transplant Flashcards

(38 cards)

1
Q

post-chronic GVHD pulm illness

A

bronchiolitis obliterans- narrowing of airways, wheeze, CXR normal, CT shows thickening, bronchiectasis. PFT- obstructive, can be stabilized with increased immunosuppression.

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2
Q

parainfluenza

A

must delay, as pneumonia is fatal in 30%; wait until PCR negative

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3
Q

re-vaccination

A

12 months post-transplant, not altered by other factors such as immunosuppression

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4
Q

AVN of hip

A

common post-Allo comp: associated with steroids and TBI

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5
Q

chronic GVHD

A

usually requires re-institution of immunosuppressants, very long slow taper, but usually possible; sicca-like symptoms, rash, higher rates in peripheral blood aloo, calcineurin inhib/prednisone can treat 50-70%,

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6
Q

acute GVHD

A

rash, n/v/diarrhea, ileus, jaundice

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7
Q

immunosuppressants

A

if no GVHD can taper at 3 months, discontinue at 6 months

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8
Q

Palifermin

A

reduces duration of GVHD

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9
Q

SCT for thalassemia

A

best results if done before hepatomegaly or fibrosis. 70-90% cure

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10
Q

alloSCT results for AML/ALL

A

50-70% 5-yr DFS.

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11
Q

CML transplant

A

restrict to progression following TKIs

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12
Q

HLA class 1 determinents

A

HLA-A, HLA-B, HLA-C. class 2: HLA-DP, DQ, DR (ch 6). low recombination frequency

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13
Q

liklihood of finding a HLA matched sibling

A

1- .75^n (n is number of siblings). if n=2, then ~45%. ABO not expressed on stem cells, so doesn’t matter

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14
Q

mismatching and outcome

A

mismatch slightly worsens leukemia relapse outcomes.

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15
Q

tolerability of HLA mismatches

A

HLAB and HLA-C are better tolerated. HLA A and DRB1 less tolerated. if peripheral CD34+ used, then HLAC mismatch less tolerated

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16
Q

marrow transplantation

A

serial aspirations- 10mL. need 1-1.5L marrow

17
Q

Peripheral marrow collection

A

faster engraftment, CD34 selection and mobilization with G-CSF or GM-CSF. can use plerixafor (CXCR4 antagonist) to mobilize cells if G-CSF insufficient. (10-20% fail to mobilize with G alone)

18
Q

umbilical transplant

A

double reduces graft failure and enhances graft v tumor

19
Q

preparative regimen before transplant for nonmalignant conditions

A

aplastic anemia- needs ATG or CTX. SCID doesn’t need because immunocompromised

20
Q

DLI dosing

A

1 x 10^7–> remission of 70% with CML

21
Q

engraftment after allo

A

marrow: 1-2 weeks after, peripheral ALC increases. day 26- ANC 1000. plts recover with neutrophils. PMBC- one week sooner, umbilical- one week later.

22
Q

graft rejection

A

more common with weaker conditioning regimens, or if a lot of transfusions were given before trx, or more mismatched, or T-cell depleted. can try to tx with GMCSF, or repeat transplant with conditioning.

23
Q

acute GVHD

A

within 3 months- rash, GI, jaundice cholestasis. classic is 100d. Tx is combination MTX/MMF and calcineurin inhibitior (cyclosporine or tacro). Tx for 3 months from Trx then taper and d/c at 6 months.

24
Q

risk factors of acute GVHD

A

mismatching, old age pt or donor, multiparous donor, more intensive conditioning regimens

25
chronic GVHD
like a collagen vascular disease. frequent in mismatched, in peripheral trx, and if prior acute GVHD. tx is steroids/calcineurin inhibitor. most pts can taper, but sometimes over months/years.
26
prophylaxis for chronic GVHD tx
bactrim + penicillin- PCP and encapsulated organism.
27
autoimmune conditions after alloSCT
5%. hemolytic anemia, ITP. tx with cyclosporine, pred, or ritux
28
Trx infection prophy
anti-fungal: flucon or voricon
29
HSV prophy after transplant, CMV prophy
IV acyclovier 250mg q8hr starteing 1 week before Trx and 1 month after Trx. can use gancyclovire st time of engraftment to reduce risk if latent CMV before. reduced risk of CMV with lymphodepleted blood products.
30
gancyclovir toxicities
granulocytopenia. responds to G-CSF. foscarnet good salvage, but causes electrolyte wasting
31
late post-trx infection
VZV (>3 months0. if chronic GVHD-->bacterial/fungal --> use propgy bactrim, penn, acyclovir.
32
post-transplant vaccination
1 year after: tetanus, diphtheria, heme inf, polio, pneumococcal. MMR/VZV/Pertussus at 24 months.
33
oral mucositis associated with preparative regimens
5-7 days post. need PCA pump. palifermin can shorten duration of mucositis
34
SOS
1-4 weeks post prepchemo. 5%. possible treat with difibrotide. prophylax with ursodeoxycholic acid.
35
idiopathic pneumonia syndrome
3-6 month post-trx related to chemo. 5% of pts. frequent following high-dose radiation. 50% mortality, no treatments.s
36
PTLD following transplant
high-dose chemoradiotherapy at increased risk, T-cell depletd at risk,.
37
DLI success by malignancy type
CR rate: CML 70%, advanced CML 12%, AML/MDS 29%, ALL 0%. half develop GVHD, 20% mortality. keep less than 10x10^7 cells.
38
CML relapse after transplant, options
DLI, interferon (35% CR)