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Today was ward rounds at Annotto Bay, which was an excellent learning experience. Typically the morning on the ward is a combination of “ward reviews” which is a brief follow up visit for (mostly) recently discharged patients who need a sooner follow up than the next available clinic date. I was able to see a baby that I had admitted for dehydration and failure to regain birthweight on my very first day of work. He was discharged a few days ago and is doing great now, has surpassed birthweight and is feeding well – I’m so happy about that! The remainder of the morning is spent discussing patients currently admitted to the ward. I never realized how much I enjoyed the whole process of reviewing management and differential diagnoses and now I realize how much more important this process becomes in a setting such as this where management decisions are largely based on your clinical judgment and a limited number of available tests.  There are quite a few patients currently admitted, most of them neonates, and quite a few admitted for jaundice.  The management of neonatal jaundice here is an interesting mix of some quite familiar therapies mixed in with some (such as giving phenobarbital and albumin) that I had never heard of, but when explained, made intuitive sense.  There is no universal bilirubin screening for newborns here and so only babies with clinical concern for jaundice end up getting a level. Even with mild jaundice, mothers are sometimes encouraged to expose the babies to sunlight and advised to return to care if jaundice does not improve. Here in Annotto Bay there is the capability for phototherapy as well as exchange transfusion if the need arises. Overall a great day, and definitely the most “academic” day so far, which is a nice contrast to the constant buzz of the clinic setting. RH
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Today was my first day of work, which was at Annotto Bay Hospital. To say I got thrown right in would be nothing short of a gross understatement, but I somehow managed to get a handle on what I was supposed to be doing by the end of the day. Today was a chronic disease follow up clinic, so I saw a mix of patients with asthma, sickle cell, epilepsy,G6PD deficiency, Trisomy 21 and a few ex-premies  – quite an impressive range, actually. I was pretty excited to see the sickle cell patients, particularly because I plan to pursue subspecialty training in pediatric hematology/oncology.  (Not so) fun fact: there are no pediatric heme/onc physicians in the entire island of Jamaica. As hard as it is to imagine there being zero, it is equally difficult for me to imagine what it would be like to be the only one. Peds heme/onc was certainly not designed to be practiced in isolation, and the extremely cooperative culture is one of the reasons I am drawn to it. So what exactly happens here?  Turns out oncology patients are treated at Bustamante Children’s Hospital in consultation with physicians from St. Jude’s for protocols and such. Hematology wise, there is a Sickle Cell Unit at the University Hospital of the West Indies that will see patients for initial consultations, for vaccines such as Pneumovax, and for management of complicated cases. However both of these institutions are in Kingston, which means often significant transportation costs for patients’ families.  So the majority of heme care takes place in clinics like the one at Annotto Bay. The patients I saw with sickle cell today brought several issues to my mind, the foremost being the lack of universal newborn screening for the disease. Given the prevalence of the sickle trait in Jamaica (1 in 10 persons), about  1 in 150 newborns will have some form of sickle cell disease.* From what I can gather, only babies born at the University Hospital of the West Indies, Victoria Jubilee and Spanish Town Hospitals get their cord blood screened for SCD. All patients that I saw today were diagnosed after some acute illness that unveiled their SCD. The first was an 11 year old boy carrying a presumptive diagnosis of SCD (in addition to his diagnosis of asthma) after CBC on an admission for respiratory distress showed Hb 5.8 and subsequent sickle screen was positive. Another was a 3 year old girl diagnosed after an episode of splenic sequestration and yet another was an 8 year old boy who presented with abdominal pain, and had an appendectomy.  His appendix was not inflamed after removal  and subsequent testing showed HbSS, so it was likely abdominal VOC all along! Overall it was a tough but exhilarating first day.  I think my favorite moment was when the dad of the 3 year old (the only dad I saw in clinic today) showed me how he palpates his daughter’s spleen, and he was spot on!  Yes, yes, yes – for so many reasons! RH *  Info from  https://www.sicklecelltrustjamaica.com/
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It has been just over 24 hours since I arrived in Jamaica. Though it seems so distant, it truly was just yesterday that I was rushing to JFK airport, struggling with my bags (how have I not realized the beauty of curbside check in until now?!).  After that, there was only the unending line to security, 3 gate changes and a 1 hour flight time delay before finally we were off.  It was only once I was suspended above NY on my way to Jamaica that I allowed myself to grasp what was happening.  And what was happening was the opportunity of a lifetime. 10 years after graduating high school and leaving Jamaica for college I was coming back as a doctor to hopefully in some small way be able to give back to the country that had given me so much. I am still in disbelief that an organization like the Issa Trust Foundation even exists and so humbled by the work they have been doing in my home country over the past several years. When I heard of the opportunity I immediately started thinking of ways to make it possible for me to be here.  And now I’m here. This month will be a curious mixture of the foreign and the familiar. The culture, as well as the actual communities I will be working in, are familiar.  In fact one of the hospitals I will work at (Port Antonio) is about a 5 minute walk from the house where I grew up and where my parents still live. So I will literally be in my own backyard.  At the same time I am acutely aware of my lack of involvement with the Jamaican medical system to date. My entire medical training has taken place in New York, and I have no doubt that the differences will be stark, and at times jarring. Despite the challenges that may arise in the work setting, the most important thing is that I am home. It feels like home, looks like home, tastes like home and there’s no place in the world like it. RH
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