Would you have Vascular purpura (Henoch-Schonlein purpura) when you have Sepsis?
Summary: Vascular purpura is reported only by a few people with Sepsis.
We study 2 people who have Vascular purpura (Henoch-Schonlein purpura) and Sepsis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
You are not alone: join a mobile support group for people who have Sepsis and Vascular purpura >>>
Sepsis (a severe blood infection that can lead to organ failure and death) (latest reports from 54,819 Sepsis patients)
Vascular purpura (haemorrhages in the skin and mucous membranes that result in the appearance of purplish spots or patches) has been reported by people with high blood pressure, rheumatoid arthritis, crohn's disease, osteoporosis, type 2 diabetes. (latest reports from 1,973 Vascular purpura patients)
On Jan, 29, 2015: 2 people who have sepsis and Vascular Purpura are studied.
Gender of people who have sepsis and experienced Vascular purpura * :
|Vascular purpura||100.00%||0.00% |
Age of people who have sepsis and experienced Vascular purpura * :
|Vascular purpura||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||100.00% |
Severity of the symptom * :
Top co-existing conditions for these people * :
- Acute myeloid leukaemia (2 people, 100.00%)
Most common drugs used by these people * :
- Piperacillin and tazobactam (2 people, 100.00%)
* Approximation only. Some reports may have incomplete information.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Do you have Sepsis and Vascular Purpura?
You are not alone! Join a mobile support group:
- support group for people who have Vascular Purpura and Sepsis
- support group for people who have Vascular Purpura
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Other conditions that could cause:
Can you answer these questions (Ask a question):
- Has anyone else acquired ecthyma as they were getting over henoch schonlein purpura?
My 11 year old daughter came down with Henoch Schonlein Purpura in September of 2013, following a sore throat. We thought maybe the throat is what caused the purpura, but she also had a black type of wound on her knee that could have very well been a spider bite, so we are not sure which of the two caused it. After months of battling and then horrid ulcers forming everywhere on her legs she was diagnosed with Henoch Schonlein Purpura with bullous hemorrhagic sores. I thought that it fit, but none of the pictures quite fit. So after going home and dealing with this and researching it for some time, we totally came to our own conclusion she did have HSP with Hemorrhagic Bullae, she had ecthyma, the pics and symptoms and way it healed all matched perfectly. Now most of them healed on their own leaving terrible, some crater type scarred areas and very dark in color. Pretty much deep brown/purple coloring in each healed ulcer. She also had necrotic tissue and eschars when the infection was at it's worst. So now the HSP has been long gone and it's now February of 2014 and she has one persistent ulcer that I am happy to report is finally making some progress, it was her largest one and it would shrink down to only needing a tiny band aid then get all the way back to half dollar size again. It is a vicious infection. At the children's hospital where she was admitted two different times for long periods of time, the learning docs were fascinated by her condition and not only the new docs but some really experienced veterans. When rounds took place, my daughter had an audience of 20-30 docs just in her room, so I know it's rare, for both to happen together. Anyhow, I just want to hear of anyone else who has even a nearly similar story! Is there anyone out there? As for the drug list, she is on nothing now. She was on all these interchanging while her infection was full blown. The ecthyma caused her so much pain, way more than the pain she felt from the HSP.She also never took the prednisone, it was given to have as a precaution if she had severe vomiting from the HSP. She never did. She did have blood in her stool. She just seems to have been sick so much since all this started, one cold after the other, she will complain her "pee" hurts one day and the next it will be okay. I just don't know which end is up for the kid and always worry about her kidneys because of the HSP. I am rambling now, any similarities? Someone please?
- Can henoch schonlein purpura cause depression after being healed 5 years later?
Hi, my husband was contracted with henoch schonlein purpura in 2008, he was serious and in ICU for 3 months. Since then he lives a normal life and has recovered very well. he is on HBP tablets and fluctuations of his kidney conditions occur now and then. He seems to have lost himself emotionally and is very depressed. has closed up on everyone in his life. could this be a cause of henoch schonlein purpura that is affecting him now?
More questions for: Sepsis, Vascular purpura
You may be interested at these reviews (Write a review):
- Sepsis hallucinations misdiagnosed
I was admitted to the hospital at 10 p.m., with a total bowel blockage caused by scar-tissue adhesions. I had first gone to the ER at 3 a.m. that morning, but the ER doc misdiagnosed my condition as constipation. I was in extreme pain and also too weak to tell my husband when he first came home that I needed to return to the ER. By the time I returned, I became violently nauseated, and vomited repeatedly. Then a gastro-nasal tube was forced down my nose and into my stomach. I began hallucinating at approximately 5 p.m. the following day. I did not realize I was hallucinating, and thought my experiences were real. Some were quite coherent, such as believing there was a book sitting on table at home with a photo on the front showing a sculpture in white marble of a woman's hands holding the Bible, with barbed wire wrapped around her hands. I thought the sculpture had won the Nobel prize, and the book was the biography of the sculptor, whose mother had gone to extraordinary lengths to keep him safe from the Nazis. Some may actually have occurred during dreams, and were wildly improbable, but I don't recall ever going to sleep. At one point, I thought I was at a rest stop on the NJ turnpike, and saw the Nobel-winning sculptor there, working on a wood sculpture. The sculptor turned out to be the maintenance man on the hospital floor. I pulled out the naso-gastral tube three times, but was unaware that I had done so, although I do remember believing that I was buried beneath peat moss and feeling suffocated as I clawed my way out. I also thought I was at a party being given by a law firm which had sold its building to a school for gifted children, but I (also a lawyer) had been deposited there by my nurse and her boyfriend, who were supposed to have taken me to the OR. Some scenes from a book I had been reading made their way into my delusions, which were so real to me that I actually called some of the people involved later on and asked if the events had really happened. The hallucinations began before surgery and continued afterward. When I awoke from anesthesia, I thought the hospital staff was painting the doors to my upstairs bathroom, a project I'd been involved with before the blockage struck. I asked them how they knew what colors to use. They thought I was joking, and confirmed that they had gotten the colors right. Finally a neurologist was summoned, and I told her I was on the passenger ramp at La Guardia airport (instead of in a hospital in NC), and that I'd been born in Havana, Cuba (instead of Baltimore, MD.) I believed myself to be a member of the ruling party in Cuba (pre-Castro) and during an outdoor ceremony, an earthquake had struck, causing ancient monuments to come tumbling down. Later, I was bobbing in harbor waters near a huge ocean liner, with plastic bottles and other detritus floating by. The foregoing are only a small sample of the multitude of hallucinations. Occasionally, I was only an observer of astonishing events, but usually I was a participant. I recognized my husband and friends, but told them about many of these events, believing they had happened. The neurologist diagnosed clonazepam withdrawal. My other doctors later said this was unlikely, as I took clonazepam in small amounts on an erratic schedule, and was not dependent on the drug, although my prescription called for 3 mg. daily. Physician friends said my symptoms were more likely the result of sepsis. I did contract a urinary-tract infection from the catheter, and was being given antibiotics. Additionally, the nature of my underlying condition, and the delay in diagnosis and treatment, may have contributed to the sepsis. Hallucinations occur in only a very small percentage of sepsis sufferers, and in only a small percentage of those withdrawing suddenly from clonazepam. However, I do fit the profile of those who do experience hallucinations with sepsis, being female and aged 62 at the time of this description. After the three-day period, I returned to normal, although believing that my hallucinations had been real persisted for some days afterward. I recovered quickly from the surgery, although the pain persisted for a while, and I was walking easily (dragging my IV with me) through the hospital halls. This was the ONLY symptom I had. Not all the hallucinations were unpleasant -- in fact, they were highly interesting -- but they were incredibly complex. I still remember all the details, better than I remember what actually happened yesterday. Except for the urinary-tract infection, I had no other adverse effects from hospitalization -- no fever, chills, nausea, sweating, headaches, trembling or anything of that kind. The bowel blockage and the surgery were of course not fun, but in a way the hallucinations were fascinating. My own feeling, and that of the doctors who know me and my medical issues, is that my experiences were caused by sepsis, not clonazepam withdrawal, and the antibiotics I was given are probably what saved me.
More reviews for: Sepsis, Vascular purpura
Comments from related studies:
From this study (9 months ago):
Appears spontaneously around eyes.
From this study (1 year ago):
Mother has made claims of illness for child since age 2. Has said Dr. thinks he has IBS - age 2. May have a liver disease - age 3. Had rashes that cleared up when with us, recurred when returned home. Told husband Dr. said he had Eczema and would have to take medication the rest of his life. Condition has not recurred since. Severe constipation (hard, dry)when comes to our home, clears up within a few days (up to age 4). Child told our niece his mother always says he's sick and gives him medicine (age 4). Has had bronchial conditions and severe nasal discharges at his mothers that cleared up when with us, she gives/gave benadryl frequently. He has had dry skin conditions, rashes clear up when with us. Fever seizures (since he was 2) at home that never occurred when with us. Child went without a Dr from December of 2012 to August 2013. Only illness during that time was a fall requiring stitches in his chin. She left the stitches in until the wound healed, keeping it covered with bandage. Became angry with husband and he received a letter from her attorney accusing him of not keeping a serious wound covered, among other false statements. After getting a doctor in August, just at the time when the child is scheduled to begin school, child becomes ill with a "rash", slurred speech, and fever seizure, took him to a local hospital who diagnosed henoch-schonlein purpura (he did not have high temp at hospital). She requested child be referred to a childrens hospital. They sent her home. Next day she went to her newly acquired doctor who gave her the referral to Children's Hospital. His mother has stated SHE has heart problems, had to have biopsies on her liver for cancer, claimed to have a "pace-maker" put in. Made/makes frequent trips to various hospitals, coming home with catheters hanging down her legs, wearing dresses so the bag is visible. Same with IV -stints? Left in her arm secured by bandages. She has told me she was almost a nurse (went to classes a few months). Was very up on medical terms and conditions, but I notice that recently she is behaving like she doesn't know anything (I've mentioned Munchhausen to my husband many times and he has told that to her recently) She told my husband after the pace maker the her Doctors say she has three years to live. That was two years ago (and just stated recently when question about her health and being able to care for the child with a bad heart, she claims it's a bladder one). Claimed she had Fibro...I am afraid she is Munchhausen and may be making the baby sick. No one listens to me. There is many more symptoms from both the mother and child. Too many to list here. Please tell me what you think is going on with the child. I tried calling hotline and all the woman said was, "Are you a doctor?" The mother called yesterday and said the child is sick again. I had talked to the mother earlier and mentioned my husband was with his other son's mother and may be staying overnight with her. She is very jealous of the other son and has made statements that my husband loves him more. A couple hours later she is calling saying the boy is sick again.
From this study (2 years ago):
Intravenous treatment with Vancomycin and zofran for crippling nausea. Five weeks treatment uneventful. Bactrim added for three days. Creatinine increasing. Severe nausea unresolved by the zofran, 4 mg. every eight hours. Changed to 8 mg. loading dose and two subsequent 8mg doses, now nausea is continuous. Is this related to renal changes, zofran resistance or something else.
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