during pregnancy, but you should speak to your doctor if you are pregnant or may become pregnant to decide the course of treatment that will be best for you. No fetal abnormalities are known to have occurred from taking hydroxychloroquine, and physicians at several major universities have used anti-malarial drugs for years to treat pregnant women with lupus without negative side effects on the fetus. Damage to the retina, the light sensitive portion of the inner eye, can occur with long-term use of Plaquenil or chloroquine Aralen.

With Plaquenil, however, the most commonly prescribed anti-malarial, this sort of damage occurs only in 1 out of 5, people who take the drug for five years or more. For this reason though, it is important that you see an ophthalmologist for an exam before starting to take an anti-malarial medication for your lupus.

Follow-up exams every 6 months or, annually at the very least are also advised. You can also monitor yourself between visits with a special grid called an Amsler grid, which can be obtained through your ophthalmologist. Thirteen days later, the patient died suddenly at home. Post-mortem examination was not carried out. Antimalarial-related cardiotoxicity most commonly manifests clinically as a restrictive or dilated cardiomyopathy or with conduction system abnormalities including atrioventricular block and bundle branch block. However, also as in our case, non-specific chest discomfort may be a presenting or co-existent feature 12 , 14 , 16 as can presyncope associated with conduction disease 12 , 14 or atrial arrhythmias.

Clinical features of other toxicities may also be present. A review by Costedoat-Chalumeau et al. In a new case reported by the same authors, concerning severe cardiotoxicity leading to heart transplantation due to use of both HCQ and CQ over a 9-year period, retinal toxicity and neuromyotoxicity were also present.

Retinopathy, the most well-known complication of these drugs, may manifest as a spectrum of changes from asymptomatic and reversible pigment changes to visual loss persisting or progressing after drug discontinuation. Prognosis in antimalarial cardiotoxicity can vary from death to cardiac transplantation to partial or complete improvement in cardiac function. In the review by Costedoat-Chalumeau et al.

Meanwhile regression of conduction disease appears to be rare — out of 15 patients with conduction disorders in which the causative agent was discontinued, only three had resolution of the disturbance. Echocardiography plays a key adjunctive role in the diagnosis of HCQ cardiotoxicity. In one report where the patient went on to undergo successful orthotopic heart transplantation, interventricular septal thickness in the explanted heart measured 20 mm.

Such findings, in the absence of significant systolic dysfunction, may be the predominant structural abnormalities seen on echocardiogram 13 , 16 , 18 or may precede the development of systolic dysfunction as in this case. Findings on imaging modalities in support of the diagnosis of hydroxychloroquine cardiomyopathy.

CMR may serve as an increasingly important diagnostic modality in antimalarial cardiotoxicity for a number of reasons. Firstly, it is the reference standard for the assessment of LV and RV function and morphology, the latter also commonly abnormal in antimalarial cardiotoxicity. Although rare, myocarditis is one of the recognized cardiovascular sequelae of RA 27 and is clearly visualized on CMR as a hyperintense area or areas on T2-weighted MRI sequences, not seen in this case.

Restrictive cardiomyopathy in particular cardiac amyloidosis was an important differential diagnosis in our case due to both the past history and echocardiographic findings; however, CMR did not show the typical imaging features suggestive of cardiac amyloid deposition. Another infiltrative cardiomyopathy, cardiac sarcoidosis, was also considered given that it has been associated with conduction system disease on presentation, female predominance, and a higher incidence of abnormal wall thickness, all relevant features to this case.

Lastly, CMR may also play a role in prognosis through its assessment of the degree of fibrosis as determined by DGE imaging. The presence of DGE in non-ischaemic cardiomyopathies predicts an 8-fold increased risk of an adverse cardiac outcome. Sudden death, most likely due to a malignant ventricular arrhythmia, occurred less than 2 months later. Endomyocardial biopsy was the key diagnostic test in this case. Histology is essential to provide an accurate diagnosis and exclude differential diagnoses, including amyloidosis, myocarditis, and sarcoidosis. Histological findings from right ventricular endomyocardial biopsy on light microscopy top panels and electron microscopy bottom panels.

Some of these vacuoles contain central nuclei arrows. A more recent case describes a year duration of therapy prior to the development of clinical heart failure. Guidelines for dosing of both CQ and HCQ are based on a large cohort study of rheumatoid patients looking at risk for developing retinal toxicity.

Avoiding the Traps of Hydroxychloroquine Use

Our patient, 58 kg at the time of her last admission, would have been above this cut-off at 6. However, serious retinal toxicity level from this study was only reported from the level of 7. It is also important to note that RA itself can be associated with a variety of cardiac manifestations, 34 some of which, including myocarditis as previously noted, could present with similar features to those noted in our case.

Impairment in renal function has been proposed as a mechanism for toxicity given that these drugs undergo renal as well as hepatic excretion.


In conclusion, we have presented, to our knowledge, only the fifth reported biopsy-proven case of HCQ cardiotoxicity, presenting as a rapidly evolving non-ischaemic biventricular dysfunction in a year-old female with RA and multiple other comorbidities on long-term HCQ therapy. Although rare, the current case and the accompanying clinically orientated literature review highlights that antimalarial cardiotoxicity can be a fatal diagnosis with cardiac dysfunction persisting despite drug discontinuation.

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  4. RA and Hydroxychloroquine: How Effective is it for Rheumatoid Arthritis?.

Given this, and the potential for reversibility, regular screening with lead ECG and transthoracic echocardiography should be considered in HCQ- or CQ-treated patients in addition to ophthalmological screening, particularly if prolonged duration of treatment or other manifestations of toxicity. Funding: This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Conflict of interest: The authors report no conflicts of interest. National Center for Biotechnology Information , U.

Author information Article notes Copyright and License information Disclaimer. Corresponding author. Email: ku. Received Oct 15; Accepted Nov This article has been cited by other articles in PMC. Abstract Cardiotoxicity is a rare but serious complication of hydroxychloroquine, a 4-aminoquinoline increasingly used in the treatment of rheumatological disorders.

Hydroxychloroquine (Plaquenil) | Coronavirus Pills UK

Keywords: Cardiomyopathy, cardiotoxicity, endomyocardial biopsy, heart failure, hydroxychloroquine. Introduction Hydroxychloroquine HCQ is a 4-aminoquinoline which differs from chloroquine CQ in the addition of a hydroxyl group. Case report A year-old woman was admitted to our tertiary referral hospital in September for further investigation and work up of progressively worsening NYHA class 2—3 dyspnoea over a period of 4—6 weeks, associated with four-pillow orthopnoea, episodic paroxysmal nocturnal dyspnoea, and profound fatigue.

Hydroxychloroquine sulphate and plaquenil review
Hydroxychloroquine sulphate and plaquenil review
Hydroxychloroquine sulphate and plaquenil review
Hydroxychloroquine sulphate and plaquenil review
Hydroxychloroquine sulphate and plaquenil review

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