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Dive into the research topics where Ajanee Mahakkanukrauh is active.

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Featured researches published by Ajanee Mahakkanukrauh.


Asian Pacific Journal of Allergy and Immunology | 2013

Pericardial fluid profiles of pericardial effusion in systemic sclerosis patients.

Patipat Kitchongcharoenying; Chingching Foocharoen; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Ratanavadee Nanagara

BACKGROUND Cardiac involvement is one of clinical presentations in systemic sclerosis (SSc). The pericardial fluid profile and the causes of pericardial effusion were our focus. OBJECTIVES To demonstrate the characteristics and causes of pericardial effusion in SSc. METHODS A descriptive retrospective study was performed on SSc patients with symptomatic pericardial effusion at Srinagarind Hospital, Khon Kaen University, Thailand, between January 1, 2000 and December 31, 2010. We excluded pericardial fluid detected by screening echocardiography. RESULTS Thirty medical records of SSc patients with pericardial effusion were reviewed. The respective mean age and median duration of disease at the time of effusion detection was 52.2±10.8 years and 11.4 months (IQR 0.03-59.1). The female to male ratio was 3.3:1. The most common signs and symptoms included tachycardia (65%) and right-sided heart failure (30%). One patient was diagnosed with cardiac tamponade due to tuberculous pericarditis. Pericardiocentesis and fluid analysis were performed in 9 patients, all of whom had pericardial fluid lactate dehydrogenase (LDH) <200 U/L and a fluid-serum LDH ratio <0.6. Most of the cases (87.5%) had a fluid-serum total protein ratio <0.5. The median white blood cell (WBC) count was 10 cell/mm3 (IQR 6-830), one-third of which was predominated by mononuclear cells. The pericardial biopsy in 8 patients revealed 4 pericardial fibrosis, 2 non-specific inflammation and 2 granuloma. CONCLUSIONS The pericardial fluid profile for SSc was similar to the exudative profile of pleural fluid. Cardiac tamponade was rare. Most pathological findings of pericardial tissue were associated with fibrosis related to the disease itself.


Rheumatology | 2015

Asymptomatic cardiac involvement in Thai systemic sclerosis: prevalence and clinical correlations with non-cardiac manifestations (preliminary report)

Chingching Foocharoen; Burabha Pussadhamma; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Ratanavadee Nanagara

OBJECTIVE To determine the prevalence of asymptomatic cardiac involvement and its correlation with non-cardiac manifestation in Thai SSc patients. METHODS A cross-sectional study was carried out between January 2012 and June 2013 at Srinagarind Hospital, Khon Kaen University, Thailand, on adult SSc patients without signs or symptoms suggestive of cardiac involvement. We excluded those with overlap syndrome, having serum creatinine >123.8 µmol/l, history of cardiac diseases, any atherosclerosis risk factors and receiving angiotensin-converting enzyme inhibitors. Non-invasive tests related to cardiac involvement were performed, including: echocardiography, ECG, chest X-ray, inflammatory biomarkers, cardiac enzymes and N-terminal prohormone of brain natriuretic peptide. RESULTS A total of 103 SSc patients were enrolled, 61.2% of whom were in the subset. Of these, 63 patients had at least one test abnormality (prevalence 61.2%; 95% CI 51.6, 70.7). The two leading cardiac abnormalities were diastolic dysfunction (44.7%) and elevation of cardiac enzymes (36.9%). The only predictor for cardiac involvement per multivariate analysis was the dcSSc subtype with a higher modified Rodnan skin score, and shorter disease duration (odds ratio = 3.37; 95% CI 1.07, 10.65). Compared with the limited subtype, dcSSc was also significantly associated with elevated cardiac enzyme and prolonged distance between a Q wave and T wave in an ECG (QT interval). CONCLUSION Asymptomatic cardiac involvement in Thai SSc was not uncommon, and the most common finding was diastolic dysfunction. Elevated cardiac enzymes were found in one-third of the patients, which correlated with the dcSSc subtype with a higher modified Rodnan skin score and shorter disease duration, suggestive of early myocardial microcirculation disruption. Long-term follow-up was performed to elucidate the clinical implication of these abnormalities.


International Journal of Rheumatic Diseases | 2011

Prognostic factors of mortality and 2-year survival analysis of systemic sclerosis with pulmonary arterial hypertension in Thailand.

Chingching Foocharoen; Ratanavadee Nanagara; Songsak Kiatchoosakun; Siraphop Suwannaroj; Ajanee Mahakkanukrauh

Aims:  Pulmonary arterial hypertension (PAH) is a major complication and cause of death in systemic sclerosis (SSc). Our objective was to identify the predictive factors of mortality and the 2‐year survival rate among Thai sufferers of PAH‐SSc.


International Journal of Rheumatic Diseases | 2016

Clinical differences between Thai systemic sclerosis patients with positive versus negative anti-topoisomerase I.

Chingching Foocharoen; Prangsuporn Suwannachat; Sittichai Netwijitpan; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Ratanavadee Nanagara

Anti‐topoisomerase I antibody (ATA) carries an increased risk of systemic sclerosis (SSc) internal organ involvement. There have been no published comparisons of the clinical characteristics of patients positive and negative for ATA in Thailand, where the positive rate for ATA is higher than among Caucasians.


International Journal of Rheumatic Diseases | 2012

Incidence rate and causes of infection in Thai systemic sclerosis patients.

Chingching Foocharoen; Yada Siriphannon; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Ratanavadee Nanagara

Infection is a common cause of death in systemic sclerosis (SSc) but despite immunosuppressant therapy, there are few reports of opportunistic infection.


Rheumatology | 2017

Effectiveness of add-on therapy with domperidone vs alginic acid in proton pump inhibitor partial response gastro-oesophageal reflux disease in systemic sclerosis: randomized placebo-controlled trial

Chingching Foocharoen; Kitti Chunlertrith; Pisaln Mairiang; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Suwassa Namvijit; Orathai Wantha; Ratanavadee Nanagara

Objectives. Twice-daily dosing of proton pump inhibitor (PPI), the standard therapy for gastro-oesophageal reflux disease (GERD), is an effective therapy for GERD in SSc. The aim of this study was to compare the efficacy of omeprazole in combination with domperidone vs in combination with algycon in reducing the severity and frequency of reflux symptoms of PPI partial response (PPI-PR) GERD in SSc. Methods. Adult SSc patients having PPI-PR GERD were randomly assigned to receive domperidone plus algycon placebo or algycon plus domperidone placebo in a 1:1 ratio plus omeprazole for 4 weeks. The assessment included severity of symptom grading by visual analogue scale, frequency of symptoms by frequency scale for symptoms of GERD and quality of life (QoL) by EuroQol five-dimensions questionnaire scoring. Results. One hundred and forty-eight SSc-GERD patients were enrolled, of whom 88 had PPI-PR. Eighty cases were randomized for either domperidone (n = 38) or algycon (n = 37) therapy. The majority in both groups had the diffuse SSc subset. At the end of the study, no significant difference in symptom grading was found between groups. After treatment and compared with baseline, the severity of symptoms, frequency scale for symptoms of GERD and QoL significantly improved in both groups. Five (13.2%) and 8 (21.6%) respective cases in the domperidone and algycon groups did not respond. Conclusion. The prevalence of PPI-PR GERD is common. Domperidone and algycon are equally effective treatments in combination with omeprazole. However, ∼17% of patients were non-responsive, so the effectiveness of domperidone, algycon and PPI combination therapy should be further investigated. Trial registration: https://clinicaltrials.gov (NCT01878526).


International Journal of Rheumatic Diseases | 2011

Survival rate among Thai systemic lupus erythematosus patients in the era of aggressive treatment

Chingching Foocharoen; Ratanavadee Nanagara; Siraphop Suwannaroj; Ajanee Mahakkanukrauh

Background:  The major cause of death in systemic lupus erythematosus (SLE) is due to the disease activity itself or infection. It is uncertain whether the treatment approach during the last decade prolonged survival in SLE.


The American Journal of the Medical Sciences | 2016

Correlation of Glomerular Filtration Rate Between Renal Scan and Estimation Equation for Patients With Scleroderma

Patcharawan Suebmee; Chingching Foocharoen; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Daris Theerakulpisut; Ratanavadee Nanagara

Background: Renal involvement in scleroderma is life‐threatening. Early detection of a deterioration of the glomerular filtration rate (GFR) is needed to preserve kidney function. Objectives: To (A) determine the correlation between (1) estimated GFR (eGFR) using 4 different formulae and (2) measured GFR (mGFR) using isotopic renal scan in Thai patients with scleroderma with normal serum creatinine and (B) to define the factors influencing eGFR. Method: A cross‐sectional study was performed in adult Thai patients with scleroderma at Srinagarind Hospital, Khon Kaen University, between December 2013 and April 2015. GFR was measured using the gold standard Tc‐99m DTPA (Tc‐99 m diethylenetriaminepentaacetic acid) renal scan. We compared the latter with the eGFR, calculated using the Cockroft‐Gault formula, Modification of Diet in Renal Disease (MDRD), Chronic Kidney Disease Epidemiology Collaboration (CKD‐EPI) equation and creatinine clearance equation. Results: A total of 76 patients with scleroderma (50 women and 26 men) with median age 54.8 years (interquartile range: 47.4 to 58.9) were enrolled. Mean disease duration was 5.6 ± 4.5 years. Median value of mGFR was 100.1 ± 27.6 mL/minute/1.73 m2. There was a correlation between mGFR from the Tc‐99m DTPA renal scan and the eGFR using the Cockroft‐Gault formula, MDRD and CKD‐EPI equation (P = 0.01, <0.001 and <0.001, respectively), but no correlation with eGFR using the creatinine clearance equation (P = 0.27). Body weight, prednisolone use and systolic blood pressure (SBP) had a negative association with mGFR (P = 0.01, 0.01 and 0.007, respectively). After multivariate analysis, SBP was the only clinical parameter that influenced mGFR (P = 0.03). Conclusions: The Cockroft‐Gault formula, MDRD study equation and CKD‐EPI were useful formulae for assessing GFR in Thai patients with scleroderma. Higher SBP was associated with a lower GFR.


International Journal of Rheumatic Diseases | 2016

Drug survival and reasons for discontinuation of the first biological disease modifying antirheumatic drugs in Thai patients with rheumatoid arthritis: Analysis from the Thai Rheumatic Disease Prior Authorization registry

Pongthorn Narongroeknawin; Parawee Chevaisrakul; Nuntana Kasitanon; Tasanee Kitumnuaypong; Ajanee Mahakkanukrauh; Boonjing Siripaitoon; Wanruchada Katchamart

To evaluate and compare the retention rate of biological disease‐modifying antirheumatic drugs (bDMARDs) in real‐life practice and identify risk factors related to remission and drug discontinuation in patients with rheumatoid arthritis (RA).


International Journal of Rheumatic Diseases | 2016

Clinical characteristics of scleroderma overlap syndromes: comparisons with pure scleroderma

Chingching Foocharoen; Sittichai Netwijitpan; Ajanee Mahakkanukrauh; Siraphop Suwannaroj; Ratanavadee Nanagara

Scleroderma with characteristics of other connective tissue diseases is called scleroderma overlap syndrome (SOV); the clinical features of which have yet to be investigated among Thai patients.

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Boonjing Siripaitoon

Prince of Songkla University

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Pongthorn Narongroeknawin

Phramongkutklao College of Medicine

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