1.A three-month follow up of musculoskeletal manifestions in chikungunya fever.
Gutierrez-Rubio Anna Kristina ; Magbitang Angeline-Therese D. ; Penserga Ester G.
Philippine Journal of Internal Medicine 2014;52(1):1-5
BACKGROUND: Chikungunya virus (CHIKV) is a mosquito- borne alphavirus of the family Togaviridae transmitted to humans by the Aedes spp. mosquitoes, causing Chikungunya Fever (CHIKF).
OBJECTIVE: This study aims to describe the course and outcome of musculoskeletal (MSK) manifestations in patients with CHIKF seen over a three-month period.
DESIGN: This is a prospective descriptive study. Seventy patients with fever, rash, and arthritis seen at the University of the Philippines-Philippine General Hospital and private arthritis clinics were collected from August - December 2012. Demographics and course of arthritis were described.
RESULTS: Seventy patients, 53 (68.6%) female, with a mean age of 39.2 ±13.50 were diagnosed with CHIKF. All cases were from the Metropolitan Manila area. Of these, 15 (21.4%) had family members affected. Twenty-four patients (34.3%) were either employed or students. The most common presenting symptoms were fever (94.3%), arthritis or athralgia (98.6%), and rash (87.1%). The most common joint areas involved were the ankles (60.0%), the wrists (40.0%) and the small joints of the hand (51.4%). Twenty-seven (47.3%) had symmetric arthritis. Thirty- seven cases (52.9%) had arthralgia or arthritis for at least six weeks. By the end of the follow-up period, only four (5.7%) had persistent musculoskeletal symptoms. Age and sex were not found to be factors in determining chronicity of arthritic symptoms (p = 0.104 and p=0.58 respectively). Of the seventy patients, 31 (44. 3%) were confirmed cases of CHIKF-- 29 had (+) CHIKV IgM by ELISA, and two had (+) CHIKV PCR. Twenty- one (67.7%) had persistent arthritis of at least six weeks. Treatment consisted of continuous NSAIDs for at least two weeks and some received steroids. In this subgroup, age and sex were not shown to correlate with chronic arthritis (p=0.47 and p=0.05 respectively).
CONCLUSION: This report on a recent outbreak of CHIKF showed the classic triad of fever, rash, and arthritis. There was no correlation between age and chronicity of arthritic symptoms. Sex, likewise, did not appear to influence chronicity. The disease occurred in family clusters. Patients required continuous treatment with NSAIDs and some had to be given steroids. Most cases resolved by 12 weeks.
Human ; Male ; Female ; Middle Aged ; Adult ; Chikungunya Fever ; Chikungunya Virus ; Togaviridae ; Anti-inflammatory Agents, Non-steroidal ; Arthralgia ; Arthritis ; Exanthema ; Enzyme-linked Immunosorbent Assay
2.In-hospital outcomes of methylprednisolone pulse therapy in the treatment of systemic lupus erythematosus.
Magbitang Angeline-Therese D. ; Rubio Anna Kristina Gutierrez ; Salido Evelyn Osio
Philippine Journal of Internal Medicine 2014;52(1):1-7
BACKGROUND: Methylprednisolone Pulse Therapy (MPPT) is standard of care in the management of severe systemic lupus erythematosus (SLE). This treatment, though, is considered a double-edged sword due to its life-threatening adverse effects. Renal disease, liver disease and high dose of the drug are factors proposed to adversely affect outcomes of patients treated with MPPT. Despite the widely accepted use of MPPT, there are no reports describing the outcomes from its use among Filipinos with SLE.
OBJECTIVE: To determine the in-hospital outcomes of patients with SLE treated with MPPT and to identify factors associated with adverse outcomes.
GENERAL STUDY DESIGN: Retrospective
POPULATION: Adult patients with SLE who were admitted in Philippine General Hospital and underwent MPPT from January 2008 to December 2012.
METHODS: Patient demographics, disease characteristics on admission, indications for MPPT and in-hospital outcomes were extracted.
ANALYSIS: Chi-square test and Fisher's exact test were used to elicit association of population characteristics to outcomes.
RESULTS: Forty-two patients with SLE who underwent MPPT were included. Majority are females (98%) and most (60%) underwent MPPT within one year of SLE diagnosis. High disease activity is seen at the time
of MPPT with a mean Mex-SLEDAI score of 14.69. Infection (83%) is the most common comorbidity. Anemia, hypoalbuminemia and significant proteinuria are the most common laboratory abnormalities. The top indication for MPPT is nephritis (83.3%). The dose received by the majority (66.7%) is one gram/day for three days, which is a high dose.
Improvement rate is 76% but the in-hospital complication rate is 64% and mortality rate is 21%. Patients with in-hospital complications have significantly lower absolute lymphocyte count (p=0.013), serum albumin (p=0.04) and greater 24-hour proteinuria (p=0.04) at baseline. High-dose MPPT is significantly associated with in-hospital complications (p=0.04) but not mortality. Nephritis (p= 0.04) and low platelet counts at baseline (p=0.01) are associated with mortality.
CONCLUSION: In this population, there is a high rate of improvement of lupus disease activity when MPPT is used but there is a corresponding high rate of in-hospital complications and mortality. High dose of MPPT seems to be associated with increased in- hospital complication, while nephritis and low platelet count showed a probable association with mortality. Further studies on a larger cohort are needed. For now, the findings of this study may be helpful in developing guidelines on the use of MPPT among Filipino patients with SLE.
Human ; Male ; Female ; Adult ; Hypoalbuminemia ; Serum Albumin ; Lupus Erythematosus, Systemic ; Nephritis ; Kidney Diseases ; Proteinuria ; Anemia ; Liver Diseases ; Lymphocyte Count ; Methylprednisolone
3.A legacy of excellence in research and service
Acta Medica Philippina 2022;56(2):5-
In 1961, Dr. Lourdes Manahan, a young internist at the Philippine General Hospital, presented her paper entitled “Rheumatic disease in the Philippines” at the Australian Rheumatism Congress in Sydney.1 This was the first time an article on the Philippine rheumatology experience was presented at an international convention. It was, however, not Dr. Manahan’s first foray into research. In 1948, she was published in this very journal – a report on familial non-hemolytic jaundice, a syndrome which would later bear her name, the Rotor-Manahan-Florentin syndrome.2 Her interest soon shifted towards a new field of study centered on diseases referred to then as “rheumatism.” After training in the United States for a year, she established an arthritis clinic to serve Filipino rheumatic patients in the PGH dispensary. For over a decade, she cared for patients alone, painstakingly documenting her findings in pages of handwritten notes and tables. These pages turned into scientific publications, and Dr. Manahan became a pioneer in research in rheumatology in the region. She was the first to describe gout in the Philippines.3, 4 She authored the COPCORD (Community Oriented Program for Control of Rheumatic Diseases) studies, a joint effort by the World Health Organization and International League Against Rheumatism to measure the burden of arthritis and disability in the community.5,6
The Division of Rheumatology continues this legacy. Research in rheumatic diseases has been one of the core disciplines of the division over its now 50 years of existence. In celebration of our founder’s 100th birth anniversary, this special issue of ACTA MEDICA PHILIPPINA republishes three of Dr. Manahan’s earlier works. The first is a report of a family with Rotor-Manahan-Florentin syndrome. 7 While not a rheumatic disease, her encounter with this condition sparked her interest in scientific inquiry. Dr. Manahan also co-authored the first clinical and laboratory description of Chikungunya in the Philippines.8 She also was one of the first to investigate HLA antigens in Ankylosing Spondylitis in Filipinos.9
This special issue in rheumatology also presents interesting cases in rheumatic diseases and original studies by the faculty of the division and its graduates. The gout registry feasibility study emphasizes the importance of databases in collecting data over time to describe the clinical profiles and outcomes of Filipino patients with gout. Penserga and Penserga’s paper shines a spotlight on the unmet need to manage rheumatoid arthritis in the Philippines, where most patients do not have access to biological treatments. Finally, Villanueva-Misa et al. demonstrate the Knee Injury and Osteoarthritis Outcome Score (KOOS) to be a valuable tool for measuring disability in Filipino patients with osteoarthritis in clinical practice and research.
As we honor the legacy of the first among us, we are reminded that the central focus of our work, both in research and clinical practice, is always in the service of the Filipino patient
Rheumatology